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Volumn 71, Issue 3, 2002, Pages 625-631

BRCA2 T2722R is a deleterious allele that causes exon skipping

Author keywords

[No Author keywords available]

Indexed keywords

BRCA1 PROTEIN; BRCA2 PROTEIN; DNA;

EID: 0036724459     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/342192     Document Type: Article
Times cited : (81)

References (41)
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    • Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy
    • (1997) J Clin Invest , vol.100 , pp. 2204-2210
    • Shiga, N.1
  • 29
    • 0032889287 scopus 로고    scopus 로고
    • BRCA1 mutations and other sequence variants in a population-based sample of Australian women with breast cancer. Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2. Australian Breast Cancer Family Study
    • (1999) Br J Cancer , vol.79 , pp. 34-39
    • Southey, M.C.1    Hopper, J.L.2
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    • The RNA binding protein YB-1 binds A/C-rich exon enhancers and stimulates splicing of the CD44 alternative exon v4 modulation of soluble CD44 concentrations by hormone and anti-hormone treatment in gynecological tumor cell lines
    • (2001) EMBO J , vol.20 , pp. 3821-3830
    • Stickeler, E.1
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    • Evidence that translation reinitiation abrogates nonsense-mediated mRNA decay in mammalian cells
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.