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Dror Sharon

Showing results (1-10 of 150) with videos related to

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Molecular Vision|August 12, 2015
Nonsyndromic retinitis pigmentosa is highly prevalent in the Jerusalem region with a high frequency of founder mutationsDror Sharon, Eyal Banin
Journal of Medical Genetics|March 27, 2019
Allele frequency analysis of variants reported to cause autosomal dominant inherited retinal diseases question the involvement of 19% of genes and 10% of reported pathogenic variantsMor Hanany, Dror Sharon
Molecular Aspects of Medicine|December 30, 2025
The potential use of anti-codon engineered tRNAs (ACE-tRNAs) to treat nonsense variants causing inherited retinal diseasesAsodu Sandeep Sarma, Dror Sharon
Proceedings of the National Academy of Sciences of the United States of America|January 23, 2020
Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseasesMor Hanany, Carlo Rivolta, Dror Sharon
Ophthalmic Genetics|February 19, 2016
OR2W3 sequence variants are unlikely to cause inherited retinal diseasesDror Sharon, Adva Kimchi, Carlo Rivolta
Advances in Experimental Medicine and Biology|July 13, 2023
Exonic Variants that Affect Splicing - An Opportunity for "Hidden" Mutations Causing Inherited Retinal DiseasesYogapriya Sundaresan, Eyal Banin, Dror Sharon
Advances in Experimental Medicine and Biology|July 13, 2023
Morphological and Functional Comparison of Mice Models for Retinitis PigmentosaPrakadeeswari Gopalakrishnan, Avigail Beryozkin, Eyal Banin, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 14, 2007
Novel USH2A mutations in Israeli patients with retinitis pigmentosa and Usher syndrome type 2Nadia Kaiserman, Alexey Obolensky, Eyal Banin, et al.
Cold Spring Harbor Perspectives in Medicine|July 17, 2023
Comparison of Worldwide Disease Prevalence and Genetic Prevalence of Inherited Retinal Diseases and Variant Interpretation ConsiderationsMor Hanany, Sapir Shalom, Tamar Ben-Yosef, et al.
Investigative Ophthalmology & Visual Science|March 12, 2010
Variable retinal phenotypes caused by mutations in the X-linked photopigment gene arrayLiliana Mizrahi-Meissonnier, Saul Merin, Eyal Banin, et al.
Pageof 15

Showing results (1-10 of 150) with videos related to

Sort By:
Pageof 15
Molecular Vision|August 12, 2015
Nonsyndromic retinitis pigmentosa is highly prevalent in the Jerusalem region with a high frequency of founder mutationsDror Sharon, Eyal Banin
Journal of Medical Genetics|March 27, 2019
Allele frequency analysis of variants reported to cause autosomal dominant inherited retinal diseases question the involvement of 19% of genes and 10% of reported pathogenic variantsMor Hanany, Dror Sharon
Molecular Aspects of Medicine|December 30, 2025
The potential use of anti-codon engineered tRNAs (ACE-tRNAs) to treat nonsense variants causing inherited retinal diseasesAsodu Sandeep Sarma, Dror Sharon
Proceedings of the National Academy of Sciences of the United States of America|January 23, 2020
Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseasesMor Hanany, Carlo Rivolta, Dror Sharon
Ophthalmic Genetics|February 19, 2016
OR2W3 sequence variants are unlikely to cause inherited retinal diseasesDror Sharon, Adva Kimchi, Carlo Rivolta
Advances in Experimental Medicine and Biology|July 13, 2023
Exonic Variants that Affect Splicing - An Opportunity for "Hidden" Mutations Causing Inherited Retinal DiseasesYogapriya Sundaresan, Eyal Banin, Dror Sharon
Advances in Experimental Medicine and Biology|July 13, 2023
Morphological and Functional Comparison of Mice Models for Retinitis PigmentosaPrakadeeswari Gopalakrishnan, Avigail Beryozkin, Eyal Banin, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 14, 2007
Novel USH2A mutations in Israeli patients with retinitis pigmentosa and Usher syndrome type 2Nadia Kaiserman, Alexey Obolensky, Eyal Banin, et al.
Cold Spring Harbor Perspectives in Medicine|July 17, 2023
Comparison of Worldwide Disease Prevalence and Genetic Prevalence of Inherited Retinal Diseases and Variant Interpretation ConsiderationsMor Hanany, Sapir Shalom, Tamar Ben-Yosef, et al.
Investigative Ophthalmology & Visual Science|March 12, 2010
Variable retinal phenotypes caused by mutations in the X-linked photopigment gene arrayLiliana Mizrahi-Meissonnier, Saul Merin, Eyal Banin, et al.
Pageof 15