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Volumn 59, Issue 2, 1999, Pages 290-293

Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHILD; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; DNA REPAIR; DNA SEQUENCE; GENE MUTATION; GENETIC ANALYSIS; HEMATOLOGIC DISEASE; HUMAN; NEUROFIBROMATOSIS; PHENOTYPE; PRIORITY JOURNAL;

EID: 0345222475     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (219)

References (22)
  • 1
    • 0030592517 scopus 로고    scopus 로고
    • Lessons from hereditary colorectal cancer
    • Kinzler, K. W., and Vogelstein, B. Lessons from hereditary colorectal cancer. Cell, 87: 159-170, 1996.
    • (1996) Cell , vol.87 , pp. 159-170
    • Kinzler, K.W.1    Vogelstein, B.2
  • 2
    • 0030882381 scopus 로고    scopus 로고
    • Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study
    • The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer
    • Peltomaki, P., and Vasen, H. F. Mutations predisposing to hereditary nonpolyposis colorectal cancer: database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer. Gastroenterology, 113: 1146-1158, 1997.
    • (1997) Gastroenterology , vol.113 , pp. 1146-1158
    • Peltomaki, P.1    Vasen, H.F.2
  • 6
    • 0031018674 scopus 로고    scopus 로고
    • Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype
    • Washington DC
    • Rampino, N., Yamamoto, H., Ionov, Y., Li, Y., Sawai, H., Reed, J. C., and Perucho, M. Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype. Science (Washington DC), 275: 967-969, 1997.
    • (1997) Science , vol.275 , pp. 967-969
    • Rampino, N.1    Yamamoto, H.2    Ionov, Y.3    Li, Y.4    Sawai, H.5    Reed, J.C.6    Perucho, M.7
  • 7
    • 0032032682 scopus 로고    scopus 로고
    • Somatic frameshift mutations in DNA mismatch repair and proapoptosis genes in hereditary nonpolyposis colorectal cancer
    • Yamamoto, H., Sawai, H., Weber, T. K., Rodriguez-Bigas, M. A., and Perucho, M. Somatic frameshift mutations in DNA mismatch repair and proapoptosis genes in hereditary nonpolyposis colorectal cancer. Cancer Res., 58: 997-1003, 1998.
    • (1998) Cancer Res. , vol.58 , pp. 997-1003
    • Yamamoto, H.1    Sawai, H.2    Weber, T.K.3    Rodriguez-Bigas, M.A.4    Perucho, M.5
  • 11
    • 0030768854 scopus 로고    scopus 로고
    • Hereditary nonpolyposis colorectal cancer (HNPCC): Eight novel germline mutations in hMSH2 or hMLH1 genes
    • Wehner, M., Buschhausen, L., Lamberti, C., Kruse, R., Caspari, R., Propping, P., and Friedl, W. Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes. Hum. Mut., 10: 241-244, 1997.
    • (1997) Hum. Mut. , vol.10 , pp. 241-244
    • Wehner, M.1    Buschhausen, L.2    Lamberti, C.3    Kruse, R.4    Caspari, R.5    Propping, P.6    Friedl, W.7
  • 12
    • 0030755372 scopus 로고    scopus 로고
    • Functional domains of the Saccharomyces cerevisiae Mlh1p and Pms1p DNA mismatch repair proteins and their relevance to human hereditary nonpolyposis colorectal cancer-associated mutations
    • Pang, Q., Prolla, T. A., and Liskay, R. M. Functional domains of the Saccharomyces cerevisiae Mlh1p and Pms1p DNA mismatch repair proteins and their relevance to human hereditary nonpolyposis colorectal cancer-associated mutations. Mol. Cell. Biol., 17: 4465-4473, 1997.
    • (1997) Mol. Cell. Biol. , vol.17 , pp. 4465-4473
    • Pang, Q.1    Prolla, T.A.2    Liskay, R.M.3
  • 15
    • 0002648901 scopus 로고
    • Neurofibromatosis: Historical perspective, classification and diagnostic criteria
    • S. M. Huson and R. A. C. Hughes (eds.), London: Chapman and Hall
    • Hudson, S. M. Neurofibromatosis: historical perspective, classification and diagnostic criteria. In: S. M. Huson and R. A. C. Hughes (eds.), The Neurofibromatoses. A Pathogenetic and Clinical Overview, pp. 1-22. London: Chapman and Hall, 1994.
    • (1994) The Neurofibromatoses. A Pathogenetic and Clinical Overview , pp. 1-22
    • Hudson, S.M.1
  • 16
    • 0003290989 scopus 로고
    • Molecular genetics of neurofibromatosis types 1 and 2
    • J. K. Cowell (ed.), Oxford: Bios Scientific Publishers
    • Colman, S. D., and Wallace, M. R. Molecular genetics of neurofibromatosis types 1 and 2. In: J. K. Cowell (ed.), Molecular Genetics of Cancer, pp. 43-70. Oxford: Bios Scientific Publishers, 1995.
    • (1995) Molecular Genetics of Cancer , pp. 43-70
    • Colman, S.D.1    Wallace, M.R.2
  • 17
    • 0029919109 scopus 로고    scopus 로고
    • Hereditary cancer: Two hits revisited
    • Knudson, A. G. Hereditary cancer: two hits revisited. J. Cancer Res. Clin. Oncol., 122: 135-140, 1996.
    • (1996) J. Cancer Res. Clin. Oncol. , vol.122 , pp. 135-140
    • Knudson, A.G.1
  • 18
    • 0025773554 scopus 로고
    • Mutator phenotype may be required for multistage carcinogenesis
    • Loeb, L. A. Mutator phenotype may be required for multistage carcinogenesis. Cancer Res., 51: 3075-3079, 1991.
    • (1991) Cancer Res. , vol.51 , pp. 3075-3079
    • Loeb, L.A.1
  • 19
  • 20
    • 0030924499 scopus 로고    scopus 로고
    • The genetics of familial leukemia
    • Baltimore
    • Horwitz, M. The genetics of familial leukemia. Leukemia (Baltimore), 11; 1347-1359, 1997.
    • (1997) Leukemia , vol.11 , pp. 1347-1359
    • Horwitz, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.