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Viruses|March 6, 2021
Characterization of the GBoV1 Capsid and Its Antibody InteractionsJennifer Chun Yu, Mario Mietzsch, Amriti Singh, et al.
Cell Stem Cell|June 4, 2016
In Vivo Hepatic Reprogramming of Myofibroblasts with AAV Vectors as a Therapeutic Strategy for Liver FibrosisMilad Rezvani, Regina Español-Suñer, Yann Malato, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 8, 2024
T-cell specific in vivo gene delivery with DART-AAVs targeted to CD8Muhammed Burak Demircan, Luca J Zinser, Alexander Michels, et al.
Journal of the American College of Cardiology|August 2, 2014
Genome editing of isogenic human induced pluripotent stem cells recapitulates long QT phenotype for drug testingYongming Wang, Ping Liang, Feng Lan, et al.
Nature Chemical Biology|April 15, 2020
Computational design of anti-CRISPR proteins with improved inhibition potencyJan Mathony, Zander Harteveld, Carolin Schmelas, et al.
Human Gene Therapy|January 24, 2025
Directed Evolution of AAV9 for Efficient Gene Expression in Cardiomyocytes In Vitro and In VivoLeonard Hüttermann, Lena C Schröder, Prithviraj M V Shetty, et al.
JCI Insight|November 15, 2019
Using a barcoded AAV capsid library to select for clinically relevant gene therapy vectorsKatja Pekrun, Gustavo De Alencastro, Qing-Jun Luo, et al.
Nature Communications|December 14, 2017
Multiplexed in vivo homology-directed repair and tumor barcoding enables parallel quantification of Kras variant oncogenicityIan P Winters, Shin-Heng Chiou, Nicole K Paulk, et al.
Blood|January 18, 2006
Host factors that impact the biodistribution and persistence of multipotent adult progenitor cellsJakub Tolar, Matthew J O'shaughnessy, Angela Panoskaltsis-Mortari, et al.
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