194 related articles for article (PubMed ID: 22711987)
1. 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]
2. 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]
3. 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]
4. 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]
5. Reduced expression and loss of heterozygosity of the SDHD gene in colorectal and gastric cancer.
Habano W; Sugai T; Nakamura S; Uesugi N; Higuchi T; Terashima M; Horiuchi S
Oncol Rep; 2003; 10(5):1375-80. PubMed ID: 12883710
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Model animals for the study of oxidative stress from complex II.
Ishii T; Miyazawa M; Onouchi H; Yasuda K; Hartman PS; Ishii N
Biochim Biophys Acta; 2013 May; 1827(5):588-97. PubMed ID: 23142169
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Carney triad, SDH-deficient tumors, and Sdhb+/- mice share abnormal mitochondria.
Szarek E; Ball ER; Imperiale A; Tsokos M; Faucz FR; Giubellino A; Moussallieh FM; Namer IJ; Abu-Asab MS; Pacak K; Taïeb D; Carney JA; Stratakis CA
Endocr Relat Cancer; 2015 Jun; 22(3):345-52. PubMed ID: 25808178
[TBL] [Abstract][Full Text] [Related]
10. Sensitivity of hematopoietic stem cells to mitochondrial dysfunction by SdhD gene deletion.
Bejarano-García JA; Millán-Uclés Á; Rosado IV; Sánchez-Abarca LI; Caballero-Velázquez T; Durán-Galván MJ; Pérez-Simón JA; Piruat JI
Cell Death Dis; 2016 Dec; 7(12):e2516. PubMed ID: 27929539
[TBL] [Abstract][Full Text] [Related]
11. Alterations of the SDHD gene locus in midgut carcinoids, Merkel cell carcinomas, pheochromocytomas, and abdominal paragangliomas.
Kytölä S; Nord B; Elder EE; Carling T; Kjellman M; Cedermark B; Juhlin C; Höög A; Isola J; Larsson C
Genes Chromosomes Cancer; 2002 Jul; 34(3):325-32. PubMed ID: 12007193
[TBL] [Abstract][Full Text] [Related]
12. Predominant expression of mutated allele of the succunate dehydrogenase D (SDHD) gene in the SDHD-related paragangliomas.
Yamashita R; Usui T; Hashimoto S; Suzuki H; Takahashi M; Honkura K; Iwamoto K; Kodama E; Tagami T; Naruse M; Shimatsu A; Kaise K
Endocr J; 2009; 56(9):1129-35. PubMed ID: 19550080
[TBL] [Abstract][Full Text] [Related]
13. Complex II subunit SDHD is critical for cell growth and metabolism, which can be partially restored with a synthetic ubiquinone analog.
Bandara AB; Drake JC; Brown DA
BMC Mol Cell Biol; 2021 Jun; 22(1):35. PubMed ID: 34118887
[TBL] [Abstract][Full Text] [Related]
14. Transgenic mice engineered to target Cre/loxP-mediated DNA recombination into catecholaminergic neurons.
Gelman DM; Noaín D; Avale ME; Otero V; Low MJ; Rubinstein M
Genesis; 2003 Aug; 36(4):196-202. PubMed ID: 12929090
[TBL] [Abstract][Full Text] [Related]
15. 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]
16.
Ashtekar A; Huk D; Magner A; La Perle K; Zhang X; Piruat JI; López-Barneo J; Jhiang SM; Kirschner LS
Endocr Relat Cancer; 2017 Nov; 24(11):579-591. PubMed ID: 28928232
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. [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]
19. Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families.
Hensen EF; Jordanova ES; van Minderhout IJ; Hogendoorn PC; Taschner PE; van der Mey AG; Devilee P; Cornelisse CJ
Oncogene; 2004 May; 23(23):4076-83. PubMed ID: 15064708
[TBL] [Abstract][Full Text] [Related]
20. Succinate dehydrogenase (SDH) D subunit (SDHD) inactivation in a growth-hormone-producing pituitary tumor: a new association for SDH?
Xekouki P; Pacak K; Almeida M; Wassif CA; Rustin P; Nesterova M; de la Luz Sierra M; Matro J; Ball E; Azevedo M; Horvath A; Lyssikatos C; Quezado M; Patronas N; Ferrando B; Pasini B; Lytras A; Tolis G; Stratakis CA
J Clin Endocrinol Metab; 2012 Mar; 97(3):E357-66. PubMed ID: 22170724
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]