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Volumn 38, Issue 3, 1996, Pages 451-453

Familial Wilms' tumor associated with a WT1 zinc finger mutation

Author keywords

[No Author keywords available]

Indexed keywords

DACTINOMYCIN; DOXORUBICIN; ETOPOSIDE; GENE PRODUCT; IFOSFAMIDE; VINCRISTINE; ZINC FINGER PROTEIN;

EID: 0030589513     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0655     Document Type: Article
Times cited : (31)

References (19)
  • 1
    • 0028302272 scopus 로고
    • Molecular genetic analysis of chromosome 11p in familial Wilms' tumour
    • 1. Baird, P. N., Pritchard, J., and Cowell, J. K. (1995). Molecular genetic analysis of chromosome 11p in familial Wilms' tumour. Br. J. Cancer 69: 1072-1077.
    • (1995) Br. J. Cancer , vol.69 , pp. 1072-1077
    • Baird, P.N.1    Pritchard, J.2    Cowell, J.K.3
  • 2
    • 0000234889 scopus 로고
    • Denys-Drash syndrome: A role for the WT1 tumour suppressor gene in urogenital development
    • 2. Bruening, W., and Pelletier, J. (1994). Denys-Drash syndrome: A role for the WT1 tumour suppressor gene in urogenital development. Semin. Dev. Biol. 5: 333-343.
    • (1994) Semin. Dev. Biol. , vol.5 , pp. 333-343
    • Bruening, W.1    Pelletier, J.2
  • 6
    • 0025098654 scopus 로고
    • Homozygous deletion in Wilms' tumors of a zinc-finger gene identified by chromosome jumping
    • 6. Gessler, M., Poustka, A., Cavenee, W., Neve, R. L., Orkin, S. H., and Bruns, G. A. P. (1990). Homozygous deletion in Wilms' tumors of a zinc-finger gene identified by chromosome jumping. Nature 343: 774-778.
    • (1990) Nature , vol.343 , pp. 774-778
    • Gessler, M.1    Poustka, A.2    Cavenee, W.3    Neve, R.L.4    Orkin, S.H.5    Bruns, G.A.P.6
  • 7
    • 0023683531 scopus 로고
    • Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11
    • 7. Grundy, P., Koufos, A., Morgan, K., Li, F. P., Meadows, A. T., and Cavenee, W. K. (1988). Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11. Nature 336: 374-377.
    • (1988) Nature , vol.336 , pp. 374-377
    • Grundy, P.1    Koufos, A.2    Morgan, K.3    Li, F.P.4    Meadows, A.T.5    Cavenee, W.K.6
  • 8
    • 0023803361 scopus 로고
    • Lack of linkage of familial Wilms' tumour to chromosomal band 11p13
    • 8. Huff, V., Compton, D. A., Chao, L.-Y., Strong, L. C., Geiser, C. F., and Saunders, G. F. (1988). Lack of linkage of familial Wilms' tumour to chromosomal band 11p13. Nature 336: 377-378.
    • (1988) Nature , vol.336 , pp. 377-378
    • Huff, V.1    Compton, D.A.2    Chao, L.-Y.3    Strong, L.C.4    Geiser, C.F.5    Saunders, G.F.6
  • 13
    • 0019497899 scopus 로고
    • Genetics of Wilms' tumor
    • 13. Matsunaga, E. (1981). Genetics of Wilms' tumor. Hum. Genet. 57: 231-246.
    • (1981) Hum. Genet. , vol.57 , pp. 231-246
    • Matsunaga, E.1
  • 16
    • 0025788974 scopus 로고
    • WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumor
    • 16. Pelletier, J., Bruening, W., Li, F. P., Haber, D. A., Glaser, T., and Housman, D. E. (1991). WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumor. Nature 353: 431-434.
    • (1991) Nature , vol.353 , pp. 431-434
    • Pelletier, J.1    Bruening, W.2    Li, F.P.3    Haber, D.A.4    Glaser, T.5    Housman, D.E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.