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Volumn 87, Issue 4, 1991, Pages 409-415

Mechanisms of insertional mutagenesis in human genes causing genetic disease

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; DNA SEQUENCE; GENE INSERTION; GENE STRUCTURE; GENETIC DISORDER; HUMAN; MUTAGENESIS; MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

EID: 0025744705     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/BF00197158     Document Type: Article
Times cited : (123)

References (43)
  • 4
    • 0023717164 scopus 로고
    • A novel β-thalassaemia frameshift mutation (codon 14/15), detectable by direct visualization of abnormal restriction fragment in amplified genomic DNA
    • (1988) Blood , vol.72 , pp. 1420-1423
    • Chan, V.1    Chan, T.K.2    Kan, Y.W.3    Todd, D.4
  • 5
    • 0025364861 scopus 로고
    • The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions
    • (1990) Hum Genet , vol.85 , pp. 55-74
    • Cooper, D.N.1    Krawczak, M.2
  • 20
    • 0025762012 scopus 로고
    • Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment
    • (1991) Hum Genet , vol.86 , pp. 425-441
    • Krawczak, M.1    Coooper, D.N.2
  • 21
    • 0021872030 scopus 로고
    • The mutational specificity of DNA polymerasebeta during in vitro DNA synthesis
    • (1985) J Biol Chem , vol.260 , pp. 5787-5796
    • Kunkel, T.A.1
  • 22
    • 0022344932 scopus 로고
    • The mutational specificity of DNA polymerases alpha and gamma during in vitro DNA synthesis
    • (1985) J Biol Chem , vol.260 , pp. 12866-12874
    • Kunkel, T.A.1
  • 23
    • 0022577219 scopus 로고
    • The base substitution fidelity of eukaryotic DNA polymerases
    • (1986) J Biol Chem , vol.261 , pp. 160-166
    • Kunkel, T.A.1
  • 28
    • 0022432381 scopus 로고
    • A Chinese G gamma+ (A-gamma-delta-beta)∘ thalassaemia deletion: comparison to other deletions in the human beta-globin gene cluster and sequence analysis of the breakpoints
    • (1985) Nucleic Acids Res , vol.13 , pp. 6559-6564
    • Mager, D.L.1    Henthorn, P.S.2    Smithies, O.3
  • 31
    • 0024259857 scopus 로고
    • The major defect in Ashkenazi Jews with Tay-Sachs disease is an insertion in the gene for the alpha chain of β-hexosaminidase
    • (1988) J Biol Chem , vol.263 , pp. 18587-18589
    • Myerowitz, R.1    Costigan, F.C.2
  • 40
    • 0024027282 scopus 로고
    • The functional significance of DNA sequence structure in a site-specific genetic recombination reaction
    • (1988) EMBO J , vol.7 , pp. 1845-1852
    • Umlauf, S.W.1    Cox, M.M.2
  • 43
    • 0024062518 scopus 로고
    • Hypothesis for testing deviations from random integration: evidence for nonrandom retroviral integration
    • (1988) Genomics , vol.3 , pp. 137-142
    • Wilson, A.F.1    Cohen, J.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.