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Edwin M Stone

Showing results (121-130 of 384) with videos related to

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Plos One|April 25, 2014
Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12Michelle J Kim, Ricardo F Frausto, George O D Rosenwasser, et al.
Investigative Ophthalmology & Visual Science|November 1, 2011
Automated discovery and quantification of image-based complex phenotypes: a twin study of drusen phenotypes in age-related macular degenerationGwenole Quellec, Stephen R Russell, Johanna M Seddon, et al.
Behavioral Neuroscience|November 3, 2010
Light aversion in mice depends on nonimage-forming irradiance detectionStewart Thompson, Ana Recober, Timothy W Vogel, et al.
Molecular Vision|July 3, 2010
T-cell infiltration in autosomal dominant neovascular inflammatory vitreoretinopathyVinit B Mahajan, John G Vallone, Jonathan H Lin, et al.
Vision Research|September 4, 2012
Phenotypic expression of Bardet-Biedl syndrome in patients homozygous for the common M390R mutation in the BBS1 geneKyle F Cox, Natalie C Kerr, Marina Kedrov, et al.
Progress in Retinal and Eye Research|December 9, 2014
Complement activation and choriocapillaris loss in early AMD: implications for pathophysiology and therapyS Scott Whitmore, Elliott H Sohn, Kathleen R Chirco, et al.
Progress in Retinal and Eye Research|December 3, 2014
Patient-specific induced pluripotent stem cells (iPSCs) for the study and treatment of retinal degenerative diseasesLuke A Wiley, Erin R Burnight, Allison E Songstad, et al.
Human Molecular Genetics|January 25, 2011
The N-terminal region of centrosomal protein 290 (CEP290) restores vision in a zebrafish model of human blindnessLisa M Baye, Xiaobai Patrinostro, Svetha Swaminathan, et al.
Investigative Ophthalmology & Visual Science|January 2, 2007
The optic nerve head in myocilin glaucomaAlex W Hewitt, Sonya L Bennett, John H Fingert, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 15, 2009
Phenotypic variability due to a novel Glu292Lys variation in exon 8 of the BEST1 gene causing best macular dystrophyElliott H Sohn, Peter J Francis, Jacque L Duncan, et al.
Pageof 39

Showing results (121-130 of 384) with videos related to

Sort By:
Pageof 39
Plos One|April 25, 2014
Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12Michelle J Kim, Ricardo F Frausto, George O D Rosenwasser, et al.
Investigative Ophthalmology & Visual Science|November 1, 2011
Automated discovery and quantification of image-based complex phenotypes: a twin study of drusen phenotypes in age-related macular degenerationGwenole Quellec, Stephen R Russell, Johanna M Seddon, et al.
Behavioral Neuroscience|November 3, 2010
Light aversion in mice depends on nonimage-forming irradiance detectionStewart Thompson, Ana Recober, Timothy W Vogel, et al.
Molecular Vision|July 3, 2010
T-cell infiltration in autosomal dominant neovascular inflammatory vitreoretinopathyVinit B Mahajan, John G Vallone, Jonathan H Lin, et al.
Vision Research|September 4, 2012
Phenotypic expression of Bardet-Biedl syndrome in patients homozygous for the common M390R mutation in the BBS1 geneKyle F Cox, Natalie C Kerr, Marina Kedrov, et al.
Progress in Retinal and Eye Research|December 9, 2014
Complement activation and choriocapillaris loss in early AMD: implications for pathophysiology and therapyS Scott Whitmore, Elliott H Sohn, Kathleen R Chirco, et al.
Progress in Retinal and Eye Research|December 3, 2014
Patient-specific induced pluripotent stem cells (iPSCs) for the study and treatment of retinal degenerative diseasesLuke A Wiley, Erin R Burnight, Allison E Songstad, et al.
Human Molecular Genetics|January 25, 2011
The N-terminal region of centrosomal protein 290 (CEP290) restores vision in a zebrafish model of human blindnessLisa M Baye, Xiaobai Patrinostro, Svetha Swaminathan, et al.
Investigative Ophthalmology & Visual Science|January 2, 2007
The optic nerve head in myocilin glaucomaAlex W Hewitt, Sonya L Bennett, John H Fingert, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 15, 2009
Phenotypic variability due to a novel Glu292Lys variation in exon 8 of the BEST1 gene causing best macular dystrophyElliott H Sohn, Peter J Francis, Jacque L Duncan, et al.
Pageof 39