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Virus Genes|August 2, 2017
Next-generation AAV vectors for clinical use: an ever-accelerating raceJonas Weinmann, Dirk GrimmJournal of Neuroscience Methods|December 26, 2021
Two engineered AAV capsid variants for efficient transduction of human cortical neurons directly converted from iPSCSandra Fischer, Benjamin Strobel, Jonas Weinmann, et al.Gene Therapy|October 19, 2019
Distinct transduction of muscle tissue in mice after systemic delivery of AAVpo1 vectorsWarut Tulalamba, Jonas Weinmann, Quang Hong Pham, et al.Human Gene Therapy|September 13, 2022
Identification of Broadly Applicable Adeno-Associated Virus Vectors by Systematic Comparison of Commonly Used Capsid Variants In VitroJonas Weinmann, Julia Söllner, Sarah Abele, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|April 23, 2025
Identification of a robust promoter in mouse and human hepatocytes by in vivo biopanning of a barcoded AAV libraryJonas Becker, Claire Domenger, Pervinder Choksi, et al.Molecular Therapy. Methods & Clinical Development|September 23, 2021
High throughput screening of novel AAV capsids identifies variants for transduction of adult NSCs within the subventricular zoneLukas P M Kremer, Santiago Cerrizuela, Sascha Dehler, et al.Nature Communications|October 29, 2020
Identification of a myotropic AAV by massively parallel in vivo evaluation of barcoded capsid variantsJonas Weinmann, Sabrina Weis, Josefine Sippel, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|February 28, 2020
Pre-arrayed Pan-AAV Peptide Display Libraries for Rapid Single-Round ScreeningKathleen Börner, Eike Kienle, Lin-Ya Huang, et al.Science Advances|September 21, 2022
Semirational bioengineering of AAV vectors with increased potency and specificity for systemic gene therapy of muscle disordersJihad El Andari, Edith Renaud-Gabardos, Warut Tulalamba, et al.Pageof 1