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Human Gene Therapy|September 12, 2015
Systemic Vascular Transduction by Capsid Mutant Adeno-Associated Virus After Intravenous InjectionDaniel M Lipinski, Chris A Reid, Sanford L Boye, et al.
Investigative Ophthalmology & Visual Science|November 1, 2011
AAV-mediated gene transfer of human X-linked inhibitor of apoptosis protects against oxidative cell death in human RPE cellsHaidong Shan, Dan Ji, Alun R Barnard, et al.
Journal of Molecular Medicine (Berlin, Germany)|June 13, 2013
Functional expression of Rab escort protein 1 following AAV2-mediated gene delivery in the retina of choroideremia mice and human cells ex vivoTanya Tolmachova, Oleg E Tolmachov, Alun R Barnard, et al.
Cell Reports|June 13, 2019
Presynaptic Expression of LRIT3 Transsynaptically Organizes the Postsynaptic Glutamate Signaling Complex Containing TRPM1Nazarul Hasan, Gobinda Pangeni, Catherine A Cobb, et al.
Investigative Ophthalmology & Visual Science|June 28, 2011
Characterization of a dominant cone degeneration in a green fluorescent protein-reporter mouse with disruption of Loci associated with human dominant retinal dystrophyDaniel M Lipinski, Mohammed Yusuf, Alun R Barnard, et al.
The American Journal of Pathology|November 26, 2018
Acid Ceramidase Deficiency in Mice Leads to Severe Ocular Pathology and Visual ImpairmentFabian P S Yu, Benjamin S Sajdak, Jakub Sikora, et al.
Plos One|April 18, 2013
Assessment of tropism and effectiveness of new primate-derived hybrid recombinant AAV serotypes in the mouse and primate retinaPeter Charbel Issa, Samantha R De Silva, Daniel M Lipinski, et al.
Stem Cell Reports|February 9, 2024
Human iPSC-derived photoreceptor transplantation in the cone dominant 13-lined ground squirrelChing Tzu Yu, Sangeetha Kandoi, Ramesh Periasamy, et al.
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