Glenn P. Lobo

Department of Ophthalmology and Visual Neurosciences, University of Minnesota

Research Area

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JoVE Journal Publications

ArticleTotal : 2	Year
Publication title Cited by 3	2024
Publication title Cited by 6	2024

Other Publications

Article	Year
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\| PubMed ID: 34064901	2021
Loss of Motor Protein MYO1C Causes Rhodopsin Mislocalization and Results in Impaired Visual Function. Cells\| PubMed ID: 34073294	2021
Lack of Association Between Polymorphisms in and and Primary Open-Angle Glaucoma in a Saudi Cohort. Frontiers in genetics\| PubMed ID: 34408771	2021
Association analysis of variants rs35934224 in and rs6478746 in in primary angle-closure and pseudoexfoliation glaucoma. European journal of ophthalmology\| PubMed ID: 34461764	2022
Vitamin A Transporters in Visual Function: A Mini Review on Membrane Receptors for Dietary Vitamin A Uptake, Storage, and Transport to the Eye. Nutrients\| PubMed ID: 34836244	2021
The role of motor proteins in photoreceptor protein transport and visual function. Ophthalmic genetics\| PubMed ID: 35470760	2022
Mice Lacking the Systemic Vitamin A Receptor RBPR2 Show Decreased Ocular Retinoids and Loss of Visual Function. Nutrients\| PubMed ID: 35745101	2022
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\| PubMed ID: 36980976	2023
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\| PubMed ID: 37099569	2023
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\| PubMed ID: 37446072	2023
Editorial: Inherited retinal dystrophies: a light at the end of the tunnel? Frontiers in cell and developmental biology\| PubMed ID: 37860821	2023
Association between Polymorphism rs61876744 in Gene and Keratoconus in a Saudi Cohort. Genes\| PubMed ID: 38136930	2023
Common Variants rs429358 and rs7412 in Gene Are Not Associated with POAG in a Saudi Cohort. Biology\| PubMed ID: 38275738	2024
The Clinical Findings, Pathogenic Variants, and Gene Therapy Qualifications Found in a Leber Congenital Amaurosis Phenotypic Spectrum Patient Cohort. International journal of molecular sciences\| PubMed ID: 38279252	2024
The Logistical Backbone of Photoreceptor Cell Function: Complementary Mechanisms of Dietary Vitamin A Receptors and Rhodopsin Transporters. International journal of molecular sciences\| PubMed ID: 38673863	2024
ε2-Carriers Are Associated with an Increased Risk of Primary Angle-Closure Glaucoma in Patients of Saudi Origin. International journal of molecular sciences\| PubMed ID: 38674156	2024
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\| PubMed ID: 39026765	2024
Polymorphism rs3742330 in microRNA Biogenesis Gene Is Associated with Pseudoexfoliation Glaucoma in Saudi Cohort. Genes\| PubMed ID: 35328042	2022
Evaluation of ABCA1 and FNDC3B Gene Polymorphisms Associated With Pseudoexfoliation Glaucoma and Primary Angle-Closure Glaucoma in a Saudi Cohort. Frontiers in genetics\| PubMed ID: 35719397	2022
Mapping of the extracellular RBP4 ligand binding domain on the RBPR2 receptor for Vitamin A transport. Frontiers in cell and developmental biology\| PubMed ID: 36910150	2023
In Silico Prediction of MYO1C-Rhodopsin Interactions and Its Significance in Protein Localization and Visual Function. Advances in experimental medicine and biology\| PubMed ID: 37440078	2023
Gender-specific association of rs2371597 polymorphism in keratoconus patients of Saudi origin. Frontiers in genetics\| PubMed ID: 39717479	2024