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Volumn 20, Issue 2, 1996, Pages 278-285

Method for multiple portal vein infusions in mice: Quantitation of adenovirus-mediated hepatic gene transfer

Author keywords

[No Author keywords available]

Indexed keywords

VIRUS DNA; VIRUS VECTOR;

EID: 0003234944     PISSN: 07366205     EISSN: None     Source Type: Journal    
DOI: 10.2144/96202rr05     Document Type: Article
Times cited : (84)

References (20)
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  • 2
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    • Long-term improvement of hypercholesterolaemia after ex vivo gene therapy in LDLR-deficient rabbits
    • Chowdhury, J.R., M. Grossman, S. Gupta, N.R. Chowdhury, J.R. Baker and J.M. Wilson. 1991. Long-term improvement of hypercholesterolaemia after ex vivo gene therapy in LDLR-deficient rabbits. Science 254:1802-1805.
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    • Chowdhury, J.R.1    Grossman, M.2    Gupta, S.3    Chowdhury, N.R.4    Baker, J.R.5    Wilson, J.M.6
  • 4
    • 0028464358 scopus 로고
    • Gene therapy for phenylketonuria: Phenotypic correction in a genetically deficient mouse model by adenovirus-mediated hepatic gene transfer
    • Fang, B., R.C. Eisensmith, X.H.C. Li, M.J. Finegold, A. Shedlovsky, W. Dove and S.L.C. Woo. 1994. Gene therapy for phenylketonuria: phenotypic correction in a genetically deficient mouse model by adenovirus-mediated hepatic gene transfer. Gene Ther. 1:247-254.
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  • 7
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    • Kay M.A., F. Graham, F. Leland and S.L.C. Woo. 1995. Therapeutic serum concentrations of human alpha-1-antitrypsin after adenovrial mediated gene transfer into mouse hepatocytes. Hepatology 21.815-819.
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    • Kay, M.A.1    Graham, F.2    Leland, F.3    Woo, S.L.C.4
  • 9
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    • Kay, M.A., Q. Li, T. Liu, F. Leland, C. Toman, M. Finegold and S.LC. Woo. 1992. Hepatic gene therapy, persistent expression of human α1-antitrypsin in mice after direct gene delivery in vivo. Hum. Gene Ther. 3:641-647.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.