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Nucleic Acids Research|September 11, 2016
TALEN/CRISPR-mediated engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locusElena Senís, Stefan Mockenhaupt, Daniel Rupp, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 17, 2022
Ex vivo and in vivo suppression of SARS-CoV-2 with combinatorial AAV/RNAi expression vectorsJonas Becker, Megan Lynn Stanifer, Sarah Rebecca Leist, et al.
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.
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.
Scientific Reports|May 19, 2022
Identification of adeno-associated virus variants for gene transfer into human neural cell types by parallel capsid screeningLea Jessica Flitsch, Kathleen Börner, Christian Stüllein, et al.
Gastroenterology|February 1, 2020
Knockdown of Virus Antigen Expression Increases Therapeutic Vaccine Efficacy in High-Titer Hepatitis B Virus Carrier MiceThomas Michler, Anna D Kosinska, Julia Festag, et al.
EMBO Molecular Medicine|January 13, 2026
Sarcomeric remodelling in human heart failure unraveled by single molecule long read sequencingJan Haas, Sarah Schudy, Benedikt Rauscher, et al.
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