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Edwin M Stone

Showing results (271-280 of 384) with videos related to

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The British Journal of Ophthalmology|November 27, 2020
Predominance of hyperopia in autosomal dominant Best vitelliform macular dystrophyRazek G Coussa, Elaine M Binkley, Mark E Wilkinson, et al.
American Journal of Ophthalmology|March 21, 2007
Familial cavitary optic disk anomalies: identification of a novel genetic locusJohn H Fingert, Robert A Honkanen, Suma P Shankar, et al.
Investigative Ophthalmology & Visual Science|January 1, 2016
Generating iPSC-Derived Choroidal Endothelial Cells to Study Age-Related Macular DegenerationAllison E Songstad, Luke A Wiley, Khahn Duong, et al.
The Journal of Clinical Investigation|August 9, 2011
Reduction of ER stress via a chemical chaperone prevents disease phenotypes in a mouse model of primary open angle glaucomaGulab S Zode, Markus H Kuehn, Darryl Y Nishimura, et al.
JAMA Ophthalmology|December 19, 2014
Comparison of retinal and choriocapillaris thicknesses following sitting to supine transition in healthy individuals and patients with age-related macular degenerationDavid R P Almeida, Li Zhang, Eric K Chin, et al.
Ophthalmic Genetics|February 22, 2014
Clinical and Electrophysiologic Characteristics of a Large Kindred with X-Linked Retinitis Pigmentosa Associated with the RPGR LocusJonathan H Tzu, Tania Arguello, Audina M Berrocal, et al.
Investigative Ophthalmology & Visual Science|October 25, 2023
Gene Expression Within a Human Choroidal Neovascular Membrane Using Spatial TranscriptomicsAndrew P Voigt, Nathaniel K Mullin, Emma M Navratil, et al.
Investigative Ophthalmology & Visual Science|December 6, 2024
Elevation of Granulocyte Colony Stimulating Factor in Human AMD Donor RPE-ChoroidKelly Mulfaul, Adnan H Khan, Samantha G Schwarte, et al.
JAMA Ophthalmology|August 17, 2023
GJA3 Genetic Variation and Autosomal Dominant Congenital Cataracts and Glaucoma Following Cataract SurgeryErin A Boese, Arlene V Drack, Benjamin R Roos, et al.
Human Molecular Genetics|July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degenerationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Pageof 39

Showing results (271-280 of 384) with videos related to

Sort By:
Pageof 39
The British Journal of Ophthalmology|November 27, 2020
Predominance of hyperopia in autosomal dominant Best vitelliform macular dystrophyRazek G Coussa, Elaine M Binkley, Mark E Wilkinson, et al.
American Journal of Ophthalmology|March 21, 2007
Familial cavitary optic disk anomalies: identification of a novel genetic locusJohn H Fingert, Robert A Honkanen, Suma P Shankar, et al.
Investigative Ophthalmology & Visual Science|January 1, 2016
Generating iPSC-Derived Choroidal Endothelial Cells to Study Age-Related Macular DegenerationAllison E Songstad, Luke A Wiley, Khahn Duong, et al.
The Journal of Clinical Investigation|August 9, 2011
Reduction of ER stress via a chemical chaperone prevents disease phenotypes in a mouse model of primary open angle glaucomaGulab S Zode, Markus H Kuehn, Darryl Y Nishimura, et al.
JAMA Ophthalmology|December 19, 2014
Comparison of retinal and choriocapillaris thicknesses following sitting to supine transition in healthy individuals and patients with age-related macular degenerationDavid R P Almeida, Li Zhang, Eric K Chin, et al.
Ophthalmic Genetics|February 22, 2014
Clinical and Electrophysiologic Characteristics of a Large Kindred with X-Linked Retinitis Pigmentosa Associated with the RPGR LocusJonathan H Tzu, Tania Arguello, Audina M Berrocal, et al.
Investigative Ophthalmology & Visual Science|October 25, 2023
Gene Expression Within a Human Choroidal Neovascular Membrane Using Spatial TranscriptomicsAndrew P Voigt, Nathaniel K Mullin, Emma M Navratil, et al.
Investigative Ophthalmology & Visual Science|December 6, 2024
Elevation of Granulocyte Colony Stimulating Factor in Human AMD Donor RPE-ChoroidKelly Mulfaul, Adnan H Khan, Samantha G Schwarte, et al.
JAMA Ophthalmology|August 17, 2023
GJA3 Genetic Variation and Autosomal Dominant Congenital Cataracts and Glaucoma Following Cataract SurgeryErin A Boese, Arlene V Drack, Benjamin R Roos, et al.
Human Molecular Genetics|July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degenerationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Pageof 39