276 related articles for article (PubMed ID: 15572694)
1. The mitochondrial SDHD gene is required for early embryogenesis, and its partial deficiency results in persistent carotid body glomus cell activation with full responsiveness to hypoxia.
Piruat JI; Pintado CO; Ortega-Sáenz P; Roche M; López-Barneo J
Mol Cell Biol; 2004 Dec; 24(24):10933-40. PubMed ID: 15572694
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Oxygen-sensing by ion channels and mitochondrial function in carotid body glomus cells.
López-Barneo J; Ortega-Sáenz P; Piruat JI; García-Fernández M
Novartis Found Symp; 2006; 272():54-64; discussion 64-72, 131-40. PubMed ID: 16686429
[TBL] [Abstract][Full Text] [Related]
4. A conditional mouse mutant in the tumor suppressor SdhD gene unveils a link between p21(WAF1/Cip1) induction and mitochondrial dysfunction.
Millán-Uclés A; Díaz-Castro B; García-Flores P; Báez A; Pérez-Simón JA; López-Barneo J; Piruat JI
PLoS One; 2014; 9(1):e85528. PubMed ID: 24465590
[TBL] [Abstract][Full Text] [Related]
5. Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma.
Gimm O; Armanios M; Dziema H; Neumann HP; Eng C
Cancer Res; 2000 Dec; 60(24):6822-5. PubMed ID: 11156372
[TBL] [Abstract][Full Text] [Related]
6. Differential impairment of catecholaminergic cell maturation and survival by genetic mitochondrial complex II dysfunction.
Díaz-Castro B; Pintado CO; García-Flores P; López-Barneo J; Piruat JI
Mol Cell Biol; 2012 Aug; 32(16):3347-57. PubMed ID: 22711987
[TBL] [Abstract][Full Text] [Related]
7. Sdhd and SDHD/H19 knockout mice do not develop paraganglioma or pheochromocytoma.
Bayley JP; van Minderhout I; Hogendoorn PC; Cornelisse CJ; van der Wal A; Prins FA; Teppema L; Dahan A; Devilee P; Taschner PE
PLoS One; 2009 Nov; 4(11):e7987. PubMed ID: 19956719
[TBL] [Abstract][Full Text] [Related]
8. The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway.
Gimenez-Roqueplo AP; Favier J; Rustin P; Mourad JJ; Plouin PF; Corvol P; Rötig A; Jeunemaitre X
Am J Hum Genet; 2001 Dec; 69(6):1186-97. PubMed ID: 11605159
[TBL] [Abstract][Full Text] [Related]
9. SDHD mutations in head and neck paragangliomas result in destabilization of complex II in the mitochondrial respiratory chain with loss of enzymatic activity and abnormal mitochondrial morphology.
Douwes Dekker PB; Hogendoorn PC; Kuipers-Dijkshoorn N; Prins FA; van Duinen SG; Taschner PE; van der Mey AG; Cornelisse CJ
J Pathol; 2003 Nov; 201(3):480-6. PubMed ID: 14595761
[TBL] [Abstract][Full Text] [Related]
10. Etiopathogenesis and clinical presentation of carotid body tumors.
Baysal BE; Myers EN
Microsc Res Tech; 2002 Nov; 59(3):256-61. PubMed ID: 12384970
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial complex II and genomic imprinting in inheritance of paraganglioma tumors.
Baysal BE
Biochim Biophys Acta; 2013 May; 1827(5):573-7. PubMed ID: 23291190
[TBL] [Abstract][Full Text] [Related]
12. Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.
Taschner PE; Jansen JC; Baysal BE; Bosch A; Rosenberg EH; Bröcker-Vriends AH; van Der Mey AG; van Ommen GJ; Cornelisse CJ; Devilee P
Genes Chromosomes Cancer; 2001 Jul; 31(3):274-81. PubMed ID: 11391798
[TBL] [Abstract][Full Text] [Related]
13. Multifocal Paraganglioma and Pheochromocytoma Due to Truncated SDHD Mutation.
Zuo Y; Li X; Wu X; Zhou J; Wang J; Wang J; Wu Z; Li H; Zhang X
Urology; 2018 Jun; 116():63-67. PubMed ID: 29545045
[TBL] [Abstract][Full Text] [Related]
14. Carotid body paraganglioma and SDHD mutation in a Greek family.
Liapis CD; Bellos JK; Halapas A; Lembessis P; Koutsilieris M; Kostakis A
Anticancer Res; 2005; 25(3c):2449-52. PubMed ID: 16080474
[TBL] [Abstract][Full Text] [Related]
15. Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss.
Badenhop RF; Cherian S; Lord RS; Baysal BE; Taschner PE; Schofield PR
Genes Chromosomes Cancer; 2001 Jul; 31(3):255-63. PubMed ID: 11391796
[TBL] [Abstract][Full Text] [Related]
16. Instability of succinate dehydrogenase in SDHD polymorphism connects reactive oxygen species production to nuclear and mitochondrial genomic mutations in yeast.
Chang YL; Hsieh MH; Chang WW; Wang HY; Lin MC; Wang CP; Lou PJ; Teng SC
Antioxid Redox Signal; 2015 Mar; 22(7):587-602. PubMed ID: 25328978
[TBL] [Abstract][Full Text] [Related]
17. Active succinate dehydrogenase (SDH) and lack of SDHD mutations in sporadic paragangliomas.
Braun S; Riemann K; Kupka S; Leistenschneider P; Sotlar K; Schmid H; Blin N
Anticancer Res; 2005; 25(4):2809-14. PubMed ID: 16080530
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial complex II regulates a distinct oxygen sensing mechanism in monocytes.
Sharma S; Wang J; Cortes Gomez E; Taggart RT; Baysal BE
Hum Mol Genet; 2017 Apr; 26(7):1328-1339. PubMed ID: 28204537
[TBL] [Abstract][Full Text] [Related]
19. A novel mutation in the SDHD gene responsible for familial paraganglioma. Medical and psychological implications.
Prontera P; Ferrando B; Giuliani V; Falcinelli F; Mencarelli A; Rogaia D; Pasini B; Donti E
Genet Couns; 2008; 19(4):413-8. PubMed ID: 19239085
[TBL] [Abstract][Full Text] [Related]
20. Mitochondrial complex II is essential for hypoxia-induced pulmonary vasoconstriction of intra- but not of pre-acinar arteries.
Paddenberg R; Tiefenbach M; Faulhammer P; Goldenberg A; Gries B; Pfeil U; Lips KS; Piruat JI; López-Barneo J; Schermuly RT; Weissmann N; Kummer W
Cardiovasc Res; 2012 Mar; 93(4):702-10. PubMed ID: 22215723
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
