Gene Therapy Preserves Vision for Fifteen Months in Retinitis Pigmentosa Mice
A subretinally delivered gene therapy vector incorporating a native untranslated regulatory region achieved fifteen months of sustained structural and functional ...
A subretinally delivered gene therapy vector incorporating a native untranslated regulatory region achieved fifteen months of sustained structural and functional ...
Delivering the transcription factor Ascl1 using an adeno-associated virus reduced photoreceptor degeneration and preserved retinal function in a mouse model ...
A five-year NIH grant will fund Upstate cell research on how PRCD and KIAA1549 support photoreceptor outer-segment formation implicated in ...
Researchers report a non-viral, OCT-guided method using gold nanorods and a 980-nm laser to deliver the opsin MCO-020 to targeted ...
The first comprehensive proteomic analysis of retinas from humanized sickle cell anemia mice reveals early downregulation of phototransduction and mitochondrial ...
An international trial led by University of Pittsburgh scientists found that an optogenetic gene therapy combined with light-projecting goggles was ...
New research shows that female mice lacking the protein quality-control gene Herc3 suffer faster retinal thinning, greater inflammatory activation, and ...
In a groundbreaking advance that could transform our understanding of neurodegenerative processes in vision loss, researchers have uncovered the pivotal ...
In the rapidly advancing field of biomedical research, there has emerged a promising avenue of exploration focused on ferroptosis—a regulated ...
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