255 related articles for article (PubMed ID: 23874847)
21. New genes and pathomechanisms in mitochondrial disorders unraveled by NGS technologies.
Legati A; Reyes A; Nasca A; Invernizzi F; Lamantea E; Tiranti V; Garavaglia B; Lamperti C; Ardissone A; Moroni I; Robinson A; Ghezzi D; Zeviani M
Biochim Biophys Acta; 2016 Aug; 1857(8):1326-1335. PubMed ID: 26968897
[TBL] [Abstract][Full Text] [Related]
22. Adaptation of respiratory chain biogenesis to cytochrome c oxidase deficiency caused by SURF1 gene mutations.
Kovářová N; Cížková Vrbacká A; Pecina P; Stránecký V; Pronicka E; Kmoch S; Houštěk J
Biochim Biophys Acta; 2012 Jul; 1822(7):1114-24. PubMed ID: 22465034
[TBL] [Abstract][Full Text] [Related]
23. Mitochondrial DNA abnormalities provide mechanistic insight and predict reactive oxygen species-stimulating drug efficacy.
Zaidieh T; Smith JR; Ball KE; An Q
BMC Cancer; 2021 Apr; 21(1):427. PubMed ID: 33865346
[TBL] [Abstract][Full Text] [Related]
24. Mitochondrial disorders of the OXPHOS system.
Fernandez-Vizarra E; Zeviani M
FEBS Lett; 2021 Apr; 595(8):1062-1106. PubMed ID: 33159691
[TBL] [Abstract][Full Text] [Related]
25. Neuron-specific specificity protein 4 bigenomically regulates the transcription of all mitochondria- and nucleus-encoded cytochrome c oxidase subunit genes in neurons.
Johar K; Priya A; Dhar S; Liu Q; Wong-Riley MT
J Neurochem; 2013 Nov; 127(4):496-508. PubMed ID: 24032355
[TBL] [Abstract][Full Text] [Related]
26. Coenzyme Q biosynthesis in health and disease.
Acosta MJ; Vazquez Fonseca L; Desbats MA; Cerqua C; Zordan R; Trevisson E; Salviati L
Biochim Biophys Acta; 2016 Aug; 1857(8):1079-1085. PubMed ID: 27060254
[TBL] [Abstract][Full Text] [Related]
27. MtBrowse: An integrative genomics browser for human mitochondrial DNA.
Singh V; Jolly B; Rajput NK; Pramanik S; Bhardwaj A
Mitochondrion; 2019 Sep; 48():31-36. PubMed ID: 30738202
[TBL] [Abstract][Full Text] [Related]
28. Assembly of nuclear DNA-encoded subunits into mitochondrial complex IV, and their preferential integration into supercomplex forms in patient mitochondria.
Lazarou M; Smith SM; Thorburn DR; Ryan MT; McKenzie M
FEBS J; 2009 Nov; 276(22):6701-13. PubMed ID: 19843159
[TBL] [Abstract][Full Text] [Related]
29. Long-lived mitochondrial cristae proteins in mouse heart and brain.
Bomba-Warczak E; Edassery SL; Hark TJ; Savas JN
J Cell Biol; 2021 Sep; 220(9):. PubMed ID: 34259807
[TBL] [Abstract][Full Text] [Related]
30. Architecture of active mammalian respiratory chain supercomplexes.
Schäfer E; Seelert H; Reifschneider NH; Krause F; Dencher NA; Vonck J
J Biol Chem; 2006 Jun; 281(22):15370-5. PubMed ID: 16551638
[TBL] [Abstract][Full Text] [Related]
31. Mitochondrial DNA mutations in disease and aging.
Wallace DC
Environ Mol Mutagen; 2010 Jun; 51(5):440-50. PubMed ID: 20544884
[TBL] [Abstract][Full Text] [Related]
32. Supramolecular organization of protein complexes in the mitochondrial inner membrane.
Vonck J; Schäfer E
Biochim Biophys Acta; 2009 Jan; 1793(1):117-24. PubMed ID: 18573282
[TBL] [Abstract][Full Text] [Related]
33. Significance of Mitochondria DNA Mutations in Diseases.
Zhu Z; Wang X
Adv Exp Med Biol; 2017; 1038():219-230. PubMed ID: 29178079
[TBL] [Abstract][Full Text] [Related]
34. Structural organization and transcription regulation of nuclear genes encoding the mammalian cytochrome c oxidase complex.
Lenka N; Vijayasarathy C; Mullick J; Avadhani NG
Prog Nucleic Acid Res Mol Biol; 1998; 61():309-44. PubMed ID: 9752724
[TBL] [Abstract][Full Text] [Related]
35. Evidence for the presence of somatic mitochondrial DNA mutations in right atrial appendage tissues of coronary artery disease patients.
Matam K; Shaik NA; Aggarwal S; Diwale S; Banaganapalli B; Al-Aama JY; Elango R; Rao P; Hasan Q
Mol Genet Genomics; 2014 Aug; 289(4):533-40. PubMed ID: 24604425
[TBL] [Abstract][Full Text] [Related]
36. Arrangement of electron transport chain components in bovine mitochondrial supercomplex I1III2IV1.
Althoff T; Mills DJ; Popot JL; Kühlbrandt W
EMBO J; 2011 Sep; 30(22):4652-64. PubMed ID: 21909073
[TBL] [Abstract][Full Text] [Related]
37. A defect in the mitochondrial complex III, but not complex IV, triggers early ROS-dependent damage in defined brain regions.
Diaz F; Garcia S; Padgett KR; Moraes CT
Hum Mol Genet; 2012 Dec; 21(23):5066-77. PubMed ID: 22914734
[TBL] [Abstract][Full Text] [Related]
38. Homozygous missense mutation in UQCRC2 associated with severe encephalomyopathy, mitochondrial complex III assembly defect and activation of mitochondrial protein quality control.
Burska D; Stiburek L; Krizova J; Vanisova M; Martinek V; Sladkova J; Zamecnik J; Honzik T; Zeman J; Hansikova H; Tesarova M
Biochim Biophys Acta Mol Basis Dis; 2021 Aug; 1867(8):166147. PubMed ID: 33865955
[TBL] [Abstract][Full Text] [Related]
39. A mutational analysis reveals new functional interactions between domains of the Oxa1 protein in Saccharomyces cerevisiae.
Mathieu L; Bourens M; Marsy S; Hlavacek O; Panozzo C; Dujardin G
Mol Microbiol; 2010 Jan; 75(2):474-88. PubMed ID: 20025673
[TBL] [Abstract][Full Text] [Related]
40. Heteroplasmic mutations of the mitochondrial genome cause paradoxical effects on mitochondrial functions.
Zhang C; Huang VH; Simon M; Sharma LK; Fan W; Haas R; Wallace DC; Bai Y; Huang T
FASEB J; 2012 Dec; 26(12):4914-24. PubMed ID: 22925728
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]