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Volumn 63, Issue 1, 1998, Pages 63-70

Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANCER CLASSIFICATION; CLINICAL ARTICLE; COLORECTAL CANCER; DNA REPAIR; FAMILIAL CANCER; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC STABILITY; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; MUIR TORRE SYNDROME; PRIORITY JOURNAL;

EID: 1642633537     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301926     Document Type: Article
Times cited : (198)

References (31)
  • 1
    • 85031595334 scopus 로고    scopus 로고
    • International Collaborative Group-HNPCC database, http:// www.nfdht.nl
  • 2
    • 85031591765 scopus 로고    scopus 로고
    • for MTS [MIM 158320] and HNPCC/Lynch syndrome [MIM 120435 and 120436]
    • Online Mendelian Inheritance in Man (OMIM), http:// www.ncbi.nlm.nih.gov/Omim (for MTS [MIM 158320] and HNPCC/Lynch syndrome [MIM 120435 and 120436])
  • 4
    • 0025878737 scopus 로고
    • Muir-Torre syndrome: A case report
    • Bisceglia M, Zenarola P (1991) Muir-Torre syndrome: a case report. Tumori 77:277-281
    • (1991) Tumori , vol.77 , pp. 277-281
    • Bisceglia, M.1    Zenarola, P.2
  • 6
    • 0022912584 scopus 로고
    • Muir-Torre syndrome: Histologic spectrum of sebaceous proliferations
    • Burgdorf WHC, Pitha J, Fahmy A (1986) Muir-Torre syndrome: histologic spectrum of sebaceous proliferations. Am J Dermatopathol 8:202-208
    • (1986) Am J Dermatopathol , vol.8 , pp. 202-208
    • Burgdorf, W.H.C.1    Pitha, J.2    Fahmy, A.3
  • 7
    • 0025755503 scopus 로고
    • Association of sebaceous gland tumors and internal malignancy: The Muir-Torre syndrome
    • Cohen PR, Kohn SR, Kurzrock R (1991) Association of sebaceous gland tumors and internal malignancy: the Muir-Torre syndrome. Am J Med 90:606-613
    • (1991) Am J Med , vol.90 , pp. 606-613
    • Cohen, P.R.1    Kohn, S.R.2    Kurzrock, R.3
  • 9
    • 0027171303 scopus 로고
    • Single-step screening method for the most common mutations in familial adenomatous polyposis
    • Friedl W, Mandl M, Sengteller M (1993) Single-step screening method for the most common mutations in familial adenomatous polyposis. Hum Mol Genet 2:1481-1482
    • (1993) Hum Mol Genet , vol.2 , pp. 1481-1482
    • Friedl, W.1    Mandl, M.2    Sengteller, M.3
  • 11
    • 0028910650 scopus 로고
    • Muir-Torre syndrome: Diagnostic criteria and review of the literature
    • Hartig C, Stieler W, Stadler R (1995) Muir-Torre syndrome: diagnostic criteria and review of the literature. Hautarzt 46:107-113
    • (1995) Hautarzt , vol.46 , pp. 107-113
    • Hartig, C.1    Stieler, W.2    Stadler, R.3
  • 13
    • 0030747145 scopus 로고    scopus 로고
    • Reduced frequency of extracolonic cancers in hereditary nonpolyposis colorectal cancer families with monoallelic hMLH1 expression
    • Jäger AC, Bisgaard ML, Myrhøj T, Bernstein I, Rehfeld JF, Nielsen FC (1997) Reduced frequency of extracolonic cancers in hereditary nonpolyposis colorectal cancer families with monoallelic hMLH1 expression. Am J Hum Genet 61: 129-138
    • (1997) Am J Hum Genet , vol.61 , pp. 129-138
    • Jäger, A.C.1    Bisgaard, M.L.2    Myrhøj, T.3    Bernstein, I.4    Rehfeld, J.F.5    Nielsen, F.C.6
  • 14
    • 0028833856 scopus 로고
    • Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal carcinoma kindred for mlh1 mutations
    • Kolodner RD, Hall NR, Lipford J, Kane MF, Morrison P, Finan PJ, Burn J, et al (1995) Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal carcinoma kindred for mlh1 mutations. Cancer Res 55:242-248
    • (1995) Cancer Res , vol.55 , pp. 242-248
    • Kolodner, R.D.1    Hall, N.R.2    Lipford, J.3    Kane, M.F.4    Morrison, P.5    Finan, P.J.6    Burn, J.7
  • 15
  • 16
    • 10544255347 scopus 로고    scopus 로고
    • Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?
    • Kruse R, Lamberti C, Wang Y, Ruelfs C, Bruns A, Esche C, Lehmann P, et al (1996) Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene? Hum Genet 98:747-750
    • (1996) Hum Genet , vol.98 , pp. 747-750
    • Kruse, R.1    Lamberti, C.2    Wang, Y.3    Ruelfs, C.4    Bruns, A.5    Esche, C.6    Lehmann, P.7
  • 19
    • 0029164415 scopus 로고
    • In vitro transcription/ translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer
    • Luce MC, Marra G, Chauhan DP, Laghi L, Carethers JM, Cherian SP, Hawn M, et al (1995) In vitro transcription/ translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer. Gastroenterology 109:1368-1374
    • (1995) Gastroenterology , vol.109 , pp. 1368-1374
    • Luce, M.C.1    Marra, G.2    Chauhan, D.P.3    Laghi, L.4    Carethers, J.M.5    Cherian, S.P.6    Hawn, M.7
  • 20
    • 0019515269 scopus 로고
    • The cancer family syndrome: Rare cutaneous phenotypic linkage of Torre's syndrome
    • Lynch HT, Lynch PM, Pester J, Fusaro RM (1981) The cancer family syndrome: rare cutaneous phenotypic linkage of Torre's syndrome. Arch Intern Med 141:607-611
    • (1981) Arch Intern Med , vol.141 , pp. 607-611
    • Lynch, H.T.1    Lynch, P.M.2    Pester, J.3    Fusaro, R.M.4
  • 21
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller SA, Dykes DD, Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16:1215
    • (1988) Nucleic Acids Res , vol.16 , pp. 1215
    • Miller, S.A.1    Dykes, D.D.2    Polesky, H.F.3
  • 23
    • 0027366970 scopus 로고
    • Obstructive jejunal adenocarcinoma in the Muir-Torre syndrome
    • Panday SC, Go IH, Mravunac M, de Koning RW (1993) Obstructive jejunal adenocarcinoma in the Muir-Torre syndrome. Neth J Med 43:116-120
    • (1993) Neth J Med , vol.43 , pp. 116-120
    • Panday, S.C.1    Go, I.H.2    Mravunac, M.3    De Koning, R.W.4
  • 24
    • 0030739106 scopus 로고    scopus 로고
    • Molecular basis of HNPCC: Mutations of MMR genes
    • Papadopoulos N, Lindblom A (1997) Molecular basis of HNPCC: mutations of MMR genes. Hum Mutat 10:89-99
    • (1997) Hum Mutat , vol.10 , pp. 89-99
    • Papadopoulos, N.1    Lindblom, A.2
  • 25
    • 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 Non-Polyposis Colorectal Cancer
    • Peltomäki P, Vasen HF (1997) Mutations predisposing to hereditary nonpolyposis colorectal cancer: database and results of a collaborative study: the International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer. Gastroenterology 113:1146-1158
    • (1997) Gastroenterology , vol.113 , pp. 1146-1158
    • Peltomäki, P.1    Vasen, H.F.2
  • 26
    • 0029013597 scopus 로고
    • The Muir-Torre syndrome: A 25-year retrospect
    • Schwartz RA, Torre DP (1995) The Muir-Torre syndrome: a 25-year retrospect. J Am Acad Dermatol 33:90-104
    • (1995) J Am Acad Dermatol , vol.33 , pp. 90-104
    • Schwartz, R.A.1    Torre, D.P.2
  • 27
    • 0025848680 scopus 로고
    • The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)
    • Vasen HFA, Mecklin J-P, Meera Khan P, Lynch HT (1991) The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC). Dis Colon Rectum 34:424-425
    • (1991) Dis Colon Rectum , vol.34 , pp. 424-425
    • Vasen, H.F.A.1    Mecklin, J.-P.2    Meera Khan, P.3    Lynch, H.T.4
  • 29
    • 0030768854 scopus 로고    scopus 로고
    • Hereditary non-polyposis colorectal cancer (HNPCC): Eight novel germline mutations in the hMSH2 or hMLH1 genes
    • Wehner M, Buschhausen L, Lamberti C, Kruse R, Caspari R, Propping P, Friedl W (1997) Hereditary non-polyposis colorectal cancer (HNPCC): eight novel germline mutations in the hMSH2 or hMLH1 genes. Hum Mutat 10:241-244
    • (1997) Hum Mutat , 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
  • 30
    • 16944364360 scopus 로고    scopus 로고
    • Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations
    • Wijnen J, Khan PM, Vasen H, van der Klift H, Mulder A, van Leeuwen-Cornelisse I, Bakker B, et al (1997) Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations. Am J Hum Genet 61:329-335
    • (1997) Am J Hum Genet , vol.61 , pp. 329-335
    • Wijnen, J.1    Khan, P.M.2    Vasen, H.3    Van Der Klift, H.4    Mulder, A.5    Van Leeuwen-Cornelisse, I.6    Bakker, B.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.