Hereditary phaeochromocytomas and paragangliomas: a study of five susceptibility genes

被引:55
作者
Bauters, C
Vantyghem, MC
Leteurtre, E
Odou, MF
Mouton, C
Porchet, N
Wemeau, JL
Proye, C
Pigny, P
机构
[1] Ctr Hosp Reg Univ Lille, Clin Endocrinol Marc Linquette, Lille, France
[2] Ctr Hosp Reg Univ Lille, Fac Med, Serv Anat Pathol, Pole Rech, Lille, France
[3] Ctr Hosp Reg Univ Lille, Hop Claude Huriez, Lab Biochim & Biol Mol, Lille, France
[4] Ctr Hosp Reg Univ Lille, Hop Claude Huriez, Serv Chirurg Gen & Endocrinienne, Lille, France
[5] Ctr Hosp Reg Univ Lille, Clin Marc Linquette, Lab Biochim Endocrinol, F-59037 Lille, France
关键词
D O I
10.1136/jmg.40.6.e75
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页数:6
相关论文
共 22 条
[1]   Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma [J].
Astuti, D ;
Latif, F ;
Dallol, A ;
Dahia, PLM ;
Douglas, F ;
George, E ;
Sköldberg, F ;
Husebye, ES ;
Eng, C ;
Maher, ER .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (01) :49-54
[2]   Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma [J].
Baysal, BE ;
Ferrell, RE ;
Willett-Brozick, JE ;
Lawrence, EC ;
Myssiorek, D ;
Bosch, A ;
van der Mey, A ;
Taschner, PEM ;
Rubinstein, WS ;
Myers, EN ;
Richard, CW ;
Cornelisse, CJ ;
Devilee, P ;
Devlin, B .
SCIENCE, 2000, 287 (5454) :848-851
[3]   Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas [J].
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 .
JOURNAL OF MEDICAL GENETICS, 2002, 39 (03) :178-183
[4]   Hereditary paraganglioma target's diverse paraganglia [J].
Baysal, BE .
JOURNAL OF MEDICAL GENETICS, 2002, 39 (09) :617-622
[5]   Genes encoding the same three subunits of respiratory complex II are present in the mitochondrial DNA of two phylogenetically distant eukaryotes [J].
Burger, G ;
Lang, BF ;
Reith, M ;
Gray, MW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (06) :2328-2332
[6]   Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma [J].
Cascon, A ;
Ruiz-Llorente, S ;
Cebrian, A ;
Telleria, D ;
Rivero, JC ;
Diez, JJ ;
Lopez-Ibarra, PJ ;
Jaunsolo, MA ;
Benitez, J ;
Robledo, M .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 (08) :457-461
[7]  
CROSSEY PA, 1994, HUM MOL GENET, V3, P1303
[8]  
Dannenberg H, 2002, CLIN CANCER RES, V8, P2061
[9]   Pheochromocytoma - Death of an axiom. [J].
Dluhy, RG .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (19) :1486-1488
[10]   Vasoactive intestinal peptide receptor-1 (VPAC-1) is a novel gene target of the hemolymphopoietic transcription factor Ikaros [J].
Dorsam, G ;
Goetzl, EJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (16) :13488-13493