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Journal of Molecular Biology|May 22, 2018
High-Throughput Dissection of AAV-Host Interactions: The Fast and the CuriousAnne-Kathrin Herrmann, Dirk GrimmBiotechnology Journal|September 25, 2020
Production, Processing, and Characterization of Synthetic AAV Gene Therapy VectorsJihad El Andari, Dirk GrimmNature Reviews. Genetics|April 7, 2011
State-of-the-art gene-based therapies: the road aheadMark A KayHuman Gene Therapy|September 26, 2007
Rapid and stable knockdown of an endogenous gene in retinal pigment epitheliumDaniel M Paskowitz, Kenneth P Greenberg, Douglas Yasumura, et al.Methods in Molecular Biology (Clifton, N.J.)|July 12, 2020
Lab-Scale Production of Recombinant Adeno-Associated Viruses (AAV) for Expression of Optogenetic ElementsJanina Haar, Chiara Krämer, Dirk GrimmMethods in Molecular Biology (Clifton, N.J.)|March 27, 2019
Rapid and Simple Screening of CRISPR Guide RNAs (gRNAs) in Cultured Cells Using Adeno-Associated Viral (AAV) VectorsJulia Fakhiri, Manuela Nickl, Dirk GrimmProgress in Molecular Biology and Translational Science|August 18, 2011
When cellular networks run out of control: global dysregulation of the RNAi machinery in human pathology and therapyStefan Mockenhaupt, Nina Schürmann, Dirk GrimmPathogens (Basel, Switzerland)|July 27, 2022
Fantastic AAV Gene Therapy Vectors and How to Find Them-Random Diversification, Rational Design and Machine LearningJonas Becker, Julia Fakhiri, Dirk GrimmHepatology (Baltimore, Md.)|January 29, 2008
Hepatic parenchymal replacement in mice by transplanted allogeneic hepatocytes is facilitated by bone marrow transplantation and mediated by CD4 cellsKonrad L Streetz, Regis Doyonnas, Dirk Grimm, et al.Hearing Research|December 3, 2020
Breaking the sound barrier: Towards next-generation AAV vectors for gene therapy of hearing disordersJulia Fakhiri, Lukas D Landegger, Dirk GrimmPageof 30