The WT1 Wilms' tumor suppressor gene: How much do we really know?

被引:144
作者
Reddy, JC
Licht, JD
机构
[1] BROOKDALE CTR MOLEC BIOL,NEW YORK,NY
[2] MT SINAI SCH MED,DEPT MED,NEW YORK,NY 10029
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 1996年 / 1287卷 / 01期
关键词
D O I
10.1016/0304-419X(95)00014-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:1 / 28
页数:28
相关论文
共 202 条
[1]   A POINT MUTATION FOUND IN THE WT1 GENE IN A SPORADIC WILMS-TUMOR WITHOUT GENITOURINARY ABNORMALITIES IS IDENTICAL WITH THE MOST FREQUENT POINT MUTATION IN DENYS-DRASH SYNDROME [J].
AKASAKA, Y ;
KIKUCHI, H ;
NAGAI, T ;
HIRAOKA, N ;
KATO, S ;
HATA, J .
FEBS LETTERS, 1993, 317 (1-2) :39-43
[2]  
AMIN KM, 1995, AM J PATHOL, V146, P344
[3]  
ANANT S, 1994, ONCOGENE, V9, P3113
[4]  
ARMSTRONG JF, 1992, MECH DEVELOP, V40, P85
[5]  
Baird Paul N., 1992, Human Molecular Genetics, V1, P301, DOI 10.1093/hmg/1.5.301
[6]  
BAIRD PN, 1992, ONCOGENE, V7, P2141
[7]   WT1 MUTATIONS ASSOCIATED WITH INCOMPLETE DENYS-DRASH SYNDROME DEFINE A DOMAIN PREDICTED TO BEHAVE IN A DOMINANT-NEGATIVE FASHION [J].
BARDEESY, N ;
ZABEL, B ;
SCHMITT, K ;
PELLETIER, J .
GENOMICS, 1994, 21 (03) :663-665
[8]  
BARDEESY N, 1995, CANCER RES, V55, P215
[9]   ANAPLASTIC WILMS-TUMOR, A SUBTYPE DISPLAYING POOR-PROGNOSIS, HARBORS P53 GENE-MUTATIONS [J].
BARDEESY, N ;
FALKOFF, D ;
PETRUZZI, MJ ;
NOWAK, N ;
ZABEL, B ;
ADAM, M ;
AGUIAR, MC ;
GRUNDY, P ;
SHOWS, T ;
PELLETIER, J .
NATURE GENETICS, 1994, 7 (01) :91-97
[10]  
BECKWITH J B, 1990, Pediatric Pathology, V10, P1