Department of Ophthalmology and Visual Neurosciences
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Conditional Loss of the Exocyst Component Exoc5 in Retinal Pigment Epithelium (RPE) Results in RPE Dysfunction, Photoreceptor Cell Degeneration, and Decreased Visual Function.
International journal of molecular sciences May, 2021 | Pubmed ID: 34064901
Loss of Motor Protein MYO1C Causes Rhodopsin Mislocalization and Results in Impaired Visual Function.
Cells May, 2021 | Pubmed ID: 34073294
Lack of Association Between Polymorphisms in and and Primary Open-Angle Glaucoma in a Saudi Cohort.
Frontiers in genetics , 2021 | Pubmed ID: 34408771
Association analysis of variants rs35934224 in and rs6478746 in in primary angle-closure and pseudoexfoliation glaucoma.
European journal of ophthalmology Jul, 2022 | Pubmed ID: 34461764
Vitamin A Transporters in Visual Function: A Mini Review on Membrane Receptors for Dietary Vitamin A Uptake, Storage, and Transport to the Eye.
Nutrients Nov, 2021 | Pubmed ID: 34836244
The role of motor proteins in photoreceptor protein transport and visual function.
Ophthalmic genetics Jun, 2022 | Pubmed ID: 35470760
Mice Lacking the Systemic Vitamin A Receptor RBPR2 Show Decreased Ocular Retinoids and Loss of Visual Function.
Nutrients Jun, 2022 | Pubmed ID: 35745101
Lack of Association of Polymorphism Located Upstream of (rs2472493), in (rs7636836), and Near - Genes (rs61275591) in Primary Open-Angle Glaucoma Patients of Saudi Origin.
Genes Mar, 2023 | Pubmed ID: 36980976
The 3' UTR polymorphisms rs3742330 in DICER1 and rs10719 in DROSHA genes are not associated with primary open-angle and angle-closure glaucoma: As case-control study.
PloS one , 2023 | Pubmed ID: 37099569
Clinical Characteristics and Genetic Variants of a Large Cohort of Patients with Retinitis Pigmentosa Using Multimodal Imaging and Next Generation Sequencing.
International journal of molecular sciences Jun, 2023 | Pubmed ID: 37446072
Editorial: Inherited retinal dystrophies: a light at the end of the tunnel?
Frontiers in cell and developmental biology , 2023 | Pubmed ID: 37860821
Association between Polymorphism rs61876744 in Gene and Keratoconus in a Saudi Cohort.
Genes Nov, 2023 | Pubmed ID: 38136930
Common Variants rs429358 and rs7412 in Gene Are Not Associated with POAG in a Saudi Cohort.
Biology Jan, 2024 | Pubmed ID: 38275738
The Clinical Findings, Pathogenic Variants, and Gene Therapy Qualifications Found in a Leber Congenital Amaurosis Phenotypic Spectrum Patient Cohort.
International journal of molecular sciences Jan, 2024 | Pubmed ID: 38279252
The Logistical Backbone of Photoreceptor Cell Function: Complementary Mechanisms of Dietary Vitamin A Receptors and Rhodopsin Transporters.
International journal of molecular sciences Apr, 2024 | Pubmed ID: 38673863
ε2-Carriers Are Associated with an Increased Risk of Primary Angle-Closure Glaucoma in Patients of Saudi Origin.
International journal of molecular sciences Apr, 2024 | Pubmed ID: 38674156
Loss of the systemic vitamin A transporter RBPR2 affects the quantitative balance between chromophore and opsins in visual pigment synthesis.
bioRxiv : the preprint server for biology Jul, 2024 | Pubmed ID: 39026765
Polymorphism rs3742330 in microRNA Biogenesis Gene Is Associated with Pseudoexfoliation Glaucoma in Saudi Cohort.
Genes Mar, 2022 | Pubmed ID: 35328042
Evaluation of ABCA1 and FNDC3B Gene Polymorphisms Associated With Pseudoexfoliation Glaucoma and Primary Angle-Closure Glaucoma in a Saudi Cohort.
Frontiers in genetics , 2022 | Pubmed ID: 35719397
Mapping of the extracellular RBP4 ligand binding domain on the RBPR2 receptor for Vitamin A transport.
Frontiers in cell and developmental biology , 2023 | Pubmed ID: 36910150
In Silico Prediction of MYO1C-Rhodopsin Interactions and Its Significance in Protein Localization and Visual Function.
Advances in experimental medicine and biology , 2023 | Pubmed ID: 37440078
Gender-specific association of rs2371597 polymorphism in keratoconus patients of Saudi origin.
Frontiers in genetics , 2024 | Pubmed ID: 39717479
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