메뉴 건너뛰기




Volumn 57, Issue 3, 1997, Pages 504-512

Structure and expression of the human FHIT gene in normal and tumor cells

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; CANCER CELL CULTURE; CHROMOSOME 8; CHROMOSOME FRAGILE SITE; CHROMOSOME TRANSLOCATION 3; CONTROLLED STUDY; EXON; GENE DELETION; GENE EXPRESSION; GENE LOCUS; GENE STRUCTURE; HUMAN; HUMAN CELL; INTRON; KIDNEY CARCINOMA; NONHUMAN; PRIORITY JOURNAL; SEQUENCE TAGGED SITE; TUMOR SUPPRESSOR GENE;

EID: 0031043860     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (213)

References (18)
  • 1
    • 13344279424 scopus 로고    scopus 로고
    • The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers
    • Ohta, M., Inoue, H., Cotticelli, M. G., Kastury, K., Baffa, R., Palazzo, J., Siprashvili, Z., Mori, M., McCue, P., Druck, T., Croce, C. M., and Huebner, K. The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers. Cell, 84: 587-597, 1996.
    • (1996) Cell , vol.84 , pp. 587-597
    • Ohta, M.1    Inoue, H.2    Cotticelli, M.G.3    Kastury, K.4    Baffa, R.5    Palazzo, J.6    Siprashvili, Z.7    Mori, M.8    McCue, P.9    Druck, T.10    Croce, C.M.11    Huebner, K.12
  • 10
    • 0003648101 scopus 로고
    • Madison, WI: Genetics Computer Group, Madison, Wisconsin
    • Genetics Computer Group. Program Manual for the Wisconsin Package, Version 8, Madison, WI: Genetics Computer Group, Madison, Wisconsin, 1994.
    • (1994) Program Manual for the Wisconsin Package, Version 8
  • 12
    • 0027953797 scopus 로고
    • Common regions of deletion in chromosome regions 3p12 and 3p14.2 in primary clear cell renal carcinomas
    • Lubinski, J., Hadaczek, P., Podolski, J., Toloczko, A., Sikorski, A., McCue, P., Druck, T., and Huebner, K. Common regions of deletion in chromosome regions 3p12 and 3p14.2 in primary clear cell renal carcinomas. Cancer Res., 54: 3710-3713, 1994.
    • (1994) Cancer Res. , vol.54 , pp. 3710-3713
    • Lubinski, J.1    Hadaczek, P.2    Podolski, J.3    Toloczko, A.4    Sikorski, A.5    McCue, P.6    Druck, T.7    Huebner, K.8
  • 13
    • 0028169985 scopus 로고
    • Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma
    • Wilke, C. M., Guo, S-W., Hall, B. K., Boldog, F., Gemmill, R. M., Chandrasekharappa, S. C., Bancroft, C. L., Drabkin, H. A., and Glover, T. W. Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma. Genomics. 22: 319-326, 1994.
    • (1994) Genomics. , vol.22 , pp. 319-326
    • Wilke, C.M.1    Guo, S.-W.2    Hall, B.K.3    Boldog, F.4    Gemmill, R.M.5    Chandrasekharappa, S.C.6    Bancroft, C.L.7    Drabkin, H.A.8    Glover, T.W.9
  • 14
    • 0029927916 scopus 로고    scopus 로고
    • Structure of the human receptor tyrosine phosphatase gamma gene (PTPRG) and relation to the familial RCC t(3;8) chromosome translocation
    • Kastury, K., Ohta, M., Lasota, J., Moir, D., Dorm an, T., LaForgia, S., Druck, T., and Huebner, K. Structure of the human receptor tyrosine phosphatase gamma gene (PTPRG) and relation to the familial RCC t(3;8) chromosome translocation. Genomics, 32: 225-235, 1996.
    • (1996) Genomics , vol.32 , pp. 225-235
    • Kastury, K.1    Ohta, M.2    Lasota, J.3    Moir, D.4    Dorm An, T.5    Laforgia, S.6    Druck, T.7    Huebner, K.8
  • 15
    • 0030060945 scopus 로고    scopus 로고
    • FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: Direct evidence for the coincidence of viral integration sites and fragile sites
    • Wilke, C. M., Hall, B. K., Hoge, A., Paradee, W., Smith, D. I., and Glover, T. W. FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites. Hum. Mol. Genet., 5: 187-195, 1996.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 187-195
    • Wilke, C.M.1    Hall, B.K.2    Hoge, A.3    Paradee, W.4    Smith, D.I.5    Glover, T.W.6
  • 16
    • 0030201105 scopus 로고    scopus 로고
    • A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints
    • Paradee, W., Wilke, C. M., Wang, L., Shridhar, R., Mullins, C. M., Hoge, A., Glover, T. W., and Smith, D. I. A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints. Genomics, 35: 87-93, 1996.
    • (1996) Genomics , vol.35 , pp. 87-93
    • Paradee, W.1    Wilke, C.M.2    Wang, L.3    Shridhar, R.4    Mullins, C.M.5    Hoge, A.6    Glover, T.W.7    Smith, D.I.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.