메뉴 건너뛰기




Volumn 59, Issue 5, 2004, Pages 242-245

Tumor supressor gene NBS1 among children patients with malignancies;Nositelé mutací NBS1 genu mezi pacienty dětské onkologie

Author keywords

NBS heterozygotes among children patients with malignancies; Slavic mutations 657del5 and R215W; Tumor supressor gene NBS1

Indexed keywords

ARTICLE; CARCINOGENESIS; CHILD; CHILDHOOD CANCER; GENE FUNCTION; GENE MUTATION; GENETIC ANALYSIS; HETEROZYGOSITY; HETEROZYGOTE; HUMAN; IONIZING RADIATION; MAJOR CLINICAL STUDY; METASTASIS; NBS1 GENE; TUMOR SUPPRESSOR GENE; X RAY ANALYSIS;

EID: 2442646395     PISSN: 00692328     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (7)

References (12)
  • 2
    • 0033380655 scopus 로고    scopus 로고
    • Cancer risk in ATM heterozygotes: A model of phenotypic and mechanistic differences between missense and truncating mutations
    • Gatti, R. A., Tward, A., Concannon. P. Cancer risk in ATM heterozygotes: a model of phenotypic and mechanistic differences between missense and truncating mutations. Molec. Genet. Metab., 1999, 68, s. 419-423.
    • (1999) Molec. Genet. Metab. , vol.68 , pp. 419-423
    • Gatti, R.A.1    Tward, A.2    Concannon, P.3
  • 3
    • 0000770165 scopus 로고    scopus 로고
    • Nijmegen breakage syndrome
    • International Nijmegen Breakage Syndrome (NBS) Study Group. Nijmegen Breakage Syndrome. Arch. Dis. Child., 2000, 82, s. 400-406.
    • (2000) Arch. Dis. Child. , vol.82 , pp. 400-406
  • 4
    • 0025268280 scopus 로고
    • An increased risk for malignant neoplasms in heterozygotes for a syndrome of microcephaly, normal intelligence, growth retardation, remarkable facies, immunodeficiency and chromosomal instability
    • Seemanová, E. An increased risk for malignant neoplasms in heterozygotes for a syndrome of microcephaly, normal intelligence, growth retardation, remarkable facies, immunodeficiency and chromosomal instability. Mutat. Res., 1990, 238, s. 321-324.
    • (1990) Mutat. Res. , vol.238 , pp. 321-324
    • Seemanová, E.1
  • 6
    • 0038074370 scopus 로고    scopus 로고
    • Multiplex single-tube screening for mutations in the Nijmegen Breakage Syndrome (NBS1) gene in Hodgkin's and non Hodgkin's lymphoma patients of Slavic origin
    • Souček, P., Gut, I., Trněný, M., Skovlund, E., Grenaker Alnaes, G., Kristensen, T., Borresen-Dale, A. L., Kristensen, V. N. Multiplex single-tube screening for mutations in the Nijmegen Breakage Syndrome (NBS1) gene in Hodgkin's and non Hodgkin's lymphoma patients of Slavic origin. Europ. J. Hum. Genet., 2003, 11, s. 416-419.
    • (2003) Europ. J. Hum. Genet. , vol.11 , pp. 416-419
    • Souček, P.1    Gut, I.2    Trněný, M.3    Skovlund, E.4    Grenaker Alnaes, G.5    Kristensen, T.6    Borresen-Dale, A.L.7    Kristensen, V.N.8
  • 9
    • 0026409331 scopus 로고
    • Incidence of cancer in 161 families affected by ataxia telangiectasia
    • Swift, M., Morrell, D., Massey, R. B., Chase, C. L. Incidence of cancer in 161 families affected by ataxia telangiectasia. New Engl. J. Med., 1991, 325, s. 1831-1836.
    • (1991) New Engl. J. Med. , vol.325 , pp. 1831-1836
    • Swift, M.1    Morrell, D.2    Massey, R.B.3    Chase, C.L.4
  • 12
    • 0242544456 scopus 로고    scopus 로고
    • Heterozygous carriers of the 657del5 mutation of the NBS1 gene in probands from families with aggregations of malignant tumors
    • roč. 141, č. 8
    • Wisniewska, A., Wojciechowska-Lacka, A., Witzak, A., Kowalska, U., Paszko, Z., Steffen, J. Heterozygous carriers of the 657del5 mutation of the NBS1 gene in probands from families with aggregations of malignant tumors. Čas. Lék. čes., 2002, roč. 141, č. 8, s. VIII.
    • (2002) Čas. Lék. Čes.
    • Wisniewska, A.1    Wojciechowska-Lacka, A.2    Witzak, A.3    Kowalska, U.4    Paszko, Z.5    Steffen, J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.