메뉴 건너뛰기




Volumn 71, Issue 3, 2000, Pages 463-469

Gene conversion-like missense mutations in the human cationic trypsinogen gene and insights into the molecular evolution of the human trypsinogen family

Author keywords

Cationic trypsinogen; Concerted evolution; Gene conversion; Hereditary pancreatitis; Human trypsinogen family; Missense mutation; Ortholog; Paralog

Indexed keywords

TRYPSINOGEN;

EID: 0033749850     PISSN: 10967192     EISSN: None     Source Type: Journal    
DOI: 10.1006/mgme.2000.3086     Document Type: Article
Times cited : (27)

References (44)
  • 10
    • 0026701193 scopus 로고
    • Gaucher disease: A G + 1 - - - - A + 1 IVS2 splice donor site mutation causing exon 2 skipping in the acid beta-glucosidase mRNA
    • (1992) Am J Hum Genet , vol.51 , pp. 810-820
    • He, G.S.1    Grabowski, G.A.2
  • 30
    • 0034062222 scopus 로고    scopus 로고
    • Origin and implication of the hereditary pancreatitis-associated N21I mutation in the cationic trypsinogen gene
    • (2000) Hum Genet , vol.106 , pp. 125-126
    • Chen, J.M.1    Ferec, C.2
  • 33
    • 0033917970 scopus 로고    scopus 로고
    • Genes, cloned cDNAs, and proteins of human trypsinogens and pancreatitis-associated cationic trypsinogen mutations
    • (2000) Pancreas , vol.21 , pp. 57-62
    • Chen, J.M.1    Ferec, C.2
  • 37
    • 0019795095 scopus 로고
    • Chi, a promoter of generalized recombination in lambda phage, is present in immunoglobulin genes
    • (1981) Nature , vol.293 , pp. 402-404
    • Kenter, A.L.1    Birshtein, B.K.2
  • 38
    • 0020965548 scopus 로고
    • Chi hotspots of generalized recombination
    • (1983) Cell , vol.34 , pp. 709-710
    • Smith, G.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.