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P50 | author | Jerzy Duszyński | Q19635956 |
Joanna Szczepanowska | Q60662489 | ||
Dominika Malińska | Q63363678 | ||
Mariusz R Wieckowski | Q38327644 | ||
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A forty-kilodalton protein of the inner membrane is the mitochondrial calcium uniporter | Q24306850 | ||
Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins. | Q24541558 | ||
Disruption of mitochondrial DNA replication in Drosophila increases mitochondrial fast axonal transport in vivo | Q27335303 | ||
The mtDNA T8993G (NARP) mutation results in an impairment of oxidative phosphorylation that can be improved by antioxidants | Q28248174 | ||
Patients with Leber hereditary optic neuropathy fail to compensate impaired oxidative phosphorylation | Q28261663 | ||
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Mitochondrial DNA rearrangements in young onset parkinsonism: two case reports | Q28362183 | ||
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Mitochondrial DNA-depleted neuroblastoma (Rho degrees) cells exhibit altered calcium signaling | Q30305575 | ||
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Altered mitochondrial structure and motion dynamics in living cells with energy metabolism defects revealed by real time microscope imaging | Q33205800 | ||
Mitochondrial mosaics in the liver of 3 infants with mtDNA defects | Q33461789 | ||
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Biochemical phenotypes associated with the mitochondrial ATP6 gene mutations at nt8993. | Q34637419 | ||
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Human extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber's hereditary optic neuropathy. | Q35593390 | ||
New insights into the bioenergetics of mitochondrial disorders using intracellular ATP reporters | Q35973374 | ||
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Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome | Q70323219 | ||
Increased activities of antioxidant enzymes and decreased ATP concentration in cultured myoblasts with the 3243A-->G mutation in mitochondrial DNA | Q73189920 | ||
An out-of-frame cytochrome b gene deletion from a patient with parkinsonism is associated with impaired complex III assembly and an increase in free radical production | Q73192853 | ||
Decreased ATP synthesis is phenotypically expressed during increased energy demand in fibroblasts containing mitochondrial tRNA mutations | Q77892921 | ||
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Calcium uptake by rat kidney mitochondria | Q36441249 | ||
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Oxidative stress, mitochondria and mtDNA-mutator mice | Q36663410 | ||
Mitochondrial control of calcium-channel gating: a mechanism for sustained signaling and transcriptional activation in T lymphocytes | Q37253977 | ||
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Multi-site control and regulation of mitochondrial energy production. | Q37708340 | ||
Mitochondrial DNA mutation-elicited oxidative stress, oxidative damage, and altered gene expression in cultured cells of patients with MERRF syndrome | Q37735748 | ||
Mitochondrial consumption of cytosolic ATP: not so fast. | Q37864389 | ||
Functional F1-ATPase essential in maintaining growth and membrane potential of human mitochondrial DNA-depleted rho degrees cells | Q38550417 | ||
The optimized allotopic expression of ND1 or ND4 genes restores respiratory chain complex I activity in fibroblasts harboring mutations in these genes | Q38914398 | ||
Effect of selenite on basic mitochondrial function in human osteosarcoma cells with chronic mitochondrial stress. | Q39509681 | ||
Antioxidant defence systems and generation of reactive oxygen species in osteosarcoma cells with defective mitochondria: effect of selenium | Q39742744 | ||
Mitochondrial ND5 gene variation associated with encephalomyopathy and mitochondrial ATP consumption | Q40067062 | ||
Impaired mitochondrial Ca2+ homeostasis in respiratory chain-deficient cells but efficient compensation of energetic disadvantage by enhanced anaerobic glycolysis due to low ATP steady state levels. | Q40131652 | ||
Mitochondrial bioenergetics and structural network organization | Q40171308 | ||
Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology | Q40227379 | ||
Involvement of protein kinase C delta in the alteration of mitochondrial mass in human cells under oxidative stress. | Q40265671 | ||
Diabetes-associated mitochondrial DNA mutation A3243G impairs cellular metabolic pathways necessary for beta cell function. | Q40273572 | ||
Enhanced ROS production and antioxidant defenses in cybrids harbouring mutations in mtDNA. | Q40373090 | ||
Influence of a mitochondrial genetic defect on capacitative calcium entry and mitochondrial organization in the osteosarcoma cells. | Q40482450 | ||
Antioxidant defences and homeostasis of reactive oxygen species in different human mitochondrial DNA-depleted cell lines. | Q40517974 | ||
Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines. | Q40519925 | ||
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations. | Q40523353 | ||
Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells | Q40749783 | ||
A calcium signaling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiency | Q40938846 | ||
Mitochondrial DNA background modifies the bioenergetics of NARP/MILS ATP6 mutant cells | Q42010130 | ||
Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations. | Q42077715 | ||
Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA. | Q42533734 | ||
Oxidative stress-dependent p66Shc phosphorylation in skin fibroblasts of children with mitochondrial disorders | Q43131078 | ||
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation | Q43885529 | ||
Extracellular pH modifies mitochondrial control of capacitative calcium entry in Jurkat cells. | Q45166513 | ||
Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy | Q45273391 | ||
Deficiency of subunits of Complex I and mitochondrial encephalomyopathy | Q48107157 | ||
MELAS: clinical features, biochemistry, and molecular genetics | Q48496312 | ||
Adult-onset MELAS. Evidence for involvement of neurons as well as cerebral vasculature in strokelike episodes | Q48958839 | ||
Quantitation and origin of the mitochondrial membrane potential in human cells lacking mitochondrial DNA. | Q50519005 | ||
Mitochondrial network complexity and pathological decrease in complex I activity are tightly correlated in isolated human complex I deficiency. | Q53675259 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1740-1746 | |
P577 | publication date | 2012-03-03 | |
P1433 | published in | Biochimica et Biophysica Acta | Q864239 |
P1476 | title | Effect of mtDNA point mutations on cellular bioenergetics | |
P478 | volume | 1817 |
Q37721601 | 53BP1 contributes to regulation of autophagic clearance of mitochondria |
Q38752245 | A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction. |
Q33843127 | A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential. |
Q40146692 | A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR). |
Q33916058 | A novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosis |
Q58749049 | Association between the T6459C point mutation of the mitochondrial MT-CO1 gene and susceptibility to sepsis among Chinese Han people |
Q46515103 | Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation. |
Q35911424 | Cumulative mtDNA damage and mutations contribute to the progressive loss of RGCs in a rat model of glaucoma |
Q64916501 | Deletion of Mtu1 (Trmu) in zebrafish revealed the essential role of tRNA modification in mitochondrial biogenesis and hearing function. |
Q93039486 | Genetic Variation for Ontogenetic Shifts in Metabolism Underlies Physiological Homeostasis in Drosophila |
Q37433859 | High Pressure-Induced mtDNA Alterations in Retinal Ganglion Cells and Subsequent Apoptosis. |
Q46376426 | Hybridization increases mitochondrial production of reactive oxygen species in sunfish. |
Q37727879 | Increased AMP-activated protein kinase in skeletal muscles of Murphy Roth Large mice and its potential role in altered metabolism |
Q35080607 | Methionine restriction slows down senescence in human diploid fibroblasts |
Q51703326 | Mitochondrial DNA (mtDNA) variants in the European haplogroups HV, JT, and U do not have a major role in schizophrenia. |
Q64891963 | Mitochondrial Transfer of Wharton's Jelly Mesenchymal Stem Cells Eliminates Mutation Burden and Rescues Mitochondrial Bioenergetics in Rotenone-Stressed MELAS Fibroblasts. |
Q50281263 | Mitochondrial genome variability: the effect on cellular functional activity. |
Q42775670 | Reduced mitochondrial activity in colonocytes facilitates AMPKα2-dependent inflammation |