3[3]KIM IH,JOZKOWICZ A,PIEDRA PA,et al.Lifetime correction of geneticdeficiency in mice with a single injection of helper-dependent adenoviral vector[J].Proc Natl Acad Sci USA,2001,98(23):13282-13287.
4[4]REDDY PS,SAKHUJA K,GANESH S,et al.Sustained human factor Ⅷexpression in hemophilia A mice following systemic delivery of a gutless adenoviralvector[J].Mol Ther,2002,5(1):63-73.
7[7]ZUFFEREY R,DONELLO JE,TRONO D,et al.Woodchuck hepatitis virus posttranscriptional regulatory element enhances expression of transgenes delivered by retroviral vectors[J].J Virol,1999,73(4):2886-2892.
8[8]POESCHLA E,CORBEAU P,WONGSTAAL F.Development of HIV vectors for antiHIV gene therapy[J].Proc Nat1 Acad Sci USA,1996,93(21):11395-11399.
9[9]YAMADA K,OLSEN JC,PATEL M,et al.Functional correction of fanconianemia group C haematopoietic cells by the use of novel lentiviral vector[J].Mol Ther,2001,3(4):485-490.
10[10]GOLDMAN MJ,LEE PS,YANG JS,et al.Lentiviral vectors for gene therapy of cystic fibrosis[J].Hum Gene Thera,1997,8(18):2261-2268.
