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Edwin M Stone

Showing results (251-260 of 384) with videos related to

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Human Molecular Genetics|May 20, 2021
Human photoreceptor cells from different macular subregions have distinct transcriptional profilesAndrew P Voigt, Nathaniel K Mullin, S Scott Whitmore, et al.
Experimental Eye Research|February 5, 2003
In vivo micropathology of Best macular dystrophy with optical coherence tomographyMichael J Pianta, Tomas S Aleman, Artur V Cideciyan, et al.
Scientific Reports|April 27, 2023
Modeling rod and cone photoreceptor cell survival in vivo using optical coherence tomographyS Scott Whitmore, Adam P DeLuca, Jeaneen L Andorf, et al.
Investigative Ophthalmology & Visual Science|January 2, 2007
RDH12 and RPE65, visual cycle genes causing leber congenital amaurosis, differ in disease expressionSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|November 23, 2013
A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 15, 2010
Anti-γ-enolase autoimmune retinopathy manifesting in early childhoodAudrey C Ko, Jasmine Hernández, Jason P Brinton, et al.
Plos One|June 9, 2016
SQSTM1 Mutations and GlaucomaTodd E Scheetz, Ben R Roos, Frances Solivan-Timpe, et al.
Experimental Eye Research|December 3, 2014
Transcriptomic analysis across nasal, temporal, and macular regions of human neural retina and RPE/choroid by RNA-SeqS Scott Whitmore, Alex H Wagner, Adam P DeLuca, et al.
Human Gene Therapy|November 25, 2003
Adeno-associated virus type 5: transduction efficiency and cell-type specificity in the primate retinaAndrew J Lotery, Grace S Yang, Robert F Mullins, et al.
Ophthalmic Genetics|January 18, 2017
Reduced penetrance in a large Caucasian pedigree with Stickler syndromeStuart W Tompson, Charles Johnson, Diana Abbott, et al.
Pageof 39

Showing results (251-260 of 384) with videos related to

Sort By:
Pageof 39
Human Molecular Genetics|May 20, 2021
Human photoreceptor cells from different macular subregions have distinct transcriptional profilesAndrew P Voigt, Nathaniel K Mullin, S Scott Whitmore, et al.
Experimental Eye Research|February 5, 2003
In vivo micropathology of Best macular dystrophy with optical coherence tomographyMichael J Pianta, Tomas S Aleman, Artur V Cideciyan, et al.
Scientific Reports|April 27, 2023
Modeling rod and cone photoreceptor cell survival in vivo using optical coherence tomographyS Scott Whitmore, Adam P DeLuca, Jeaneen L Andorf, et al.
Investigative Ophthalmology & Visual Science|January 2, 2007
RDH12 and RPE65, visual cycle genes causing leber congenital amaurosis, differ in disease expressionSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|November 23, 2013
A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 15, 2010
Anti-γ-enolase autoimmune retinopathy manifesting in early childhoodAudrey C Ko, Jasmine Hernández, Jason P Brinton, et al.
Plos One|June 9, 2016
SQSTM1 Mutations and GlaucomaTodd E Scheetz, Ben R Roos, Frances Solivan-Timpe, et al.
Experimental Eye Research|December 3, 2014
Transcriptomic analysis across nasal, temporal, and macular regions of human neural retina and RPE/choroid by RNA-SeqS Scott Whitmore, Alex H Wagner, Adam P DeLuca, et al.
Human Gene Therapy|November 25, 2003
Adeno-associated virus type 5: transduction efficiency and cell-type specificity in the primate retinaAndrew J Lotery, Grace S Yang, Robert F Mullins, et al.
Ophthalmic Genetics|January 18, 2017
Reduced penetrance in a large Caucasian pedigree with Stickler syndromeStuart W Tompson, Charles Johnson, Diana Abbott, et al.
Pageof 39