Genetically modified adenoviral vector with the protein transduction domain of Tat improves gene transfer to CAR-deficient cells

Bioscience Reports

Volumn 29, Issue 2, 2009, Pages 103-109

  Liu, Shihai ^a   Mao, Qinwen ^b   Zhang, Weifeng ^a   Zheng, Xiaojing ^a   Bian, Ye ^a   Wang, Dongyang ^a   Li, Huijin ^a   Chai, Lihong ^a   Zhao, Junli ^a   Xia, Haibin ^a  

^a SHAANXI NORMAL UNIVERSITY   (China)

^b UNIVERSITY OF TEXAS AT DALLAS   (United States)

Author keywords

Adenovirus (Ad); Cancer; Fibre protein; Gene delivery; Protein transduction domain (PTD); Tat

Indexed keywords

CAR RECEPTOR; TRANSACTIVATOR PROTEIN; VIRUS RECEPTOR;

ARTICLE; CELL LINE; CHEMISTRY; CYTOLOGY; FIBROBLAST; GENE THERAPY; GENE TRANSFER; GENETIC TRANSDUCTION; GENETICS; HUMAN; HUMAN ADENOVIRUS; KIDNEY; METABOLISM; METHODOLOGY; PROTEIN TERTIARY STRUCTURE; UMBILICAL VEIN;

ADENOVIRUSES, HUMAN; CELL LINE; FIBROBLASTS; GENE PRODUCTS, TAT; GENE THERAPY; GENE TRANSFER TECHNIQUES; HUMANS; KIDNEY; PROTEIN STRUCTURE, TERTIARY; RECEPTORS, VIRUS; TRANSDUCTION, GENETIC; UMBILICAL VEINS;

EID: 66349092921     PISSN: 01448463     EISSN: 15734935     Source Type: Journal    
DOI: 10.1042/BSR20080023     Document Type: Article

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