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S Hanlon

Showing results (61-70 of 64) with videos related to

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Gene Therapy|June 10, 2025
Engineered AAV capsids mediate transduction of murine neurofibroma and sciatic nerveEdwina Abou Haidar, Shilpa Prabhakar, Pike See Cheah, et al.
Molecular Therapy. Methods & Clinical Development|December 25, 2018
Gene Transfer with AAV9-PHP.B Rescues Hearing in a Mouse Model of Usher Syndrome 3A and Transduces Hair Cells in a Non-human PrimateBence György, Elise J Meijer, Maryna V Ivanchenko, et al.
Nature Communications|October 2, 2019
High levels of AAV vector integration into CRISPR-induced DNA breaksKillian S Hanlon, Benjamin P Kleinstiver, Sara P Garcia, et al.
Nature|March 30, 2023
Genomic investigations of unexplained acute hepatitis in childrenSofia Morfopoulou, Sarah Buddle, Oscar Enrique Torres Montaguth, et al.
Pageof 7

Showing results (61-70 of 64) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 64 results.
Gene Therapy|June 10, 2025
Engineered AAV capsids mediate transduction of murine neurofibroma and sciatic nerveEdwina Abou Haidar, Shilpa Prabhakar, Pike See Cheah, et al.
Molecular Therapy. Methods & Clinical Development|December 25, 2018
Gene Transfer with AAV9-PHP.B Rescues Hearing in a Mouse Model of Usher Syndrome 3A and Transduces Hair Cells in a Non-human PrimateBence György, Elise J Meijer, Maryna V Ivanchenko, et al.
Nature Communications|October 2, 2019
High levels of AAV vector integration into CRISPR-induced DNA breaksKillian S Hanlon, Benjamin P Kleinstiver, Sara P Garcia, et al.
Nature|March 30, 2023
Genomic investigations of unexplained acute hepatitis in childrenSofia Morfopoulou, Sarah Buddle, Oscar Enrique Torres Montaguth, et al.
Pageof 7