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Edwin M Stone

Showing results (291-300 of 384) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|November 13, 2004
Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsinDarryl Y Nishimura, Melissa Fath, Robert F Mullins, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
Metabolic Analysis of Human Retinal Pigment Epithelium and Choroid Tissue in Aging and Macular DegenerationEmma M Navratil, Xiuying Liu, Luke A Wiley, et al.
Human Molecular Genetics|February 26, 2015
Protein misfolding and the pathogenesis of ABCA4-associated retinal degenerationsNing Zhang, Yaroslav Tsybovsky, Alexander V Kolesnikov, et al.
Ophthalmology|June 1, 2017
Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal DiseaseEdwin M Stone, Jeaneen L Andorf, S Scott Whitmore, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutationsTomas S Aleman, Artur V Cideciyan, Alexander Sumaroka, et al.
Retina (Philadelphia, Pa.)|October 26, 2012
Proteomic analysis of vitreous biopsy techniquesJessica M Skeie, Eric N Brown, Harryl D Martinez, et al.
Human Molecular Genetics|November 6, 2023
Demonstration of the pathogenicity of a common non-exomic mutation in ABCA4 using iPSC-derived retinal organoids and retrospective clinical dataErin R Burnight, Beau J Fenner, Ian C Han, et al.
Human Mutation|May 12, 2009
Predicting the pathogenicity of RPE65 mutationsA R Philp, M Jin, S Li, et al.
Molecular Vision|April 18, 2012
Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucomaMao Mao, Frances Solivan-Timpe, Ben R Roos, et al.
Investigative Ophthalmology & Visual Science|November 24, 2011
Autosomal recessive retinitis pigmentosa caused by mutations in the MAK geneEdwin M Stone, Xunda Luo, Elise Héon, et al.
Pageof 39

Showing results (291-300 of 384) with videos related to

Sort By:
Pageof 39
Proceedings of the National Academy of Sciences of the United States of America|November 13, 2004
Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsinDarryl Y Nishimura, Melissa Fath, Robert F Mullins, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
Metabolic Analysis of Human Retinal Pigment Epithelium and Choroid Tissue in Aging and Macular DegenerationEmma M Navratil, Xiuying Liu, Luke A Wiley, et al.
Human Molecular Genetics|February 26, 2015
Protein misfolding and the pathogenesis of ABCA4-associated retinal degenerationsNing Zhang, Yaroslav Tsybovsky, Alexander V Kolesnikov, et al.
Ophthalmology|June 1, 2017
Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal DiseaseEdwin M Stone, Jeaneen L Andorf, S Scott Whitmore, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutationsTomas S Aleman, Artur V Cideciyan, Alexander Sumaroka, et al.
Retina (Philadelphia, Pa.)|October 26, 2012
Proteomic analysis of vitreous biopsy techniquesJessica M Skeie, Eric N Brown, Harryl D Martinez, et al.
Human Molecular Genetics|November 6, 2023
Demonstration of the pathogenicity of a common non-exomic mutation in ABCA4 using iPSC-derived retinal organoids and retrospective clinical dataErin R Burnight, Beau J Fenner, Ian C Han, et al.
Human Mutation|May 12, 2009
Predicting the pathogenicity of RPE65 mutationsA R Philp, M Jin, S Li, et al.
Molecular Vision|April 18, 2012
Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucomaMao Mao, Frances Solivan-Timpe, Ben R Roos, et al.
Investigative Ophthalmology & Visual Science|November 24, 2011
Autosomal recessive retinitis pigmentosa caused by mutations in the MAK geneEdwin M Stone, Xunda Luo, Elise Héon, et al.
Pageof 39