PCDH15 Dual-AAV Gene Therapy for Deafness and Blindness in Usher Syndrome Type 1F Models

Oct 23, 2024 | Government, News, Science

Bookmark (0) Please login to bookmarkClose Username or Email Address Password Remember Me J Clin Invest. 2024 Oct 15:e177700. doi: 10.1172/JCI177700. Online ahead of print.ABSTRACTUsher syndrome type 1F (USH1F), resulting from mutations in the protocadherin-15...

Real-life neovascular AMD treatment considering reimbursement in Turkiye: One-year comparison of switching to intravitreal ranibizumab or aflibercept after treatment failure with three loading intravitreal bevacizumab injections

Oct 21, 2024 | Government, News, Science

Bookmark (0) Please login to bookmarkClose Username or Email Address Password Remember Me North Clin Istanb. 2024 Oct 3;11(5):451-459. doi: 10.14744/nci.2024.75688. eCollection 2024.ABSTRACTOBJECTIVE: To compare one-year anatomical and functional results of switching...

Methodology for Studying Interactions of Vitamin A Membrane Receptors and Opsin Protein with their Ligands in Generating the Retinylidene Protein

Oct 21, 2024 | Government, News, Science

Bookmark (0) Please login to bookmarkClose Username or Email Address Password Remember Me J Vis Exp. 2024 Oct 4;(212). doi: 10.3791/67036.ABSTRACTDistribution of dietary vitamin A/all-trans retinol (ROL) throughout the body is critical for maintaining retinoid...

Translational Research and Therapies for Neuroprotection and Regeneration of the Optic Nerve and Retina: A Narrative Review

Oct 16, 2024 | Government, News, Science

Bookmark (0) Please login to bookmarkClose Username or Email Address Password Remember Me Int J Mol Sci. 2024 Sep 29;25(19):10485. doi: 10.3390/ijms251910485.ABSTRACTMost retinal and optic nerve diseases pose significant threats to vision, primarily due to...

Strabismus in an Adolescent With Stargardt Disease: An Atypical Presentation

Oct 14, 2024 | Government, News, Science

Bookmark (0) Please login to bookmarkClose Username or Email Address Password Remember Me Cureus. 2024 Sep 13;16(9):e69325. doi: 10.7759/cureus.69325. eCollection 2024 Sep.ABSTRACTWe report on the case of a 19-year-old male with Stargardt disease (STGD1) who presented...

Generation of a gene-corrected isogenic human iPSC line (CSUASOi006-A-1) from a retinitis pigmentosa patient with heterozygous c.5792C > T mutation in the PRPF8 gene

Oct 10, 2024 | Government, News, Science

Bookmark (0) Please login to bookmarkClose Username or Email Address Password Remember Me Stem Cell Res. 2024 Oct 5;81:103572. doi: 10.1016/j.scr.2024.103572. Online ahead of print.ABSTRACTRetinitis pigmentosa (RP) is a common inherited retinal disease characterized...