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Molecular Therapy. Methods & Clinical Development|February 13, 2025
A versatile cell line for establishing potency of cell type-specific AAV transgenesRefugio A Martinez, Yemeserach M Bishaw, Meagan A Quinlan, et al.
Molecular Therapy. Methods & Clinical Development|December 24, 2025
AAV-PHP.eB achieves superior neuronal transduction over AAV9 in pigtail macaques following intracerebroventricular administrationMichal G Fortuna, Lyle H Nyberg, Naz Taskin, et al.
Nature Biotechnology|April 28, 2026
Pool-packaged AAV libraries exhibit extensive length-dependent and homology-dependent chimerismJean-Benoît Lalanne, Chau Huynh, John K Mich, et al.
Nature Methods|November 3, 2015
Fixed single-cell transcriptomic characterization of human radial glial diversityElliot R Thomsen, John K Mich, Zizhen Yao, et al.
Nature Communications|September 26, 2022
Single cell atlas of spinal cord injury in mice reveals a pro-regenerative signature in spinocerebellar neuronsKaya J E Matson, Daniel E Russ, Claudia Kathe, et al.
Nature Medicine|January 16, 2026
Single-cell atlas of the developing Down syndrome brain cortexMichael Lattke, Wee Leng Tan, Salil Kalarikkal Sukumaran, et al.
Biorxiv : the Preprint Server for Biology|January 3, 2024
AAV-mediated interneuron-specific gene replacement for Dravet syndromeJohn K Mich, Jiyun Ryu, Aguan D Wei, et al.
Science Translational Medicine|March 19, 2025
Interneuron-specific dual-AAV SCN1A gene replacement corrects epileptic phenotypes in mouse models of Dravet syndromeJohn K Mich, Jiyun Ryu, Aguan D Wei, et al.
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