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Edwin M Stone

Showing results (311-320 of 384) with videos related to

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Genomics|August 30, 2006
Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humansBarbara Zangerl, Orly Goldstein, Alisdair R Philp, et al.
The American Journal of Pathology|May 4, 2019
Choriocapillaris Degeneration in Geographic AtrophyElliott H Sohn, Miles J Flamme-Wiese, S Scott Whitmore, et al.
Stem Cell Research & Therapy|November 18, 2025
Production of clinical grade patient iPSC-derived 3D retinal organoids containing transplantable photoreceptor cellsLaura R Bohrer, Luke A Wiley, Allison T Wright, et al.
Ophthalmology|January 19, 2010
Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosaSaloni Walia, Gerald A Fishman, Samuel G Jacobson, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 7, 2002
Variations in the myocilin gene in patients with open-angle glaucomaWallace L M Alward, Young H Kwon, Cheryl L Khanna, et al.
The Journal of Clinical Investigation|February 16, 2008
Increased expression of the WNT antagonist sFRP-1 in glaucoma elevates intraocular pressureWan-Heng Wang, Loretta G McNatt, Iok-Hou Pang, et al.
Ophthalmic Genetics|March 26, 2008
Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathySuma P Shankar, John H Fingert, Valerio Carelli, et al.
American Journal of Ophthalmology|March 19, 2013
A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Alice E Davidson, et al.
Journal of Translational Medicine|March 1, 2023
Automating iPSC generation to enable autologous photoreceptor cell replacement therapyLaura R Bohrer, Nicholas E Stone, Nathaniel K Mullin, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
Single-Cell Gene Expression and eQTL Analyses in the Human Retina, RPE, and Choroid in Macular DegenerationAndrew P Voigt, Nathaniel K Mullin, Kelly Mulfaul, et al.
Pageof 39

Showing results (311-320 of 384) with videos related to

Sort By:
Pageof 39
Genomics|August 30, 2006
Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humansBarbara Zangerl, Orly Goldstein, Alisdair R Philp, et al.
The American Journal of Pathology|May 4, 2019
Choriocapillaris Degeneration in Geographic AtrophyElliott H Sohn, Miles J Flamme-Wiese, S Scott Whitmore, et al.
Stem Cell Research & Therapy|November 18, 2025
Production of clinical grade patient iPSC-derived 3D retinal organoids containing transplantable photoreceptor cellsLaura R Bohrer, Luke A Wiley, Allison T Wright, et al.
Ophthalmology|January 19, 2010
Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosaSaloni Walia, Gerald A Fishman, Samuel G Jacobson, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 7, 2002
Variations in the myocilin gene in patients with open-angle glaucomaWallace L M Alward, Young H Kwon, Cheryl L Khanna, et al.
The Journal of Clinical Investigation|February 16, 2008
Increased expression of the WNT antagonist sFRP-1 in glaucoma elevates intraocular pressureWan-Heng Wang, Loretta G McNatt, Iok-Hou Pang, et al.
Ophthalmic Genetics|March 26, 2008
Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathySuma P Shankar, John H Fingert, Valerio Carelli, et al.
American Journal of Ophthalmology|March 19, 2013
A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Alice E Davidson, et al.
Journal of Translational Medicine|March 1, 2023
Automating iPSC generation to enable autologous photoreceptor cell replacement therapyLaura R Bohrer, Nicholas E Stone, Nathaniel K Mullin, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
Single-Cell Gene Expression and eQTL Analyses in the Human Retina, RPE, and Choroid in Macular DegenerationAndrew P Voigt, Nathaniel K Mullin, Kelly Mulfaul, et al.
Pageof 39