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Human Gene Therapy|August 17, 2017
Driving CARs on the Highway to Solid Cancer: Some Considerations on the Adoptive Therapy with CAR T CellsHinrich AbkenHuman Gene Therapy|August 17, 2017
Optimization of Human NK Cell Manufacturing: Fully Automated Separation, Improved Ex Vivo Expansion Using IL-21 with Autologous Feeder Cells, and Generation of Anti-CD123-CAR-Expressing Effector CellsStephan Klöß, Olaf Oberschmidt, Michael Morgan, et al.Human Gene Therapy|September 1, 2017
Capsid Engineering of Adenovirus Vectors: Overcoming Early Vector-Host Interactions for TherapyClaudia Hagedorn, Florian KreppelHuman Gene Therapy|September 12, 2015
Systemic Vascular Transduction by Capsid Mutant Adeno-Associated Virus After Intravenous InjectionDaniel M Lipinski, Chris A Reid, Sanford L Boye, et al.Human Gene Therapy|September 29, 2015
Interplay of Promoter Usage and Intragenic CpG Content: Impact on GFP Reporter Gene ExpressionSimone Krinner, Asli Heitzer, Benedikt Asbach, et al.Human Gene Therapy|August 7, 2015
Gene Therapy Fully Restores Vision to the All-Cone Nrl(-/-) Gucy2e(-/-) Mouse Model of Leber Congenital Amaurosis-1Sanford L Boye, James J Peterson, Shreyasi Choudhury, et al.Human Gene Therapy|July 21, 2017
Steerable Induction of the Thymosin β4/MRTF-A Pathway via AAV-Based Overexpression Induces Therapeutic NeovascularizationTilman Ziegler, Markus Kraus, Wira Husada, et al.Human Gene Therapy|June 9, 2016
Adeno-Associated Virus-Based Gene Therapy for CNS DiseasesMichaël Hocquemiller, Laura Giersch, Mickael Audrain, et al.Human Gene Therapy|August 11, 2017
Making Oncolytic Virotherapy a Clinical Reality: The European ContributionMargaret R Duffy, Kerry D Fisher, Len W SeymourHuman Gene Therapy|September 19, 2015
Efficient Reprogramming of Human Fibroblasts and Blood-Derived Endothelial Progenitor Cells Using Nonmodified RNA for Reprogramming and Immune EvasionMarco Alexander Poleganov, Sarah Eminli, Tim Beissert, et al.Pageof 413