메뉴 건너뛰기




Volumn 70, Issue 3, 2006, Pages 250-252

Large genomic alterations in hMSH2 and hMLH1 in early-onset colorectal cancer: Identification of a large complex de novo hMLH1 alteration [1]

Author keywords

[No Author keywords available]

Indexed keywords

MISMATCH REPAIR PROTEIN PMS2; PROTEIN MLH1; PROTEIN MSH2; PROTEIN MSH6;

EID: 33747141723     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2006.00662.x     Document Type: Letter
Times cited : (12)

References (13)
  • 1
    • 0037058317 scopus 로고    scopus 로고
    • After hMSH2 and hMLH1 - What next? Analysis of three-generational, population-based, early-onset colorectal cancer families
    • Jenkins MA, Baglietto L, Dite GS et al. After hMSH2 and hMLH1 - what next? Analysis of three-generational, population-based, early-onset colorectal cancer families. Int J Cancer 2002: 102: 166-171.
    • (2002) Int J Cancer , vol.102 , pp. 166-171
    • Jenkins, M.A.1    Baglietto, L.2    Dite, G.S.3
  • 2
    • 26644441586 scopus 로고    scopus 로고
    • Use of molecular tumour characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer
    • Epub 22 August 2005
    • Southey MC, Jenkins MA, Mead L et al. Use of molecular tumour characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer. J Clin Oncol 2005: 23 (27): 6524-6532. Epub 22 August 2005.
    • (2005) J Clin Oncol , vol.23 , Issue.27 , pp. 6524-6532
    • Southey, M.C.1    Jenkins, M.A.2    Mead, L.3
  • 3
    • 0032534069 scopus 로고    scopus 로고
    • A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal cancer
    • Review
    • Boland CR, Thibodeau SN, Hamilton SR et al. A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res 1998: 58 (22): 5248-5257. Review.
    • (1998) Cancer Res , vol.58 , Issue.22 , pp. 5248-5257
    • Boland, C.R.1    Thibodeau, S.N.2    Hamilton, S.R.3
  • 4
    • 0034956758 scopus 로고    scopus 로고
    • Molecular pathologic analysis enhances the diagnosis and management of Muir-Torre syndrome and gives insight into its underlying molecular pathogenesis
    • Southey MC, Young MA, Whitty J et al. Molecular pathologic analysis enhances the diagnosis and management of Muir-Torre syndrome and gives insight into its underlying molecular pathogenesis. Am J Surg Pathol 2001: 25: 936-941.
    • (2001) Am J Surg Pathol , vol.25 , pp. 936-941
    • Southey, M.C.1    Young, M.A.2    Whitty, J.3
  • 6
    • 0033358556 scopus 로고    scopus 로고
    • De novo BRCA1 mutation in a patient with breast cancer and an inherited BRCA2 mutation
    • Tesoriero A, Andersen C, Southey M et al. De novo BRCA1 mutation in a patient with breast cancer and an inherited BRCA2 mutation. Am J Hum Genet 1999: 65 (2): 567-569.
    • (1999) Am J Hum Genet , vol.65 , Issue.2 , pp. 567-569
    • Tesoriero, A.1    Andersen, C.2    Southey, M.3
  • 7
    • 20444419055 scopus 로고    scopus 로고
    • Large genomic aberrations in MSH2 and MLH1 genes are frequent in Chinese colorectal cancer
    • Zhu M, Li J, Zhang X et al. Large genomic aberrations in MSH2 and MLH1 genes are frequent in Chinese colorectal cancer. Cancer Genet Cytogenet 2005: 160 (1): 61-67.
    • (2005) Cancer Genet Cytogenet , vol.160 , Issue.1 , pp. 61-67
    • Zhu, M.1    Li, J.2    Zhang, X.3
  • 8
    • 24944480082 scopus 로고    scopus 로고
    • Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC)
    • van der Klift H, Wijnen J, Wagner A et al. Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC). Genes Chromosomes Cancer 2005: 44 (2): 123-138.
    • (2005) Genes Chromosomes Cancer , vol.44 , Issue.2 , pp. 123-138
    • van der Klift, H.1    Wijnen, J.2    Wagner, A.3
  • 9
    • 21044452350 scopus 로고    scopus 로고
    • Deletions account for 17% of pathogenic germline alterations in MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer (HNPCC) families
    • Grabowski M, Mueller-Koch Y, Grasbon-Frodl E et al. Deletions account for 17% of pathogenic germline alterations in MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer (HNPCC) families. Genet Test 2005: 9 (2): 138-146.
    • (2005) Genet Test , vol.9 , Issue.2 , pp. 138-146
    • Grabowski, M.1    Mueller-Koch, Y.2    Grasbon-Frodl, E.3
  • 10
    • 21144444336 scopus 로고    scopus 로고
    • Gastrointestinal Oncology Group of the Spanish Gastroenterological Association. Genomic rearrangements in MSH2 and MLH1 are rare mutational events in Spanish patients with hereditary nonpolyposis colorectal cancer
    • Castellvi-Bel S, Castells A, Strunk M. et al. Gastrointestinal Oncology Group of the Spanish Gastroenterological Association. Genomic rearrangements in MSH2 and MLH1 are rare mutational events in Spanish patients with hereditary nonpolyposis colorectal cancer. Cancer Lett 2005: 225 (1): 93-98.
    • (2005) Cancer Lett , vol.225 , Issue.1 , pp. 93-98
    • Castellvi-Bel, S.1    Castells, A.2    Strunk, M.3
  • 11
    • 33644904579 scopus 로고    scopus 로고
    • First report of a de novo germline mutation in the MLH1 gene
    • Stulp RP, Vos YJ, Mol B et al. First report of a de novo germline mutation in the MLH1 gene. World J Gastroenterol 2006: 12 (5): 809-811.
    • (2006) World J Gastroenterol , vol.12 , Issue.5 , pp. 809-811
    • Stulp, R.P.1    Vos, Y.J.2    Mol, B.3
  • 12
    • 33645826906 scopus 로고    scopus 로고
    • Cancer risks for mismatch repair gene mutation carriers: A population-based early onset case-family study
    • Jenkins MA, Baglietto L, Dowty JG et al. Cancer risks for mismatch repair gene mutation carriers: A population-based early onset case-family study. Clin Gastroenterol Hepatol 2006: 4 (4): 489-498.
    • (2006) Clin Gastroenterol Hepatol , vol.4 , Issue.4 , pp. 489-498
    • Jenkins, M.A.1    Baglietto, L.2    Dowty, J.G.3
  • 13
    • 0346363771 scopus 로고    scopus 로고
    • Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: Identification of novel and recurrent deletions by MLPA
    • Taylor CF, Charlton RS, Burn J, Sheridan E, Taylor GR. Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: Identification of novel and recurrent deletions by MLPA. Hum Mutat 2003: 22 (6): 428-433.
    • (2003) Hum Mutat , vol.22 , Issue.6 , pp. 428-433
    • Taylor, C.F.1    Charlton, R.S.2    Burn, J.3    Sheridan, E.4    Taylor, G.R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.