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Proceedings of the National Academy of Sciences of the United States of America
|
August 10, 2011
Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosa
Budd A Tucker, Todd E Scheetz, Robert F Mullins, et al.
Diabetes
|
March 29, 2005
Nonhuman primate models for diabetic ocular neovascularization using AAV2-mediated overexpression of vascular endothelial growth factor
Corinna Lebherz, Albert M Maguire, Alberto Auricchio, et al.
Nature Medicine
|
April 2, 2021
Durable vision improvement after a single treatment with antisense oligonucleotide sepofarsen: a case report
Artur V Cideciyan, Samuel G Jacobson, Allen C Ho, et al.
Investigative Ophthalmology & Visual Science
|
November 24, 2005
ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retina
Artur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science
|
August 29, 2006
Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutations
Samuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
International Journal of Molecular Sciences
|
May 24, 2019
Short-Wavelength Sensitive Cone (S-cone) Testing as an Outcome Measure for <i>NR2E3</i> Clinical Treatment Trials
Alejandro J Roman, Christian A Powers, Evelyn P Semenov, et al.
Molecular Vision
|
October 26, 2007
Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosis
Alejandro J Roman, Sanford L Boye, Tomas S Aleman, et al.
Visual Neuroscience
|
January 12, 2001
Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man
Artur V Cideciyan, Françoise Haeseleer, Robert N Fariss, et al.
Investigative Ophthalmology & Visual Science
|
December 17, 2008
Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations
Samuel G Jacobson, Tomas S Aleman, Alexander Sumaroka, et al.
Plos One
|
November 24, 2011
Characterisation of a C1qtnf5 Ser163Arg knock-in mouse model of late-onset retinal macular degeneration
Xinhua Shu, Ulrich F O Luhmann, Tomas S Aleman, et al.
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Search research articles
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Showing results (91-100 of 224) with videos related to
Sort By:
Page
of 23
Proceedings of the National Academy of Sciences of the United States of America
|
August 10, 2011
Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosa
Budd A Tucker, Todd E Scheetz, Robert F Mullins, et al.
Diabetes
|
March 29, 2005
Nonhuman primate models for diabetic ocular neovascularization using AAV2-mediated overexpression of vascular endothelial growth factor
Corinna Lebherz, Albert M Maguire, Alberto Auricchio, et al.
Nature Medicine
|
April 2, 2021
Durable vision improvement after a single treatment with antisense oligonucleotide sepofarsen: a case report
Artur V Cideciyan, Samuel G Jacobson, Allen C Ho, et al.
Investigative Ophthalmology & Visual Science
|
November 24, 2005
ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retina
Artur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science
|
August 29, 2006
Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutations
Samuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
International Journal of Molecular Sciences
|
May 24, 2019
Short-Wavelength Sensitive Cone (S-cone) Testing as an Outcome Measure for <i>NR2E3</i> Clinical Treatment Trials
Alejandro J Roman, Christian A Powers, Evelyn P Semenov, et al.
Molecular Vision
|
October 26, 2007
Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosis
Alejandro J Roman, Sanford L Boye, Tomas S Aleman, et al.
Visual Neuroscience
|
January 12, 2001
Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man
Artur V Cideciyan, Françoise Haeseleer, Robert N Fariss, et al.
Investigative Ophthalmology & Visual Science
|
December 17, 2008
Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations
Samuel G Jacobson, Tomas S Aleman, Alexander Sumaroka, et al.
Plos One
|
November 24, 2011
Characterisation of a C1qtnf5 Ser163Arg knock-in mouse model of late-onset retinal macular degeneration
Xinhua Shu, Ulrich F O Luhmann, Tomas S Aleman, et al.
Page
of 23