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Dror Sharon

Showing results (11-20 of 150) with videos related to

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Progress in Retinal and Eye Research|October 25, 2017
Genotype-functional-phenotype correlations in photoreceptor guanylate cyclase (GC-E) encoded by GUCY2DDror Sharon, Hanna Wimberg, Yael Kinarty, et al.
Advances in Experimental Medicine and Biology|July 13, 2023
Factors Affecting Readthrough of Natural Versus Premature Termination CodonsAvigail Beryozkin, Kerstin Nagel-Wolfum, Eyal Banin, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 2, 2022
Ultra-widefield fundus autofluorescence imaging in patients with autosomal recessive retinitis pigmentosa reveals a genotype-phenotype correlationRani Patal, Eyal Banin, Tomer Batash, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
Profile of the genes expressed in the human peripheral retina, macula, and retinal pigment epithelium determined through serial analysis of gene expression (SAGE)Dror Sharon, Seth Blackshaw, Constance L Cepko, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 11, 2009
The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patientsDikla Bandah, Saul Merin, Munther Ashhab, et al.
Human Molecular Genetics|May 17, 2002
Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patternsCarlo Rivolta, Dror Sharon, Margaret M DeAngelis, et al.
Human Genetics|June 16, 2010
An ancient autosomal haplotype bearing a rare achromatopsia-causing founder mutation is shared among Arab Muslims and Oriental JewsLina Zelinger, Alex Greenberg, Susanne Kohl, et al.
American Journal of Ophthalmology|May 29, 2012
Frequency, genotype, and clinical spectrum of best vitelliform macular dystrophy: data from a national center in DenmarkHanna Bitner, Patrik Schatz, Liliana Mizrahi-Meissonnier, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 6, 2015
Retinal structure in young patients aged 10 years or less with Best vitelliform macular dystrophyPatrik Schatz, Dror Sharon, Sermed Al-Hamdani, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 21, 2008
Microarray-based gene expression analysis during retinal maturation of albino ratsGil Ben-Shlomo, Ron Ofri, Dikla Bandah, et al.
Pageof 15

Showing results (11-20 of 150) with videos related to

Sort By:
Pageof 15
Progress in Retinal and Eye Research|October 25, 2017
Genotype-functional-phenotype correlations in photoreceptor guanylate cyclase (GC-E) encoded by GUCY2DDror Sharon, Hanna Wimberg, Yael Kinarty, et al.
Advances in Experimental Medicine and Biology|July 13, 2023
Factors Affecting Readthrough of Natural Versus Premature Termination CodonsAvigail Beryozkin, Kerstin Nagel-Wolfum, Eyal Banin, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 2, 2022
Ultra-widefield fundus autofluorescence imaging in patients with autosomal recessive retinitis pigmentosa reveals a genotype-phenotype correlationRani Patal, Eyal Banin, Tomer Batash, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
Profile of the genes expressed in the human peripheral retina, macula, and retinal pigment epithelium determined through serial analysis of gene expression (SAGE)Dror Sharon, Seth Blackshaw, Constance L Cepko, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 11, 2009
The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patientsDikla Bandah, Saul Merin, Munther Ashhab, et al.
Human Molecular Genetics|May 17, 2002
Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patternsCarlo Rivolta, Dror Sharon, Margaret M DeAngelis, et al.
Human Genetics|June 16, 2010
An ancient autosomal haplotype bearing a rare achromatopsia-causing founder mutation is shared among Arab Muslims and Oriental JewsLina Zelinger, Alex Greenberg, Susanne Kohl, et al.
American Journal of Ophthalmology|May 29, 2012
Frequency, genotype, and clinical spectrum of best vitelliform macular dystrophy: data from a national center in DenmarkHanna Bitner, Patrik Schatz, Liliana Mizrahi-Meissonnier, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 6, 2015
Retinal structure in young patients aged 10 years or less with Best vitelliform macular dystrophyPatrik Schatz, Dror Sharon, Sermed Al-Hamdani, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 21, 2008
Microarray-based gene expression analysis during retinal maturation of albino ratsGil Ben-Shlomo, Ron Ofri, Dikla Bandah, et al.
Pageof 15