H. Uri Saragovi
Affiliations: | Pharmacology | McGill University, Montreal, QC, Canada |
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| Guo X, Kazanova A, Thurmond S, et al. (2021) Effective chimeric antigen receptor T cells against SARS-CoV-2. Iscience. 24: 103295 |
| Brahimi F, Galan A, Siegel S, et al. (2021) . Molecular Pharmacology |
| Brahimi F, Galan A, Jmaeff S, et al. (2020) Alternative Splicing of a Receptor Intracellular Domain Yields Different Ectodomain Conformations, Enabling Isoform-Selective Functional Ligands. Iscience. 23: 101447 |
| Mossa AH, Galan A, Cammisotto PG, et al. (2020) Antagonism of proNGF or its receptor p75 reverses remodelling and improves bladder function in a mouse model of diabetic voiding dysfunction. Diabetologia |
| Jmaeff S, Sidorova Y, Lippiatt H, et al. (2020) Small-molecule ligands that bind the RET receptor activate neuroprotective signals independent of but modulated by co-receptor GFRα1. Molecular Pharmacology |
| Jmaeff S, Sidorova Y, Nedev H, et al. (2020) Small-molecule agonists of the RET receptor tyrosine kinase activate biased trophic signals that are influenced by the presence of GFRa1 co-receptors. The Journal of Biological Chemistry. 295: 6532-6542 |
| Saragovi HU, Galan A, Levin LA. (2019) Neuroprotection: Pro-survival and Anti-neurotoxic Mechanisms as Therapeutic Strategies in Neurodegeneration. Frontiers in Cellular Neuroscience. 13: 231 |
| Josephy-Hernandez S, Jmaeff S, Pirvulescu I, et al. (2016) Neurotrophin receptor agonists and antagonists as therapeutic agents: An evolving paradigm. Neurobiology of Disease. 97: 139-155 |
| Tong W, Maira M, Gagnon M, et al. (2015) Ligands Binding to Cell Surface Ganglioside GD2 Cause Src-Dependent Activation of N-Methyl-D-Aspartate Receptor Signaling and Changes in Cellular Morphology. Plos One. 10: e0134255 |
| Barcelona PF, Saragovi HU. (2015) A Pro-Nerve Growth Factor (proNGF) and NGF Binding Protein, α2-Macroglobulin, Differentially Regulates p75 and TrkA Receptors and Is Relevant to Neurodegeneration Ex Vivo and In Vivo. Molecular and Cellular Biology. 35: 3396-408 |