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Human Gene Therapy|December 24, 2022
Development of an Inducible, Replication-Competent Assay Cell Line for Titration of Infectious Recombinant Adeno-Associated Virus VectorsZion Lee, Min Lu, Eesha Irfanullah, et al.Human Gene Therapy|December 14, 2022
Genome Editing of Pik3cd Impedes Abnormal Retinal AngiogenesisWenyi Wu, Gaoen Ma, Hui Qi, et al.Human Gene Therapy|November 26, 2019
Conditional Immortalization of Lymphoid Progenitors via Tetracycline-Regulated LMO2 ExpressionEkaterina Koniaeva, Maike Stahlhut, Lucas Lange, et al.Human Gene Therapy|November 28, 2019
Differential Transgene Silencing of Myeloid-Specific Promoters in the AAVS1 Safe Harbor Locus of Induced Pluripotent Stem Cell-Derived Myeloid CellsDenise Klatt, Erica Cheng, Dirk Hoffmann, et al.Human Gene Therapy|January 12, 2019
(Pro)renin Receptor RNA Interference Silencing Attenuates Diabetic Cardiomyopathy Pathological Process in RatsShiran Yu, Hai Yuan, Min Yang, et al.Human Gene Therapy|June 18, 2021
An Improved Lentiviral Fluorescent Genetic Barcoding Approach Distinguishes Hematopoietic Stem Cell Properties in Multiplexed In Vivo ExperimentsAnna Lieske, Teng Cheong Ha, Axel Schambach, et al.Human Gene Therapy|July 6, 2021
Adenosine Deaminase 1 Overexpression Enhances the Antitumor Efficacy of Chimeric Antigen Receptor-Engineered T CellsYun Qu, Zachary S Dunn, Xianhui Chen, et al.Human Gene Therapy|December 22, 2020
Combining Oncolytic Viruses with Chimeric Antigen Receptor T Cell TherapyKyle McGrath, Gianpietro DottiHuman Gene Therapy|January 7, 2021
Lack of Toxicity in Nonhuman Primates Receiving Clinically Relevant Doses of an AAV9.U7snRNA Vector Designed to Induce DMD Exon 2 SkippingLiubov V Gushchina, Emma C Frair, Natalie Rohan, et al.Human Gene Therapy|December 10, 2020
AAV1-Mediated shRNA Knockdown of SASH1 in Rat Bronchus Attenuates Hypoxia-Induced Pulmonary Artery RemodelingHong Liu, Ning Wang, Jun Li, et al.Pageof 413