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Edwin M Stone

Showing results (171-180 of 384) with videos related to

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Investigative Ophthalmology & Visual Science|March 8, 2012
Autosomal recessive retinitis pigmentosa due to ABCA4 mutations: clinical, pathologic, and molecular characterizationRobert F Mullins, Markus H Kuehn, Roxana A Radu, et al.
Case Reports in Ophthalmology|September 26, 2022
Vascular Findings in the Choriocapillaris in a Case of Radiation Retinopathy Secondary to Choroidal MelanomaElaine M Binkley, Lola P Lozano, Megan J Riker, et al.
Investigative Ophthalmology & Visual Science|June 30, 2004
Dark adaptation of rod photoreceptors in normal subjects, and in patients with Stargardt disease and an ABCA4 mutationJennifer J Kang Derwent, Deborah J Derlacki, John R Hetling, et al.
Current Eye Research|January 5, 2013
Identification of proteins that interact with TANK binding kinase 1 and testing for mutations associated with glaucomaSeongjin Seo, Frances Solivan-Timpe, Ben R Roos, et al.
American Journal of Ophthalmology|March 22, 2018
Expanded Retinal Disease Spectrum Associated With Autosomal Recessive Mutations in GUCY2DMaria L Stunkel, Scott E Brodie, Artur V Cideciyan, et al.
Molecular Vision|September 23, 2015
Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmosDavid Khorram, Michael Choi, Ben R Roos, et al.
Current Protocols in Stem Cell Biology|August 15, 2017
Generation of Xeno-Free, cGMP-Compliant Patient-Specific iPSCs from Skin BiopsyLuke A Wiley, Kristin R Anfinson, Cathryn M Cranston, et al.
Ophthalmic Genetics|September 27, 2017
Evaluation of sFLT1 protein levels in human eyes with the FLT1 rs9943922 polymorphismKathleen R Chirco, Carly J Lewis, Todd E Scheetz, et al.
Ophthalmic Genetics|September 25, 2012
Confirmation of the association between the TCF4 risk allele and Fuchs endothelial corneal dystrophy in patients from the Midwestern United StatesJohn F Stamler, Ben R Roos, Michael D Wagoner, et al.
Molecular Vision|November 23, 2013
Altered gene expression in dry age-related macular degeneration suggests early loss of choroidal endothelial cellsS Scott Whitmore, Terry A Braun, Jessica M Skeie, et al.
Pageof 39

Showing results (171-180 of 384) with videos related to

Sort By:
Pageof 39
Investigative Ophthalmology & Visual Science|March 8, 2012
Autosomal recessive retinitis pigmentosa due to ABCA4 mutations: clinical, pathologic, and molecular characterizationRobert F Mullins, Markus H Kuehn, Roxana A Radu, et al.
Case Reports in Ophthalmology|September 26, 2022
Vascular Findings in the Choriocapillaris in a Case of Radiation Retinopathy Secondary to Choroidal MelanomaElaine M Binkley, Lola P Lozano, Megan J Riker, et al.
Investigative Ophthalmology & Visual Science|June 30, 2004
Dark adaptation of rod photoreceptors in normal subjects, and in patients with Stargardt disease and an ABCA4 mutationJennifer J Kang Derwent, Deborah J Derlacki, John R Hetling, et al.
Current Eye Research|January 5, 2013
Identification of proteins that interact with TANK binding kinase 1 and testing for mutations associated with glaucomaSeongjin Seo, Frances Solivan-Timpe, Ben R Roos, et al.
American Journal of Ophthalmology|March 22, 2018
Expanded Retinal Disease Spectrum Associated With Autosomal Recessive Mutations in GUCY2DMaria L Stunkel, Scott E Brodie, Artur V Cideciyan, et al.
Molecular Vision|September 23, 2015
Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmosDavid Khorram, Michael Choi, Ben R Roos, et al.
Current Protocols in Stem Cell Biology|August 15, 2017
Generation of Xeno-Free, cGMP-Compliant Patient-Specific iPSCs from Skin BiopsyLuke A Wiley, Kristin R Anfinson, Cathryn M Cranston, et al.
Ophthalmic Genetics|September 27, 2017
Evaluation of sFLT1 protein levels in human eyes with the FLT1 rs9943922 polymorphismKathleen R Chirco, Carly J Lewis, Todd E Scheetz, et al.
Ophthalmic Genetics|September 25, 2012
Confirmation of the association between the TCF4 risk allele and Fuchs endothelial corneal dystrophy in patients from the Midwestern United StatesJohn F Stamler, Ben R Roos, Michael D Wagoner, et al.
Molecular Vision|November 23, 2013
Altered gene expression in dry age-related macular degeneration suggests early loss of choroidal endothelial cellsS Scott Whitmore, Terry A Braun, Jessica M Skeie, et al.
Pageof 39