242 related articles for article (PubMed ID: 12082502)
1. Succinate dehydrogenase and human diseases: new insights into a well-known enzyme.
Rustin P; Munnich A; Rötig A
Eur J Hum Genet; 2002 May; 10(5):289-91. PubMed ID: 12082502
[TBL] [Abstract][Full Text] [Related]
2. Mutations in the C. elegans succinate dehydrogenase iron-sulfur subunit promote superoxide generation and premature aging.
Huang J; Lemire BD
J Mol Biol; 2009 Apr; 387(3):559-69. PubMed ID: 19233206
[TBL] [Abstract][Full Text] [Related]
3. Phenotypic dichotomy in mitochondrial complex II genetic disorders.
Baysal BE; Rubinstein WS; Taschner PE
J Mol Med (Berl); 2001 Sep; 79(9):495-503. PubMed ID: 11692162
[TBL] [Abstract][Full Text] [Related]
4. Effects of site-directed mutations in Escherichia coli succinate dehydrogenase on the enzyme activity and production of superoxide radicals.
Zhao Z; Rothery RA; Weiner JH
Biochem Cell Biol; 2006 Dec; 84(6):1013-21. PubMed ID: 17215887
[TBL] [Abstract][Full Text] [Related]
5. A role for mitochondrial enzymes in inherited neoplasia and beyond.
Eng C; Kiuru M; Fernandez MJ; Aaltonen LA
Nat Rev Cancer; 2003 Mar; 3(3):193-202. PubMed ID: 12612654
[TBL] [Abstract][Full Text] [Related]
6. Inborn errors of complex II--unusual human mitochondrial diseases.
Rustin P; Rötig A
Biochim Biophys Acta; 2002 Jan; 1553(1-2):117-22. PubMed ID: 11803021
[TBL] [Abstract][Full Text] [Related]
7. Succinate dehydrogenase deficiency in human.
Brière JJ; Favier J; El Ghouzzi V; Djouadi F; Bénit P; Gimenez AP; Rustin P
Cell Mol Life Sci; 2005 Oct; 62(19-20):2317-24. PubMed ID: 16143825
[TBL] [Abstract][Full Text] [Related]
8. Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma.
Bayley JP; van Minderhout I; Weiss MM; Jansen JC; Oomen PH; Menko FH; Pasini B; Ferrando B; Wong N; Alpert LC; Williams R; Blair E; Devilee P; Taschner PE
BMC Med Genet; 2006 Jan; 7():1. PubMed ID: 16405730
[TBL] [Abstract][Full Text] [Related]
9. The SDHB Arg230His mutation causing familial paraganglioma alters glycolysis in a new
Saskői É; Hujber Z; Nyírő G; Likó I; Mátyási B; Petővári G; Mészáros K; Kovács AL; Patthy L; Supekar S; Fan H; Sváb G; Tretter L; Sarkar A; Nazir A; Sebestyén A; Patócs A; Mehta A; Takács-Vellai K
Dis Model Mech; 2020 Oct; 13(10):. PubMed ID: 32859697
[TBL] [Abstract][Full Text] [Related]
10. The ubiquinone-binding site of the Saccharomyces cerevisiae succinate-ubiquinone oxidoreductase is a source of superoxide.
Guo J; Lemire BD
J Biol Chem; 2003 Nov; 278(48):47629-35. PubMed ID: 13129931
[TBL] [Abstract][Full Text] [Related]
11. Succinate dehydrogenase: the complex roles of a simple enzyme.
Huang S; Millar AH
Curr Opin Plant Biol; 2013 Jun; 16(3):344-9. PubMed ID: 23453781
[TBL] [Abstract][Full Text] [Related]
12. Accumulation of Krebs cycle intermediates and over-expression of HIF1alpha in tumours which result from germline FH and SDH mutations.
Pollard PJ; Brière JJ; Alam NA; Barwell J; Barclay E; Wortham NC; Hunt T; Mitchell M; Olpin S; Moat SJ; Hargreaves IP; Heales SJ; Chung YL; Griffiths JR; Dalgleish A; McGrath JA; Gleeson MJ; Hodgson SV; Poulsom R; Rustin P; Tomlinson IP
Hum Mol Genet; 2005 Aug; 14(15):2231-9. PubMed ID: 15987702
[TBL] [Abstract][Full Text] [Related]
13. Free-living nematodes Caenorhabditis elegans possess in their mitochondria an additional rhodoquinone, an essential component of the eukaryotic fumarate reductase system.
Takamiya S; Matsui T; Taka H; Murayama K; Matsuda M; Aoki T
Arch Biochem Biophys; 1999 Nov; 371(2):284-9. PubMed ID: 10545216
[TBL] [Abstract][Full Text] [Related]
14. [Complex II (succinate-ubiquinone reductase) deficiency].
Nonaka I
Ryoikibetsu Shokogun Shirizu; 2001; (36):132-4. PubMed ID: 11596343
[No Abstract] [Full Text] [Related]
15. K40E: a novel succinate dehydrogenase (SDH)B mutation causing familial phaeochromocytoma and paraganglioma.
McDonnell CM; Benn DE; Marsh DJ; Robinson BG; Zacharin MR
Clin Endocrinol (Oxf); 2004 Oct; 61(4):510-4. PubMed ID: 15473885
[TBL] [Abstract][Full Text] [Related]
16. Architecture of succinate dehydrogenase and reactive oxygen species generation.
Yankovskaya V; Horsefield R; Törnroth S; Luna-Chavez C; Miyoshi H; Léger C; Byrne B; Cecchini G; Iwata S
Science; 2003 Jan; 299(5607):700-4. PubMed ID: 12560550
[TBL] [Abstract][Full Text] [Related]
17. Mutations in the Saccharomyces cerevisiae succinate dehydrogenase result in distinct metabolic phenotypes revealed through (1)H NMR-based metabolic footprinting.
Szeto SS; Reinke SN; Sykes BD; Lemire BD
J Proteome Res; 2010 Dec; 9(12):6729-39. PubMed ID: 20964315
[TBL] [Abstract][Full Text] [Related]
18. Late-onset optic atrophy, ataxia, and myopathy associated with a mutation of a complex II gene.
Birch-Machin MA; Taylor RW; Cochran B; Ackrell BA; Turnbull DM
Ann Neurol; 2000 Sep; 48(3):330-5. PubMed ID: 10976639
[TBL] [Abstract][Full Text] [Related]
19. Assembly of mitochondrial succinate dehydrogenase in human health and disease.
Cao K; Xu J; Cao W; Wang X; Lv W; Zeng M; Zou X; Liu J; Feng Z
Free Radic Biol Med; 2023 Oct; 207():247-259. PubMed ID: 37490987
[TBL] [Abstract][Full Text] [Related]
20. Succinate dehydrogenase - Assembly, regulation and role in human disease.
Rutter J; Winge DR; Schiffman JD
Mitochondrion; 2010 Jun; 10(4):393-401. PubMed ID: 20226277
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]