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Virus Genes|August 2, 2017
Next-generation AAV vectors for clinical use: an ever-accelerating raceJonas Weinmann, Dirk GrimmGene 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.Methods (San Diego, Calif.)|November 5, 2002
Production methods for gene transfer vectors based on adeno-associated virus serotypesDirk GrimmSilence|October 28, 2011
The dose can make the poison: lessons learned from adverse in vivo toxicities caused by RNAi overexpressionDirk GrimmPlos Biology|July 17, 2024
When size matters: A novel compact Cas12a variant for in vivo genome editingFelix Bubeck, Dirk GrimmCytotherapy|August 23, 2022
Boosters for adeno-associated virus (AAV) vector (r)evolutionJoanna Szumska, Dirk GrimmFrontiers in Immunology|November 15, 2021
Adeno-Associated Viruses (AAV) and Host Immunity - A Race Between the Hare and the HedgehogKleopatra Rapti, Dirk GrimmBiotechnology Journal|January 10, 2018
Split Cas9, Not Hairs - Advancing the Therapeutic Index of CRISPR TechnologyCarolin Schmelas, Dirk GrimmMolecular Therapy : the Journal of the American Society of Gene Therapy|April 8, 2021
Best of most possible worlds: Hybrid gene therapy vectors based on parvoviruses and heterologous virusesJulia Fakhiri, Dirk GrimmPageof 15