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Human Molecular Genetics
|
May 20, 2021
Human photoreceptor cells from different macular subregions have distinct transcriptional profiles
Andrew 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 tomography
Michael 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 tomography
S 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 expression
Samuel 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 correlations
Kaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
December 15, 2010
Anti-γ-enolase autoimmune retinopathy manifesting in early childhood
Audrey C Ko, Jasmine Hernández, Jason P Brinton, et al.
Plos One
|
June 9, 2016
SQSTM1 Mutations and Glaucoma
Todd 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-Seq
S 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 retina
Andrew J Lotery, Grace S Yang, Robert F Mullins, et al.
Ophthalmic Genetics
|
January 18, 2017
Reduced penetrance in a large Caucasian pedigree with Stickler syndrome
Stuart W Tompson, Charles Johnson, Diana Abbott, et al.
Page
of 39
Search research articles
Search
Showing results (251-260 of 384) with videos related to
Sort By:
Page
of 39
Human Molecular Genetics
|
May 20, 2021
Human photoreceptor cells from different macular subregions have distinct transcriptional profiles
Andrew 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 tomography
Michael 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 tomography
S 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 expression
Samuel 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 correlations
Kaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
December 15, 2010
Anti-γ-enolase autoimmune retinopathy manifesting in early childhood
Audrey C Ko, Jasmine Hernández, Jason P Brinton, et al.
Plos One
|
June 9, 2016
SQSTM1 Mutations and Glaucoma
Todd 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-Seq
S 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 retina
Andrew J Lotery, Grace S Yang, Robert F Mullins, et al.
Ophthalmic Genetics
|
January 18, 2017
Reduced penetrance in a large Caucasian pedigree with Stickler syndrome
Stuart W Tompson, Charles Johnson, Diana Abbott, et al.
Page
of 39