| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Wallace DC | |
| P2860 | cites work | The genome sequence of Rickettsia prowazekii and the origin of mitochondria | Q22122428 |
| Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation | Q29614475 | ||
| P433 | issue | 5407 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | mitochondrion | Q39572 |
| P304 | page(s) | 1482-8 | |
| P577 | publication date | 1999-03-05 | |
| P1433 | published in | Science | Q192864 |
| P1476 | title | Mitochondrial diseases in man and mouse | |
| P478 | volume | 283 |
| Q30452893 | "Ping-pong" interactions between mitochondrial tRNA import receptors within a multiprotein complex |
| Q59800426 | 'Governor vessel-unblocking and mind-regulating' acupuncture therapy ameliorates cognitive dysfunction in a rat model of middle cerebral artery occlusion |
| Q45790850 | (-)-Epicatechin enhances fatigue resistance and oxidative capacity in mouse muscle |
| Q41586241 | 1,8-Naphthalimide Derivative Dyes with Large Stokes Shifts for Targeting Live-Cell Mitochondria. |
| Q43725921 | 3,4-Dihydroxyphenylacetaldehyde and hydrogen peroxide generate a hydroxyl radical: possible role in Parkinson's disease pathogenesis |
| Q56901042 | 5 S rRNA and tRNA import into human mitochondria. Comparison of in vitro requirements |
| Q58697245 | A Cultural Algorithm for the Representation of Mitochondrial Population |
| Q57974100 | A Preliminary Fastview of Mitochondrial Protein Profile from Healthy and Type 2 Diabetic Subjects |
| Q35770976 | A TAT-frataxin fusion protein increases lifespan and cardiac function in a conditional Friedreich's ataxia mouse model |
| Q28204133 | A big development for a small RNA |
| Q36499104 | A brief overview of mechanisms of mitochondrial toxicity from NRTIs |
| Q35671810 | A causal link between respiration and senescence in Podospora anserina |
| Q43600883 | A central functional role for the 49-kDa subunit within the catalytic core of mitochondrial complex I. |
| Q34551734 | A cluster of metabolic defects caused by mutation in a mitochondrial tRNA. |
| Q34362301 | A comparative proteomic strategy for subcellular proteome research: ICAT approach coupled with bioinformatics prediction to ascertain rat liver mitochondrial proteins and indication of mitochondrial localization for catalase. |
| Q36372760 | A compositional segmentation of the human mitochondrial genome is related to heterogeneities in the guanine mutation rate. |
| Q73035318 | A debut for mito-mouse |
| Q53537772 | A follow-up study in a Taiwanese family with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome. |
| Q24540271 | A human mitochondrial GTP binding protein related to tRNA modification may modulate phenotypic expression of the deafness-associated mitochondrial 12S rRNA mutation |
| Q24537551 | A human mitochondrial transcription factor is related to RNA adenine methyltransferases and binds S-adenosylmethionine |
| Q38081957 | A matter of life, death and diseases: mitochondria from a proteomic perspective |
| Q44550168 | A metabolic model for life span determination in Caenorhabditis elegans |
| Q33749557 | A method to identify and validate mitochondrial modulators using mammalian cells and the worm C. elegans |
| Q39126039 | A mitochondria-specific visible-light sensitized europium β-diketonate complex with red emission |
| Q55143303 | A mitochondria-targeted nanoradiosensitizer activating reactive oxygen species burst for enhanced radiation therapy. |
| Q30903931 | A mitochondria-targeted triphenylphosphonium-conjugated nitroxide functions as a radioprotector/mitigator |
| Q37117512 | A mitochondrial DNA mutation linked to colon cancer results in proton leaks in cytochrome c oxidase |
| Q24308718 | A mitochondrial enzyme degrades carotenoids and protects against oxidative stress |
| Q29547303 | A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine |
| Q21090760 | A multi-platform draft de novo genome assembly and comparative analysis for the Scarlet Macaw (Ara macao) |
| Q34616018 | A mutation in the ATP2 gene abrogates the age asymmetry between mother and daughter cells of the yeast Saccharomyces cerevisiae. |
| Q28594190 | A mutation in the inner mitochondrial membrane peptidase 2-like gene (Immp2l) affects mitochondrial function and impairs fertility in mice |
| Q47740260 | A novel defense system of mitochondria in mice and human subjects for preventing expression of mitochondrial dysfunction by pathogenic mutant mtDNAs |
| Q34144436 | A novel homoplasmic mutation in mtDNA with a single evolutionary origin as a risk factor for cardiomyopathy |
| Q42500837 | A novel mutation in the mitochondrial tRNA(Ser(AGY)) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency |
| Q36652792 | A phenotypic perspective on Mammalian oxygen sensor candidates |
| Q51555505 | A phosphinate-based near-infrared fluorescence probe for imaging the superoxide radical anion in vitro and in vivo. |
| Q37392524 | A potential impact of DNA repair on ageing and lifespan in the ageing model organism Podospora anserina: decrease in mitochondrial DNA repair activity during ageing |
| Q48498598 | A proteomic analysis of liver mitochondria during acute endotoxemia. |
| Q42605611 | A putative mitochondrial fission gene from the ectomycorrhizal ascomycete Tuber borchii Vittad.: cloning, characterisation and phylogeny. |
| Q44122038 | A replicating module as the unit of mitochondrial structure and functioning |
| Q35535022 | A review comparing deoxyribonucleoside triphosphate (dNTP) concentrations in the mitochondrial and cytoplasmic compartments of normal and transformed cells |
| Q39607639 | A role for MHR1, a gene required for mitochondrial genetic recombination, in the repair of damage spontaneously introduced in yeast mtDNA. |
| Q35147910 | A specific nuclear DNA background is required for high frequency lymphoma development in transmitochondrial mice with G13997A mtDNA |
| Q36391379 | A structural model for the large subunit of the mammalian mitochondrial ribosome. |
| Q36854153 | A switch in metabolism precedes increased mitochondrial biogenesis in respiratory chain-deficient mouse hearts |
| Q29614550 | A systematic RNAi screen identifies a critical role for mitochondria in C. elegans longevity |
| Q48608470 | A systematic analysis of the suitability of preimplantation genetic diagnosis for mitochondrial diseases in a heteroplasmic mitochondrial mouse model. |
| Q38962365 | A systematic assessment of mitochondrial function identified novel signatures for drug-induced mitochondrial disruption in cells |
| Q54447301 | A systems approach for decoding mitochondrial retrograde signaling pathways. |
| Q34768108 | A targeted mass spectrometry-based approach for the identification and characterization of proteins containing α-aminoadipic and γ-glutamic semialdehyde residues |
| Q46964172 | A transgenic model to study the pathogenesis of somatic mtDNA mutation accumulation in beta-cells |
| Q51039707 | A two-channel responsive fluorescent probe with AIE characteristics and its application for selective imaging of superoxide anions in living cells. |
| Q37358186 | A zebrafish model for pyruvate dehydrogenase deficiency: rescue of neurological dysfunction and embryonic lethality using a ketogenic diet |
| Q41942673 | ATP controls neuronal apoptosis triggered by microtubule breakdown or potassium deprivation |
| Q36525469 | ATP synthase: a molecular therapeutic drug target for antimicrobial and antitumor peptides |
| Q43707852 | ATP synthesis is coupled to rat liver mitochondrial RNA synthesis |
| Q81305741 | ATRA promotes alpha tocopherol succinate-induced apoptosis in freshly isolated leukemic cells from chronic myeloid leukemic patients |
| Q34008821 | Ablation of TSC2 enhances insulin secretion by increasing the number of mitochondria through activation of mTORC1 |
| Q35737647 | Abnormal mitochondrial dynamics and synaptic degeneration as early events in Alzheimer's disease: implications to mitochondria-targeted antioxidant therapeutics |
| Q50660726 | Abnormal mitochondrial structure in human unfertilized oocytes and arrested embryos. |
| Q30479303 | Absolute quantitation of a heteroplasmic mitochondrial DNA deletion using a multiplex three-primer real-time PCR assay |
| Q33280200 | Accumulation of mitochondrial DNA deletion mutations in aged muscle fibers: evidence for a causal role in muscle fiber loss |
| Q78468478 | Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism? |
| Q36103535 | Accumulation of oxidatively generated DNA damage in the brain: a mechanism of neurotoxicity |
| Q44116932 | Acetyl-L-carnitine protects against amyloid-beta neurotoxicity: roles of oxidative buffering and ATP levels |
| Q36703656 | Acknowledging selection at sub-organismal levels resolves controversy on pro-cooperation mechanisms |
| Q36452743 | Acrolein-mediated injury in nervous system trauma and diseases |
| Q43224778 | Activation of oxidative stress response by hydroxyl substituted chalcones and cyclic chalcone analogues in mitochondria. |
| Q37771263 | Adenine nucleotide translocator as a regulator of mitochondrial function: implication in the pathogenesis of metabolic syndrome |
| Q39371961 | Adeno-associated virus-mediated gene transfer of the heart/muscle adenine nucleotide translocator (ANT) in mouse |
| Q36319041 | Adenylate kinase phosphotransfer communicates cellular energetic signals to ATP-sensitive potassium channels |
| Q34572695 | Administration of an antioxidant prevents lymphoma development in transmitochondrial mice overproducing reactive oxygen species |
| Q28253831 | Adrenodoxin (Adx) and CYP11A1 (P450scc) induce apoptosis by the generation of reactive oxygen species in mitochondria |
| Q33374303 | Advanced In Vivo Heteronuclear MRS Approaches for Studying Brain Bioenergetics Driven by Mitochondria |
| Q35059090 | Advances in the analysis of single mitochondria |
| Q58762661 | Age-Dependent Loss of Mitochondrial Function in Epithelial Tissue Can Be Reversed by Coenzyme Q |
| Q73327397 | Age-associated changes in mitochondrial parameters on peripheral human lymphocytes |
| Q35621362 | Ageing, repetitive genomes and DNA damage |
| Q46127059 | Ageing: beneficial miscommunication |
| Q33722192 | Aging: Dial M for Mitochondria |
| Q48772008 | Aim24 stabilizes respiratory chain supercomplexes and is required for efficient respiration. |
| Q34676867 | Alcohol and mitochondria: a dysfunctional relationship |
| Q39936180 | Allosteric regulation of tRNA import: interactions between tRNA domains at the inner membrane of Leishmania mitochondria |
| Q34560275 | Alteration of liver cell function and proliferation: differentiation between adaptation and toxicity |
| Q63385550 | Alteration of mitochondrial calcium homeostasis by ammonia-induced activation of NMDA receptors in rat brain in vivo |
| Q44203656 | Alterations in mitochondrial function in a mouse model of hypertrophic cardiomyopathy |
| Q44024811 | Alterations in renal mitochondrial respiration in response to the reactive oxoaldehyde methylglyoxal |
| Q35947731 | Altered Mitochondrial Function, Mitochondrial DNA and Reduced Metabolic Flexibility in Patients With Diabetic Nephropathy |
| Q27000255 | Alzheimer's pathogenesis and its link to the mitochondrion |
| Q34365724 | Aminoacylation properties of pathology-related human mitochondrial tRNA(Lys) variants |
| Q37039531 | Amyloid-beta overproduction causes abnormal mitochondrial dynamics via differential modulation of mitochondrial fission/fusion proteins |
| Q35908707 | An Essential Role of the Mitochondrial Electron Transport Chain in Cell Proliferation Is to Enable Aspartate Synthesis |
| Q54941702 | An alternative approach to medical genetics based on modern evolutionary biology. Part 1: mutation and symbiogenesis. |
| Q48971303 | An examination of the effects of the antioxidant Pycnogenol on cognitive performance, serum lipid profile, endocrinological and oxidative stress biomarkers in an elderly population. |
| Q36072568 | An extracellular Zn-only superoxide dismutase from Puccinia striiformis confers enhanced resistance to host-derived oxidative stress |
| Q33341058 | Analysis of mitochondrial function in situ in permeabilized muscle fibers, tissues and cells |
| Q46541827 | Analysis of reactive oxygen species and antioxidant defenses in complex I deficient patients revealed a specific increase in superoxide dismutase activity. |
| Q45145366 | Analysis of the biological response of mouse liver (Mus musculus) exposed to As2O3 based on integrated -omics approaches |
| Q37785713 | Angiotensin II blockade: a strategy to slow ageing by protecting mitochondria? |
| Q35645375 | Animal models of human mitochondrial DNA mutations |
| Q47666076 | Anti- and pro-oxidative properties of PADMA 28, a Tibetan herbal formulation |
| Q36108255 | Anti-apoptotic MCL-1 localizes to the mitochondrial matrix and couples mitochondrial fusion to respiration |
| Q36421608 | Antibiotic use and abuse: a threat to mitochondria and chloroplasts with impact on research, health, and environment |
| Q36239807 | Antibody-based approaches to diagnosis and characterization of oxidative phosphorylation diseases |
| Q40370929 | Anticancer activity of sodium caffeate and its mechanism |
| Q48243994 | Antioxidant-mediated reversal of oxidative damage in mouse modeling of complex I inhibition. |
| Q34214558 | Apoptosis and its clinical impact |
| Q58782665 | Application of the obligate aerobic yeast Yarrowia lipolytica as a eucaryotic model to analyse Leigh syndrome mutations in the complex I core subunits PSST and TYKY |
| Q46025850 | Are rod outer segment ATP-ase and ATP-synthase activity expression of the same protein? |
| Q43623412 | Assaying mitochondrial respiratory complex activity in mitochondria isolated from human cells and tissues. |
| Q33445097 | Assessing the genotoxicity of chronic environmental irradiation by using mitochondrial DNA heteroplasmy in the bank vole (Clethrionomys glareolus) at Chornobyl, Ukraine |
| Q36168711 | Assessment and treatment in autism spectrum disorders: a focus on genetics and psychiatry |
| Q34459104 | Association of leukocyte mitochondrial DNA copy number with colorectal cancer risk: Results from the Shanghai Women's Health Study |
| Q40365390 | Association of mitochondrial DNA transversion mutations with familial medullary thyroid carcinoma/multiple endocrine neoplasia type 2 syndrome |
| Q34170799 | Association of mitochondrial DNA variations with lung cancer risk in a Han Chinese population from southwestern China |
| Q46493926 | Association of mitochondrial function and sperm progressivity in slow- and fast-growing roosters |
| Q33449191 | Association of superoxide anions with retinal pigment epithelial cell apoptosis induced by mononuclear phagocytes |
| Q55331854 | Associations of blood mitochondrial DNA copy number with social-demographics and cancer risk: results from the Mano-A-Mano Mexican American Cohort. |
| Q34961939 | Associations of mitochondrial haplogroups b4 and e with biliary atresia and differential susceptibility to hydrophobic bile Acid. |
| Q35891859 | Astrocyte mitochondria in in vitro models of ischemia |
| Q35097295 | Asymmetric segregation of damaged cellular components in spatially structured multicellular organisms |
| Q40407433 | Attenuation of UV-induced apoptosis by coenzyme Q10 in human cells harboring large-scale deletion of mitochondrial DNA. |
| Q34101070 | BMCP1: a mitochondrial uncoupling protein in neurons which regulates mitochondrial function and oxidant production |
| Q42057928 | Baculovirus expression reconstitutes Drosophila mitochondrial DNA polymerase |
| Q32161682 | Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation). |
| Q37202353 | Bcl-x L increases mitochondrial fission, fusion, and biomass in neurons |
| Q36677229 | Beyond retrograde and anterograde signalling: mitochondrial-nuclear interactions as a means for evolutionary adaptation and contemporary disease susceptibility |
| Q35083362 | Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors |
| Q42702308 | Biochemical and Molecular Alterations Following Arsenic-Induced Oxidative Stress and Mitochondrial Dysfunction in Rat Brain |
| Q34987772 | Bioenergetics, mitochondria, and cardiac myocyte differentiation |
| Q91870162 | Biogenic Aldehyde-Mediated Mechanisms of Toxicity in Neurodegenerative Disease |
| Q45847143 | Biological function through network topology: a survey of the human diseasome |
| Q64885849 | Blockage of glutamine-dependent anaplerosis affects mTORC1/2 activity and ultimately leads to cellular senescence-like response. |
| Q47070209 | Bonsaï, a ribosomal protein S15 homolog, involved in gut mitochondrial activity and systemic growth |
| Q39162782 | Boosting antioxidants by lipophilization: a strategy to increase cell uptake and target mitochondria |
| Q34464761 | Brain metabolism and brain disease: is metabolic deficiency the proximate cause of Alzheimer dementia? |
| Q49072984 | Brain testosterone deficiency leads to down-regulation of mitochondrial gene expression in rat hippocampus accompanied by a decline in peroxisome proliferator-activated receptor-γ coactivator 1α expression. |
| Q48328371 | Brain uptake of Tc99m-HMPAO correlates with clinical response to the novel redox modulating agent EPI-743 in patients with mitochondrial disease |
| Q33264159 | CE-LIF analysis of mitochondria using uncoated and dynamically coated capillaries |
| Q34085469 | CREB activation induced by mitochondrial dysfunction is a new signaling pathway that impairs cell proliferation |
| Q40443282 | Ca2+-induced permeability transition in human lymphoblastoid cell mitochondria from normal and Huntington's disease individuals. |
| Q33736292 | Caenorhabditis elegans: A useful model for studying metabolic disorders in which oxidative stress is a contributing factor. |
| Q30234815 | Can Mitochondria DNA Provide a Novel Biomarker for Evaluating the Risk and Prognosis of Colorectal Cancer? |
| Q36228895 | Cancer cell growth and survival as a system-level property sustained by enhanced glycolysis and mitochondrial metabolic remodeling |
| Q33782145 | Capillary isoelectric focusing of individual mitochondria |
| Q28372167 | Cardiac dysfunction occurs in the HIV-1 transgenic mouse treated with zidovudine |
| Q33987941 | Cardiac mitochondria and reactive oxygen species generation |
| Q37823035 | Cardiotoxicity associated with targeting kinase pathways in cancer |
| Q33678876 | Casiopeína IIgly-induced oxidative stress and mitochondrial dysfunction in human lung cancer A549 and H157 cells |
| Q35958844 | Caspase cleavage of cytochrome c1 disrupts mitochondrial function and enhances cytochrome c release |
| Q34264459 | Cationic bolasomes with delocalized charge centers as mitochondria-specific DNA delivery systems |
| Q42377883 | Cdkal1, a type 2 diabetes susceptibility gene, regulates mitochondrial function in adipose tissue. |
| Q58366560 | Cell Biology of Diabetic Kidney Disease |
| Q35054667 | Cell Penetrating Peptoids (CPPos): Synthesis of a Small Combinatorial Library by Using IRORI MiniKans. |
| Q28276493 | Cell and tissue autofluorescence research and diagnostic applications |
| Q53660053 | Cell cycle dependent morphology changes and associated mitochondrial DNA redistribution in mitochondria of human cell lines. |
| Q92922603 | Cellular Aging Characteristics and Their Association with Age-Related Disorders |
| Q38061270 | Cellular and molecular mechanisms of mitochondrial function |
| Q52716227 | Cellular and molecular mechanisms of various types of oocyte aging. |
| Q74000730 | Cellular phenotypes of age-associated skeletal muscle mitochondrial abnormalities in rhesus monkeys |
| Q42810724 | Cellular stress responses, mitostress and carnitine insufficiencies as critical determinants in aging and neurodegenerative disorders: role of hormesis and vitagenes |
| Q89683589 | Central and Peripheral Metabolic Defects Contribute to the Pathogenesis of Alzheimer's Disease: Targeting Mitochondria for Diagnosis and Prevention |
| Q36078791 | Central role of mitofusin 2 in autophagosome-lysosome fusion in cardiomyocytes |
| Q47786265 | Centrifugation-Free Magnetic Isolation of Functional Mitochondria Using Paramagnetic Iron Oxide Nanoparticles |
| Q52028452 | Cerebral oligaemia episode triggers free radical formation and late cognitive deficiencies. |
| Q74210559 | Cerebrovascular disorders and genetic polymorphisms: mitochondrial DNA5178C is predominant in cerebrovascular disorders |
| Q37508421 | Changes in mitochondrial homeostasis and redox status in astronauts following long stays in space |
| Q51681184 | Changes in the human mitochondrial genome after treatment of malignant disease. |
| Q52100796 | Chaperonin 60 and mitochondrial disease in Dictyostelium. |
| Q51733057 | Chapter 18 Analysis of respiratory chain complex assembly with radiolabeled nuclear- and mitochondrial-encoded subunits. |
| Q38465729 | Characterization and expression analysis of prohibitin in the testis of Chinese mitten crab Eriocheir sinensis. |
| Q81380046 | Characterization and prevalence of a circular mitochondrial plasmid in senescence-prone isolates of Neurospora intermedia |
| Q59194228 | Characterization and prognostic significance of mitochondrial DNA variations in acute myeloid leukemia |
| Q34146570 | Characterization of a human import component of the mitochondrial outer membrane, TOMM70A. |
| Q47929695 | Characterization of the human SDHD gene encoding the small subunit of cytochrome b (cybS) in mitochondrial succinate-ubiquinone oxidoreductase |
| Q27990522 | Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients |
| Q42699753 | Chronic Arsenic Exposure-Induced Oxidative Stress is Mediated by Decreased Mitochondrial Biogenesis in Rat Liver. |
| Q46699416 | Chronic Effects of Realistic Concentrations of Non-essential and Essential Metals (Lead and Zinc) on Oxidative Stress Biomarkers of the Mosquitofish, Gambusia holbrooki. |
| Q37358098 | Circle-to-circle amplification for precise and sensitive DNA analysis |
| Q38028131 | Citrulline and arginine utility in treating nitric oxide deficiency in mitochondrial disorders |
| Q48328105 | Clk1-regulated aerobic glycolysis is involved in glioma chemoresistance |
| Q47135441 | Co-expression Network Approach Reveals Functional Similarities among Diseases Affecting Human Skeletal Muscle |
| Q73632873 | Coculture of human oviductal cells maintains mitochondrial function and decreases caspase activity of cleavage-stage mouse embryos |
| Q33892701 | Coexpression within Integrated Mitochondrial Pathways Reveals Different Networks in Normal and Chemically Treated Transcriptomes. |
| Q43797774 | Combined antiretroviral therapy causes cardiomyopathy and elevates plasma lactate in transgenic AIDS mice |
| Q40488655 | Common and cell type-specific responses of human cells to mitochondrial dysfunction |
| Q28289016 | Comparative mitochondrial proteomic analysis of hepatocellular carcinoma from patients |
| Q33621981 | Comparison of anti-oxidant activities of seventy herbs that have been used in Korean traditional medicine |
| Q36638620 | Complementation between polymerase- and exonuclease-deficient mitochondrial DNA polymerase mutants in genomically engineered flies |
| Q24292254 | Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c |
| Q58853759 | Complex II inactivation is lethal in the nematode Caenorhabditis elegans |
| Q36504889 | Complex disease-associated pharmacogenetics: drug efficacy, drug safety, and confirmation of a pathogenetic hypothesis (Alzheimer's disease). |
| Q64069439 | Concentration of mitochondrial DNA mutations by cytoplasmic transfer from platelets to cultured mouse cells |
| Q34087251 | Conceptualisation and measurement of frailty in elderly people |
| Q34203306 | Condensation of plasmid DNA enhances mitochondrial association in skeletal muscle following hydrodynamic limb vein injection |
| Q30308887 | Conflicting levels of selection in the accumulation of mitochondrial defects in Saccharomyces cerevisiae |
| Q42385487 | Confounding by linkage disequilibrium |
| Q92423968 | Coniferaldehyde attenuates Alzheimer's pathology via activation of Nrf2 and its targets |
| Q36207366 | Consequences of zygote injection and germline transfer of mutant human mitochondrial DNA in mice. |
| Q38906439 | Constitutional and functional genetics of human alcohol-related hepatocellular carcinoma. |
| Q24670800 | Control of mitochondrial membrane permeabilization by adenine nucleotide translocator interacting with HIV-1 viral protein rR and Bcl-2 |
| Q34803503 | Control region mtDNA variants: longevity, climatic adaptation, and a forensic conundrum |
| Q37813021 | Controlling subcellular delivery to optimize therapeutic effect |
| Q43116476 | Convergence of multiple signaling pathways is required to coordinately up-regulate mtDNA and mitochondrial biogenesis during T cell activation |
| Q34075210 | Coordinated patterns of gene expression for substrate and energy metabolism in skeletal muscle of diabetic mice |
| Q35882344 | Correcting human mitochondrial mutations with targeted RNA import |
| Q40477028 | Correction of translational defects in patient-derived mutant mitochondria by complex-mediated import of a cytoplasmic tRNA. |
| Q35625442 | Coupled reductions in brain oxidative phosphorylation and synaptic function can be quantified and staged in the course of Alzheimer disease |
| Q41123555 | Covalent, Non-Covalent, Encapsulated Nanodrug Regulate the Fate of Intra- and Extracellular Trafficking: Impact on Cancer and Normal Cells. |
| Q37307399 | Cr(VI) induces premature senescence through ROS-mediated p53 pathway in L-02 hepatocytes |
| Q30697610 | Creatine kinase B-driven energy transfer in the brain is important for habituation and spatial learning behaviour, mossy fibre field size and determination of seizure susceptibility |
| Q26859194 | Critical pathogenic events underlying progression of neurodegeneration in glaucoma |
| Q43948129 | Cultivation in glucose-deprived medium stimulates mitochondrial biogenesis and oxidative metabolism in HepG2 hepatoma cells |
| Q35911424 | Cumulative mtDNA damage and mutations contribute to the progressive loss of RGCs in a rat model of glaucoma |
| Q42732590 | Curcumin attenuates aluminum-induced oxidative stress and mitochondrial dysfunction in rat brain |
| Q36707796 | Cybrid models of mtDNA disease and transmission, from cells to mice |
| Q43559588 | Cyclopentenone prostaglandins as potential inducers of intracellular oxidative stress |
| Q46742920 | Cyclophilin D regulates the dynamic assembly of mitochondrial ATP synthase into synthasomes. |
| Q33610590 | Cytokine and nitric oxide levels in patients with sepsis--temporal evolvement and relation to platelet mitochondrial respiratory function |
| Q52168246 | Cytoplasm mediates both development and oxidation-induced apoptotic cell death in mouse zygotes. |
| Q34235748 | Cytoplasmic inheritance and its implications for animal biotechnology |
| Q33361448 | Cytoplasmic signaling in the control of mitochondrial uproar? |
| Q77368564 | Cytosolic thioredoxin peroxidase I is essential for the antioxidant defense of yeast with dysfunctional mitochondria |
| Q36976707 | D-beta-hydroxybutyrate protects neurons in models of Alzheimer's and Parkinson's disease |
| Q44175688 | DBGSA: a novel method of distance-based gene set analysis |
| Q38589212 | DNA Damage, DNA Repair, Aging, and Neurodegeneration |
| Q34224979 | DNA double-strand breaks activate ATM independent of mitochondrial dysfunction in A549 cells |
| Q33838032 | DNA polymerases in the mitochondria: A critical review of the evidence. |
| Q33935962 | DNA precursor asymmetries in mammalian tissue mitochondria and possible contribution to mutagenesis through reduced replication fidelity. |
| Q27933718 | DNA recombination-initiation plays a role in the extremely biased inheritance of yeast [rho-] mitochondrial DNA that contains the replication origin ori5. |
| Q49981106 | DNA repair deficiency sensitizes lung cancer cells to NAD+ biosynthesis blockade. |
| Q34396940 | DNA sequences proximal to human mitochondrial DNA deletion breakpoints prevalent in human disease form G-quadruplexes, a class of DNA structures inefficiently unwound by the mitochondrial replicative Twinkle helicase |
| Q92191656 | Data on heteroplasmic mutations in mitochondrial genomes of loggerhead and hawksbill sea turtles: First approach |
| Q80064819 | De Toni-Debré-Fanconi syndrome due to a palindrome-flanked deletion in mitochondrial DNA |
| Q37356290 | De novo mutation in POLG leads to haplotype insufficiency and Alpers syndrome. |
| Q49794628 | Deciphering the Spectrum of Mitochondrial DNA Mutations in Hepatocellular Carcinoma Using High-Throughput Sequencing. |
| Q36503796 | Decreased aminoacylation in pathology-related mutants of mitochondrial tRNATyr is associated with structural perturbations in tRNA architecture. |
| Q41811395 | Decreased exhaled nitric oxide levels in patients with mitochondrial disorders |
| Q44839444 | Decreased susceptibility to antifungals in respiratory-deficient Kluyveromyces lactis mutants |
| Q44598592 | Defective hepatic mitochondrial respiratory chain in patients with nonalcoholic steatohepatitis |
| Q43685968 | Defective mitochondrial protein translocation precludes normal Caenorhabditis elegans development |
| Q34241192 | Defects in mitochondrial DNA replication and human disease |
| Q34098312 | Defects of mitochondrial DNA replication. |
| Q42523283 | Deficiency or inhibition of oxygen sensor Phd1 induces hypoxia tolerance by reprogramming basal metabolism |
| Q36392678 | Deficient mitochondrial biogenesis in critical illness: cause, effect, or epiphenomenon? |
| Q33773866 | Degree of glutathione deficiency and redox imbalance depend on subtype of mitochondrial disease and clinical status |
| Q36981764 | Deletion of MCL-1 causes lethal cardiac failure and mitochondrial dysfunction |
| Q33406263 | Deletion of the mitochondrial flavoprotein apoptosis inducing factor (AIF) induces beta-cell apoptosis and impairs beta-cell mass |
| Q36416150 | Deletion-mutant mtDNA increases in somatic tissues but decreases in female germ cells with age. |
| Q34983135 | Delivery of bioactive molecules to mitochondria in vivo. |
| Q38015903 | Delivery to mitochondria: a narrower approach for broader therapeutics |
| Q37029870 | Denervation induces cytosolic phospholipase A2-mediated fatty acid hydroperoxide generation by muscle mitochondria |
| Q53688741 | Deoxyribonucleotide Triphosphate Metabolism in Cancer and Metabolic Disease. |
| Q36293799 | Desmin cytoskeleton linked to muscle mitochondrial distribution and respiratory function. |
| Q39681978 | Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR. |
| Q35754839 | Detection of Ultra-Rare Mitochondrial Mutations in Breast Stem Cells by Duplex Sequencing. |
| Q83292765 | Detection of mitochondrial fission with orientation-dependent optical Fourier filters |
| Q35086454 | Detection of mitochondrial single nucleotide polymorphisms using a primer elongation reaction on oligonucleotide microarrays |
| Q46902442 | Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations |
| Q35192906 | Development of gene therapy for treatment of age-related macular degeneration |
| Q34827699 | Development of insulin resistance and obesity in mice overexpressing cellular glutathione peroxidase |
| Q34452604 | Development of lipophilic cations as therapies for disorders due to mitochondrial dysfunction |
| Q39304113 | Developmental plasticity shapes synaptic phenotypes of autism-associated neuroligin-3 mutations in the calyx of Held |
| Q51892557 | Developmental regulation of mitochondrial biogenesis and function in the mouse mammary gland during a prolonged lactation cycle. |
| Q40273572 | Diabetes-associated mitochondrial DNA mutation A3243G impairs cellular metabolic pathways necessary for beta cell function. |
| Q30956250 | Diagnosis and management of MELAS. |
| Q44768021 | Diagnostic criteria for pediatric multiple sclerosis |
| Q47804981 | Diagnostic value of mitochondrial DNA mutation analysis in juvenile unilateral ptosis |
| Q43971159 | Dietary restriction initiated in late adulthood can reverse age-related alterations of protein and protein metabolism |
| Q48670791 | Differential distribution of human mitochondrial DNA in somatic tissues and hairs. |
| Q42485472 | Differential effects of specific amino acid restriction on glucose metabolism, reduction/oxidation status and mitochondrial damage in DU145 and PC3 prostate cancer cells |
| Q33265042 | Differential expression of mitochondrial and extramitochondrial proteins in lymphocytes of male broilers with low and high feed efficiency |
| Q44838381 | Differential expression of oxidative phosphorylation genes in patients with Alzheimer's disease: implications for early mitochondrial dysfunction and oxidative damage. |
| Q36494335 | Differential mitochondrial protein expression profiling in neurodegenerative diseases |
| Q34025440 | Differential roles of Epac in regulating cell death in neuronal and myocardial cells |
| Q30831407 | Differentiation and the cytomorphology of salivary gland tumors with specific reference to oncocytic metaplasia |
| Q38884808 | Differentiation of Human Neural Stem Cells into Motor Neurons Stimulates Mitochondrial Biogenesis and Decreases Glycolytic Flux |
| Q60636832 | Dilated cardiomyopathy and mitochondrial dysfunction in Sirt1-deficient mice: A role for Sirt1-Mef2 in adult heart |
| Q43099702 | Disease-causing mitochondrial heteroplasmy segregated within induced pluripotent stem cell clones derived from a patient with MELAS. |
| Q33757397 | Disease-related versus polymorphic mutations in human mitochondrial tRNAs. Where is the difference? |
| Q33948563 | Disorders related to mitochondrial membranes: pathology of the respiratory chain and neurodegeneration |
| Q35661396 | Disruption of Mitochondrion-To-Nucleus Interaction in Deceased Cloned Piglets |
| Q91130209 | Disruption of the mouse Shmt2 gene confers embryonic anaemia via foetal liver-specific metabolomic disorders |
| Q28139177 | Disruption of the uncoupling protein-2 gene in mice reveals a role in immunity and reactive oxygen species production |
| Q33763691 | Distinct functions of junD in cardiac hypertrophy and heart failure |
| Q42913202 | Distinct retinal deficits in a zebrafish pyruvate dehydrogenase-deficient mutant. |
| Q46802337 | Distribution of androstenedione and its effects on total free fatty acids in pregnant rats |
| Q27940132 | Division of mitochondria requires a novel DMN1-interacting protein, Net2p |
| Q36255314 | Does mitochondrial dysfunction during antiretroviral therapy in human immunodeficiency virus infection suggest antioxidant supplementation as a beneficial option? |
| Q51702976 | Down-regulation of mitochondrial cytochrome c oxidase in senescent porcine pulmonary artery endothelial cells. |
| Q34413967 | Downregulation of NDUFA1 and other oxidative phosphorylation-related genes is a consistent feature of basal cell carcinoma. |
| Q35590585 | Drosophila melanogaster and the future of 'evo-devo' biology in space. Challenges and problems in the path of an eventual colonization project outside the earth |
| Q46750400 | Drosophila melanogaster homolog of Down syndrome critical region 1 is critical for mitochondrial function |
| Q33853014 | Drug delivery to mitochondria: the key to mitochondrial medicine |
| Q24535778 | Dual localization of human DNA topoisomerase IIIalpha to mitochondria and nucleus |
| Q24291421 | Dual trafficking of Slit3 to mitochondria and cell surface demonstrates novel localization for Slit protein |
| Q40605991 | Dynamics of protein nitration in cells and mitochondria |
| Q52692095 | Dynamin-Related Protein 1 at the Crossroads of Cancer. |
| Q36206064 | Dysregulation of Mitochondrial Functions and Osteogenic Differentiation in Cisd2-Deficient Murine Induced Pluripotent Stem Cells |
| Q43115530 | EMBO WORKSHOP REPORT: Molecular and cellular gerontology Serpiano, Switzerland, September 18-22, 1999. |
| Q47074213 | Early developmental pathology due to cytochrome c oxidase deficiency is revealed by a new zebrafish model |
| Q52712869 | Early life benefits and later life costs of a two amino acid deletion in Drosophila simulans. |
| Q47389009 | Echinococcus granulosus strain differentiation based on sequence heterogeneity in mitochondrial genes of cytochrome c oxidase-1 and NADH dehydrogenase-1. |
| Q36388176 | Effect of a Fusion Peptide by Covalent Conjugation of a Mitochondrial Cell-Penetrating Peptide and a Glutathione Analog Peptide |
| Q37662353 | Effect of acute xanthine oxidase inhibition on myocardial energetics during basal and very high cardiac workstates |
| Q28565106 | Effect of ischemic preconditioning on mitochondrial dysfunction and mitochondrial p53 translocation after transient global cerebral ischemia in rats |
| Q35002406 | Effect of structural modulation of polyphenolic compounds on the inhibition of Escherichia coli ATP synthase |
| Q45138789 | Effect of treating induced mitochondrial damage on embryonic development and epigenesis |
| Q73455558 | Effects of aerobic training on lactate and catecholaminergic exercise responses in mitochondrial myopathies |
| Q39086053 | Effects of airborne toxicants on pulmonary function and mitochondrial DNA damage in rodent lungs |
| Q37418521 | Effects of benzo[a]pyrene on mitochondrial and nuclear DNA damage in Atlantic killifish (Fundulus heteroclitus) from a creosote-contaminated and reference site |
| Q40068903 | Effects of imaging conditions on mitochondrial transport and length in larval motor axons of Drosophila |
| Q39733739 | Efficient cloning and engineering of entire mitochondrial genomes in Escherichia coli and transfer into transcriptionally active mitochondria |
| Q46856395 | Efficient execution of cell death in non-glycolytic cells requires the generation of ROS controlled by the activity of mitochondrial H+-ATP synthase |
| Q34623673 | Electron transport chain defects in heart failure |
| Q37488246 | Emerging roles of mitochondrial membrane dynamics in health and disease. |
| Q36967723 | Emerging therapies for mitochondrial disorders |
| Q42143277 | Endogenous mitochondrial oxidative stress in MnSOD-deficient mouse embryonic fibroblasts promotes mitochondrial DNA glycation |
| Q35131161 | Endonuclease III and endonuclease VIII conditionally targeted into mitochondria enhance mitochondrial DNA repair and cell survival following oxidative stress |
| Q38112040 | Endothelial cell energy metabolism, proliferation, and apoptosis in pulmonary hypertension. |
| Q77648336 | Enhanced apoptosis in prolonged cultures of senescent porcine pulmonary artery endothelial cells |
| Q44024800 | Enhanced mtDNA repair capacity protects pulmonary artery endothelial cells from oxidant-mediated death |
| Q40407402 | Enhancement of cisplatin-induced apoptosis and caspase 3 activation by depletion of mitochondrial DNA in a human osteosarcoma cell line. |
| Q46325293 | Environmental Tobacco Smoke Alters Metabolic Systems in Adult Rats. |
| Q92357155 | Environmental factors modulated ancient mitochondrial DNA variability and the prevalence of rheumatic diseases in the Basque Country |
| Q41439002 | Enzymatic activities linked to cardiac energy metabolism of Trypanosoma evansi-infected rats and their possible functional correlations to disease pathogenesis |
| Q34367235 | Enzymology of mitochondrial base excision repair |
| Q34386766 | Epidemiology and treatment of mitochondrial disorders |
| Q90221699 | Epigenetic Modifications Compromise Mitochondrial DNA Quality Control in the Development of Diabetic Retinopathy |
| Q37734460 | Epigenetic regulation of the nuclear-coded GCAT and SHMT2 genes confers human age-associated mitochondrial respiration defects. |
| Q92093237 | Epigenetics and Mitochondrial Stability in the Metabolic Memory Phenomenon Associated with Continued Progression of Diabetic Retinopathy |
| Q35069310 | Eukaryotic genome evolution: rearrangement and coevolution of compartmentalized genetic information |
| Q63977301 | Evaluation and treatment of the human immunodeficiency virus-1-exposed infant |
| Q44329063 | Evaluation of (4-[18F]Fluorophenyl)triphenylphosphonium ion. A potential myocardial blood flow agent for PET. |
| Q35672377 | Evaluation of quantitative and qualitative aspects of mitochondrial function in human skeletal and cardiac muscles |
| Q46414184 | Evaluation of the ROS Inhibiting Activity and Mitochondrial Targeting of Phenolic Compounds in Fibroblast Cells Model System and Enhancement of Efficiency by Natural Deep Eutectic Solvent (NADES) Formulation. |
| Q43963313 | Events upstream of mitochondrial protein import limit the oxidative capacity of fibroblasts in multiple mitochondrial disease |
| Q27939094 | Evidence for a role of FEN1 in maintaining mitochondrial DNA integrity |
| Q22241227 | Evidence linking oxidative stress, mitochondrial dysfunction, and inflammation in the brain of individuals with autism |
| Q46908915 | Evidence of adaptive evolution of alpine pheasants to high-altitude environment from mitogenomic perspective |
| Q38263989 | Evidence to support mitochondrial neuroprotection, in severe traumatic brain injury |
| Q35064205 | Evolution of the mitochondrial fusion-fission cycle and its role in aging |
| Q54706275 | Evolutionary diversification of mitochondrial proteomes: implications for human disease. |
| Q51963096 | Evolvability suppression to stabilize far-sighted adaptations. |
| Q43869563 | Exogenous phospholipids specifically affect transmembrane potential of brain mitochondria and cytochrome C release. |
| Q44547134 | Experimental evidence against the mitochondrial theory of aging. A study of isolated human skeletal muscle mitochondria |
| Q34429365 | Exploring the catalytic core of complex I by Yarrowia lipolytica yeast genetics |
| Q40866706 | Expression of Rattus norvegicus mtDNA in Mus musculus cells results in multiple respiratory chain defects |
| Q46424917 | Expression of VDAC Regulated by Extracts of Limonium sinense Ktze root Against CCl4-induced Liver Damage |
| Q34601641 | Expression of a mitochondrial peroxiredoxin prevents programmed cell death in Leishmania donovani |
| Q30839671 | Extraction and annotation of human mitochondrial genomes from 1000 Genomes Whole Exome Sequencing data |
| Q35999424 | FABP4 reversed the regulation of leptin on mitochondrial fatty acid oxidation in mice adipocytes |
| Q40990028 | Faster and stronger manifestation of mitochondrial diseases in skeletal muscle than in heart related to cytosolic inorganic phosphate (Pi) accumulation |
| Q35459603 | Females with a mutation in a nuclear-encoded mitochondrial protein pay a higher cost of survival than do males in Drosophila. |
| Q64926601 | Fishing in the Cell Powerhouse: Zebrafish as A Tool for Exploration of Mitochondrial Defects Affecting the Nervous System. |
| Q46667460 | Flow cytometry in the study of mitochondrial respiratory chain disorders. |
| Q34500668 | Flow cytometry of isolated mitochondria during development and under some pathological conditions |
| Q43744100 | Fluorometric detection of ADP/ATP carrier deficiency in human muscle. |
| Q31920157 | Flux-balance analysis of mitochondrial energy metabolism: consequences of systemic stoichiometric constraints |
| Q37715192 | Foxo1 integrates insulin signaling with mitochondrial function in the liver |
| Q24674610 | Frequency and phenotypic implications of mitochondrial DNA mutations in human squamous cell cancers of the head and neck |
| Q35212591 | From genotype to phenotype: genetics and medical practice in the new millennium |
| Q36929305 | From mitochondria to disease: role of the renin-angiotensin system |
| Q33827866 | From sideroblastic anemia to the role of mitochondrial DNA mutations in myelodysplastic syndromes |
| Q37446931 | From structure to function: mitochondrial morphology, motion and shaping in vascular smooth muscle |
| Q36137537 | Function of GRIM-19, a mitochondrial respiratory chain complex I protein, in innate immunity |
| Q28552632 | Functional Characterization of Three Concomitant MtDNA LHON Mutations Shows No Synergistic Effect on Mitochondrial Activity |
| Q52867091 | Functional Mitochondria Are Important for the Effect of Resveratrol. |
| Q38213198 | Functional annotation of introns in mitochondrial genome--a brief review |
| Q33836224 | Functional brain imaging in the resting state and during activation in Alzheimer's disease. Implications for disease mechanisms involving oxidative phosphorylation |
| Q34540620 | Functional differences between mitochondrial haplogroup T and haplogroup H in HEK293 cybrid cells |
| Q46212405 | Functional expression of plant alternative oxidase decreases antimycin A-induced reactive oxygen species production in human cells |
| Q34142478 | Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases |
| Q51598419 | Functionalized self-assembled monolayer on gold for detection of human mitochondrial tRNA gene mutations. |
| Q28273169 | Further evidence for paternal inheritance of mitochondrial DNA in the sheep (Ovis aries) |
| Q24561759 | GRIM-19, a cell death regulatory protein, is essential for assembly and function of mitochondrial complex I |
| Q44306254 | Ganglioside GT1B and melatonin inhibit brain mitochondrial DNA damage and seizures induced by kainic acid in mice |
| Q30514129 | Gene delivery to mitochondria by targeting modified adenoassociated virus suppresses Leber's hereditary optic neuropathy in a mouse model. |
| Q34623700 | Gene regulatory mechanisms governing energy metabolism during cardiac hypertrophic growth |
| Q34264448 | Gene therapy by mitochondrial transfer |
| Q34133279 | Gene therapy for progeny of mito-mice carrying pathogenic mtDNA by nuclear transplantation |
| Q36688667 | Gene therapy of the other genome: the challenges of treating mitochondrial DNA defects |
| Q34435173 | GeneFriends: an online co-expression analysis tool to identify novel gene targets for aging and complex diseases. |
| Q73035349 | Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes |
| Q42950686 | Generation of trans-mitochondrial mito-mice by the introduction of a pathogenic G13997A mtDNA from highly metastatic lung carcinoma cells. |
| Q37764795 | Generation, function, and prognostic utility of somatic mitochondrial DNA mutations in cancer |
| Q34688103 | Genes, mitochondria and aging in filamentous fungi |
| Q50203938 | Genetic Variants in the Manganese Superoxide Dismutase 2 Gene and in the Catalase Gene are not Associated With Alcoholic Chronic Pancreatitis. |
| Q93012161 | Genetic and morphometric categorization of Taenia ovis from Sheep in Iran |
| Q58490420 | Genetic characterization of Egyptian and Italian sheep breeds using mitochondrial DNA. |
| Q35112849 | Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathy |
| Q61764128 | Genetic risk markers for hepatocellular carcinoma in patients with alcoholic liver disease |
| Q28397261 | Genetic variability of respiratory complex abundance, organization and activity in mouse brain |
| Q54349886 | Genetic variants of MnSOD and GPX1 and susceptibility to bladder cancer in a Turkish population. |
| Q33691714 | Genetic variation in PARL influences mitochondrial content |
| Q35132741 | Genetics and mitochondrial abnormalities in autism spectrum disorders: a review |
| Q34369881 | Genetics of familial paragangliomas: past, present, and future |
| Q27935978 | Genome-wide responses to mitochondrial dysfunction |
| Q35111415 | Geriatric oncology: a clinical approach to the older patient with cancer. |
| Q34576588 | Germline bottlenecks, biparental inheritance and selection on mitochondrial variants: a two-level selection model |
| Q94464138 | Gerontoxanthone I and Macluraxanthone Induce Mitophagy and Attenuate Ischemia/Reperfusion Injury |
| Q33991794 | Glia are critical for the neuropathology of complex I deficiency in Drosophila |
| Q34615869 | Glucose metabolism derangements in adults with the MELAS m.3243A>G mutation |
| Q51377105 | Glucose transporter type I deficiency causing mitochondrial dysfunction. |
| Q28505776 | Glutamyl-tRNAGln amidotransferase is essential for mammalian mitochondrial translation in vivo |
| Q46425686 | Glycation of mitochondrial proteins from diabetic rat kidney is associated with excess superoxide formation |
| Q43998719 | Glycerophosphate-dependent hydrogen peroxide production by brown adipose tissue mitochondria and its activation by ferricyanide |
| Q30152650 | Granzyme B enters the mitochondria in a Sam50-, Tim22- and mtHsp70-dependent manner to induce apoptosis. |
| Q41918189 | Guidelines for the use of flow cytometry and cell sorting in immunological studies |
| Q37715573 | HSP72 is a mitochondrial stress sensor critical for Parkin action, oxidative metabolism, and insulin sensitivity in skeletal muscle |
| Q37424675 | Hallmarks of a new era in mitochondrial biochemistry |
| Q80611167 | Handling mammalian mitochondrial tRNAs and aminoacyl-tRNA synthetases for functional and structural characterization |
| Q35165702 | Have environmental mutagens caused oncomutations in people? |
| Q57458095 | Hepatocyte miR-33a mediates mitochondrial dysfunction and hepatosteatosis by suppressing NDUFA5 |
| Q46712412 | Hepatoprotection of oleanolic acid is related to its inhibition on mitochondrial permeability transition |
| Q45138383 | Hepatoprotective activity of Terminalia catappa L. leaves and its two triterpenoids |
| Q37713095 | Heterogeneity in Cancer Metabolism: New Concepts in an Old Field |
| Q36501296 | Heteroplasmy as a common state of mitochondrial genetic information in plants and animals |
| Q34020757 | Heteroplasmy of the human mtDNA control region remains constant during life |
| Q34692062 | Heterozygous Polg mutation causes motor dysfunction due to mtDNA deletions |
| Q40479130 | High frequency of somatic mitochondrial DNA mutations in human thyroid carcinomas and complex I respiratory defect in thyroid cancer cell lines. |
| Q38494582 | High levels of gene expression explain the strong evolutionary constraint of mitochondrial protein-coding genes |
| Q55981909 | High-Resolution Genomic Analysis of Human Mitochondrial RNA Sequence Variation |
| Q46667465 | High-throughput assessment of mitochondrial membrane potential in situ using fluorescence resonance energy transfer |
| Q35208534 | High-throughput screening of FDA-approved drugs using oxygen biosensor plates reveals secondary mitofunctional effects |
| Q36129409 | Hitting the brakes: termination of mitochondrial transcription |
| Q32138928 | How understanding the control of energy metabolism can help investigation of mitochondrial dysfunction, regulation and pharmacology |
| Q38968532 | HtrA2/Omi influences the stability of LON protease 1 and prohibitin, proteins involved in mitochondrial homeostasis |
| Q28115572 | Human Myo19 is a novel myosin that associates with mitochondria |
| Q37322422 | Human mitochondrial DNA replication machinery and disease |
| Q38247491 | Human mitochondrial genome flaws and risk of cancer |
| Q42537947 | Human mitochondrial tRNAMet is exported to the cytoplasm and associates with the Argonaute 2 protein |
| Q33943662 | Human mitochondrial topoisomerase I |
| Q28215338 | Human mitochondrial transcription factor A binds preferentially to oxidatively damaged DNA |
| Q24313359 | Human mitochondrial transcription factor B1 interacts with the C-terminal activation region of h-mtTFA and stimulates transcription independently of its RNA methyltransferase activity |
| Q74159658 | Human quadriceps muscle mitochondria: a functional characterization |
| Q44435551 | Human skeletal muscle mitochondrial metabolism in youth and senescence: no signs of functional changes in ATP formation and mitochondrial oxidative capacity. |
| Q48784381 | Human-animal cytoplasmic hybrid embryos, mitochondria, and an energetic debate. |
| Q90598570 | HyPer2 imaging reveals temporal and heterogeneous hydrogen peroxide changes in denervated and aged skeletal muscle fibers in vivo |
| Q38894828 | Hydrophobized triphenyl phosphonium derivatives for the preparation of mitochondriotropic liposomes: choice of hydrophobic anchor influences cytotoxicity but not mitochondriotropic effect. |
| Q37034432 | Hyperglycemic Conditions Prime Cells for RIP1-dependent Necroptosis. |
| Q35113389 | Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion |
| Q93105365 | Hypoxia induces rapid, STAT3 and ROS dependent, mitochondrial translocation of RelA(p65) and IκBα |
| Q37036607 | IGF-1 protects intestinal epithelial cells from oxidative stress-induced apoptosis |
| Q37855570 | IP(3) Receptors, Mitochondria, and Ca Signaling: Implications for Aging |
| Q35370058 | IRS2 increases mitochondrial dysfunction and oxidative stress in a mouse model of Huntington disease |
| Q64963573 | Identification and Characterization of New RNASEH1 Mutations Associated With PEO Syndrome and Multiple Mitochondrial DNA Deletions. |
| Q34547595 | Identification and characterization of mitochondrial abasic (AP)-endonuclease in mammalian cells |
| Q35908442 | Identification of 14-3-3γ as a Mieap-interacting protein and its role in mitochondrial quality control |
| Q33231204 | Identification of a putative mitochondrial RNA polymerase from Physarum polycephalum: characterization, expression, purification, and transcription in vitro |
| Q33942032 | Identification of a ryanodine receptor in rat heart mitochondria |
| Q37413833 | Identification of mitochondrial disease genes through integrative analysis of multiple datasets |
| Q33325706 | Identification of molecular pathways affected by pterostilbene, a natural dimethylether analog of resveratrol |
| Q92924523 | Imaging Mitochondrial Functions: from Fluorescent Dyes to Genetically-Encoded Sensors |
| Q90332429 | Iminosugars Spiro-Linked with Morpholine-Fused 1,2,3-Triazole: Synthesis, Conformational Analysis, Glycosidase Inhibitory Activity, Antifungal Assay, and Docking Studies |
| Q36615718 | Immature Rubus coreanus Shows a Free Radical-Scavenging Effect and Inhibits Cholesterol Synthesis and Secretion in Liver Cells |
| Q90016261 | Immunosuppressant drug tacrolimus induced mitochondrial nephrotoxicity, modified PCNA and Bcl-2 expression attenuated by Ocimum basilicum L. in CD1 mice |
| Q28578564 | Impaired expression of NADH dehydrogenase subunit 1 and PPARgamma coactivator-1 in skeletal muscle of ZDF rats: restoration by troglitazone |
| Q52541455 | Impaired insulin secretion and beta-cell loss in tissue-specific knockout mice with mitochondrial diabetes. |
| Q84987787 | Impaired mitochondrial respiration and decreased fatigue resistance followed by severe muscle weakness in skeletal muscle of mitochondrial DNA mutator mice |
| Q35252601 | Impaired respiratory function in MELAS-induced pluripotent stem cells with high heteroplasmy levels. |
| Q34793219 | Import and assembly of proteins into mitochondria of mammalian cells |
| Q39693264 | In Saccharomyces cerevisiae, ATP2 mRNA sorting to the vicinity of mitochondria is essential for respiratory function |
| Q81554465 | In situ genotyping individual DNA molecules by target-primed rolling-circle amplification of padlock probes |
| Q39227742 | In vitro 3'-end endonucleolytic processing defect in a human mitochondrial tRNA(Ser(UCN)) precursor with the U7445C substitution, which causes non-syndromic deafness |
| Q44298045 | In vitro effects of polyglutamine tracts on Ca2+-dependent depolarization of rat and human mitochondria: relevance to Huntington's disease. |
| Q41807410 | In vivo and in vitro assessment of brain bioenergetics in aging rats |
| Q34777508 | In vivo effects of dietary quercetin and quercetin-rich red onion extract on skeletal muscle mitochondria, metabolism, and insulin sensitivity |
| Q34057751 | In vivo oxygen-17 NMR for imaging brain oxygen metabolism at high field |
| Q34405677 | In vivo quantification reveals extensive natural variation in mitochondrial form and function in Caenorhabditis briggsae |
| Q27931938 | Inactivation of Saccharomyces cerevisiae OGG1 DNA repair gene leads to an increased frequency of mitochondrial mutants. |
| Q57537758 | Increase in mitochondrial DNA mutations impairs retinal function and renders the retina vulnerable to injury |
| Q43628476 | Increased calcium vulnerability of senescent cardiac mitochondria: protective role for a mitochondrial potassium channel opener |
| Q34381144 | Increased mitochondrial mass in mitochondrial myopathy mice |
| Q48910103 | Increased oxidative damage in nuclear and mitochondrial DNA in Alzheimer's disease. |
| Q46888735 | Increased oxidative damage in nuclear and mitochondrial DNA in mild cognitive impairment |
| Q46555080 | Increased oxidative damage with altered antioxidative status in type 2 diabetic patients harboring the 16189 T to C variant of mitochondrial DNA. |
| Q24542578 | Induced overexpression of mitochondrial Mn-superoxide dismutase extends the life span of adult Drosophila melanogaster |
| Q34184643 | Inducible expression of a dominant negative DNA polymerase-gamma depletes mitochondrial DNA and produces a rho0 phenotype. |
| Q40482450 | Influence of a mitochondrial genetic defect on capacitative calcium entry and mitochondrial organization in the osteosarcoma cells. |
| Q39991458 | Influence of mitochondrial DNA level on cellular energy metabolism: implications for mitochondrial diseases |
| Q40394628 | Inheritance of mitochondrial disorders |
| Q37129457 | Inherited disorders affecting mitochondrial function are associated with glutathione deficiency and hypocitrullinemia |
| Q34692482 | Inherited mitochondrial diseases of DNA replication |
| Q38649815 | Inherited mitochondrial genomic instability and chemical exposures |
| Q39704890 | Inhibition of complex I of the electron transport chain causes O2-. -mediated mitochondrial outgrowth. |
| Q51642781 | Inhibition of mitochondrial complex-1 restores the downregulation of aquaporins in obstructive nephropathy. |
| Q35042398 | Inhibition of mitochondrial proton F0F1-ATPase/ATP synthase by polyphenolic phytochemicals |
| Q21296696 | Inhibition of the Mitochondrial Permeability Transition for Cytoprotection: Direct versus Indirect Mechanisms |
| Q44152179 | Inhibition of the mitochondrial respiratory chain by alanine in rat cerebral cortex |
| Q44027584 | Inhibition of the mitochondrial respiratory chain by phenylalanine in rat cerebral cortex |
| Q43921784 | Inhibition of the mitochondrial respiratory chain complex activities in rat cerebral cortex by methylmalonic acid. |
| Q42134189 | Inhibition sites in F1-ATPase from bovine heart mitochondria. |
| Q34633928 | Initial experience in the treatment of inherited mitochondrial disease with EPI-743. |
| Q38802167 | Innovative Technologies in Nanomedicines: From Passive Targeting to Active Targeting/From Controlled Pharmacokinetics to Controlled Intracellular Pharmacokinetics. |
| Q34127625 | Insight into nanoparticle cellular uptake and intracellular targeting |
| Q35776712 | Insulin resistance is associated with epigenetic and genetic regulation of mitochondrial DNA in obese humans |
| Q37715179 | Insulin signaling meets mitochondria in metabolism |
| Q44532294 | Insulin-like growth factor-1 prevents loss of electrochemical gradient in cardiac muscle mitochondria via activation of PI 3 kinase/Akt pathway. |
| Q28593536 | Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria |
| Q98177448 | Integrating Ultra-Weak Photon Emission Analysis in Mitochondrial Research |
| Q24793149 | Integrative analysis of the mitochondrial proteome in yeast |
| Q27629213 | Integrity ofthermus thermophiluscytochrome c552Synthesized byescherichia colicells expressing the host-specific cytochromecmaturation genes,ccmABCDEFGH: Biochemical, spectral, and structural characterization of the recombinant protein |
| Q45878904 | Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA. |
| Q24314111 | Interactions between PBEF and oxidative stress proteins--a potential new mechanism underlying PBEF in the pathogenesis of acute lung injury |
| Q88442582 | Intraspecific mitochondrial genome comparison identified CYTB as a high-resolution population marker in a new pest Athetis lepigone |
| Q46457362 | Introgression of mtDNA in Urosaurus lizards: historical and ecological processes |
| Q41549302 | Iron Deprivation Induces Transcriptional Regulation of Mitochondrial Biogenesis |
| Q34013010 | Iron deficiency and iron excess damage mitochondria and mitochondrial DNA in rats. |
| Q36031463 | Is There a Link between Mitochondrial Reserve Respiratory Capacity and Aging? |
| Q43886867 | Ischemic preconditioning and Na+/H+ exchange inhibition improve reperfusion ion homeostasis |
| Q28217558 | Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation |
| Q73944610 | Isolation and subfractionation of mitochondria from the yeast Saccharomyces cerevisiae |
| Q40828951 | Isolation of a bi-directional promoter directing expression of the mouse GABPalpha and ATP synthase coupling factor 6 genes. |
| Q42160127 | Japanese Alzheimer's disease and other complex disorders diagnosis based on mitochondrial SNP haplogroups |
| Q39363091 | Junctophilin 2 knockdown interfere with mitochondrium status in ESC-CMs and cardiogenesis of ES cells |
| Q35109723 | KIOM-4 Protects against Oxidative Stress-Induced Mitochondrial Damage in Pancreatic β-cells via Its Antioxidant Effects |
| Q35755707 | Kidney-Specific Reduction of Oxidative Phosphorylation Genes Derived from Spontaneously Hypertensive Rat. |
| Q28283648 | L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1 |
| Q36826689 | LC-MS Analysis of Human Platelets as a Platform for Studying Mitochondrial Metabolism |
| Q33974957 | LETM1, a gene deleted in Wolf-Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein |
| Q34627398 | Laboratory diagnosis of metabolic myopathies |
| Q43757469 | Late-onset corticohippocampal neurodepletion attributable to catastrophic failure of oxidative phosphorylation in MILON mice. |
| Q26863599 | Leber hereditary optic neuropathy: current perspectives |
| Q28768948 | Likelihood Analysis of Asymmetrical Mutation Bias Gradients in Vertebrate Mitochondrial Genomes |
| Q33893542 | Linking chemical electron-proton transfer to proton pumping in cytochrome c oxidase: broken-symmetry DFT exploration of intermediates along the catalytic reaction pathway of the iron-copper dinuclear complex |
| Q51660260 | Lipopolysaccharide stimulates mitochondrial biogenesis via activation of nuclear respiratory factor-1. |
| Q35947255 | Liposomes loaded with paclitaxel and modified with novel triphenylphosphonium-PEG-PE conjugate possess low toxicity, target mitochondria and demonstrate enhanced antitumor effects in vitro and in vivo |
| Q34447070 | Localization of mitochondrial DNA encoded cytochrome c oxidase subunits I and II in rat pancreatic zymogen granules and pituitary growth hormone granules |
| Q37634512 | Long term adverse effects related to nucleoside reverse transcriptase inhibitors: clinical impact of mitochondrial toxicity |
| Q54467516 | Loss of a primordial identity element for a mammalian mitochondrial aminoacylation system. |
| Q36382575 | Loss of the respiratory enzyme citrate synthase directly links the Warburg effect to tumor malignancy. |
| Q33679205 | Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation |
| Q94352872 | L’évaluation et le traitement du nourrisson exposé au virus d’immunodéficience humaine de type 1 |
| Q45861723 | MITO-Porter for Mitochondrial Delivery and Mitochondrial Functional Analysis |
| Q38504142 | MITOCHONDRIAL REDOX IMAGING FOR CANCER DIAGNOSTIC AND THERAPEUTIC STUDIES |
| Q39541857 | MITOP, the mitochondrial proteome database: 2000 update |
| Q30384428 | MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: new patients and novel mutations. |
| Q36129109 | MaGelLAn 1.0: a software to facilitate quantitative and population genetic analysis of maternal inheritance by combination of molecular and pedigree information. |
| Q42374188 | Macropinocytic entry of isolated mitochondria in epidermal growth factor-activated human osteosarcoma cells |
| Q33334641 | Maintenance and integrity of the mitochondrial genome: a plethora of nuclear genes in the budding yeast |
| Q37763932 | Mammalian mitochondrial proteomics: insights into mitochondrial functions and mitochondria-related diseases |
| Q28140976 | Mammalian mitochondrial ribosomal proteins (4). Amino acid sequencing, characterization, and identification of corresponding gene sequences |
| Q33778100 | Manganese superoxide dismutase V16A single-nucleotide polymorphism in the mitochondrial targeting sequence is associated with reduced enzymatic activity in cryopreserved human hepatocytes |
| Q44122031 | Manipulation of mitochondrial DNA gene expression in the mouse |
| Q47612283 | Marked mitochondrial DNA sequence heterogeneity in single CD34+ cell clones from normal adult bone marrow |
| Q57282162 | Maternal component in the familial aggregation of hypertension |
| Q35845825 | Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice. |
| Q26849450 | Maternal inheritance of mitochondrial DNA by diverse mechanisms to eliminate paternal mitochondrial DNA |
| Q43664500 | Measurements of protein carbonyls, ortho- and meta-tyrosine and oxidative phosphorylation complex activity in mitochondria from young and old rats |
| Q43001982 | Mechanism in the reaction of cytochrome c oxidase with organic hydroperoxides: an ESR spin-trapping investigation |
| Q27647277 | Mechanism of inhibition of bovine F1-ATPase by resveratrol and related polyphenols |
| Q28131760 | Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1 |
| Q37468328 | Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD). |
| Q37511851 | Mechanotransduction and Metabolism in Cardiomyocyte Microdomains. |
| Q36525492 | Medicinal chemistry of ATP synthase: a potential drug target of dietary polyphenols and amphibian antimicrobial peptides |
| Q48223108 | Melas with point mutations involving tRNALeu (A3243G) and tRNAGlu(A14693g) |
| Q35001051 | Melatonin in mitochondrial dysfunction and related disorders |
| Q40121244 | Metabolic and antioxidant system alterations in an astrocytoma cell line challenged with mitochondrial DNA deletion |
| Q37217309 | Metabolic control analysis: a tool for designing strategies to manipulate metabolic pathways. |
| Q37617074 | Metabolic imaging in multiple time scales |
| Q28384779 | Metabolic regulation of manganese superoxide dismutase expression via essential amino acid deprivation |
| Q92685482 | Metabolic switching in pluripotent stem cells reorganizes energy metabolism and subcellular organelles |
| Q34132623 | Metabolism and lifespan |
| Q36693111 | Metabolism pathways in chronic lymphocytic leukemia |
| Q37701655 | Metabolite measurements in the caudate nucleus, anterior cingulate cortex and hippocampus among patients with mitochondrial disorders: a case-control study using proton magnetic resonance spectroscopy |
| Q36056367 | Metalloprotease OMA1 Fine-tunes Mitochondrial Bioenergetic Function and Respiratory Supercomplex Stability |
| Q26863224 | Metals, oxidative stress and neurodegeneration: a focus on iron, manganese and mercury |
| Q46327960 | Methylene blue and its analogues as antidepressant compounds. |
| Q47660144 | Mice deficient in the Shmt2 gene have mitochondrial respiration defects and are embryonic lethal |
| Q30484862 | Mice with mitochondrial complex I deficiency develop a fatal encephalomyopathy |
| Q51553464 | MicroRNA array analysis of microRNAs related to systemic scleroderma. |
| Q30634345 | Microphotometric analysis of NADH-tetrazolium reductase deficiency in fibroblasts of patients with Leber hereditary optic neuropathy. |
| Q42799263 | Mild mitochondrial uncoupling does not affect mitochondrial biogenesis but downregulates pyruvate carboxylase in adipocytes: role for triglyceride content reduction |
| Q89422097 | Mito-mice∆ and mitochondrial DNA mutator mice as models of human osteoporosis caused not by aging but by hyperparathyroidism |
| Q42175820 | MitoBlue: a nontoxic and photostable blue-emitting dye that selectively labels functional mitochondria |
| Q34667750 | MitoLSDB: a comprehensive resource to study genotype to phenotype correlations in human mitochondrial DNA variations |
| Q41878294 | MitoLoc: A method for the simultaneous quantification of mitochondrial network morphology and membrane potential in single cells |
| Q34084587 | MitoMiner: a data warehouse for mitochondrial proteomics data |
| Q24671804 | Mitochondria |
| Q38741503 | Mitochondria and Mitochondrial ROS in Cancer: Novel Targets for Anticancer Therapy |
| Q37431693 | Mitochondria and cancer |
| Q35894464 | Mitochondria and mind |
| Q35540388 | Mitochondria and vascular lesions as a central target for the development of Alzheimer's disease and Alzheimer disease-like pathology in transgenic mice |
| Q36359505 | Mitochondria as a target for early detection and diagnosis of cancer |
| Q34264441 | Mitochondria as subcellular targets for clinically useful anthracyclines |
| Q42487268 | Mitochondria buffer non-toxic calcium loads and release calcium through the mitochondrial permeability transition pore and sodium/calcium exchanger in rat basal forebrain neurons |
| Q33737272 | Mitochondria harbouring mutant mtDNA--a cuckoo in the nest? |
| Q28394886 | Mitochondria in the pathogenesis of diabetes: a proteomic view |
| Q37990817 | Mitochondria in vascular disease |
| Q64245244 | Mitochondria-Responsive Drug Release along with Heat Shock Mediated by Multifunctional Glycolipid Micelles for Precise Cancer Chemo-Phototherapy |
| Q35164499 | Mitochondria-mediated nuclear mutator phenotype in Saccharomyces cerevisiae |
| Q35108107 | Mitochondria-related male infertility |
| Q36262408 | Mitochondria-related miR-141-3p contributes to mitochondrial dysfunction in HFD-induced obesity by inhibiting PTEN. |
| Q36846818 | Mitochondria: a hub of redox activities and cellular distress control |
| Q35071387 | Mitochondria: releasing power for life and unleashing the machineries of death |
| Q36671535 | Mitochondrial "swirls" induced by oxygen stress and in the Drosophila mutant hyperswirl |
| Q37316455 | Mitochondrial (dys)function in adipocyte (de)differentiation and systemic metabolic alterations |
| Q35577705 | Mitochondrial Bioenergetics, Aging, and Aging-Related Disease |
| Q45144296 | Mitochondrial DNA 3644T-->C mutation associated with bipolar disorder |
| Q64230639 | Mitochondrial DNA Fitness Depends on Nuclear Genetic Background in |
| Q37030177 | Mitochondrial DNA aberrations of bone marrow cells from patients with aplastic anemia |
| Q73721797 | Mitochondrial DNA alteration in esophageal cancer |
| Q28141431 | Mitochondrial DNA and disease |
| Q37621771 | Mitochondrial DNA and functional investigations into the radiosensitivity of four mouse strains. |
| Q35789945 | Mitochondrial DNA as a cancer biomarker |
| Q35418164 | Mitochondrial DNA content varies with pathological characteristics of breast cancer |
| Q30760899 | Mitochondrial DNA deletion mutations are concomitant with ragged red regions of individual, aged muscle fibers: analysis by laser-capture microdissection |
| Q35645470 | Mitochondrial DNA deletions and differential mitochondrial DNA content in Rhesus monkeys: implications for aging |
| Q40877362 | Mitochondrial DNA depletion causes morphological changes in the mitochondrial reticulum of cultured human cells |
| Q28649392 | Mitochondrial DNA disease and developmental implications for reproductive strategies |
| Q58912088 | Mitochondrial DNA haplogroups modulate the radiographic progression of Spanish patients with osteoarthritis |
| Q57174226 | Mitochondrial DNA heteroplasmy in cloned cattle produced by fetal and adult cell cloning |
| Q49605186 | Mitochondrial DNA in Lung Cancer. |
| Q34106586 | Mitochondrial DNA inheritance in Saccharomyces cerevisiae |
| Q34264471 | Mitochondrial DNA metabolism targeting drugs |
| Q48224759 | Mitochondrial DNA modifies cognition in interaction with the nuclear genome and age in mice |
| Q37735748 | Mitochondrial DNA mutation-elicited oxidative stress, oxidative damage, and altered gene expression in cultured cells of patients with MERRF syndrome |
| Q28304162 | Mitochondrial DNA mutations and mitochondrial DNA depletion in breast cancer |
| Q28250500 | Mitochondrial DNA mutations and mitochondrial DNA depletion in gastric cancer |
| Q38889446 | Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men. |
| Q34589585 | Mitochondrial DNA mutations in mutator mice confer respiration defects and B-cell lymphoma development |
| Q51661489 | Mitochondrial DNA mutations in primary leukemia cells after chemotherapy: clinical significance and therapeutic implications. |
| Q35582417 | Mitochondrial DNA mutations in the hematopoietic system |
| Q33997161 | Mitochondrial DNA mutations regulate metastasis of human breast cancer cells. |
| Q74394247 | Mitochondrial DNA mutations, oxidative stress, and aging |
| Q53624950 | Mitochondrial DNA oxidative damage contributes to cardiomyocyte ischemia/reperfusion-injury in rats: cardioprotective role of lycopene. |
| Q21144317 | Mitochondrial DNA polymorphism A4917G is independently associated with age-related macular degeneration |
| Q36960466 | Mitochondrial DNA polymorphisms specifically modify cerebral β-amyloid proteostasis |
| Q34994585 | Mitochondrial DNA repair and aging |
| Q39140349 | Mitochondrial DNA sequence and phylogenetic evaluation of geographically disparate Sus scrofa breeds. |
| Q92586273 | Mitochondrial DNA somatic mutation burden and heteroplasmy are associated with chronological age, smoking, and HIV infection |
| Q35848412 | Mitochondrial DNA spectra of single human CD34+ cells, T cells, B cells, and granulocytes |
| Q54938047 | Mitochondrial DNA transmission and confounding mitochondrial influences in cloned cattle and pigs. |
| Q80923272 | Mitochondrial DNA turnover occurs during preimplantation development and can be modulated by environmental factors |
| Q73692274 | Mitochondrial DNA variant 16189T>C is associated with susceptibility to endometrial cancer |
| Q37128695 | Mitochondrial DNA with a large-scale deletion causes two distinct mitochondrial disease phenotypes in mice |
| Q47974460 | Mitochondrial DNA-Induced Inflammatory Responses and Lung Injury in Thermal Injury Rat Model: Protective Effect of Epigallocatechin Gallate |
| Q73701269 | Mitochondrial Disease |
| Q62397450 | Mitochondrial Disorders |
| Q42226725 | Mitochondrial Dynamics in Mitochondrial Diseases |
| Q73627919 | Mitochondrial Genetics...and a new way to rescue them |
| Q35969962 | Mitochondrial Haplotypes Influence Metabolic Traits in Porcine Transmitochondrial Cybrids. |
| Q40726482 | Mitochondrial K(ATP) channel openers activate the ERK kinase by an oxidant-dependent mechanism |
| Q57847919 | Mitochondrial Membrane Potential and ATP Production in Primary Disorders of ATP Synthase |
| Q38678063 | Mitochondrial Mutations in Cardiac Disorders |
| Q40067062 | Mitochondrial ND5 gene variation associated with encephalomyopathy and mitochondrial ATP consumption |
| Q36702313 | Mitochondrial NDUFS3 regulates the ROS-mediated onset of metabolic switch in transformed cells |
| Q33820008 | Mitochondrial Nucleoid: Shield and Switch of the Mitochondrial Genome |
| Q41927221 | Mitochondrial Oxidative Phosphorylation System (OXPHOS) Deficits in Schizophrenia: Possible Interactions with Cellular Processes |
| Q91914273 | Mitochondrial Respiratory Disorders: A Perspective on their Metabolite Biomarkers and Implications for Clinical Diagnosis and Therapeutic Intervention |
| Q41786761 | Mitochondrial Sensorineural Hearing Loss: A Retrospective Study and a Description of Cochlear Implantation in a MELAS Patient |
| Q77291654 | Mitochondrial Toxicity Associated with Nucleoside Reverse Transcriptase Inhibitor Therapy |
| Q41617454 | Mitochondrial and nuclear DNA damage and repair in age-related macular degeneration |
| Q37692490 | Mitochondrial biogenesis by NO yields functionally active mitochondria in mammals |
| Q33876294 | Mitochondrial biogenesis defects and neuromuscular disorders |
| Q36499708 | Mitochondrial biogenesis in the pulmonary vasculature during inhalational lung injury and fibrosis |
| Q42015474 | Mitochondrial biogenesis restores oxidative metabolism during Staphylococcus aureus sepsis |
| Q36771650 | Mitochondrial biogenesis: a therapeutic target for neurodevelopmental disorders and neurodegenerative diseases |
| Q57287805 | Mitochondrial biology and prostate cancer ethnic disparity |
| Q55072954 | Mitochondrial biology in reproduction. |
| Q34264422 | Mitochondrial contributions to cancer cell physiology: potential for drug development |
| Q29617739 | Mitochondrial control of cell death |
| Q37534178 | Mitochondrial control region alterations and breast cancer risk: a study in South Indian population |
| Q50858174 | Mitochondrial cytochrome c oxidase subunit II variations predict adverse prognosis in cytogenetically normal acute myeloid leukaemia. |
| Q38180688 | Mitochondrial cytopathies and cardiovascular disease |
| Q24799964 | Mitochondrial defects in cancer |
| Q34366678 | Mitochondrial defects in neurodegenerative disease |
| Q28510070 | Mitochondrial deficiency and cardiac sudden death in mice lacking the MEF2A transcription factor |
| Q34660403 | Mitochondrial diabetes mellitus |
| Q34737294 | Mitochondrial diabetes: pathophysiology, clinical presentation, and genetic analysis |
| Q79341034 | Mitochondrial disorders and ataxia |
| Q33793717 | Mitochondrial disorders. A diagnostic challenge in clinical chemistry |
| Q91618895 | Mitochondrial division inhibitor 1 reduces dynamin-related protein 1 and mitochondrial fission activity |
| Q34545756 | Mitochondrial dynamics in mammals |
| Q38625440 | Mitochondrial dynamics, mitophagy and cardiovascular disease. |
| Q34811509 | Mitochondrial dysfunction and Down's syndrome. |
| Q36239813 | Mitochondrial dysfunction and antiretroviral nucleoside analog toxicities: what is the evidence? |
| Q50432740 | Mitochondrial dysfunction and myoclonic epilepsy: cause or effect or both? |
| Q35136214 | Mitochondrial dysfunction and nucleoside reverse transcriptase inhibitor therapy: experimental clarifications and persistent clinical questions |
| Q34137363 | Mitochondrial dysfunction and pathology in bipolar disorder and schizophrenia |
| Q35232104 | Mitochondrial dysfunction can connect the diverse medical symptoms associated with autism spectrum disorders |
| Q34282032 | Mitochondrial dysfunction due to oxidative mitochondrial DNA damage is reduced through cooperative actions of diverse proteins |
| Q34990992 | Mitochondrial dysfunction during sepsis: still more questions than answers. |
| Q24630557 | Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis |
| Q35903564 | Mitochondrial dysfunction in cancer |
| Q37455446 | Mitochondrial dysfunction in human breast cancer cells and their transmitochondrial cybrids |
| Q35557675 | Mitochondrial dysfunction, apoptotic cell death, and Alzheimer's disease |
| Q34144271 | Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene |
| Q30890554 | Mitochondrial encephalopathy |
| Q46361960 | Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes syndrome with hypothyroidism and focal segmental glomerulosclerosis in a paediatric patient |
| Q36070074 | Mitochondrial energy metabolism in heart failure: a question of balance |
| Q26824822 | Mitochondrial function and dysfunction: an update |
| Q34462332 | Mitochondrial function in normal and diabetic beta-cells |
| Q34594198 | Mitochondrial functions and aging |
| Q51656021 | Mitochondrial fusion provides an 'initial metabolic complementation' controlled by mtDNA. |
| Q35120186 | Mitochondrial gene history and mRNA localization: is there a correlation? |
| Q36740555 | Mitochondrial gene polymorphisms alter hepatic cellular energy metabolism and aggravate diet-induced non-alcoholic steatohepatitis. |
| Q33821051 | Mitochondrial genome maintenance in health and disease. |
| Q33873854 | Mitochondrial genotype segregation and effects during mammalian development: applications to biotechnology |
| Q34163287 | Mitochondrial haplogroups and control region polymorphisms in age-related macular degeneration: a case-control study |
| Q51788256 | Mitochondrial haplogroups associated with Japanese Alzheimer's patients. |
| Q53303487 | Mitochondrial haplogroups associated with Japanese centenarians, Alzheimer's patients, Parkinson's patients, type 2 diabetic patients and healthy non-obese young males. |
| Q35952222 | Mitochondrial haplogroups define two phenotypes of osteoarthritis. |
| Q24804344 | Mitochondrial inhibition of uracil-DNA glycosylase is not mutagenic |
| Q34344644 | Mitochondrial involvement in brain function and dysfunction: relevance to aging, neurodegenerative disorders and longevity |
| Q37362132 | Mitochondrial iron accumulation with age and functional consequences |
| Q35606693 | Mitochondrial medicine for aging and neurodegenerative diseases |
| Q33836633 | Mitochondrial membrane perturbations in cholestasis. |
| Q33609715 | Mitochondrial metabolism and diabetes |
| Q33214287 | Mitochondrial mutagenesis and oxidative stress in human prostate cancer |
| Q33732618 | Mitochondrial mutagenesis in human cells and tissues |
| Q37311021 | Mitochondrial mutations contribute to HIF1alpha accumulation via increased reactive oxygen species and up-regulated pyruvate dehydrogenease kinase 2 in head and neck squamous cell carcinoma |
| Q43628481 | Mitochondrial mutations differentially affect aging, mutability and anesthetic sensitivity in Caenorhabditis elegans |
| Q34561515 | Mitochondrial mutations may drive Y chromosome evolution |
| Q53675259 | Mitochondrial network complexity and pathological decrease in complex I activity are tightly correlated in isolated human complex I deficiency. |
| Q37015652 | Mitochondrial nuclear receptors and transcription factors: who's minding the cell? |
| Q36270598 | Mitochondrial oxidant generation and oxidative damage in Ames dwarf and GH transgenic mice |
| Q36626374 | Mitochondrial oxidative damage in aging and Alzheimer's disease: implications for mitochondrially targeted antioxidant therapeutics |
| Q45001313 | Mitochondrial oxidative phosphorylation transcriptome alterations in human amyotrophic lateral sclerosis spinal cord and blood |
| Q28593572 | Mitochondrial oxidative stress in mice lacking the glutathione peroxidase-1 gene |
| Q34423769 | Mitochondrial peroxiredoxins are critical for the maintenance of redox state and the survival of adult Drosophila |
| Q33943645 | Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy |
| Q42748320 | Mitochondrial protection by the thioredoxin-2 and glutathione systems in an in vitro endothelial model of sepsis |
| Q36735868 | Mitochondrial protein import and human health and disease |
| Q36697530 | Mitochondrial rRNA and tRNA and hearing function |
| Q38821544 | Mitochondrial remodeling: Rearranging, recycling, and reprogramming |
| Q36119450 | Mitochondrial respiration defects in cancer cells cause activation of Akt survival pathway through a redox-mediated mechanism |
| Q38299817 | Mitochondrial respiratory chain deficiency in Caenorhabditis elegans results in developmental arrest and increased life span |
| Q50584261 | Mitochondrial respiratory dysfunction caused by a heteroplasmic mitochondrial DNA mutation blocks cellular reprogramming. |
| Q27348908 | Mitochondrial structure and function are disrupted by standard isolation methods |
| Q35914830 | Mitochondrial tRNA 3' end metabolism and human disease. |
| Q26828352 | Mitochondrial tRNA mutations and disease |
| Q36668719 | Mitochondrial targeting of recombinant RNAs modulates the level of a heteroplasmic mutation in human mitochondrial DNA associated with Kearns Sayre Syndrome |
| Q35017647 | Mitochondrial threshold effects. |
| Q46881541 | Mitochondrial toxicity in hearts of CD-1 mice following perinatal exposure to AZT, 3TC, or AZT/3TC in combination. |
| Q35550221 | Mitochondrial toxicity of nrti antiviral drugs: an integrated cellular perspective |
| Q24299860 | Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNA |
| Q30476644 | Mitochondrial transfer between cells can rescue aerobic respiration |
| Q37347784 | Mitochondrial-Nuclear Interactions Mediate Sex-Specific Transcriptional Profiles in Drosophila. |
| Q33836653 | Mitochondrial-nuclear interactions and lifespan control in fungi |
| Q33991805 | Mitochondrially targeted antioxidants and thiol reagents |
| Q41108935 | Mitochondrially-imported RNA in drug discovery |
| Q36522646 | Mitoenergetic failure in Alzheimer disease |
| Q43478776 | Mitonuclear Interactions Mediate Transcriptional Responses to Hypoxia in Drosophila |
| Q39132336 | Mitophagy and Alzheimer's Disease: Cellular and Molecular Mechanisms. |
| Q92633565 | Mitophagy in Alzheimer's Disease and Other Age-Related Neurodegenerative Diseases |
| Q39149860 | Mitophagy in neurodegeneration and aging. |
| Q26776469 | Mitophagy programs: mechanisms and physiological implications of mitochondrial targeting by autophagy |
| Q44771659 | Mobilization of adenine nucleotide translocators as molecular bases of the biochemical threshold effect observed in mitochondrial diseases |
| Q33796387 | Model systems for redox cofactor activity |
| Q45221017 | Modification of radiation damage to mitochondrial system in vivo by Podophyllum hexandrum: mechanistic aspects. |
| Q77876813 | Modulating heteroplasmy |
| Q44234584 | Modulation of Lon protease activity and aconitase turnover during aging and oxidative stress. |
| Q33833886 | Modulation of mitochondrial transcription in response to mtDNA depletion and repletion in HeLa cells |
| Q38016561 | Modulation of telomere binding proteins: a future area of research for skin protection and anti-aging target |
| Q34615857 | Molecular bases of cellular iron toxicity |
| Q28508683 | Molecular characterization of mitocalcin, a novel mitochondrial Ca2+-binding protein with EF-hand and coiled-coil domains |
| Q37785514 | Molecular genetics of mitochondrial disorders |
| Q33841122 | Molecular interactions of cancer and age. |
| Q33875611 | Molecular oncology focus - is carcinogenesis a 'mitochondriopathy'? |
| Q34373141 | Morphological dynamics of mitochondria--a special emphasis on cardiac muscle cells |
| Q36479150 | Mother's curse: the effect of mtDNA on individual fitness and population viability |
| Q52021400 | Mother's mitochondria and optimal offspring sex ratio. |
| Q33503932 | MtSNPscore: a combined evidence approach for assessing cumulative impact of mitochondrial variations in disease |
| Q35198793 | Multiphoton excited fluorescent materials for frequency upconversion emission and fluorescent probes. |
| Q28594703 | Multiple organ pathology, metabolic abnormalities and impaired homeostasis of reactive oxygen species in Epas1-/- mice |
| Q49578903 | Multiple ways to prevent transmission of paternal mitochondrial DNA for maternal inheritance in animals. |
| Q37404541 | Multisystem manifestations of mitochondrial disorders |
| Q34150861 | Muscle-specific loss of apoptosis-inducing factor leads to mitochondrial dysfunction, skeletal muscle atrophy, and dilated cardiomyopathy |
| Q43098981 | Musings about the effects of environment on photosynthesis |
| Q44957600 | Mutagenesis by transient misalignment in the human mitochondrial DNA control region |
| Q34478495 | Mutagenic analysis of the F0 stator subunits |
| Q40231756 | Mutant huntingtin expression induces mitochondrial calcium handling defects in clonal striatal cells: functional consequences |
| Q24794136 | Mutation in mitochondrial complex I ND6 subunit is associated with defective response to hypoxia in human glioma cells |
| Q38334427 | Mutations in the spacer region of Drosophila mitochondrial DNA polymerase affect DNA binding, processivity, and the balance between Pol and Exo function |
| Q33210189 | Mutations of mitochondrial 12S rRNA in gastric carcinoma and their significance |
| Q35587467 | My approach to oncocytic tumours of the thyroid |
| Q43280918 | Myeloperoxidase and superoxide dismutase 2 polymorphisms comodulate the risk of hepatocellular carcinoma and death in alcoholic cirrhosis. |
| Q90371571 | NDUFV2 pseudogene (NDUFV2P1) contributes to mitochondrial complex I deficits in schizophrenia |
| Q34074236 | NO synthase and NO-dependent signal pathways in brain aging and neurodegenerative disorders: the role of oxidant/antioxidant balance. |
| Q37176104 | NOX enzymes as novel targets for drug development |
| Q35985407 | NOX2 As a Target for Drug Development: Indications, Possible Complications, and Progress |
| Q36703351 | Nanotechnology inspired tools for mitochondrial dysfunction related diseases |
| Q34162430 | Natural radioactivity and human mitochondrial DNA mutations |
| Q47112971 | Neural-specific deletion of mitochondrial p32/C1qbp leads to leukoencephalopathy due to undifferentiated oligodendrocyte and axon degeneration |
| Q36762857 | Neuroimaging in mitochondrial disorders |
| Q42908536 | Neuroinflammation, Oxidative Stress and the Pathogenesis of Parkinson's Disease |
| Q37408409 | Neurometabolic disorders and dysfunction in autism spectrum disorders |
| Q64079076 | Neuronal Redox-Imbalance in Rett Syndrome Affects Mitochondria as Well as Cytosol, and Is Accompanied by Intensified Mitochondrial O Consumption and ROS Release |
| Q35196229 | Neuronal ageing from an intraneuronal perspective: roles of endoplasmic reticulum and mitochondria |
| Q33881866 | Neurotoxicity associated with neuroleptic-induced oral dyskinesias in rats. Implications for tardive dyskinesia? |
| Q33892767 | New features of mitochondrial DNA replication system in yeast and man. |
| Q37291226 | New insights in the pathogenesis of multiple sclerosis--role of acrolein in neuronal and myelin damage |
| Q46990994 | New variants in the mitochondrial genomes of schizophrenic patients |
| Q28709961 | Next generation sequencing and comparative analyses of Xenopus mitogenomes |
| Q39499163 | Nickel exposure induces oxidative damage to mitochondrial DNA in Neuro2a cells: the neuroprotective roles of melatonin |
| Q31115741 | Nitric oxide-dependent generation of reactive species in sickle cell disease. Actin tyrosine induces defective cytoskeletal polymerization |
| Q37121433 | Normal mitochondrial respiratory function is essential for spatial remote memory in mice |
| Q90661779 | Novel biallelic variants in MSTO1 associated with mitochondrial myopathy |
| Q46009324 | Novel human mitochondrial tRNA phe mutation in a patient with hearing impairment: a case study. |
| Q41813058 | Novel m.15434C>A (p.230L>I) Mitochondrial Cytb Gene Missense Mutation Associated with Dilated Cardiomyopathy |
| Q93352759 | Novel mutations in the mitochondrial complex I assembly gene NDUFAF5 reveal heterogeneous phenotypes |
| Q34116250 | Novel role of p53 in maintaining mitochondrial genetic stability through interaction with DNA Pol gamma |
| Q28396642 | Nuclear DNA damage signalling to mitochondria in ageing |
| Q45022855 | Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells. |
| Q39236946 | Nuclear but not mitochondrial-encoded oxidative phosphorylation genes are altered in aging, mild cognitive impairment, and Alzheimer's disease |
| Q37112850 | Nucleoid localization of Hsp40 Mdj1 is important for its function in maintenance of mitochondrial DNA |
| Q37068704 | Nucleotide incorporation by human DNA polymerase gamma opposite benzo[a]pyrene and benzo[c]phenanthrene diol epoxide adducts of deoxyguanosine and deoxyadenosine. |
| Q89877024 | Nutritional geometry of mitochondrial genetic effects on male fertility |
| Q34805446 | Obesity and hepatosteatosis in mice with enhanced oxidative DNA damage processing in mitochondria |
| Q53341563 | Oncogene-specific gene expression signatures at preneoplastic stage in mice define distinct mechanisms of hepatocarcinogenesis. |
| Q35663083 | Oocyte quality is decreased in women with minimal or mild endometriosis |
| Q27334237 | Opa1 is required for proper mitochondrial metabolism in early development |
| Q38212813 | Ophthalmic manifestations of inherited neurodegenerative disorders |
| Q42165515 | Oral administration of orthovanadate and Trigonella foenum graecum seed power restore the activities of mitochondrial enzymes in tissues of alloxan-induced diabetic rats |
| Q35690379 | Outer mitochondrial membrane permeability can regulate coupled respiration and cell survival |
| Q24298232 | Overexpressed human mitochondrial thioredoxin confers resistance to oxidant-induced apoptosis in human osteosarcoma cells |
| Q34571312 | Overexpression of peroxisome proliferator-activated receptor gamma co-activator-1alpha leads to muscle atrophy with depletion of ATP |
| Q51724662 | Overexpression of the alternative oxidase restores senescence and fertility in a long-lived respiration-deficient mutant of Podospora anserina. |
| Q58581080 | Overriding Phthalate Decomposition When Exploring Mycophenolic Acid Intermediates as Selenium-Based ROS Biological Probes |
| Q34114363 | Oxidant-NO dependent gene regulation in dogs with type I diabetes: impact on cardiac function and metabolism |
| Q42839708 | Oxidative DNA damage causes mitochondrial genomic instability in Saccharomyces cerevisiae |
| Q35023216 | Oxidative DNA damage in lung tissue from patients with COPD is clustered in functionally significant sequences |
| Q38818702 | Oxidative Stress Induced Mitochondrial Failure and Vascular Hypoperfusion as a Key Initiator for the Development of Alzheimer Disease. |
| Q35606429 | Oxidative Stress and Down Syndrome: A Route toward Alzheimer-Like Dementia |
| Q41141816 | Oxidative Stress in Neurodegenerative Diseases: From Molecular Mechanisms to Clinical Applications |
| Q41526360 | Oxidative Stress-Mediated Atherosclerosis: Mechanisms and Therapies |
| Q33774187 | Oxidative damage and age-related macular degeneration |
| Q58726639 | Oxidative status of cardinal ligament in pelvic organ prolapse |
| Q37566969 | Oxidative status predicts quality in human mesenchymal stem cells |
| Q74341665 | Oxidative stress and apoptosis |
| Q36019900 | Oxidative stress in atherogenesis and arterial thrombosis: the disconnect between cellular studies and clinical outcomes. |
| Q33921185 | Oxidative stress induced age dependent meibomian gland dysfunction in Cu, Zn-superoxide dismutase-1 (Sod1) knockout mice |
| Q53266394 | Oxidative stress level in circulating neutrophils is linked to neurodegenerative diseases. |
| Q37956881 | Oxidative stress, frailty and cognitive decline |
| Q38094613 | Oxidative stress: the mitochondria-dependent and mitochondria-independent pathways of apoptosis |
| Q37355397 | Oxygen control of intracellular distribution of mitochondria in muscle fibers |
| Q43606174 | Oxygen radical-induced mitochondrial DNA damage and repair in pulmonary vascular endothelial cell phenotypes |
| Q34000773 | PARP inhibition delays progression of mitochondrial encephalopathy in mice. |
| Q35691132 | PGC-1beta controls mitochondrial metabolism to modulate circadian activity, adaptive thermogenesis, and hepatic steatosis |
| Q35705486 | PNPASE and RNA trafficking into mitochondria |
| Q35613347 | POS5 gene of Saccharomyces cerevisiae encodes a mitochondrial NADH kinase required for stability of mitochondrial DNA. |
| Q28508508 | PRELI (protein of relevant evolutionary and lymphoid interest) is located within an evolutionarily conserved gene cluster on chromosome 5q34-q35 and encodes a novel mitochondrial protein |
| Q92901825 | PUMILIO1 Links Epilepsy to Spinocerebellar Ataxia |
| Q28506059 | Pancreatic beta cells lack a low glucose and O2-inducible mitochondrial protein that augments cell survival |
| Q74554779 | Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenarians |
| Q44833660 | Paradoxical decrease of mitochondrial DNA deletions in epithelial cells of active ulcerative colitis patients |
| Q35113387 | Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction |
| Q48202720 | Pathogenic mitochondrial DNA-induced respiration defects in hematopoietic cells result in anemia by suppressing erythroid differentiation |
| Q58040388 | Pathways related to mitochondrial dysfunction in cartilage of endemic osteoarthritis patients in China |
| Q35814781 | Patterns of natural selection acting on the mitochondrial genome of a locally adapted fish species |
| Q34884970 | Peptide-based carbon nanotubes for mitochondrial targeting |
| Q33373844 | Performance of mitochondrial DNA mutations detecting early stage cancer |
| Q37526796 | Peroxisome proliferator-activated receptor gamma coactivator-1 promotes cardiac mitochondrial biogenesis |
| Q37497833 | Pharmacological approaches to restore mitochondrial function |
| Q34807192 | Pharmacological control of cellular calcium handling in dystrophic skeletal muscle |
| Q33993644 | Pharmacology of nucleoside and nucleotide reverse transcriptase inhibitor-induced mitochondrial toxicity. |
| Q40643080 | Phyllanthus Suppresses Prostate Cancer Cell, PC-3, Proliferation and Induces Apoptosis through Multiple Signalling Pathways (MAPKs, PI3K/Akt, NFκB, and Hypoxia). |
| Q49887032 | Physiological Mitochondrial Fragmentation Is a Normal Cardiac Adaptation to Increased Energy Demand. |
| Q38587871 | Physiological roles of mitochondrial fission in cultured cells and mouse development |
| Q27935689 | Pir1p mediates translocation of the yeast Apn1p endonuclease into the mitochondria to maintain genomic stability |
| Q92665725 | Polycystic ovary syndrome and mitochondrial dysfunction |
| Q33604703 | Polymorphisms in the mitochondrial DNA control region and frailty in older adults |
| Q44602602 | Possible antioxidant and neuroprotective mechanisms of FK506 in attenuating haloperidol-induced orofacial dyskinesia |
| Q24338278 | Possible existence of lysosome-like organella within mitochondria and its role in mitochondrial quality control |
| Q44248025 | Postlipopolysaccharide oxidative damage of mitochondrial DNA. |
| Q79154601 | Potential clinical applications using stem cells derived from human umbilical cord blood |
| Q36700182 | Power and SNP tagging in whole mitochondrial genome association studies |
| Q98291826 | Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study |
| Q36103197 | Preimplantation death of xenomitochondrial mouse embryo harbouring bovine mitochondria |
| Q50761333 | Prevention of apoptosis by deferoxamine during 4 hours of cold cardioplegia and reperfusion: in vitro study of isolated working rat heart model. |
| Q40900379 | Prevention of neurodegeneration by a neuroprotective radical scavenger |
| Q26797996 | Primer removal during mammalian mitochondrial DNA replication |
| Q39753791 | Pro-oxidant properties of AZT and other thymidine analogues in macrophages: implication of the azido moiety in oxidative stress |
| Q80341733 | Proliferation of mitochondria in chronically stimulated rabbit skeletal muscle--transcription of mitochondrial genes and copy number of mitochondrial DNA |
| Q35117918 | Prooxidant properties of p66shc are mediated by mitochondria in human cells |
| Q43593930 | Protective effect of carvedilol on chenodeoxycholate induction of the permeability transition pore. |
| Q90699227 | Protective effect of theaflavin on glycoprotein components and TCA cycle enzymes in high-fat diet and streptozotocin-induced diabetic rats |
| Q36387714 | Protective effects of sirtuins in cardiovascular diseases: from bench to bedside |
| Q38359199 | Protective role of melatonin in mitochondrial dysfunction and related disorders |
| Q33690022 | Proteogenomics Reveals Enriched Ribosome Assembly and Protein Translation in Pectoralis major of High Feed Efficiency Pedigree Broiler Males. |
| Q44280967 | Proteome analysis reveals phosphorylation of ATP synthase beta -subunit in human skeletal muscle and proteins with potential roles in type 2 diabetes. |
| Q44417232 | Proteomic Consequences of a Human Mitochondrial tRNA Mutation beyond the Frame of Mitochondrial Translation |
| Q54687587 | Proteomic analysis of cancer-cell mitochondria |
| Q42065903 | Proteomic analysis of mitochondrial protein turnover: identification of novel substrate proteins of the matrix protease pim1. |
| Q53241728 | Proteomic approaches in understanding a detected relationship between chemotherapy-induced nephrotoxicity and cell respiration in HK-2 cells. |
| Q33947294 | Proteomic method identifies proteins nitrated in vivo during inflammatory challenge |
| Q33799381 | Proteomic survey towards the tissue-specific proteins of mouse mitochondria |
| Q35241298 | Proteomics in neurodegenerative diseases: Methods for obtaining a closer look at the neuronal proteome |
| Q58857942 | Proteomics in the Systems-Level Study of the Metabolic Syndrome |
| Q36591226 | Psychiatric symptoms correlate with metabolic indices in the hippocampus and cingulate in patients with mitochondrial disorders. |
| Q36595558 | Purity matters: A workflow for the valid high-resolution lipid profiling of mitochondria from cell culture samples |
| Q42277191 | Quality control of mitochondria during aging: is there a good and a bad side of mitochondrial dynamics? |
| Q26862395 | Quality matters: how does mitochondrial network dynamics and quality control impact on mtDNA integrity? |
| Q48445579 | Quantification of oxygen metabolic rates in Human brain with dynamic 17 O MRI: Profile likelihood analysis. |
| Q48324144 | Quantification of total mitochondrial DNA and mitochondrial common deletion in the frontal cortex of patients with schizophrenia and bipolar disorder |
| Q39016138 | Quantitative PCR-based measurement of nuclear and mitochondrial DNA damage and repair in mammalian cells. |
| Q73606018 | Quantitative plasmid mixture analysis using the fluorogenic 5'-nuclease polymerase chain reaction assay |
| Q34264482 | RNA delivery into mitochondria |
| Q28586228 | RNA silencing of mitochondrial m-Nfs1 reduces Fe-S enzyme activity both in mitochondria and cytosol of mammalian cells |
| Q40636632 | Radiation protection of HepG2 cells by Podophyllum hexandrum Royale |
| Q36955833 | Radical-free biology of oxidative stress |
| Q39413342 | Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age. |
| Q36025504 | Rapid mitochondrial DNA segregation in primate preimplantation embryos precedes somatic and germline bottleneck |
| Q34156841 | Re-engineering the mitochondrial genomes in mammalian cells |
| Q26851203 | Reactive oxygen species in health and disease |
| Q36459995 | Reactive oxygen species-mediated mitochondria-to-nucleus signaling: a key to aging and radical-caused diseases |
| Q26821921 | Receptor-mediated mitophagy in yeast and mammalian systems |
| Q38282362 | Recovery of hibernating myocardium: what is the role of surgical revascularization? |
| Q88930712 | Redox Equivalents and Mitochondrial Bioenergetics |
| Q36646486 | Redox control of leukemia: from molecular mechanisms to therapeutic opportunities |
| Q37446110 | Redox signaling in cardiovascular health and disease. |
| Q28582920 | Reduced activity of mtTFA decreases the transcription in mitochondria isolated from diabetic rat heart |
| Q55172169 | Reduction of the ATPase inhibitory factor 1 (IF1) leads to visual impairment in vertebrates. |
| Q33208704 | Regulating cell survival by controlling cellular energy production: novel functions for ancient signaling pathways? |
| Q24296720 | Regulation of cytochrome c oxidase activity by c-Src in osteoclasts |
| Q33531334 | Regulation of metabolism in Caenorhabditis elegans longevity |
| Q38034936 | Regulation of metastasis; mitochondrial DNA mutations have appeared on stage |
| Q34119796 | Regulation of mitochondrial biogenesis |
| Q35213424 | Regulation of mitochondrial biogenesis in muscle by endurance exercise |
| Q53392996 | Relation of functional and morphological changes in mitochondria to myocardial contractile and relaxation reserves in asymptomatic to mildly symptomatic patients with hypertrophic cardiomyopathy. |
| Q37344137 | Renal angiotensin II type 1 receptor expression and associated hypertension in rats with minimal SHR nuclear genome |
| Q34167978 | Repair of 8-oxoG is slower in endogenous nuclear genes than in mitochondrial DNA and is without strand bias. |
| Q34583753 | Replication and preferential inheritance of hypersuppressive petite mitochondrial DNA. |
| Q33873936 | Reproductive biotechnology and "big" biological questions |
| Q44195721 | Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy |
| Q39347930 | Resolution of mitochondrial oxidative stress rescues coronary collateral growth in Zucker obese fatty rats. |
| Q51766326 | Resolving the Enigma of the Clonal Expansion of mtDNA Deletions. |
| Q43207647 | Respiration in adipocytes is inhibited by reactive oxygen species |
| Q40601891 | Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation |
| Q43672495 | Restoration of Ca2+-inhibited oxidative phosphorylation in cardiac mitochondria by mitochondrial Ca2+ unloading |
| Q34662316 | Retinal Function and Structure in Ant1-Deficient Mice |
| Q49632281 | Retinal energy demands control vascular supply of the retina in development and disease: The role of neuronal lipid and glucose metabolism. |
| Q34808624 | Retinal ganglion cell disorders: types and treatments |
| Q33805623 | Reverse genetic studies of mitochondrial DNA-based diseases using a mouse model |
| Q33705828 | Revolution in mitochondrial medicine |
| Q42369764 | Role of Cardiolipin in Mitochondrial Signaling Pathways |
| Q58599968 | Role of GTPases in the Regulation of Mitochondrial Dynamics in Alzheimer's Disease and CNS-Related Disorders |
| Q41070215 | Role of mitochondrial DNA damage and dysfunction in veterans with Gulf War Illness. |
| Q34976262 | Role of mitochondrial dysfunction in Alzheimer's disease |
| Q38824997 | Role of the mitochondrial DNA replication machinery in mitochondrial DNA mutagenesis, aging and age-related diseases |
| Q35625434 | Role of vascular hypoperfusion-induced oxidative stress and mitochondria failure in the pathogenesis of Azheimer disease |
| Q38917412 | Roles of mitophagy in cellular physiology and development |
| Q55007822 | Rotenone ameliorates chronic renal injury caused by acute ischemia/reperfusion. |
| Q34033183 | Rotenone remarkably attenuates oxidative stress, inflammation, and fibrosis in chronic obstructive uropathy |
| Q44840186 | SOCS2 inhibited mitochondria biogenesis via inhibiting p38 MAPK/ATF2 pathway in C2C12 cells |
| Q33822264 | SOD2 deficient erythroid cells up-regulate transferrin receptor and down-regulate mitochondrial biogenesis and metabolism |
| Q34049463 | SOD2 protects against oxidation-induced apoptosis in mouse retinal pigment epithelium: implications for age-related macular degeneration |
| Q38957347 | Schwann cell mitochondria as key regulators in the development and maintenance of peripheral nerve axons |
| Q44512801 | Screening and comparison of antioxidant activity of solvent extracts of herbal medicines used in Korea |
| Q88930281 | Sdha+/- Rats Display Minimal Muscle Pathology Without Significant Behavioral or Biochemical Abnormalities |
| Q34363047 | Search for characteristic structural features of mammalian mitochondrial tRNAs. |
| Q33843176 | Secondary carnitine deficiency and impaired docosahexaenoic (22:6n-3) acid synthesis: a common denominator in the pathophysiology of diseases of oxidative phosphorylation and beta-oxidation |
| Q37066699 | Selection by drug resistance proteins located in the mitochondria of mammalian cells |
| Q45869262 | Selective DNA release from DQAsome/DNA complexes at mitochondria-like membranes |
| Q36777340 | Selective imaging of mitochondrial surfaces with novel fluorescent probes |
| Q47616286 | Sequence polymorphism in the coding region of mitochondrial genome encompassing position 8389-8865. |
| Q83047794 | Sequence polymorphisms of the mtDNA control region in a human isolate: the Georgians from Swanetia |
| Q35012267 | Sequence variation and the biological function of genes: methodological and biological considerations |
| Q43564487 | Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chain |
| Q50059988 | Sequencing and analysis of the whole genome of Indian Gujarati male. |
| Q46040648 | Sequencing and comparing whole mitochondrial genomes of animals |
| Q49920428 | Serine Catabolism by SHMT2 Is Required for Proper Mitochondrial Translation Initiation and Maintenance of Formylmethionyl-tRNAs. |
| Q35006906 | Sexual dimorphism in the expression of mitochondria-related genes in rat heart at different ages |
| Q64229710 | Shortage of Cellular ATP as a Cause of Diseases and Strategies to Enhance ATP |
| Q40394633 | Signal transduction to mitochondrial ATP synthase: evidence that PDGF-dependent phosphorylation of the delta-subunit occurs in several cell lines, involves tyrosine, and is modulated by lysophosphatidic acid |
| Q73205704 | Simultaneous detection of mitochondrial respiratory chain activity and reactive oxygen in digitonin-permeabilized cells using flow cytometry |
| Q51133421 | Simultaneous fluorescence visualization of mitochondrial hydrogen peroxide and zinc ions in live cells and in vivo. |
| Q28242165 | Single nucleotide polymorphisms over the entire mtDNA genome that increase the power of forensic testing in Caucasians |
| Q38137835 | Single-nucleotide polymorphisms of GPX1 and MnSOD and susceptibility to bladder cancer: a systematic review and meta-analysis |
| Q35420953 | Site-specific proteomic analysis of lipoxidation adducts in cardiac mitochondria reveals chemical diversity of 2-alkenal adduction |
| Q34614061 | Sls1p is a membrane-bound regulator of transcription-coupled processes involved in Saccharomyces cerevisiae mitochondrial gene expression |
| Q34739211 | So close and yet so far: mitochondria and peroxisomes are one but with specific talents. |
| Q46265496 | Social Origins of Developmental Risk for Mental and Physical Illness. |
| Q47862133 | Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours |
| Q79108457 | Somatic mitochondrial DNA mutations in adult-onset leukaemia |
| Q64134314 | Somatic mitochondrial DNA mutations in primary and metastatic ovarian cancer |
| Q37736575 | Species identification through mitochondrial rRNA genetic analysis. |
| Q30501631 | Specific biomarkers for stochastic division patterns and starvation-induced quiescence under limited glucose levels in fission yeast |
| Q36069084 | Specific mitochondrial DNA mutation in mice regulates diabetes and lymphoma development |
| Q36918606 | Specific polymorphic variation in the mitochondrial genome and increased in-hospital mortality after severe trauma |
| Q44489239 | Specific targeting of a DNA-alkylating reagent to mitochondria. Synthesis and characterization of [4-((11aS)-7-methoxy-1,2,3,11a-tetrahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-on-8-oxy)butyl]-triphenylphosphonium iodide |
| Q57688071 | Specificity of mtDNA-directed PCR—influence of NUclear MTDNA insertion (NUMT) contamination in routine samples and techniques |
| Q49971097 | Spectral properties of ionic benzotristhiazole based donor-acceptor NLO-phores in polymer matrices and their one- and two-photon cellular imaging ability. |
| Q56689113 | Sperm Mitochondrial Mutations as a Cause of Low Sperm Motility |
| Q36414411 | Stability of the mitochondrial genome requires an amino-terminal domain of yeast mitochondrial RNA polymerase |
| Q35131099 | Stable heteroplasmy at the single-cell level is facilitated by intercellular exchange of mtDNA. |
| Q27077073 | Starvation induced cell death in autophagy-defective yeast mutants is caused by mitochondria dysfunction |
| Q30451005 | Stem cell-based models and therapies for neurodegenerative diseases |
| Q34478955 | Stochastic modelling, Bayesian inference, and new in vivo measurements elucidate the debated mtDNA bottleneck mechanism. |
| Q28272479 | Structure-function defects of human mitochondrial DNA polymerase in autosomal dominant progressive external ophthalmoplegia |
| Q47667899 | Subcellular Fractionation for DIGE-Based Proteomics |
| Q37136773 | Sulfiredoxin Translocation into Mitochondria Plays a Crucial Role in Reducing Hyperoxidized Peroxiredoxin III. |
| Q28397283 | Sulfite Oxidase Activity of Cytochrome c: Role of Hydrogen Peroxide |
| Q44583900 | Superoxide activates uncoupling proteins by generating carbon-centered radicals and initiating lipid peroxidation: studies using a mitochondria-targeted spin trap derived from alpha-phenyl-N-tert-butylnitrone. |
| Q45857435 | Suppression of disease phenotypes of adult mito-mice carrying pathogenic mtDNA by bone marrow transplantation. |
| Q36642278 | Suppression of manganese superoxide dismutase augments sensitivity to radiation, hyperthermia and doxorubicin in colon cancer cell lines by inducing apoptosis |
| Q34217027 | Surface conjugation of triphenylphosphonium to target poly(amidoamine) dendrimers to mitochondria |
| Q41352849 | Surface modification of liposomes with rhodamine-123-conjugated polymer results in enhanced mitochondrial targeting |
| Q34416995 | Surveyor Nuclease: a new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defects. |
| Q36530909 | Synergistic Effects of Cilostazol and Probucol on ER Stress-Induced Hepatic Steatosis via Heme Oxygenase-1-Dependent Activation of Mitochondrial Biogenesis |
| Q46438642 | Synthesis and characterization of a triphenylphosphonium-conjugated peroxidase mimetic. Insights into the interaction of ebselen with mitochondria. |
| Q42591986 | Synthesis of a mitochondria-targeted spin trap using a novel Parham-type cyclization. |
| Q41188746 | Synthesis of triphenylphosphonium vitamin E derivatives as mitochondria-targeted antioxidants |
| Q29617873 | Systematic screen for human disease genes in yeast |
| Q37030590 | Systematic screens for human disease genes, from yeast to human and back |
| Q92309378 | Systemic Lupus Erythematosus: Pathogenesis at the Functional Limit of Redox Homeostasis |
| Q34339371 | TAT opens the door |
| Q64883288 | TEFM regulates both transcription elongation and RNA processing in mitochondria. |
| Q38802165 | TUFM downregulation induces epithelial-mesenchymal transition and invasion in lung cancer cells via a mechanism involving AMPK-GSK3β signaling |
| Q48760407 | Tacrine and its analogues impair mitochondrial function and bioenergetics: a lipidomic analysis in rat brain. |
| Q51067188 | Targetable phosphorescent oxygen nanosensors for the assessment of tumor mitochondrial dysfunction by monitoring the respiratory activity. |
| Q43963405 | Targeted myocardial transgenic expression of HIV Tat causes cardiomyopathy and mitochondrial damage. |
| Q55017371 | Targeting Mitochondrial Bioenergetics as a Therapeutic Strategy for Chronic Lymphocytic Leukemia. |
| Q38622293 | Targeting autophagy and mitophagy for mitochondrial diseases treatment. |
| Q46774788 | Targeting human 8-oxoguanine DNA glycosylase to mitochondria protects cells from 2-methoxyestradiol-induced-mitochondria-dependent apoptosis |
| Q34264476 | Targeting large molecules to mitochondria |
| Q81110470 | Targeting of tRNA into yeast and human mitochondria: the role of anticodon nucleotides |
| Q37049208 | Targeting peptide nucleic acid (PNA) oligomers to mitochondria within cells by conjugation to lipophilic cations: implications for mitochondrial DNA replication, expression and disease |
| Q44624372 | Targeting proteins to mitochondria using TAT. |
| Q46453448 | Targeting the NAD7 subunit to mitochondria restores a functional complex I and a wild type phenotype in the Nicotiana sylvestris CMS II mutant lacking nad7. |
| Q43632344 | The (Holey) study of mitochondria in apoptosis |
| Q35137172 | The Broad Impact of TOM40 on Neurodegenerative Diseases in Aging |
| Q36228346 | The Degradation Pathway of the Mitophagy Receptor Atg32 Is Re-Routed by a Posttranslational Modification |
| Q38945146 | The Mitochondrial Permeability Transition Pore and ATP Synthase. |
| Q34879429 | The Mitoscriptome in Aging and Disease. |
| Q24543580 | The PET1-CMS mitochondrial mutation in sunflower is associated with premature programmed cell death and cytochrome c release |
| Q90568414 | The Role of Mitochondria in the Mechanisms of Cardiac Ischemia-Reperfusion Injury |
| Q60695086 | The T9176G mutation of human mtDNA gives a fully assembled but inactive ATP synthase when modeled in Escherichia coli |
| Q28661634 | The Trojan female technique: a novel, effective and humane approach for pest population control |
| Q35127771 | The Use of Denaturing High-Performance Liquid Chromatography (DHPLC) for the Analysis of Genetic Variations: Impact for Diagnostics and Pharmacogenetics |
| Q35926921 | The absence of a mitochondrial genome in rho0 yeast cells extends lifespan independently of retrograde regulation |
| Q28754651 | The adaptive evolution of the mammalian mitochondrial genome |
| Q33826111 | The age-related accumulation of a mitochondrial DNA control region mutation in muscle, but not brain, detected by a sensitive PNA-directed PCR clamping based method |
| Q24618241 | The complete sequence of the zebrafish (Danio rerio) mitochondrial genome and evolutionary patterns in vertebrate mitochondrial DNA |
| Q33655973 | The costs of being male: are there sex-specific effects of uniparental mitochondrial inheritance? |
| Q36470441 | The creation of cybrids harboring mitochondrial haplogroups in the Taiwanese population of ethnic Chinese background: an extensive in vitro tool for the study of mitochondrial genomic variations |
| Q35083432 | The dynamin-related GTPase Opa1 is required for glucose-stimulated ATP production in pancreatic beta cells |
| Q34380418 | The effect of citrulline and arginine supplementation on lactic acidemia in MELAS syndrome |
| Q42427505 | The effect of mitochondrial dysfunction on cytosolic nucleotide metabolism |
| Q39625453 | The effects of antidepressants on mitochondrial function in a model cell system and isolated mitochondria. |
| Q44651953 | The effects of nuclear reprogramming on mitochondrial DNA replication. |
| Q33904974 | The emergence of modern neuroscience: some implications for neurology and psychiatry |
| Q38866179 | The evolution and role of mitochondrial fusion and fission in aging and disease |
| Q55039234 | The evolutionary processes of mitochondrial and chloroplast genomes differ from those of nuclear genomes. |
| Q35948562 | The formation and functional consequences of heterogeneous mitochondrial distributions in skeletal muscle |
| Q34237999 | The genetics and pathology of oxidative phosphorylation |
| Q37142417 | The genetics you never knew: a genetics primer |
| Q24291646 | The human mitochondrial ribosomal protein genes: mapping of 54 genes to the chromosomes and implications for human disorders |
| Q34974582 | The importance of mitochondrial DNA in aging and cancer |
| Q39182036 | The induction of mitochondria-mediated apoptosis in cancer cells by ruthenium(II) asymmetric complexes |
| Q73179332 | The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both? |
| Q24623671 | The innate immune system in host mice targets cells with allogenic mitochondrial DNA |
| Q24546038 | The mechanism of superoxide production by NADH:ubiquinone oxidoreductase (complex I) from bovine heart mitochondria |
| Q37651211 | The mitochondrial DNA polymerase in health and disease. |
| Q33813322 | The mitochondrial T16189C polymorphism is associated with coronary artery disease in Middle European populations |
| Q34442309 | The mitochondrial genome and mitochondrial muscle disorders. |
| Q38034189 | The mitochondrial genome and psychiatric illness |
| Q28681826 | The mitochondrial genome encodes abundant small noncoding RNAs |
| Q36844086 | The mitochondrial genome sequence of Mus terricolor: comparison with Mus musculus domesticus and implications for xenomitochondrial mouse modeling. |
| Q22010971 | The mitochondrial p55 accessory subunit of human DNA polymerase gamma enhances DNA binding, promotes processive DNA synthesis, and confers N-ethylmaleimide resistance |
| Q80761703 | The mitochondrial pharmacogenomics of haplogroup T: MTND2*LHON4917G and antiretroviral therapy-associated peripheral neuropathy |
| Q30480776 | The mitochondrial respiratory chain controls intracellular calcium signaling and NFAT activity essential for heart formation in Xenopus laevis |
| Q43873241 | The mitochondrial toxin 3-nitropropionic acid aggravates reserpine-induced oral dyskinesia in rats |
| Q36693924 | The mitochondrion as a primary site of action of regulatory agents involved in neuroimmunomodulation. |
| Q33829445 | The molecular diagnosis of metabolic myopathies |
| Q37684132 | The multiple mechanisms of cell death triggered by resveratrol in lymphoma and leukemia |
| Q34338783 | The neuro-ophthalmology of mitochondrial disease |
| Q33870484 | The neurogenic basic helix-loop-helix transcription factor NeuroD6 confers tolerance to oxidative stress by triggering an antioxidant response and sustaining the mitochondrial biomass. |
| Q43887789 | The nuclear genome is involved in heteroplasmy control in a mitochondrial mutant strain of Drosophila subobscura |
| Q34562809 | The organization and inheritance of the mitochondrial genome |
| Q35647363 | The potential risks of abnormal transmission of mtDNA through assisted reproductive technologies. |
| Q37418894 | The power of yeast to model diseases of the powerhouse of the cell. |
| Q93000726 | The primitive growth factor NME7AB induces mitochondrially active naïve-like pluripotent stem cells |
| Q27653963 | The proteome of Saccharomyces cerevisiae mitochondria |
| Q35019244 | The role of maternal mitochondria during oogenesis, fertilization and embryogenesis |
| Q37606811 | The role of mitochondria in health and disease |
| Q37878430 | The role of mitochondria in neurodegenerative diseases |
| Q37825773 | The role of mitochondria in osteoarthritis |
| Q35174458 | The role of mitochondria in the life of the nematode, Caenorhabditis elegans |
| Q36910241 | The role of mitochondrial DNA mutations and free radicals in disease and ageing |
| Q34327375 | The role of mitochondrial genome in essential hypertension in a Chinese Han population |
| Q28509993 | The role of mitochondrial porins and the permeability transition pore in learning and synaptic plasticity |
| Q24595895 | The role of the TIM8-13 complex in the import of Tim23 into mitochondria |
| Q34591630 | The role of the mitochondrial genome in ageing and carcinogenesis |
| Q89791052 | The spatio-temporal features of chicken mitochondrial ND2 gene heteroplasmy and the effects of nutrition factors on this gene |
| Q33927048 | The strength and timing of the mitochondrial bottleneck in salmon suggests a conserved mechanism in vertebrates |
| Q38152284 | The systems biology of mitochondrial fission and fusion and implications for disease and aging |
| Q48328769 | The typically mitochondrial DNA-encoded ATP6 subunit of the F1F0-ATPase is encoded by a nuclear gene in Chlamydomonas reinhardtii |
| Q37915809 | The use of individual patient's fibroblasts in the search for personalized treatment of nuclear encoded OXPHOS diseases. |
| Q36707801 | The use of micromanipulation methods as a tool to prevention of transmission of mutated mitochondrial DNA. |
| Q40663427 | The yeast counterparts of human 'MELAS' mutations cause mitochondrial dysfunction that can be rescued by overexpression of the mitochondrial translation factor EF-Tu. |
| Q38793825 | Therapeutic Potential of Resveratrol in Lymphoid Malignancies. |
| Q59793891 | Therapeutic potential of the mitochondria-targeted antioxidant MitoQ in mitochondrial-ROS induced sensorineural hearing loss caused by Idh2 deficiency |
| Q36505451 | Thymidine analogues suppress autophagy and adipogenesis in cultured adipocytes |
| Q45230300 | Time-course of mitochondrial gene expressions in mice brains: implications for mitochondrial dysfunction, oxidative damage, and cytochrome c in aging |
| Q40420581 | To use MIBI or not to use MIBI? That is the question when assessing tumour cells |
| Q28649774 | Toward a mtDNA locus-specific mutation database using the LOVD platform |
| Q34265156 | Towards mitochondrial gene therapy: DQAsomes as a strategy |
| Q44428732 | Towards understanding human mitochondrial leucine aminoacylation identity. |
| Q51126217 | Toxicity of new emerging pollutant tris-(2,3-dibromopropyl) isocyanurate on BALB/c mice. |
| Q36633152 | Trace amounts of 8-oxo-dGTP in mitochondrial dNTP pools reduce DNA polymerase gamma replication fidelity. |
| Q43138065 | Trading mtDNA uncovers its role in metastasis. |
| Q51686616 | Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mitochondrial diseases. |
| Q35923008 | Transcriptional control of cardiac fuel metabolism and mitochondrial function |
| Q37030759 | Transcriptional quiescence of paternal mtDNA in cyprinid fish embryos |
| Q24532032 | Transformation of isolated mammalian mitochondria by bacterial conjugation |
| Q37358162 | Transient oxidative stress damages mitochondrial machinery inducing persistent beta-cell dysfunction |
| Q52115273 | Transmission of the mitochondrial t8993c mutation in a new family. |
| Q37612665 | Transmitochondrial mice as models for primary prevention of diseases caused by mutation in the tRNA(Lys) gene |
| Q35912030 | Transmitochondrial mice: proof of principle and promises |
| Q24200432 | Treatment for mitochondrial disorders |
| Q24244543 | Treatment for mitochondrial disorders |
| Q24247852 | Treatment for mitochondrial myopathy |
| Q46489599 | Troxerutin attenuates diet-induced oxidative stress, impairment of mitochondrial biogenesis and respiratory chain complexes in mice heart |
| Q36619848 | Two-dimensional intact mitochondrial DNA agarose electrophoresis reveals the structural complexity of the mammalian mitochondrial genome. |
| Q30833030 | Two-photon fluorescence spectroscopy and microscopy of NAD(P)H and flavoprotein |
| Q52319318 | Tying Trafficking to Fusion and Fission at the Mighty Mitochondria. |
| Q52971206 | Tyrosine-derived stimuli responsive, fluorescent amino acids. |
| Q40218393 | UV-irradiation induces oxidative damage to mitochondrial DNA primarily through hydrogen peroxide: analysis of 8-oxodGuo by HPLC. |
| Q50488724 | UVB irradiation as a tool to assess ROS-induced damage in human spermatozoa. |
| Q35004513 | Ultra-sensitive sequencing reveals an age-related increase in somatic mitochondrial mutations that are inconsistent with oxidative damage |
| Q37049152 | Ultrastructural definition of apoptosis in heart failure |
| Q44530003 | Ultrastructure of the gingiva in cardiac patients treated with or without calcium channel blockers |
| Q42733812 | Uncoupling protein 1 decreases superoxide production in brown adipose tissue mitochondria |
| Q34035403 | Uncoupling protein 2 plays an important role in nitric oxide production of lipopolysaccharide-stimulated macrophages |
| Q37198638 | Unique quadruple immunofluorescence assay demonstrates mitochondrial respiratory chain dysfunction in osteoblasts of aged and PolgA(-/-) mice |
| Q33567299 | Up-regulation of avian uncoupling protein in cold-acclimated and hyperthyroid ducklings prevents reactive oxygen species production by skeletal muscle mitochondria |
| Q46555077 | Upregulation of matrix metalloproteinase 1 and disruption of mitochondrial network in skin fibroblasts of patients with MERRF syndrome |
| Q27940072 | Uracil-DNA glycosylase-deficient yeast exhibit a mitochondrial mutator phenotype |
| Q45297227 | Usage of mitochondrial D-loop variation to predict risk for Huntington disease. |
| Q46160383 | Use of the NADH-quinone oxidoreductase (NDI1) gene of Saccharomyces cerevisiae as a possible cure for complex I defects in human cells |
| Q42036779 | Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia |
| Q36309165 | Variations of mitochondrial D-loop region plus downstream gene 1 2S rRNA-tRNA(phe) and gastric carcinomas |
| Q38714209 | Viral symbiosis and the holobiontic nature of the human genome |
| Q37676789 | Vitrification of in vitro matured oocytes: effects on meiotic spindle configuration and mitochondrial function |
| Q33655960 | What cost mitochondria? The maintenance of functional mitochondrial DNA within and across generations. |
| Q64228827 | When a common biological role does not imply common disease outcomes: Disparate pathology linked to human mitochondrial aminoacyl-tRNA synthetases |
| Q29615672 | Why do we age? |
| Q34422404 | Xenomitochondrial mice: investigation into mitochondrial compensatory mechanisms |
| Q34136226 | Yeast mitochondrial dynamics: fusion, division, segregation, and shape |
| Q73587274 | [Mitochondrial diseases: still a difficult diagnosis] |
| Q48165533 | iPSCs, a Future Tool for Therapeutic Intervention in Mitochondrial Disorders: Pros and Cons. |
| Q37164369 | miRNAs in mtDNA-less cell mitochondria |
| Q34101830 | mtDNA haplogroup J modulates telomere length and nitric oxide production |
| Q34574948 | mtDNA phylogeny and evolution of laboratory mouse strains |
| Q35875202 | mtDNA variation, climatic adaptation, degenerative diseases, and longevity |
| Q34318143 | tRNA and cytochrome c in cell death and beyond. |
| Q26740355 | Generation of reactive oxygen species in the anterior eye segment. Synergistic codrugs of N-acetylcarnosine lubricant eye drops and mitochondria-targeted antioxidant act as a powerful therapeutic platform for the treatment of cataracts and primary o |
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