scholarly article | Q13442814 |
P2093 | author name string | Sarika Srivastava | |
Carlos T Moraes | |||
John N Barrett | |||
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Multiple environmental and genetic factors influence skeletal muscle PGC-1alpha and PGC-1beta gene expression in twins | Q24561604 | ||
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 | ||
A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis | Q27860471 | ||
Cloning and characterization of COX14, whose product is required for assembly of yeast cytochrome oxidase | Q27933346 | ||
COX15 codes for a mitochondrial protein essential for the assembly of yeast cytochrome oxidase | Q27935360 | ||
SHY1, the yeast homolog of the mammalian SURF-1 gene, encodes a mitochondrial protein required for respiration | Q27939004 | ||
A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy | Q28118731 | ||
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Facile detection of mitochondrial DNA mutations in tumors and bodily fluids | Q28138849 | ||
Peroxisome proliferator-activated receptor gamma coactivator 1beta (PGC-1beta ), a novel PGC-1-related transcription coactivator associated with host cell factor | Q28208668 | ||
Control of hepatic gluconeogenesis through the transcriptional coactivator PGC-1 | Q28216275 | ||
Peroxisome proliferator-activated receptor gamma coactivator 1 coactivators, energy homeostasis, and metabolism | Q28266830 | ||
Mitochondria-to-nucleus stress signaling induces phenotypic changes, tumor progression and cell invasion | Q28362221 | ||
The mtDNA-encoded ND6 subunit of mitochondrial NADH dehydrogenase is essential for the assembly of the membrane arm and the respiratory function of the enzyme | Q28368398 | ||
PGC-1beta in the regulation of hepatic glucose and energy metabolism | Q28566796 | ||
Pattern of organization of human mitochondrial pseudogenes in the nuclear genome | Q28768380 | ||
Transcriptional co-activator PGC-1 alpha drives the formation of slow-twitch muscle fibres | Q29555845 | ||
Suppression of reactive oxygen species and neurodegeneration by the PGC-1 transcriptional coactivators | Q29617353 | ||
mtDNA mutations increase tumorigenicity in prostate cancer | Q33757050 | ||
Transcriptional activators and coactivators in the nuclear control of mitochondrial function in mammalian cells | Q34122975 | ||
Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA. | Q34386122 | ||
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV. | Q34390115 | ||
Somatic mutations of the mitochondrial genome in human colorectal tumours | Q34478926 | ||
Bcl-xL promotes the open configuration of the voltage-dependent anion channel and metabolite passage through the outer mitochondrial membrane | Q34647032 | ||
The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle | Q35195556 | ||
Transcriptional regulatory circuits controlling mitochondrial biogenesis and function | Q35683727 | ||
Mitochondrial DNA mutations in human cancer | Q36557982 | ||
Oxidative phosphorylation dysfunction modulates expression of extracellular matrix--remodeling genes and invasion | Q37423893 | ||
Peroxisome proliferator-activated receptor gamma coactivator-1 promotes cardiac mitochondrial biogenesis | Q37526796 | ||
Tight control of respiration by NADH dehydrogenase ND5 subunit gene expression in mouse mitochondria | Q39450692 | ||
Efficient selection and characterization of mutants of a human cell line which are defective in mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase | Q40021624 | ||
A disease-associated G5703A mutation in human mitochondrial DNA causes a conformational change and a marked decrease in steady-state levels of mitochondrial tRNA(Asn). | Q40023968 | ||
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III. | Q40267043 | ||
Nuclear suppression of mitochondrial defects in cells without the ND6 subunit | Q40326435 | ||
Bioenergetic analysis of peroxisome proliferator-activated receptor gamma coactivators 1alpha and 1beta (PGC-1alpha and PGC-1beta) in muscle cells | Q40649634 | ||
In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I. | Q40775533 | ||
Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background | Q40953651 | ||
Low reserve of cytochrome c oxidase capacity in vivo in the respiratory chain of a variety of human cell types. | Q40993797 | ||
In vivo labeling and analysis of human mitochondrial translation products | Q41244321 | ||
The kinetic basis of threshold effects observed in mitochondrial diseases: a systemic approach | Q42173118 | ||
Sequential serum-dependent activation of CREB and NRF-1 leads to enhanced mitochondrial respiration through the induction of cytochrome c. | Q42802810 | ||
Endogenous oxygen radicals modulate protein tyrosine phosphorylation and JNK-1 activation in lectin-stimulated thymocytes. | Q42996261 | ||
Mitochondrial stress-induced calcium signaling, phenotypic changes and invasive behavior in human lung carcinoma A549 cells | Q44208147 | ||
BCL-2 improves oxidative phosphorylation and modulates adenine nucleotide translocation in mitochondria of cells harboring mutant mtDNA. | Q44216665 | ||
The signal for a leaky UAG stop codon in several plant viruses includes the two downstream codons | Q44362876 | ||
Frameshifting in the synthesis of Escherichia coli polypeptide chain release factor two on eukaryotic ribosomes | Q44798061 | ||
Bcl-2 and the outer mitochondrial membrane in the inactivation of cytochrome c during Fas-mediated apoptosis | Q46500722 | ||
Positive contribution of pathogenic mutations in the mitochondrial genome to the promotion of cancer by prevention from apoptosis | Q47836751 | ||
Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours | Q47862133 | ||
Low mitochondrial respiratory chain content correlates with tumor aggressiveness in renal cell carcinoma. | Q51716676 | ||
Control of oxidative phosphorylation in rat muscle mitochondria: implications for mitochondrial myopathies. | Q52545278 | ||
Lack of oxidative phosphorylation and low mitochondrial membrane potential decrease susceptibility to apoptosis and do not modulate the protective effect of Bcl-x(L) in osteosarcoma cells. | Q54060881 | ||
Extracellular ATP stimulates adenylyl cyclase and phospholipase C through distinct purinoceptors in NG108-15 cells. | Q55480924 | ||
Frameshifting at the internal stop codon within the mRNA for bacterial release factor-2 on eukaryotic ribosomes | Q68544849 | ||
Differential regulation of respiratory chain subunits by a CREB-dependent signal transduction pathway. Role of cyclic AMP in cytochrome c and COXIV gene expression | Q72695013 | ||
Mitochondrial DNA alteration in esophageal cancer | Q73721797 | ||
High incidence of somatic mitochondrial DNA mutations in human ovarian carcinomas | Q74379476 | ||
Regulation of mitochondrial biogenesis in skeletal muscle by CaMK | Q77932716 | ||
Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women | Q81158816 | ||
Nuclear respiratory factors and the pathways of nuclear-mitochondrial interaction | Q83200046 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | phosphorylation | Q242736 |
P304 | page(s) | 993-1005 | |
P577 | publication date | 2007-04-15 | |
P1433 | published in | Human Molecular Genetics | Q2720965 |
P1476 | title | PGC-1alpha/beta upregulation is associated with improved oxidative phosphorylation in cells harboring nonsense mtDNA mutations | |
P478 | volume | 16 |
Q35786077 | A method for mutagenesis of mouse mtDNA and a resource of mouse mtDNA mutations for modeling human pathological conditions |
Q37153804 | A role of mitochondrial complex II defects in genetic models of Huntington's disease expressing N-terminal fragments of mutant huntingtin |
Q47114888 | Alterations in PGC1α expression levels are involved in colorectal cancer risk: a qualitative systematic review. |
Q34904962 | An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells |
Q33772820 | Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression |
Q38743834 | Bromodomain Inhibitors Correct Bioenergetic Deficiency Caused by Mitochondrial Disease Complex I Mutations |
Q50597504 | Chapter 7 Tracing human mitochondrial complex I assembly by use of GFP-tagged subunits. |
Q39330883 | Contractile activity-induced mitochondrial biogenesis and mTORC1. |
Q51344073 | Current strategies towards therapeutic manipulation of mtDNA heteroplasmy. |
Q55008290 | Deciphering the Dichotomous Effects of PGC-1α on Tumorigenesis and Metastasis. |
Q39295659 | Defining the action spectrum of potential PGC-1α activators on a mitochondrial and cellular level in vivo |
Q53193157 | Effects of treadmill running and rutin on lipolytic signaling pathways and TRPV4 protein expression in the adipose tissue of diet-induced obese mice. |
Q26741300 | Emerging therapeutic roles for NAD(+) metabolism in mitochondrial and age-related disorders |
Q37094802 | Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular Atrophy. |
Q97093163 | Maternally inherited mitochondrial respiratory disorders: from pathogenetic principles to therapeutic implications |
Q34590193 | Mitochondrial biogenesis and turnover |
Q36771650 | Mitochondrial biogenesis: a therapeutic target for neurodevelopmental disorders and neurodegenerative diseases |
Q35632864 | Mitochondrial energetics and therapeutics |
Q36784219 | Nicotinamide riboside restores cognition through an upregulation of proliferator-activated receptor-γ coactivator 1α regulated β-secretase 1 degradation and mitochondrial gene expression in Alzheimer's mouse models |
Q37292951 | PGC-1alpha/beta induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders. |
Q28583359 | PGC-1{alpha} and PGC-1{beta} regulate mitochondrial density in neurons |
Q39586801 | PPARGC1B gene is associated with Kashin-Beck disease in Han Chinese |
Q53076500 | Peroxisome Proliferator-Activated Receptor γ and PGC-1α in Cancer: Dual Actions as Tumor Promoter and Suppressor. |
Q64068471 | Quantitative Variation in m.3243A > G Mutation Produce Discrete Changes in Energy Metabolism |
Q34390683 | Regulatory role of mitochondria in oxidative stress and atherosclerosis |
Q28301918 | Sequence homology at the breakpoint and clinical phenotype of mitochondrial DNA deletion syndromes |
Q37101634 | Suppression mechanisms of COX assembly defects in yeast and human: insights into the COX assembly process |
Q37394160 | Synthesis of cytochrome c oxidase subunit 1 is translationally downregulated in the absence of functional F1F0-ATP synthase |
Q33840188 | The role of PGC-1 coactivators in aging skeletal muscle and heart |
Q27317003 | X-linked intellectual disability gene CASK regulates postnatal brain growth in a non-cell autonomous manner |
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