Year: 2024
Type: article
Source: Nature Chemical Biology
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Funders: U.S. Department of Health and Human Services, Oregon Health and Science University, National Institutes of Health, University of California, San Francisco, National Institute on Aging, National Institute on Drug Abuse, National Eye Institute, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke, Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco
Awards: G1419896738, G2335736519, G2342450115, G2535433541, G2764442335, Molecular basis for ligand and cell type specific regulation of opioid receptors, G3668112890, G3869190629, G4374229610, G4768255817, MEMBRANE TRAFFICKING OF OPIOID RECEPTORS, G524481016, LTQ Orbitrap Velos, G6003464827, G7022274240, MEMBRANE TRAFFICKING OF OPIOID RECEPTORS, G7249880227, G7585305919, G839201715, Endosomes as a multifunctional hub to control GPCR function, Membrane Trafficking of Opioid and Adrenergic Receptors, Systematic elucidation of endosomal trafficking as a therapeutic opportunity in AD using CRISPR-based functional genomics, Molecular basis for ligand and cell type specific regulation of opioid receptors, G9000284826, G9000346595, Mechanisms and Cellular Function of Opioid Receptor Endocytosis, Chemical Physiology Training Program, Program in Biomedical Sciences, Cancer Center Support Grant, Characterization of Compartmentalized GPCR Signaling in Neurons, Molecular and Cellular Biophysics Training Grant, Ophthalmology Core Facility, OHSU Knight Cancer Institute
OpenAlex ID: W4402135302