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Journal of Precision Medicine (Amsterdam, Netherlands)|July 8, 2026
Precision therapeutic tRNA rescue of nonsense mutation R166X in KCNJ13 to restore K+ channel functionAllison Spillane, Enes Akyuz, Meha Kabra, et al.
Biorxiv : the Preprint Server for Biology|July 17, 2025
Preventing vision loss in a mouse model of Leber Congenital Amaurosis by engineered tRNAEnes Akyuz, Pawan K Shahi, Lionel Gissot, et al.
Ophthalmology Science|May 27, 2026
Association of Autosomal Dominant Snowflake Vitreoretinal Degeneration with RetinoschisisBikash R Pattnaik, Ken K Nischal, Oleg Alekseev, et al.
International Journal of Biological Sciences|May 20, 2026
Synonymous editing alters ion channel function, favoring prime editing for retinal disease correctionMeha Kabra, Mariya Moosajee, Ana Navarrete, et al.
Signal Transduction and Targeted Therapy|June 9, 2026
Engineered tRNA reduces vision loss in a mouse model of Leber congenital amaurosisPawan K Shahi, Enes Akyuz, Lionel Gissot, et al.
Investigative Ophthalmology & Visual Science|February 14, 2020
Vigabatrin-Induced Retinal Functional Alterations and Second-Order Neuron Plasticity in C57BL/6J MiceKore Chan, Mrinalini Hoon, Bikash R Pattnaik, et al.
The Journal of Clinical Investigation|August 10, 2023
Nonviral base editing of KCNJ13 mutation preserves vision in a model of inherited retinal channelopathyMeha Kabra, Pawan K Shahi, Yuyuan Wang, et al.
American Journal of Human Genetics|July 25, 2020
Human iPSC Modeling Reveals Mutation-Specific Responses to Gene Therapy in a Genotypically Diverse Dominant MaculopathyDivya Sinha, Benjamin Steyer, Pawan K Shahi, et al.
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