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Edwin M Stone

Showing results (211-220 of 384) with videos related to

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Experimental Eye Research|September 1, 2025
Sialoglycoconjugate profiling of human choroid, retinal pigment epithelium, and basal laminar depositsEmma M Navratil, Piper A Wenzel, Miles J Flamme-Wiese, et al.
BMC Medical Genetics|April 28, 2011
Evaluation of variants in the selectin genes in age-related macular degenerationRobert F Mullins, Jessica M Skeie, James C Folk, et al.
American Journal of Human Genetics|July 20, 2004
Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)Annie P Chiang, Darryl Nishimura, Charles Searby, et al.
Experimental Eye Research|May 9, 2006
Retinal synthesis and deposition of complement components induced by ocular hypertensionMarkus H Kuehn, Chan Y Kim, Jelena Ostojic, et al.
Investigative Ophthalmology & Visual Science|April 27, 2007
Bestrophin gene mutations cause canine multifocal retinopathy: a novel animal model for best diseaseKarina E Guziewicz, Barbara Zangerl, Sarah J Lindauer, et al.
Experimental Eye Research|October 17, 2024
Ghost vessels in the eye: Cell free choriocapillaris domains in atrophic age-related macular degenerationRobert F Mullins, Miles J Flamme-Wiese, Emma M Navratil, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2011
Three-dimensional distribution of the vitelliform lesion, photoreceptors, and retinal pigment epithelium in the macula of patients with best vitelliform macular dystrophyChristine N Kay, Michael D Abramoff, Robert F Mullins, et al.
Cells|February 20, 2020
Single-Cell RNA Sequencing in Human Retinal Degeneration Reveals Distinct Glial Cell PopulationsAndrew P Voigt, Elaine Binkley, Miles J Flamme-Wiese, et al.
Human Molecular Genetics|January 20, 2011
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathyArtur V Cideciyan, Rivka A Rachel, Tomas S Aleman, et al.
Advances in Experimental Medicine and Biology|January 26, 2007
Genetic factors modifying clinical expression of autosomal dominant RPStephen P Daiger, Suma P Shankar, Alice B Schindler, et al.
Pageof 39

Showing results (211-220 of 384) with videos related to

Sort By:
Pageof 39
Experimental Eye Research|September 1, 2025
Sialoglycoconjugate profiling of human choroid, retinal pigment epithelium, and basal laminar depositsEmma M Navratil, Piper A Wenzel, Miles J Flamme-Wiese, et al.
BMC Medical Genetics|April 28, 2011
Evaluation of variants in the selectin genes in age-related macular degenerationRobert F Mullins, Jessica M Skeie, James C Folk, et al.
American Journal of Human Genetics|July 20, 2004
Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)Annie P Chiang, Darryl Nishimura, Charles Searby, et al.
Experimental Eye Research|May 9, 2006
Retinal synthesis and deposition of complement components induced by ocular hypertensionMarkus H Kuehn, Chan Y Kim, Jelena Ostojic, et al.
Investigative Ophthalmology & Visual Science|April 27, 2007
Bestrophin gene mutations cause canine multifocal retinopathy: a novel animal model for best diseaseKarina E Guziewicz, Barbara Zangerl, Sarah J Lindauer, et al.
Experimental Eye Research|October 17, 2024
Ghost vessels in the eye: Cell free choriocapillaris domains in atrophic age-related macular degenerationRobert F Mullins, Miles J Flamme-Wiese, Emma M Navratil, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2011
Three-dimensional distribution of the vitelliform lesion, photoreceptors, and retinal pigment epithelium in the macula of patients with best vitelliform macular dystrophyChristine N Kay, Michael D Abramoff, Robert F Mullins, et al.
Cells|February 20, 2020
Single-Cell RNA Sequencing in Human Retinal Degeneration Reveals Distinct Glial Cell PopulationsAndrew P Voigt, Elaine Binkley, Miles J Flamme-Wiese, et al.
Human Molecular Genetics|January 20, 2011
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathyArtur V Cideciyan, Rivka A Rachel, Tomas S Aleman, et al.
Advances in Experimental Medicine and Biology|January 26, 2007
Genetic factors modifying clinical expression of autosomal dominant RPStephen P Daiger, Suma P Shankar, Alice B Schindler, et al.
Pageof 39