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Human Gene Therapy|March 7, 2009
Lentiviral vector design for optimal T cell receptor gene expression in the transduction of peripheral blood lymphocytes and tumor-infiltrating lymphocytesStephanie Jones, Peter D Peng, Shicheng Yang, et al.Human Gene Therapy|March 11, 2009
Treatment with LL-37 peptide enhances antitumor effects induced by CpG oligodeoxynucleotides against ovarian cancerChi-Mu Chuang, Archana Monie, Annie Wu, et al.Human Gene Therapy|March 14, 2009
Antitumor therapy based on cellular competitionJordi Martinez-Quintanilla, Manel Cascallo, Cristina Fillat, et al.Human Gene Therapy|February 28, 2009
Transduction of liver metastases after intravenous injection of Ad5/35 or Ad35 vectors with and without factor X-binding protein pretreatmentYing Liu, Hongjie Wang, Roma Yumul, et al.Human Gene Therapy|May 7, 2009
Acute toxicity study of a simian immunodeficiency virus-based lentiviral vector for retinal gene transfer in nonhuman primatesYasuhiro Ikeda, Yoshikazu Yonemitsu, Masanori Miyazaki, et al.Human Gene Therapy|May 8, 2009
Avidin fusion protein-expressing lentiviral vector for targeted drug deliveryHanna P Lesch, Jere T Pikkarainen, Minna U Kaikkonen, et al.Human Gene Therapy|May 8, 2009
Scalable recombinant adeno-associated virus production using recombinant herpes simplex virus type 1 coinfection of suspension-adapted mammalian cellsDarby L Thomas, Lijun Wang, Justine Niamke, et al.Human Gene Therapy|May 28, 2009
Dosing regimen has a significant impact on the efficiency of morpholino oligomer-induced exon skipping in mdx miceAlberto Malerba, Francesca C Thorogood, George Dickson, et al.Human Gene Therapy|June 23, 2009
Thermosensitivity of the reverse transcription process as an inactivation mechanism of lentiviral vectorsM Carmo, J D Dias, A Panet, et al.Human Gene Therapy|June 25, 2009
Inhibition of acidic mammalian chitinase by RNA interference suppresses ovalbumin-sensitized allergic asthmaChing-Jen Yang, Yu-Kuo Liu, Chao-Lin Liu, et al.Pageof 413