169 related articles for article (PubMed ID: 12231007)
1. Cytopathies involving mitochondrial complex II.
Ackrell BA
Mol Aspects Med; 2002 Oct; 23(5):369-84. PubMed ID: 12231007
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Two hydrophobic subunits are essential for the heme b ligation and functional assembly of complex II (succinate-ubiquinone oxidoreductase) from Escherichia coli.
Nakamura K; Yamaki M; Sarada M; Nakayama S; Vibat CR; Gennis RB; Nakayashiki T; Inokuchi H; Kojima S; Kita K
J Biol Chem; 1996 Jan; 271(1):521-7. PubMed ID: 8550613
[TBL] [Abstract][Full Text] [Related]
4. Localization of histidine residues responsible for heme axial ligation in cytochrome b556 of complex II (succinate:ubiquinone oxidoreductase) in Escherichia coli.
Vibat CR; Cecchini G; Nakamura K; Kita K; Gennis RB
Biochemistry; 1998 Mar; 37(12):4148-59. PubMed ID: 9521736
[TBL] [Abstract][Full Text] [Related]
5. Retention of heme in axial ligand mutants of succinate-ubiquinone xxidoreductase (complex II) from Escherichia coli.
Maklashina E; Rothery RA; Weiner JH; Cecchini G
J Biol Chem; 2001 Jun; 276(22):18968-76. PubMed ID: 11259408
[TBL] [Abstract][Full Text] [Related]
6. The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency.
Bayley JP; Devilee P; Taschner PE
BMC Med Genet; 2005 Nov; 6():39. PubMed ID: 16288654
[TBL] [Abstract][Full Text] [Related]
7. [From gene to disease; from SDHD, a defect in the respiratory chain, to paragangliomas and pheochromocytomas].
Taschner PE; Bröcker-Vriends AH; van der Mey AG
Ned Tijdschr Geneeskd; 2002 Nov; 146(46):2188-90. PubMed ID: 12467161
[TBL] [Abstract][Full Text] [Related]
8. Genes encoding the same three subunits of respiratory complex II are present in the mitochondrial DNA of two phylogenetically distant eukaryotes.
Burger G; Lang BF; Reith M; Gray MW
Proc Natl Acad Sci U S A; 1996 Mar; 93(6):2328-32. PubMed ID: 8637872
[TBL] [Abstract][Full Text] [Related]
9. Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas.
Baysal BE; Willett-Brozick JE; Lawrence EC; Drovdlic CM; Savul SA; McLeod DR; Yee HA; Brackmann DE; Slattery WH; Myers EN; Ferrell RE; Rubinstein WS
J Med Genet; 2002 Mar; 39(3):178-83. PubMed ID: 11897817
[TBL] [Abstract][Full Text] [Related]
10. [Complex II (succinate-ubiquinone reductase) deficiency].
Nonaka I
Ryoikibetsu Shokogun Shirizu; 2001; (36):132-4. PubMed ID: 11596343
[No Abstract] [Full Text] [Related]
11. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas.
Benn DE; Croxson MS; Tucker K; Bambach CP; Richardson AL; Delbridge L; Pullan PT; Hammond J; Marsh DJ; Robinson BG
Oncogene; 2003 Mar; 22(9):1358-64. PubMed ID: 12618761
[TBL] [Abstract][Full Text] [Related]
12. Cytochrome b in human complex II (succinate-ubiquinone oxidoreductase): cDNA cloning of the components in liver mitochondria and chromosome assignment of the genes for the large (SDHC) and small (SDHD) subunits to 1q21 and 11q23.
Hirawake H; Taniwaki M; Tamura A; Kojima S; Kita K
Cytogenet Cell Genet; 1997; 79(1-2):132-8. PubMed ID: 9533030
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Resolution and reconstitution of succinate-ubiquinone reductase from Escherichia coli.
Yang X; Yu L; Yu CA
J Biol Chem; 1997 Apr; 272(15):9683-9. PubMed ID: 9092498
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
Baysal BE; Ferrell RE; Willett-Brozick JE; Lawrence EC; Myssiorek D; Bosch A; van der Mey A; Taschner PE; Rubinstein WS; Myers EN; Richard CW; Cornelisse CJ; Devilee P; Devlin B
Science; 2000 Feb; 287(5454):848-51. PubMed ID: 10657297
[TBL] [Abstract][Full Text] [Related]
17. Succinate dehydrogenase and fumarate reductase from Escherichia coli.
Cecchini G; Schröder I; Gunsalus RP; Maklashina E
Biochim Biophys Acta; 2002 Jan; 1553(1-2):140-57. PubMed ID: 11803023
[TBL] [Abstract][Full Text] [Related]
18. Mutations in SDHC cause autosomal dominant paraganglioma, type 3.
Niemann S; Müller U
Nat Genet; 2000 Nov; 26(3):268-70. PubMed ID: 11062460
[TBL] [Abstract][Full Text] [Related]
19. [Mitochondrial cytopathies: identification of responsible nuclear genes].
Paquis V
Arch Pediatr; 1996 Sep; 3(9):915-6. PubMed ID: 8949357
[No Abstract] [Full Text] [Related]
20. Hereditary paraganglioma targets diverse paraganglia.
Baysal BE
J Med Genet; 2002 Sep; 39(9):617-22. PubMed ID: 12205103
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
