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Ala Moshiri

Showing results (71-80 of 92) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|June 30, 2025
Genome-Wide Insights into the Genes and Pathways Shaping Human Foveal DevelopmentCallum Hunt, Ha-Jun Yoon, Alvin Lirio, et al.
Developmental Biology|October 22, 2019
Cytoglobin deficiency potentiates Crb1-mediated retinal degeneration in rd8 miceYoung Sam Kwon, Addy Tham, Antonio Jacobo Lopez, et al.
Scientific Reports|December 5, 2025
Spontaneous refractive error, ocular biometry and age related lens changes in a population of geriatric rhesus macaquesJonathon M Ross, Karolina Roszak, Ana Ripolles-Garcia, et al.
Experimental Eye Research|March 26, 2026
Zfp503 haploinsufficiency causes optic nerve coloboma in miceJenna Wong-Fortunato, Benjamin Yang, Louise Lanoue, et al.
Investigative Ophthalmology & Visual Science|January 23, 2023
A Spontaneous Nonhuman Primate Model of Myopic FoveoschisisTzu-Ni Sin, Sangbae Kim, Yumei Li, et al.
Nature Communications|July 5, 2024
Genetic diversity of 1,845 rhesus macaques improves genetic variation interpretation and identifies disease modelsJun Wang, Meng Wang, Ala Moshiri, et al.
The Journal of Clinical Investigation|January 23, 2019
A nonhuman primate model of inherited retinal diseaseAla Moshiri, Rui Chen, Soohyun Kim, et al.
Investigative Ophthalmology & Visual Science|September 9, 2025
Genome-Wide Insights Into the Genes and Pathways Shaping Human Foveal Development: Redefining the Genetic Landscape of Foveal HypoplasiaCallum Hunt, Ha-Jun Yoon, Alvin Lirio, et al.
Investigative Ophthalmology & Visual Science|November 3, 2022
Zfp503/Nlz2 Is Required for RPE Differentiation and Optic Fissure ClosureElangovan Boobalan, Amy H Thompson, Ramakrishna P Alur, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2021
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delayUirá Souto Melo, Devon Bonner, Kevin C Kent Lloyd, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Medrxiv : the Preprint Server for Health Sciences|June 30, 2025
Genome-Wide Insights into the Genes and Pathways Shaping Human Foveal DevelopmentCallum Hunt, Ha-Jun Yoon, Alvin Lirio, et al.
Developmental Biology|October 22, 2019
Cytoglobin deficiency potentiates Crb1-mediated retinal degeneration in rd8 miceYoung Sam Kwon, Addy Tham, Antonio Jacobo Lopez, et al.
Scientific Reports|December 5, 2025
Spontaneous refractive error, ocular biometry and age related lens changes in a population of geriatric rhesus macaquesJonathon M Ross, Karolina Roszak, Ana Ripolles-Garcia, et al.
Experimental Eye Research|March 26, 2026
Zfp503 haploinsufficiency causes optic nerve coloboma in miceJenna Wong-Fortunato, Benjamin Yang, Louise Lanoue, et al.
Investigative Ophthalmology & Visual Science|January 23, 2023
A Spontaneous Nonhuman Primate Model of Myopic FoveoschisisTzu-Ni Sin, Sangbae Kim, Yumei Li, et al.
Nature Communications|July 5, 2024
Genetic diversity of 1,845 rhesus macaques improves genetic variation interpretation and identifies disease modelsJun Wang, Meng Wang, Ala Moshiri, et al.
The Journal of Clinical Investigation|January 23, 2019
A nonhuman primate model of inherited retinal diseaseAla Moshiri, Rui Chen, Soohyun Kim, et al.
Investigative Ophthalmology & Visual Science|September 9, 2025
Genome-Wide Insights Into the Genes and Pathways Shaping Human Foveal Development: Redefining the Genetic Landscape of Foveal HypoplasiaCallum Hunt, Ha-Jun Yoon, Alvin Lirio, et al.
Investigative Ophthalmology & Visual Science|November 3, 2022
Zfp503/Nlz2 Is Required for RPE Differentiation and Optic Fissure ClosureElangovan Boobalan, Amy H Thompson, Ramakrishna P Alur, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2021
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delayUirá Souto Melo, Devon Bonner, Kevin C Kent Lloyd, et al.
Pageof 10