Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastoma-Reference-Cited by-同舟云学术

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Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastoma

Published:2004-10-26 Issue:10 Volume:91 Page:1835-1841
ISSN:0007-0920
Container-title:British Journal of Cancer
language:en
Short-container-title:Br J Cancer

Author:

Astuti D,Morris M,Krona C,Abel F,Gentle D,Martinsson T,Kogner P,Neumann H P H,Voutilainen R,Eng C,Rustin P,Latif F,Maher E R

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology

Link

http://www.nature.com/articles/6602202.pdf

Reference47 articles.

1. Abel F, Sjöberg RM, Ejeskär K, Krona C, Martinsson T (2002) Analyses of apoptotic regulators CASP9 and DFFA at 1P36.2, reveal rare allele variants in human neuroblastoma tumours. Br J Cancer 86: 596–604

2. Agathanggelou A, Honorio S, Macartney DP, Martinez A, Dallol A, Rader J, Fullwood P, Chauhan A, Walker R, Shaw JA, Hosoe S, Lerman MI, Minna JD, Maher ER, Latif F (2001) Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumours. Oncogene 20: 1509–1518

3. An WG, Kanekal M, Simon MC, Maltepe E, Blagosklonny MV, Neckers LM (1998) Stabilization of wild-type p53 by hypoxia-inducible factor 1alpha. Nature 392: 405–408

4. Astuti D, Douglas F, Lennard TW, Aligianis IA, Woodward ER, Evans DG, Eng C, Latif F, Maher ER (2001a) Germline SDHD mutation in familial phaeochromocytoma. Lancet 357: 1181–1182

5. Astuti D, Latif F, Dallol A, Dahia PL, Douglas F, George E, Skoldberg F, Husebye ES, Eng C, Maher ER (2001b) Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Am J Hum Genet 69: 49–54

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