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Human Gene Therapy Methods|January 30, 2019
Standardized, Scalable, and Timely Flexible Adeno-Associated Virus Vector Production Using Frozen High-Density HEK-293 Cell Stocks and CELLdiscsBenjamin Strobel, Kai Zuckschwerdt, Gudrun Zimmermann, et al.
Nature Communications|February 7, 2020
High-throughput identification of synthetic riboswitches by barcode-free amplicon-sequencing in human cellsBenjamin Strobel, Maike Spöring, Holger Klein, et al.
Molecular Therapy. Advances|May 20, 2026
MicroRNA-based targeting strategies enable AAV-mediated, tissue-selective gene expression in adipose tissue and skeletal muscle of miceGina Blahetek, Sarah Abele, Emilia Schmierer, et al.
Translational Vision Science & Technology|September 14, 2021
AAV-Mediated Expression of Human VEGF, TNF-α, and IL-6 Induces Retinal Pathology in MiceCarina M Weigelt, Holger Fuchs, Tanja Schönberger, et al.
Frontiers in Cell and Developmental Biology|September 12, 2022
Transcriptional comparison of adult human primary Retinal Pigment Epithelium, human pluripotent stem cell-derived Retinal Pigment Epithelium, and ARPE19 cellsElke K Markert, Holger Klein, Coralie Viollet, et al.
Iscience|April 20, 2026
STARR-CRAAVT: A platform to identify cell type-specific regulatory elements for next-generation gene therapyRobert Becker, Priyanka Choudhury, Martin Oti, et al.
ACS Synthetic Biology|May 20, 2020
A Small-Molecule-Responsive Riboswitch Enables Conditional Induction of Viral Vector-Mediated Gene Expression in MiceBenjamin Strobel, Matthias J Düchs, Dragica Blazevic, et al.
American Journal of Respiratory Cell and Molecular Biology|April 7, 2015
Modeling Pulmonary Disease Pathways Using Recombinant Adeno-Associated Virus 6.2Benjamin Strobel, Matthias J Duechs, Ramona Schmid, et al.
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