The MEN II syndromes and the role of the ret proto-oncogene

被引:56
作者
Ponder, BAJ
Smith, D
机构
来源
ADVANCES IN CANCER RESEARCH, VOL 70 | 1996年 / 70卷
关键词
D O I
10.1016/S0065-230X(08)60875-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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页码:179 / 222
页数:44
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共 149 条
[1]   CELL FATE DETERMINATION IN THE PERIPHERAL NERVOUS-SYSTEM - THE SYMPATHOADRENAL PROGENITOR [J].
ANDERSON, DJ .
JOURNAL OF NEUROBIOLOGY, 1993, 24 (02) :185-198
[2]   MUTATION ANALYSIS OF THE RET RECEPTOR TYROSINE KINASE IN HIRSCHSPRUNG DISEASE [J].
ANGRIST, M ;
BOLK, S ;
THIEL, B ;
PUFFENBERGER, EG ;
HOFSTRA, RM ;
BUYS, CHCM ;
CASS, DT ;
CHAKRAVARTI, A .
HUMAN MOLECULAR GENETICS, 1995, 4 (05) :821-830
[3]  
ASAI N, 1995, MOL CELL BIOL, V15, P1613
[4]   DIVERSITY OF RET PROTOONCOGENE MUTATIONS IN FAMILIAL AND SPORADIC HIRSCHSPRUNG DISEASE [J].
ATTIE, T ;
PELET, A ;
EDERY, P ;
ENG, C ;
MULLIGAN, LM ;
AMIEL, J ;
BOUTRAND, L ;
BELDJORD, C ;
NIHOULFEKETE, C ;
MUNNICH, A ;
PONDER, BAJ ;
LYONNET, S .
HUMAN MOLECULAR GENETICS, 1995, 4 (08) :1381-1386
[5]  
BADNER JA, 1990, AM J HUM GENET, V46, P568
[6]   CLONAL ORIGIN OF INHERITED MEDULLARY-THYROID CARCINOMA AND PHEOCHROMOCYTOMA [J].
BAYLIN, SB ;
GANN, DS ;
HSU, SH .
SCIENCE, 1976, 193 (4250) :321-323
[7]   THE RET PROTOONCOGENE IN SPORADIC PHEOCHROMOCYTOMAS - FREQUENT MEN 2-LIKE MUTATIONS AND NEW MOLECULAR DEFECTS [J].
BELDJORD, C ;
DESCLAUXARRAMOND, F ;
RAFFINSANSON, M ;
CORVOL, JC ;
DEKEYZER, Y ;
LUTON, JP ;
PLOUIN, PF ;
BERTAGNA, X .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (07) :2063-2068
[8]  
BLAIKIE P, 1994, J BIOL CHEM, V269, P32031
[9]  
BLOCK MA, 1980, ARCH SURG-CHICAGO, V115, P142
[10]  
BOLINO A, 1995, ONCOGENE, V10, P2415