314 related articles for article (PubMed ID: 26014388)
21. Human NADH:ubiquinone oxidoreductase deficiency: radical changes in mitochondrial morphology?
Koopman WJ; Verkaart S; Visch HJ; van Emst-de Vries S; Nijtmans LG; Smeitink JA; Willems PH
Am J Physiol Cell Physiol; 2007 Jul; 293(1):C22-9. PubMed ID: 17428841
[TBL] [Abstract][Full Text] [Related]
22. The effect of small molecules on nuclear-encoded translation diseases.
Soiferman D; Ayalon O; Weissman S; Saada A
Biochimie; 2014 May; 100():184-91. PubMed ID: 24012549
[TBL] [Abstract][Full Text] [Related]
23. Pro-oxidant effect of ALA is implicated in mitochondrial dysfunction of HepG2 cells.
Laafi J; Homedan C; Jacques C; Gueguen N; Schmitt C; Puy H; Reynier P; Carmen Martinez M; Malthièry Y
Biochimie; 2014 Nov; 106():157-66. PubMed ID: 25220386
[TBL] [Abstract][Full Text] [Related]
24. Evaluation of mitochondrial bioenergetics, dynamics, endoplasmic reticulum-mitochondria crosstalk, and reactive oxygen species in fibroblasts from patients with complex I deficiency.
Leipnitz G; Mohsen AW; Karunanidhi A; Seminotti B; Roginskaya VY; Markantone DM; Grings M; Mihalik SJ; Wipf P; Van Houten B; Vockley J
Sci Rep; 2018 Jan; 8(1):1165. PubMed ID: 29348607
[TBL] [Abstract][Full Text] [Related]
25.
Thompson K; Mai N; Oláhová M; Scialó F; Formosa LE; Stroud DA; Garrett M; Lax NZ; Robertson FM; Jou C; Nascimento A; Ortez C; Jimenez-Mallebrera C; Hardy SA; He L; Brown GK; Marttinen P; McFarland R; Sanz A; Battersby BJ; Bonnen PE; Ryan MT; Chrzanowska-Lightowlers ZM; Lightowlers RN; Taylor RW
EMBO Mol Med; 2018 Nov; 10(11):. PubMed ID: 30201738
[TBL] [Abstract][Full Text] [Related]
26. Differential expression of oxidative phosphorylation genes in patients with Alzheimer's disease: implications for early mitochondrial dysfunction and oxidative damage.
Manczak M; Park BS; Jung Y; Reddy PH
Neuromolecular Med; 2004; 5(2):147-62. PubMed ID: 15075441
[TBL] [Abstract][Full Text] [Related]
27. Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defects.
Fernández-Vizarra E; Tiranti V; Zeviani M
Biochim Biophys Acta; 2009 Jan; 1793(1):200-11. PubMed ID: 18620006
[TBL] [Abstract][Full Text] [Related]
28. A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative disease.
Potluri P; Davila A; Ruiz-Pesini E; Mishmar D; O'Hearn S; Hancock S; Simon M; Scheffler IE; Wallace DC; Procaccio V
Mol Genet Metab; 2009 Apr; 96(4):189-95. PubMed ID: 19185523
[TBL] [Abstract][Full Text] [Related]
29. Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.
Bonora E; Porcelli AM; Gasparre G; Biondi A; Ghelli A; Carelli V; Baracca A; Tallini G; Martinuzzi A; Lenaz G; Rugolo M; Romeo G
Cancer Res; 2006 Jun; 66(12):6087-96. PubMed ID: 16778181
[TBL] [Abstract][Full Text] [Related]
30. Extension of chronological life span by reduced TOR signaling requires down-regulation of Sch9p and involves increased mitochondrial OXPHOS complex density.
Pan Y; Shadel GS
Aging (Albany NY); 2009 Jan; 1(1):131-45. PubMed ID: 20157595
[TBL] [Abstract][Full Text] [Related]
31. Alternative oxidase rescues mitochondria-mediated dopaminergic cell loss in Drosophila.
Humphrey DM; Parsons RB; Ludlow ZN; Riemensperger T; Esposito G; Verstreken P; Jacobs HT; Birman S; Hirth F
Hum Mol Genet; 2012 Jun; 21(12):2698-712. PubMed ID: 22398207
[TBL] [Abstract][Full Text] [Related]
32. Reduced mitochondrial Ca(2+) transients stimulate autophagy in human fibroblasts carrying the 13514A>G mutation of the ND5 subunit of NADH dehydrogenase.
Granatiero V; Giorgio V; Calì T; Patron M; Brini M; Bernardi P; Tiranti V; Zeviani M; Pallafacchina G; De Stefani D; Rizzuto R
Cell Death Differ; 2016 Feb; 23(2):231-41. PubMed ID: 26206091
[TBL] [Abstract][Full Text] [Related]
33. Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation.
Tabebi M; Charfi N; Kallabi F; Alila-Fersi O; Ben Mahmoud A; Tlili A; Keskes-Ammar L; Kamoun H; Abid M; Mnif M; Fakhfakh F
J Diabetes Complications; 2017 Jan; 31(1):253-259. PubMed ID: 27422531
[TBL] [Abstract][Full Text] [Related]
34. Aging-associated mitochondrial DNA mutations alter oxidative phosphorylation machinery and cause mitochondrial dysfunctions.
Li H; Shen L; Hu P; Huang R; Cao Y; Deng J; Yuan W; Liu D; Yang J; Gu H; Bai Y
Biochim Biophys Acta Mol Basis Dis; 2017 Sep; 1863(9):2266-2273. PubMed ID: 28559044
[TBL] [Abstract][Full Text] [Related]
35. Bromodomain Inhibitors Correct Bioenergetic Deficiency Caused by Mitochondrial Disease Complex I Mutations.
Barrow JJ; Balsa E; Verdeguer F; Tavares CD; Soustek MS; Hollingsworth LR; Jedrychowski M; Vogel R; Paulo JA; Smeitink J; Gygi SP; Doench J; Root DE; Puigserver P
Mol Cell; 2016 Oct; 64(1):163-175. PubMed ID: 27666594
[TBL] [Abstract][Full Text] [Related]
36. A novel mutation in
Diquigiovanni C; Bergamini C; Diaz R; Liparulo I; Bianco F; Masin L; Baldassarro VA; Rizzardi N; Tranchina A; Buscherini F; Wischmeijer A; Pippucci T; Scarano E; Cordelli DM; Fato R; Seri M; Paracchini S; Bonora E
FASEB J; 2019 Oct; 33(10):11284-11302. PubMed ID: 31314595
[TBL] [Abstract][Full Text] [Related]
37. Mechanistic insights into mitochondrial tRNA
Ji Y; Nie Z; Meng F; Hu C; Chen H; Jin L; Chen M; Zhang M; Zhang J; Liang M; Wang M; Guan MX
J Biol Chem; 2021 Jul; 297(1):100816. PubMed ID: 34023389
[TBL] [Abstract][Full Text] [Related]
38. Expression patterns of mitochondrial OXPHOS components, mitofusin 1 and dynamin-related protein 1 are associated with human embryo fragmentation.
Otasevic V; Surlan L; Vucetic M; Tulic I; Buzadzic B; Stancic A; Jankovic A; Velickovic K; Golic I; Markelic M; Korac A; Korac B
Reprod Fertil Dev; 2016 Mar; 28(3):319-27. PubMed ID: 25033890
[TBL] [Abstract][Full Text] [Related]
39. Genetic and functional analysis of mitochondrial DNA-encoded complex I genes.
Bai Y; Hu P; Park JS; Deng JH; Song X; Chomyn A; Yagi T; Attardi G
Ann N Y Acad Sci; 2004 Apr; 1011():272-83. PubMed ID: 15126303
[TBL] [Abstract][Full Text] [Related]
40. Biallelic pathogenic variants in COX11 are associated with an infantile-onset mitochondrial encephalopathy.
Rius R; Bennett NK; Bhattacharya K; Riley LG; Yüksel Z; Formosa LE; Compton AG; Dale RC; Cowley MJ; Gayevskiy V; Al Tala SM; Almehery AA; Ryan MT; Thorburn DR; Nakamura K; Christodoulou J
Hum Mutat; 2022 Dec; 43(12):1970-1978. PubMed ID: 36030551
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]