ZFIN ID: ZDB-PERS-140916-1
Lobo, Glenn
Email: lobo@musc.edu
URL: http://academicdepartments.musc.edu/facultydirectory/Lobo-Glenn
Affiliation: Lobo Lab
Address: Medical University of South Carolina Department of Medicine Drug Discovery Building DDB513 70 President Street, MSC 629 Charleston, SC 29425
Country: United States
Phone: 843-876-2371
Fax:
ORCID ID:


BIOGRAPHY AND RESEARCH INTERESTS


PUBLICATIONS
Radhakrishnan, R., Leung, M., Roehrich, H., Walterhouse, S., Kondkar, A.A., Fitzgibbon, W., Biswal, M.R., Lobo, G.P. (2022) Mice Lacking the Systemic Vitamin A Receptor RBPR2 Show Decreased Ocular Retinoids and Loss of Visual Function. Nutrients. 14(12)
Rohrer, B., Biswal, M.R., Obert, E., Dang, Y., Su, Y., Zuo, X., Fogelgren, B., Kondkar, A.A., Lobo, G.P., Lipschutz, J.H. (2021) 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. 22(10):
Solanki, A.K., Kondkar, A.A., Fogerty, J., Su, Y., Kim, S.H., Lipschutz, J.H., Nihalani, D., Perkins, B.D., Lobo, G.P. (2020) A Functional Binding Domain in the Rbpr2 Receptor Is Required for Vitamin A Transport, Ocular Retinoid Homeostasis, and Photoreceptor Cell Survival in Zebrafish. Cells. 9(5):
Fulmer, D., Toomer, K., Guo, L., Moore, K., Glover, J., Moore, R., Stairley, R., Lobo, G., Zuo, X., Dang, Y., Su, Y., Fogelgren, B., Gerard, P., Chung, D., Heydarpour, M., Mukherjee, R., Body, S.C., Norris, R.A., Lipschutz, J.H. (2019) Defects in the Exocyst-Cilia Machinery Cause Bicuspid Aortic Valve Disease and Aortic Stenosis. Circulation. 140(16):1331-1341
Zuo, X., Lobo, G., Fulmer, D., Guo, L., Dang, Y., Su, Y., Ilatovskaya, D.V., Nihalani, D., Rohrer, B., Body, S.C., Norris, R.A., Lipschutz, J.H. (2019) The exocyst acting through the primary cilium is necessary for renal ciliogenesis, cystogenesis, and tubulogenesis. The Journal of biological chemistry. 294(17):6710-6718
Lobo, G.P., Pauer, G., Lipschutz, J.H., Hagstrom, S.A. (2018) The Retinol-Binding Protein Receptor 2 (Rbpr2) Is Required for Photoreceptor Survival and Visual Function in the Zebrafish. Advances in experimental medicine and biology. 1074:569-576
Shi, Y., Su, Y., Lipschutz, J.H., Lobo, G.P. (2017) Zebrafish as models to study ciliopathies of the eye and kidney. Clinical nephrology and research. 1:6-9
Shi, Y., Obert, E., Rahman, B., Rohrer, B., Lobo, G.P. (2017) The Retinol Binding Protein Receptor 2 (Rbpr2) is required for Photoreceptor Outer Segment Morphogenesis and Visual Function in Zebrafish. Scientific Reports. 7:16207
Lobo, G.P., Fulmer, D., Guo, L., Zuo, X., Dang, Y., Kim, S.H., Su, Y., George, K., Obert, E., Fogelgren, B., Nihalani, D., Norris, R.A., Rohrer, B., Lipschutz, J.H. (2017) The exocyst is required for photoreceptor ciliogenesis and retinal development. The Journal of biological chemistry. 292(36):14814-14826
Daniele, L.L., Emran, F., Lobo, G.P., Gaivin, R.J., Perkins, B.D. (2016) Mutation of wrb, a Component of the Guided Entry of Tail-Anchored Protein Pathway, Disrupts Photoreceptor Synapse Structure and Function. Investigative ophthalmology & visual science. 57:2942-54
Lobo, G.P., Isken, A., Hoff, S., Babino, D., and von Lintig, J. (2012) BCDO2 acts as a carotenoid scavenger and gatekeeper for the mitochondrial apoptotic pathway. Development (Cambridge, England). 139(16):2966-2977

NON-ZEBRAFISH PUBLICATIONS