메뉴 건너뛰기




Volumn 37, Issue 3, 1996, Pages 310-315

Mapping of a putative tumor suppressor locus to proximal 7p in Wilms tumors

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 7P; CLINICAL ARTICLE; GENE LOCATION; GENE MAPPING; HUMAN; HUMAN TISSUE; KARYOTYPE; NEPHROBLASTOMA; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 0030297969     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0565     Document Type: Article
Times cited : (37)

References (45)
  • 1
    • 0026907525 scopus 로고
    • Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome
    • Baird, P. N., Santos, A., Groves, N., Jadresic, L., and Cowell, J. K. (1992). Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome. Hum. Mol. Genet. 1: 301-305.
    • (1992) Hum. Mol. Genet. , vol.1 , pp. 301-305
    • Baird, P.N.1    Santos, A.2    Groves, N.3    Jadresic, L.4    Cowell, J.K.5
  • 9
    • 0028147486 scopus 로고
    • The molecular genetics of Wilms tumor
    • Coppes, M. J., and Williams, B. R. G. (1994). The molecular genetics of Wilms tumor. Cancer Invest. 12: 57-65.
    • (1994) Cancer Invest. , vol.12 , pp. 57-65
    • Coppes, M.J.1    Williams, B.R.G.2
  • 10
    • 0025098654 scopus 로고
    • Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping
    • Gessler, M., Poustka, A., Cavenee, W., Neve, R. L., Orkin, S. H., and Bruns, G. A. P. (1990). Homozygous deletion in Wilms tumours 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
  • 12
    • 0028351728 scopus 로고
    • Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome
    • Grundy, P. E., Telzerow, P. E., Breslow, N., Moksness, J., Huff, V., and Paterson, M. C. (1994). Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome. Cancer Res. 54: 2331-2333.
    • (1994) Cancer Res. , vol.54 , pp. 2331-2333
    • Grundy, P.E.1    Telzerow, P.E.2    Breslow, N.3    Moksness, J.4    Huff, V.5    Paterson, M.C.6
  • 16
    • 0026341035 scopus 로고
    • Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors
    • Kaneko, Y., Homma, C., Maseki, N., Sakurai, M., and Hata, J.-i. (1991). Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors. Cancer Res. 51: 5937-5942.
    • (1991) Cancer Res. , vol.51 , pp. 5937-5942
    • Kaneko, Y.1    Homma, C.2    Maseki, N.3    Sakurai, M.4    Hata, J.-I.5
  • 22
    • 0026339877 scopus 로고
    • Report of the committee on chromosome changes in neoplasia. Human Gene Mapping 11
    • Mitelman, F., Kaneko, Y., and Trent, J. (1991). Report of the committee on chromosome changes in neoplasia. Human Gene Mapping 11. Cytogenet. Cell Genet. 58: 1053-1079.
    • (1991) Cytogenet. Cell Genet. , vol.58 , pp. 1053-1079
    • Mitelman, F.1    Kaneko, Y.2    Trent, J.3
  • 23
    • 0027285258 scopus 로고
    • Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
    • Ogawa, O., Eccles, M. R., Szeto, J., McNoe, L. A., Yun, K., Maw, M. A., Smith, P. J., and Reeve, A. E. (1993a). Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour. Nature 362: 749-751.
    • (1993) Nature , vol.362 , pp. 749-751
    • Ogawa, O.1    Eccles, M.R.2    Szeto, J.3    McNoe, L.A.4    Yun, K.5    Maw, M.A.6    Smith, P.J.7    Reeve, A.E.8
  • 24
    • 0027422302 scopus 로고
    • Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism
    • Ogawa, O., Becroft, D. M., Morison, I. M., Eccles, M. R., Skeen, J. E., Mauger, D. C., and Reeve, A. E. (1993b). Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism. Nature Genet. 5: 408-412.
    • (1993) Nature Genet. , vol.5 , pp. 408-412
    • Ogawa, O.1    Becroft, D.M.2    Morison, I.M.3    Eccles, M.R.4    Skeen, J.E.5    Mauger, D.C.6    Reeve, A.E.7
  • 28
    • 0025788974 scopus 로고
    • WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour
    • Pelletier, J., Bruening, W., Li, F. P., Haber, D. A., Glaser, T., and Housman, D. E. (1991b). WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour. 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
  • 30
    • 0022446922 scopus 로고
    • Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization
    • Pinkel, D., Straume, T., and Gray, J. W. (1986). Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proc. Natl. Acad. Sci. USA 83: 2934-2938.
    • (1986) Proc. Natl. Acad. Sci. USA , vol.83 , pp. 2934-2938
    • Pinkel, D.1    Straume, T.2    Gray, J.W.3
  • 34
    • 0024505754 scopus 로고
    • Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells
    • Reeve, A. E., Sih, S. A., Raizis, A. M., and Feinberg, A. P. (1989). Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells. Mol. Cell. Biol. 9: 1799-1803.
    • (1989) Mol. Cell. Biol. , vol.9 , pp. 1799-1803
    • Reeve, A.E.1    Sih, S.A.2    Raizis, A.M.3    Feinberg, A.P.4
  • 35
    • 0029011076 scopus 로고
    • Constitutional and acquired rearrangements of chromosome 7 in Wilms tumor
    • Rivera, H. (1995). Constitutional and acquired rearrangements of chromosome 7 in Wilms tumor. Cancer Genet. Cytogenet. 81: 97-98.
    • (1995) Cancer Genet. Cytogenet. , vol.81 , pp. 97-98
    • Rivera, H.1
  • 37
    • 0026689597 scopus 로고
    • Cytogenetics and molecular genetics of Wilms' tumor of childhood
    • Slater, R. M., and Mannens, M. M. A. M. (1992). Cytogenetics and molecular genetics of Wilms' tumor of childhood. Cancer Genet. Cytogenet. 61: 111-121.
    • (1992) Cancer Genet. Cytogenet. , vol.61 , pp. 111-121
    • Slater, R.M.1    Mannens, M.M.A.M.2
  • 38
    • 0029042877 scopus 로고
    • Report of the second international workshop on human chromosome 7 mapping 1994
    • Tsui, L.-C., Donis-Keller, H., and Grzeschik, K-H. (1995). Report of the second international workshop on human chromosome 7 mapping 1994. Cytogenet. Cell Genet. 71: 2-21.
    • (1995) Cytogenet. Cell Genet. , vol.71 , pp. 2-21
    • Tsui, L.-C.1    Donis-Keller, H.2    Grzeschik, K.-H.3
  • 40
    • 0027131705 scopus 로고
    • Infrequency of ras, p53, WT1, or RB gene alterations in Wilms tumors
    • Waber, P. G., Chen, J., and Nisen, P. D. (1993). Infrequency of ras, p53, WT1, or RB gene alterations in Wilms tumors. Cancer 72: 3732-3738.
    • (1993) Cancer , vol.72 , pp. 3732-3738
    • Waber, P.G.1    Chen, J.2    Nisen, P.D.3
  • 41
    • 0025346754 scopus 로고
    • Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11
    • Wadey, R. B., Pal, N., Buckle, B., Yeomans, E., Pritchard, J., and Cowell, J. K. (1990). Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11. Oncogene 5: 901-907.
    • (1990) Oncogene , vol.5 , pp. 901-907
    • Wadey, R.B.1    Pal, N.2    Buckle, B.3    Yeomans, E.4    Pritchard, J.5    Cowell, J.K.6
  • 43
    • 0000739916 scopus 로고
    • The use of PCR and ethidium bromide staining to detect length variation in short repeat units
    • Watkins, C., Warne, D., Kelsell, D., Beckmann, J., Nyberg, K., and Spurr, N. (1991). The use of PCR and ethidium bromide staining to detect length variation in short repeat units. Technique 3:175-178.
    • (1991) Technique , vol.3 , pp. 175-178
    • Watkins, C.1    Warne, D.2    Kelsell, D.3    Beckmann, J.4    Nyberg, K.5    Spurr, N.6
  • 44
    • 0027420362 scopus 로고
    • Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome
    • Weksberg, R., Shen, D. R., Fei, Y. L., Song, Q. L., and Squire, J. (1993). Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome. Nature Genet. 5: 143-150.
    • (1993) Nature Genet. , vol.5 , pp. 143-150
    • Weksberg, R.1    Shen, D.R.2    Fei, Y.L.3    Song, Q.L.4    Squire, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.