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Alejandro J Roman

Showing results (21-30 of 96) with videos related to

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Investigative Ophthalmology & Visual Science|June 19, 2019
Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis Due to CEP290 or NPHP5 Mutations: Predictions From Artificial IntelligenceAlexander Sumaroka, Alexandra V Garafalo, Evelyn P Semenov, et al.
Nature Genetics|October 30, 2004
Lifespan and mitochondrial control of neurodegenerationAlan F Wright, Samuel G Jacobson, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|February 20, 2014
Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutationsWei Chieh Huang, Artur V Cideciyan, Alejandro J Roman, et al.
International Journal of Molecular Sciences|March 6, 2021
Leber Congenital Amaurosis Due to <i>GUCY2D</i> Mutations: Longitudinal Analysis of Retinal Structure and Visual FunctionSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Investigative Ophthalmology & Visual Science|July 5, 2018
Cone Vision Changes in the Enhanced S-Cone Syndrome Caused by NR2E3 Gene MutationsAlexandra V Garafalo, Giacomo Calzetti, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|June 30, 2017
Pupillary Light Reflexes in Severe Photoreceptor Blindness Isolate the Melanopic Component of Intrinsically Photosensitive Retinal Ganglion CellsJason Charng, Samuel G Jacobson, Elise Heon, et al.
The Journal of Biological Chemistry|January 13, 2011
Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutationsSanae Sakami, Tadao Maeda, Grzegorz Bereta, et al.
American Journal of Ophthalmology|June 29, 2018
Efficacy Outcome Measures for Clinical Trials of USH2A Caused by the Common c.2299delG MutationGiacomo Calzetti, Richard A Levy, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|September 23, 2015
Molecular Heterogeneity Within the Clinical Diagnosis of Pericentral Retinal DegenerationRodrigo Matsui, Artur V Cideciyan, Sharon B Schwartz, et al.
Investigative Ophthalmology & Visual Science|August 13, 2010
Human retinal disease from AIPL1 gene mutations: foveal cone loss with minimal macular photoreceptors and rod function remainingSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Pageof 10

Showing results (21-30 of 96) with videos related to

Sort By:
Pageof 10
Investigative Ophthalmology & Visual Science|June 19, 2019
Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis Due to CEP290 or NPHP5 Mutations: Predictions From Artificial IntelligenceAlexander Sumaroka, Alexandra V Garafalo, Evelyn P Semenov, et al.
Nature Genetics|October 30, 2004
Lifespan and mitochondrial control of neurodegenerationAlan F Wright, Samuel G Jacobson, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|February 20, 2014
Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutationsWei Chieh Huang, Artur V Cideciyan, Alejandro J Roman, et al.
International Journal of Molecular Sciences|March 6, 2021
Leber Congenital Amaurosis Due to <i>GUCY2D</i> Mutations: Longitudinal Analysis of Retinal Structure and Visual FunctionSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Investigative Ophthalmology & Visual Science|July 5, 2018
Cone Vision Changes in the Enhanced S-Cone Syndrome Caused by NR2E3 Gene MutationsAlexandra V Garafalo, Giacomo Calzetti, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|June 30, 2017
Pupillary Light Reflexes in Severe Photoreceptor Blindness Isolate the Melanopic Component of Intrinsically Photosensitive Retinal Ganglion CellsJason Charng, Samuel G Jacobson, Elise Heon, et al.
The Journal of Biological Chemistry|January 13, 2011
Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutationsSanae Sakami, Tadao Maeda, Grzegorz Bereta, et al.
American Journal of Ophthalmology|June 29, 2018
Efficacy Outcome Measures for Clinical Trials of USH2A Caused by the Common c.2299delG MutationGiacomo Calzetti, Richard A Levy, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|September 23, 2015
Molecular Heterogeneity Within the Clinical Diagnosis of Pericentral Retinal DegenerationRodrigo Matsui, Artur V Cideciyan, Sharon B Schwartz, et al.
Investigative Ophthalmology & Visual Science|August 13, 2010
Human retinal disease from AIPL1 gene mutations: foveal cone loss with minimal macular photoreceptors and rod function remainingSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
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