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Brian P Brooks

Showing results (71-80 of 158) with videos related to

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Molecular Therapy. Advances|May 15, 2026
Gene therapy induces pigmentation in induced pluripotent stem cell-derived retinal pigment epithelium of OCA1A patients and albino rat eyeAman George, Arnold Leigh, Evan Selzer, et al.
Neuroimage. Clinical|January 31, 2021
In vivo assessment of neurodegeneration in Spinocerebellar Ataxia type 7Jacob A Parker, Shabbir H Merchant, Sanaz Attaripour-Isfahani, et al.
Birth Defects Research|November 12, 2024
Epidemiology of Coloboma: Prevalence and Patterns in Texas, 1999-2014Danielle L Mitchell, Tiffany M Chambers, A J Agopian, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 6, 2017
Genetic background-dependent role of <i>Egr1</i> for eyelid developmentJangsuk Oh, Yujuan Wang, Shida Chen, et al.
Stem Cell Reports|January 29, 2021
Gene Therapy of Dominant CRX-Leber Congenital Amaurosis using Patient Stem Cell-Derived Retinal OrganoidsKamil Kruczek, Zepeng Qu, James Gentry, et al.
Genes|May 28, 2022
Clinical Phenotypes of <i>CDHR1</i>-Associated Retinal DystrophiesVolha V Malechka, Catherine A Cukras, Emily Y Chew, et al.
Investigative Ophthalmology & Visual Science|March 19, 2024
High Clinical Exome Sequencing Diagnostic Rates and Novel Phenotypic Expansions for Nonisolated Microphthalmia, Anophthalmia, and ColobomaBhavana Kunisetty, Bailey A Martin-Giacalone, Xiaonan Zhao, et al.
Plos Genetics|March 12, 2010
Papillorenal syndrome-causing missense mutations in PAX2/Pax2 result in hypomorphic alleles in mouse and humanRamakrishna P Alur, Camasamudram Vijayasarathy, Jacob D Brown, et al.
Investigative Ophthalmology & Visual Science|July 28, 2022
Photoreceptor and Retinal Pigment Epithelium Relationships in Eyes With Vitelliform Macular Dystrophy Revealed by Multimodal Adaptive Optics ImagingTao Liu, Nancy Aguilera, Andrew J Bower, et al.
Molecular Genetics and Metabolism|March 6, 2017
Clinical and molecular phenotyping of a child with Hermansky-Pudlak syndrome-7, an uncommon genetic type of HPSMelanie M Bryan, Nathanial J Tolman, Karen L Simon, et al.
Pageof 16

Showing results (71-80 of 158) with videos related to

Sort By:
Pageof 16
Molecular Therapy. Advances|May 15, 2026
Gene therapy induces pigmentation in induced pluripotent stem cell-derived retinal pigment epithelium of OCA1A patients and albino rat eyeAman George, Arnold Leigh, Evan Selzer, et al.
Neuroimage. Clinical|January 31, 2021
In vivo assessment of neurodegeneration in Spinocerebellar Ataxia type 7Jacob A Parker, Shabbir H Merchant, Sanaz Attaripour-Isfahani, et al.
Birth Defects Research|November 12, 2024
Epidemiology of Coloboma: Prevalence and Patterns in Texas, 1999-2014Danielle L Mitchell, Tiffany M Chambers, A J Agopian, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 6, 2017
Genetic background-dependent role of <i>Egr1</i> for eyelid developmentJangsuk Oh, Yujuan Wang, Shida Chen, et al.
Stem Cell Reports|January 29, 2021
Gene Therapy of Dominant CRX-Leber Congenital Amaurosis using Patient Stem Cell-Derived Retinal OrganoidsKamil Kruczek, Zepeng Qu, James Gentry, et al.
Genes|May 28, 2022
Clinical Phenotypes of <i>CDHR1</i>-Associated Retinal DystrophiesVolha V Malechka, Catherine A Cukras, Emily Y Chew, et al.
Investigative Ophthalmology & Visual Science|March 19, 2024
High Clinical Exome Sequencing Diagnostic Rates and Novel Phenotypic Expansions for Nonisolated Microphthalmia, Anophthalmia, and ColobomaBhavana Kunisetty, Bailey A Martin-Giacalone, Xiaonan Zhao, et al.
Plos Genetics|March 12, 2010
Papillorenal syndrome-causing missense mutations in PAX2/Pax2 result in hypomorphic alleles in mouse and humanRamakrishna P Alur, Camasamudram Vijayasarathy, Jacob D Brown, et al.
Investigative Ophthalmology & Visual Science|July 28, 2022
Photoreceptor and Retinal Pigment Epithelium Relationships in Eyes With Vitelliform Macular Dystrophy Revealed by Multimodal Adaptive Optics ImagingTao Liu, Nancy Aguilera, Andrew J Bower, et al.
Molecular Genetics and Metabolism|March 6, 2017
Clinical and molecular phenotyping of a child with Hermansky-Pudlak syndrome-7, an uncommon genetic type of HPSMelanie M Bryan, Nathanial J Tolman, Karen L Simon, et al.
Pageof 16