High-efficiency Transduction and Correction of Murine Hemophilia B Using AAV2 Vectors Devoid of Multiple Surface-exposed Tyrosines

Author:

Markusic David M,Herzog Roland W,Aslanidi George V,Hoffman Brad E,Li Baozheng,Li Mengxin,Jayandharan Giridhara R.,Ling Chen,Zolotukhin Irene,Ma Wenqin,Zolotukhin Sergei,Srivastava Arun,Zhong Li

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine

Reference45 articles.

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3. Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vector;Flotte;Proc Natl Acad Sci USA,1993

4. Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors;Snyder;Nat Genet,1997

5. Efficient long-term gene transfer into muscle tissue of immunocompetent mice by adeno-associated virus vector;Xiao;J Virol,1996

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