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Investigative Ophthalmology & Visual Science|March 11, 2016
Genetic Analysis of the Rhodopsin Gene Identifies a Mosaic Dominant Retinitis Pigmentosa Mutation in a Healthy IndividualAvigail Beryozkin, Gal Levy, Anat Blumenfeld, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|August 15, 2023
Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retinitis pigmentosaChen Matsevich, Prakadeeswari Gopalakrishnan, Ning Chang, et al.Investigative Ophthalmology & Visual Science|May 20, 2026
Comparative Analysis of Intravitreal Diffusion Patterns Across Ex Vivo Human and In Vivo/Ex Vivo Animal ModelsAnfisa Ayalon, Avigail Beryozkin, Katherine A Davoli, et al.Investigative Ophthalmology & Visual Science|January 30, 2014
Identification of mutations causing inherited retinal degenerations in the israeli and palestinian populations using homozygosity mappingAvigail Beryozkin, Lina Zelinger, Dikla Bandah-Rozenfeld, et al.Journal of Medical Genetics|May 22, 2016
Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing dataSamer Khateb, Mor Hanany, Ayat Khalaileh, et al.International Journal of Molecular Sciences|September 10, 2021
Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy EfficacyMartial Mbefo, Adeline Berger, Karine Schouwey, et al.Ophthalmology|December 26, 2017
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical AspectsAdva Kimchi, Samer Khateb, Rong Wen, et al.Scientific Reports|September 17, 2020
Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutationsAvigail Beryozkin, Samer Khateb, Carlos Alberto Idrobo-Robalino, et al.American Journal of Human Genetics|February 8, 2011
A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi JewsLina Zelinger, Eyal Banin, Alexey Obolensky, et al.Frontiers in Cell and Developmental Biology|November 1, 2021
Retinal Degeneration Associated With RPGRIP1: A Review of Natural History, Mutation Spectrum, and Genotype-Phenotype Correlation in 228 PatientsAvigail Beryozkin, Hamzah Aweidah, Roque Daniel Carrero Valenzuela, et al.Pageof 3