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Frontiers in Genome Editing|April 1, 2022
Promoterless Gene Targeting Approach Combined to CRISPR/Cas9 Efficiently Corrects Hemophilia B Phenotype in Neonatal MiceMichela Lisjak, Alessia De Caneva, Thibaut Marais, et al.Nucleic Acids Research|December 4, 2016
Regulated complex assembly safeguards the fidelity of Sleeping Beauty transpositionYongming Wang, Diana Pryputniewicz-Dobrinska, Enikö Éva Nagy, et al.Nature Chemical Biology|April 3, 2019
An orange calcium-modulated bioluminescent indicator for non-invasive activity imagingYounghee Oh, Yunhee Park, Julia H Cho, et al.EMBO Molecular Medicine|April 9, 2025
Clinically translatable mitochondrial gene therapy in muscle using tandem mtZFN architecturePavel A Nash, Keira M Turner, Christopher A Powell, et al.Nature Genetics|January 17, 2019
Publisher Correction: Immune genes are primed for robust transcription by proximal long noncoding RNAs located in nuclear compartmentsStephanie Fanucchi, Ezio T Fok, Emiliano Dalla, 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 Methods|November 1, 2018
Engineered anti-CRISPR proteins for optogenetic control of CRISPR-Cas9Felix Bubeck, Mareike D Hoffmann, Zander Harteveld, et al.Molecular Therapy. Methods & Clinical Development|February 16, 2019
Novel Chimeric Gene Therapy Vectors Based on Adeno-Associated Virus and Four Different Mammalian BocavirusesJulia Fakhiri, Marc A Schneider, Jens Puschhof, et al.Nature Medicine|April 12, 2016
RNA interference-induced hepatotoxicity results from loss of the first synthesized isoform of microRNA-122 in micePaul N Valdmanis, Shuo Gu, Kirk Chu, et al.Cell Transplantation|November 9, 2010
Immunogenicity and immunomodulatory properties of umbilical cord lining mesenchymal stem cellsTobias Deuse, Mandy Stubbendorff, Karis Tang-Quan, et al.Pageof 30