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Volumn 4, Issue 2, 2007, Pages 130-134

Medulloblastoma, acute myelocytic leukemia and colonic carcinomas in a child with biallelic MSH6 mutations

Author keywords

[No Author keywords available]

Indexed keywords

BUSULFAN; CAPECITABINE; CARBOPLATIN; CYCLOPHOSPHAMIDE; CYTARABINE; DAUNORUBICIN; ETOPOSIDE; PROTEIN MSH6; VINCRISTINE;

EID: 33846660119     PISSN: 17434254     EISSN: 17434262     Source Type: Journal    
DOI: 10.1038/ncponc0719     Document Type: Article
Times cited : (76)

References (18)
  • 1
    • 16544395180 scopus 로고    scopus 로고
    • A homozygous MSH6 mutation in a child with cafe-au-lait spots, oligodendroglioma and rectal cancer
    • Menko FH et al. (2004) A homozygous MSH6 mutation in a child with cafe-au-lait spots, oligodendroglioma and rectal cancer. Fam Cancer 3: 123-127
    • (2004) Fam Cancer , vol.3 , pp. 123-127
    • Menko, F.H.1
  • 2
    • 27644596327 scopus 로고    scopus 로고
    • A homozygous mutation in MSH6 causes Turcot syndrome
    • Hegde MR et al. (2005) A homozygous mutation in MSH6 causes Turcot syndrome. Clin Cancer Res 11: 4689-4693
    • (2005) Clin Cancer Res , vol.11 , pp. 4689-4693
    • Hegde, M.R.1
  • 3
    • 33644892563 scopus 로고    scopus 로고
    • Neurofibromatosis von Recklinghausen type I phenotype and early onset of cancers in siblings compound heterozygous for mutations in MSH6
    • Ostergaard JR et al. (2005) Neurofibromatosis von Recklinghausen type I phenotype and early onset of cancers in siblings compound heterozygous for mutations in MSH6. Am J Med Genet A 139:96-105
    • (2005) Am J Med Genet A , vol.139 , pp. 96-105
    • Ostergaard, J.R.1
  • 4
    • 33646044700 scopus 로고    scopus 로고
    • Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without haematological malignancy and brain tumor
    • Plaschke J et al. (2006) Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without haematological malignancy and brain tumor. Eur J Hum Genet 14:561-566
    • (2006) Eur J Hum Genet , vol.14 , pp. 561-566
    • Plaschke, J.1
  • 5
    • 14644396669 scopus 로고    scopus 로고
    • Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: The German Hereditary Nonpolyposis Colorectal Cancer Consortium
    • Plaschke J et al. (2004) Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: The German Hereditary Nonpolyposis Colorectal Cancer Consortium. J Clin Oncol 22: 4486-4494
    • (2004) J Clin Oncol , vol.22 , pp. 4486-4494
    • Plaschke, J.1
  • 6
    • 0033556009 scopus 로고    scopus 로고
    • Neurofibromatosis and early onset of cancers in hMLH1-deficient children
    • Wang Q et al. (1999) Neurofibromatosis and early onset of cancers in hMLH1-deficient children. Cancer Res 59: 294-297
    • (1999) Cancer Res , vol.59 , pp. 294-297
    • Wang, Q.1
  • 7
    • 0034094731 scopus 로고    scopus 로고
    • Use of the national institutes of health criteria for diagnosis of neurofibromatosis 1 in children
    • DeBella K et al. (2000) Use of the national institutes of health criteria for diagnosis of neurofibromatosis 1 in children. Pediatrics 105: 608-614
    • (2000) Pediatrics , vol.105 , pp. 608-614
    • DeBella, K.1
  • 8
    • 0028970197 scopus 로고
    • The molecular basis of Turcot's syndrome
    • Hamilton SR et al. (1995) The molecular basis of Turcot's syndrome. N Engl J Med 332: 839-847
    • (1995) N Engl J Med , vol.332 , pp. 839-847
    • Hamilton, S.R.1
  • 9
    • 13444274594 scopus 로고    scopus 로고
    • Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour
    • Reid S et al. (2005) Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour. J Med Genet 42: 147-151
    • (2005) J Med Genet , vol.42 , pp. 147-151
    • Reid, S.1
  • 10
    • 0037337734 scopus 로고    scopus 로고
    • Medulloblastoma with adverse reaction to radiation therapy in nijmegen breakage syndrome
    • Bakhshi S et al. (2003) Medulloblastoma with adverse reaction to radiation therapy in nijmegen breakage syndrome. J Pediatr Hematol Oncol 25: 248-251
    • (2003) J Pediatr Hematol Oncol , vol.25 , pp. 248-251
    • Bakhshi, S.1
  • 11
    • 0031052108 scopus 로고    scopus 로고
    • Bloom's syndrome. XX. The first 100 cancers
    • German J (1997) Bloom's syndrome. XX. The first 100 cancers. Cancer Genet Cytogenet 93: 100-106
    • (1997) Cancer Genet Cytogenet , vol.93 , pp. 100-106
    • German, J.1
  • 12
    • 79959316443 scopus 로고    scopus 로고
    • Colorectal cancer screening: Clinical practice guidelines in oncology
    • National Comprehensive Cancer Network
    • National Comprehensive Cancer Network (2003) Colorectal cancer screening: Clinical practice guidelines in oncology. J Nat Comp Cancer Net 1: 72-93
    • (2003) J Nat Comp Cancer Net , vol.1 , pp. 72-93
  • 13
    • 28944450748 scopus 로고    scopus 로고
    • Mechanisms of therapy-related carcinogenesis
    • Allan JM and Travis LB (2005) Mechanisms of therapy-related carcinogenesis. Nat Rev Cancer 5: 943-955
    • (2005) Nat Rev Cancer , vol.5 , pp. 943-955
    • Allan, J.M.1    Travis, L.B.2
  • 14
    • 1842841660 scopus 로고    scopus 로고
    • Mutations in DNA mismatch repair genes: Implications for DNA damage signaling and drug sensitivity
    • Fedier A and Fink D (2004) Mutations in DNA mismatch repair genes: implications for DNA damage signaling and drug sensitivity. Int J Oncol 24: 1039-1047
    • (2004) Int J Oncol , vol.24 , pp. 1039-1047
    • Fedier, A.1    Fink, D.2
  • 15
    • 33646256145 scopus 로고    scopus 로고
    • A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy
    • Hunter C et al. (2006) A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy. Cancer Res 66: 3987-3991
    • (2006) Cancer Res , vol.66 , pp. 3987-3991
    • Hunter, C.1
  • 16
    • 0031855988 scopus 로고    scopus 로고
    • Enrichment for DNA mismatch repair-deficient cells during treatment with cisplatin
    • Fink D et al. (1998) Enrichment for DNA mismatch repair-deficient cells during treatment with cisplatin. Int J Cancer 77: 741-746
    • (1998) Int J Cancer , vol.77 , pp. 741-746
    • Fink, D.1
  • 17
    • 3242756741 scopus 로고    scopus 로고
    • Defective DNA mismatch repair in acute myeloid leukemia/myelodysplastic syndrome after organ transplantation
    • Offman J et al. (2004) Defective DNA mismatch repair in acute myeloid leukemia/myelodysplastic syndrome after organ transplantation. Blood 104: 822-828
    • (2004) Blood , vol.104 , pp. 822-828
    • Offman, J.1
  • 18
    • 33646798052 scopus 로고    scopus 로고
    • Mismatch repair status in prediction of benefit from adjuvant fluorouracil chemotherapy in colorectal cancer
    • Jover R et al. (2006) Mismatch repair status in prediction of benefit from adjuvant fluorouracil chemotherapy in colorectal cancer. Gut 55: 848-855
    • (2006) Gut , vol.55 , pp. 848-855
    • Jover, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.