These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
393 related articles for article (PubMed ID: 28173120)
21. Mic10, a Core Subunit of the Mitochondrial Contact Site and Cristae Organizing System, Interacts with the Dimeric F Rampelt H; Bohnert M; Zerbes RM; Horvath SE; Warscheid B; Pfanner N; van der Laan M J Mol Biol; 2017 Apr; 429(8):1162-1170. PubMed ID: 28315355 [TBL] [Abstract][Full Text] [Related]
22. TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndrome. Spiegel R; Khayat M; Shalev SA; Horovitz Y; Mandel H; Hershkovitz E; Barghuti F; Shaag A; Saada A; Korman SH; Elpeleg O; Yatsiv I J Med Genet; 2011 Mar; 48(3):177-82. PubMed ID: 21147908 [TBL] [Abstract][Full Text] [Related]
24. Milder clinical course of Type IV 3-methylglutaconic aciduria due to a novel mutation in TMEM70. Shchelochkov OA; Li FY; Wang J; Zhan H; Towbin JA; Jefferies JL; Wong LJ; Scaglia F Mol Genet Metab; 2010; 101(2-3):282-5. PubMed ID: 20728387 [TBL] [Abstract][Full Text] [Related]
25. Kinetic coupling of the respiratory chain with ATP synthase, but not proton gradients, drives ATP production in cristae membranes. Toth A; Meyrat A; Stoldt S; Santiago R; Wenzel D; Jakobs S; von Ballmoos C; Ott M Proc Natl Acad Sci U S A; 2020 Feb; 117(5):2412-2421. PubMed ID: 31964824 [TBL] [Abstract][Full Text] [Related]
26. A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo-cardiomyopathy. Atay Z; Bereket A; Turan S; Haliloglu B; Memisoglu A; Khayat M; Shalev SA; Spiegel R Gene; 2013 Feb; 515(1):197-9. PubMed ID: 23235116 [TBL] [Abstract][Full Text] [Related]
27. Who and how in the regulation of mitochondrial cristae shape and function. Quintana-Cabrera R; Mehrotra A; Rigoni G; Soriano ME Biochem Biophys Res Commun; 2018 May; 500(1):94-101. PubMed ID: 28438601 [TBL] [Abstract][Full Text] [Related]
28. Knockdown of F1 epsilon subunit decreases mitochondrial content of ATP synthase and leads to accumulation of subunit c. Havlícková V; Kaplanová V; Nůsková H; Drahota Z; Houstek J Biochim Biophys Acta; 2010; 1797(6-7):1124-9. PubMed ID: 20026007 [TBL] [Abstract][Full Text] [Related]
29. MICOS assembly controls mitochondrial inner membrane remodeling and crista junction redistribution to mediate cristae formation. Stephan T; Brüser C; Deckers M; Steyer AM; Balzarotti F; Barbot M; Behr TS; Heim G; Hübner W; Ilgen P; Lange F; Pacheu-Grau D; Pape JK; Stoldt S; Huser T; Hell SW; Möbius W; Rehling P; Riedel D; Jakobs S EMBO J; 2020 Jul; 39(14):e104105. PubMed ID: 32567732 [TBL] [Abstract][Full Text] [Related]
30. An evidence based hypothesis on the existence of two pathways of mitochondrial crista formation. Harner ME; Unger AK; Geerts WJ; Mari M; Izawa T; Stenger M; Geimer S; Reggiori F; Westermann B; Neupert W Elife; 2016 Nov; 5():. PubMed ID: 27849155 [TBL] [Abstract][Full Text] [Related]
32. Deregulation of mitochondrial F1FO-ATP synthase via OSCP in Alzheimer's disease. Beck SJ; Guo L; Phensy A; Tian J; Wang L; Tandon N; Gauba E; Lu L; Pascual JM; Kroener S; Du H Nat Commun; 2016 May; 7():11483. PubMed ID: 27151236 [TBL] [Abstract][Full Text] [Related]
33. Biochemical consequences in yeast of the human mitochondrial DNA 8993T>C mutation in the ATPase6 gene found in NARP/MILS patients. Kucharczyk R; Rak M; di Rago JP Biochim Biophys Acta; 2009 May; 1793(5):817-24. PubMed ID: 19269308 [TBL] [Abstract][Full Text] [Related]
34. Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation. Honzík T; Tesarová M; Mayr JA; Hansíková H; Jesina P; Bodamer O; Koch J; Magner M; Freisinger P; Huemer M; Kostková O; van Coster R; Kmoch S; Houstêk J; Sperl W; Zeman J Arch Dis Child; 2010 Apr; 95(4):296-301. PubMed ID: 20335238 [TBL] [Abstract][Full Text] [Related]
35. Mitochondrial diseases and genetic defects of ATP synthase. Houstek J; Pícková A; Vojtísková A; Mrácek T; Pecina P; Jesina P Biochim Biophys Acta; 2006; 1757(9-10):1400-5. PubMed ID: 16730639 [TBL] [Abstract][Full Text] [Related]
36. Knockdown of human Oxa1l impairs the biogenesis of F1Fo-ATP synthase and NADH:ubiquinone oxidoreductase. Stiburek L; Fornuskova D; Wenchich L; Pejznochova M; Hansikova H; Zeman J J Mol Biol; 2007 Nov; 374(2):506-16. PubMed ID: 17936786 [TBL] [Abstract][Full Text] [Related]
37. [Structure, biogenesis and mechanism of function of the mitochondrial ATP synthase complex]. Wysocka-Kapcińska M; Kucharczyk R Postepy Biochem; 2012; 58(3):344-52. PubMed ID: 23373419 [TBL] [Abstract][Full Text] [Related]