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Edwin M Stone

Showing results (321-330 of 384) with videos related to

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Human Molecular Genetics|February 19, 2022
Choroidal endothelial and macrophage gene expression in atrophic and neovascular macular degenerationAndrew P Voigt, Nathaniel K Mullin, Kelly Mulfaul, et al.
Frontiers in Medicine|July 3, 2023
Long-term functional and structural outcomes in X-linked retinoschisis: implications for clinical trialsBeau J Fenner, Jonathan F Russell, Arlene V Drack, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 20, 2006
Regulation of gene expression in the mammalian eye and its relevance to eye diseaseTodd E Scheetz, Kwang-Youn A Kim, Ruth E Swiderski, et al.
The CRISPR Journal|April 26, 2019
CRISPR-Cas9-Mediated Correction of the 1.02 kb Common Deletion in <i>CLN3</i> in Induced Pluripotent Stem Cells from Patients with Batten DiseaseErin R Burnight, Laura R Bohrer, Joseph C Giacalone, et al.
Investigative Ophthalmology & Visual Science|October 27, 2006
Retinal disease expression in Bardet-Biedl syndrome-1 (BBS1) is a spectrum from maculopathy to retina-wide degenerationAmir A Azari, Tomas S Aleman, Artur V Cideciyan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 23, 2009
Visual impairment in the absence of dystroglycanJakob S Satz, Alisdair R Philp, Huy Nguyen, et al.
Biomacromolecules|July 26, 2018
Effect of Molecular Weight and Functionality on Acrylated Poly(caprolactone) for Stereolithography and Biomedical ApplicationsBrian J Green, Kristan S Worthington, Jessica R Thompson, et al.
Journal of Vitreoretinal Diseases|May 1, 2026
A Single-Center Analysis of Variables Used to Select a Vitreoretinal Surgery Training ProgramTimothy M Boyce, Kyle M Green, Ian C Han, et al.
Investigative Ophthalmology & Visual Science|January 27, 2005
Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotypeSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Stem Cells Translational Medicine|May 6, 2017
Connective Tissue Growth Factor Promotes Efficient Generation of Human Induced Pluripotent Stem Cell-Derived Choroidal EndotheliumAllison E Songstad, Kristan S Worthington, Kathleen R Chirco, et al.
Pageof 39

Showing results (321-330 of 384) with videos related to

Sort By:
Pageof 39
Human Molecular Genetics|February 19, 2022
Choroidal endothelial and macrophage gene expression in atrophic and neovascular macular degenerationAndrew P Voigt, Nathaniel K Mullin, Kelly Mulfaul, et al.
Frontiers in Medicine|July 3, 2023
Long-term functional and structural outcomes in X-linked retinoschisis: implications for clinical trialsBeau J Fenner, Jonathan F Russell, Arlene V Drack, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 20, 2006
Regulation of gene expression in the mammalian eye and its relevance to eye diseaseTodd E Scheetz, Kwang-Youn A Kim, Ruth E Swiderski, et al.
The CRISPR Journal|April 26, 2019
CRISPR-Cas9-Mediated Correction of the 1.02 kb Common Deletion in <i>CLN3</i> in Induced Pluripotent Stem Cells from Patients with Batten DiseaseErin R Burnight, Laura R Bohrer, Joseph C Giacalone, et al.
Investigative Ophthalmology & Visual Science|October 27, 2006
Retinal disease expression in Bardet-Biedl syndrome-1 (BBS1) is a spectrum from maculopathy to retina-wide degenerationAmir A Azari, Tomas S Aleman, Artur V Cideciyan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 23, 2009
Visual impairment in the absence of dystroglycanJakob S Satz, Alisdair R Philp, Huy Nguyen, et al.
Biomacromolecules|July 26, 2018
Effect of Molecular Weight and Functionality on Acrylated Poly(caprolactone) for Stereolithography and Biomedical ApplicationsBrian J Green, Kristan S Worthington, Jessica R Thompson, et al.
Journal of Vitreoretinal Diseases|May 1, 2026
A Single-Center Analysis of Variables Used to Select a Vitreoretinal Surgery Training ProgramTimothy M Boyce, Kyle M Green, Ian C Han, et al.
Investigative Ophthalmology & Visual Science|January 27, 2005
Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotypeSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Stem Cells Translational Medicine|May 6, 2017
Connective Tissue Growth Factor Promotes Efficient Generation of Human Induced Pluripotent Stem Cell-Derived Choroidal EndotheliumAllison E Songstad, Kristan S Worthington, Kathleen R Chirco, et al.
Pageof 39