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One or more keywords matched the following properties of Stokes, Alexander J.
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overview My laboratory is interested in the study of ion channels as mechanistic components and druggable targets in complex human disease. My career has spanned the initial cloning, electrophysiological and biochemical characterization and, more recently, the in vivo and translational study of ion channels. I have worked in immunological, cardiovascular and cancer disease settings, following lines of investigation that seek to demystify these often enigmatic proteins and work towards a complete understanding of their roles in health and disease. My recent work has combined ion channel regulatory and mechanistic studies with powerful in vivo approaches to study their contributions in cardiovascular physiology and disease. I have a proven track record of pre-clinical and translational studies of TRP ion channels in complex human disease states, such as cardiovascular disease. Ion channels control complex cellular responses, and offer insights into disease mechanisms as well as potential therapeutic approaches. Their study requires a multi-dimensional approach, where their biophysics is understood in the context of their protein-protein interactions, the net outcomes of the ionic fluxes they conduct, and their tissue-specific expression. This work also requires interdisciplinary collaborations and the ability to work across in vitro and in vivo model systems, a strength of my laboratory. The projects in my laboratory are empowered by senior collaborators at Kyoto University, Harvard Medical School, the Universities of Aarhus, Nebraska and British Columbia, Rockefeller University, Wisconsin Institutes for Medical Research, and the Air Force Research Laboratories (AFRL). My contributions include roles in the initial cloning of TRPM2 and TRPM7 and the Orai1 ICRAC subunit. I have produced electrophysiological and biochemical characterization of ion channels and linked them to functional roles in immune system cells (exemplified by the role of TRPV2 and TRPA1 in mast cells). More recently, I have broken ground in the in vivo and translational study of TRP and CRAC family members in the setting of cardiovascular disease, leading to publications and an issued 2015 U.S. Patent. I am also Director of the University of Hawaii Biorepository. http://uhbio.jabsom.hawaii.edu/Home.html This resource is funded by : National Institutes of Health - National Institute on Minority Health and Health Disparities • RMATRIX - 3U54MD007584-03S1 (Dr. J Hedges) & RCMI BRIDGES • G12 MD007601 (Dr. M. Berry), and The National Institute General Medical Sciences • INBRE III • P20GM10346612 (Dr. R Nichols).
One or more keywords matched the following items that are connected to Stokes, Alexander J.
Item TypeName
Academic Article Pacific island 'Awa (Kava) extracts, but not isolated kavalactones, promote proinflammatory responses in model mast cells.
Academic Article Lipid body accumulation alters calcium signaling dynamics in immune cells.
Academic Article Single-walled carbon nanotube exposure induces membrane rearrangement and suppression of receptor-mediated signalling pathways in model mast cells.
Academic Article Beyond apoptosis: the mechanism and function of phosphatidylserine asymmetry in the membrane of activating mast cells.
Academic Article Transcriptional and Functional Plasticity Induced by Chronic Insulin Exposure in a Mast Cell-Like Basophilic Leukemia Cell Model.
Academic Article Insulin-induced lipid body accumulation is accompanied by lipid remodelling in model mast cells.
Academic Article Differential roles of CB1 and CB2 cannabinoid receptors in mast cells.
Academic Article A TRPV2-PKA signaling module for transduction of physical stimuli in mast cells.
Academic Article Formation of a physiological complex between TRPV2 and RGA protein promotes cell surface expression of TRPV2.
Academic Article Fcepsilon RI control of Ras via inositol (1,4,5) trisphosphate 3-kinase and inositol tetrakisphosphate.
Academic Article Secretogranin III directs secretory vesicle biogenesis in mast cells in a manner dependent upon interaction with chromogranin A.
Concept Leukemia, Mast-Cell
Concept Mast Cells
Academic Article Link between TRPV channels and mast cell function.
Search Criteria
  • Mast Cells
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