메뉴 건너뛰기




Volumn 59, Issue 15, 1999, Pages 3570-3575

Unbalanced germ-line expression of hMLH1 and hMSH2 alleles in hereditary nonpolyposis colorectal cancer

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CLINICAL ARTICLE; COLORECTAL CANCER; GENE EXPRESSION; GENE SEQUENCE; GENETIC TRANSCRIPTION; HUMAN; HUMAN TISSUE; MICROSATELLITE INSTABILITY; PRIORITY JOURNAL;

EID: 17444395546     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (52)

References (26)
  • 1
    • 0031470414 scopus 로고    scopus 로고
    • Etiology, natural history, management, and molecular genetics of hereditary nonpolyposis colorectal cancer (Lynch syndromes): Genetic counselling implications
    • Lynch, H. T., Lemon, S. J., Karr, B., Franklin, B., Lynch, J., Watson, P., Tinley, S., Lerman, C., and Carter, C. Etiology, natural history, management, and molecular genetics of hereditary nonpolyposis colorectal cancer (Lynch syndromes): genetic counselling implications. Cancer Epidemiol. Biomark. Prev., 6: 987-991, 1997.
    • (1997) Cancer Epidemiol. Biomark. Prev. , vol.6 , pp. 987-991
    • Lynch, H.T.1    Lemon, S.J.2    Karr, B.3    Franklin, B.4    Lynch, J.5    Watson, P.6    Tinley, S.7    Lerman, C.8    Carter, C.9
  • 2
    • 0028061678 scopus 로고
    • Hereditary gastrointestinal polyposis and nonpolyposis syndromes
    • Rustgi, A. K. Hereditary gastrointestinal polyposis and nonpolyposis syndromes. N. Engl. J. Med., 331: 1694-1702, 1994.
    • (1994) N. Engl. J. Med. , vol.331 , pp. 1694-1702
    • Rustgi, A.K.1
  • 5
    • 0030870631 scopus 로고    scopus 로고
    • Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred
    • Akiyama, Y., Sato, H., Yamada, T., Nagasaki, H., Tsuchiya, A., Abe, R., and Yuasa, Y. Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred. Cancer Res., 57: 3920-3923, 1997.
    • (1997) Cancer Res. , vol.57 , pp. 3920-3923
    • Akiyama, Y.1    Sato, H.2    Yamada, T.3    Nagasaki, H.4    Tsuchiya, A.5    Abe, R.6    Yuasa, Y.7
  • 7
    • 0030882381 scopus 로고    scopus 로고
    • Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study
    • Peltomäki, P., Vasen, H. F. A., and The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer. Mutations predisposing to hereditary nonpolyposis colorectal cancer: database and results of a collaborative study. Gastroenterology, 113: 1146-1158, 1997.
    • (1997) Gastroenterology , vol.113 , pp. 1146-1158
    • Peltomäki, P.1    Vasen, H.F.A.2
  • 11
    • 0031017268 scopus 로고    scopus 로고
    • Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines
    • Kane, M. F., Loda, M., Gaida, G. M., Lipman, J., Mishra, R., Goldman, H., Jessup, J. M., and Kolodner, R. D. Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines. Cancer Res., 57: 808-811, 1997.
    • (1997) Cancer Res. , vol.57 , pp. 808-811
    • Kane, M.F.1    Loda, M.2    Gaida, G.M.3    Lipman, J.4    Mishra, R.5    Goldman, H.6    Jessup, J.M.7    Kolodner, R.D.8
  • 14
    • 0023277545 scopus 로고
    • Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
    • Chomczynski, P., and Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem., 162; 156-159, 1987.
    • (1987) Anal. Biochem. , vol.162 , pp. 156-159
    • Chomczynski, P.1    Sacchi, N.2
  • 18
    • 0028861609 scopus 로고
    • Two mutant alleles of the insulin receptor gene in a family with a genetic form of insulin resistance: A 10 base pair deletion in exon 1 and a mutation substituting serine for asparagine-462
    • Cama, A., de la Luz Sierra, M., Kadowaki, T., Kadowaki, H., Quon, M. J., Rudiger, H. W., Dreyer, M., and Taylor, S. I. Two mutant alleles of the insulin receptor gene in a family with a genetic form of insulin resistance: a 10 base pair deletion in exon 1 and a mutation substituting serine for asparagine-462. Hum. Genet., 95: 174-182, 1995.
    • (1995) Hum. Genet. , vol.95 , pp. 174-182
    • Cama, A.1    De La Luz Sierra, M.2    Kadowaki, T.3    Kadowaki, H.4    Quon, M.J.5    Rudiger, H.W.6    Dreyer, M.7    Taylor, S.I.8
  • 19
    • 0027271806 scopus 로고
    • Differential expression of mutant and normal β T3 receptor alleles in kindreds with generalized resistance to thyroid hormone
    • Mixson, A. J., Hauser, P., Tennyson, G., Renault, J. C., Bodenner, D. L., and Weintraub, B. D. Differential expression of mutant and normal β T3 receptor alleles in kindreds with generalized resistance to thyroid hormone. J. Clin. Invest., 91: 2296-2300, 1993.
    • (1993) J. Clin. Invest. , vol.91 , pp. 2296-2300
    • Mixson, A.J.1    Hauser, P.2    Tennyson, G.3    Renault, J.C.4    Bodenner, D.L.5    Weintraub, B.D.6
  • 26
    • 0023790820 scopus 로고
    • Molecular basis and prenatal diagnosis of β-thalassemia
    • Kazazian, H. H., and Boehm, C. D. Molecular basis and prenatal diagnosis of β-thalassemia. Blood, 72: 1107-1116, 1988.
    • (1988) Blood , vol.72 , pp. 1107-1116
    • Kazazian, H.H.1    Boehm, C.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.