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Volumn 57, Issue 23, 1997, Pages 5207-5212

Absence of Fhit protein in primary lung tumors and cell lines with FHIT gene abnormalities

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBODY PRODUCTION; ANTIBODY SPECIFICITY; ARTICLE; DNA DETERMINATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENE MUTATION; HUMAN; HUMAN CELL; IMMUNOCYTOCHEMISTRY; LUNG CARCINOGENESIS; LUNG TUMOR; PRIORITY JOURNAL;

EID: 15444345047     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (130)

References (16)
  • 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
    • 0022446922 scopus 로고
    • Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization
    • Pinkel, D., Straume, T., and Gray, J. W. Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proc. Natl. Acad. Sci. USA, 83: 2934-2938, 1986.
    • (1986) Proc. Natl. Acad. Sci. USA , vol.83 , pp. 2934-2938
    • Pinkel, D.1    Straume, T.2    Gray, J.W.3
  • 14
    • 0029903698 scopus 로고    scopus 로고
    • The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14
    • Panagopoulos, I., Pandis, N., Thelin, S., Petersson, C., Mertens, F., Borg, A., Kristoffersson, U., Mitelman, F., and Aman, P. The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14. Cancer Res., 56: 4871-4875, 1996.
    • (1996) Cancer Res. , vol.56 , pp. 4871-4875
    • Panagopoulos, I.1    Pandis, N.2    Thelin, S.3    Petersson, C.4    Mertens, F.5    Borg, A.6    Kristoffersson, U.7    Mitelman, F.8    Aman, P.9
  • 15
    • 0029830791 scopus 로고    scopus 로고
    • Frequent abnormalities of FHIT, a candidate tumor suppressor gene, in head and neck cancer cell lines
    • Mao, L., Fan, Y-H., Lotan, R., and Hong, W. K. Frequent abnormalities of FHIT, a candidate tumor suppressor gene, in head and neck cancer cell lines. Cancer Res., 56: 5128-5131, 1996.
    • (1996) Cancer Res. , vol.56 , pp. 5128-5131
    • Mao, L.1    Fan, Y.-H.2    Lotan, R.3    Hong, W.K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.