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Auteur
Michael Xi Zhu is a professor in the Department of Integrative Biology and Pharmacology, McGovern Medical School, The University of Texas Health Science Center at Houston, Texas. He received his BS from Fudan University, Shanghai, China, in 1984, and his MS and PhD degrees from the University of Houston in 1988 and 1991, respectively. He was a postdoctoral fellow in the Department of Cell Biology at Baylor College of Medicine, Houston, Texas, from 1991 to 1994 and an assistant researcher in the Department of Anesthesiology, University of California at Los Angeles, from 1994 to 1997. In 1997, he became assistant professor in the Department of Pharmacology and Neurobiotechnology Center at The Ohio State University. In 2000, he transferred his appointment to the Department of Neuroscience and Center for Molecular Neurobiology at The Ohio State University, where was promoted to associate professor in 2003 and to professor in 2010. In 2010, he moved to his current position. Dr. Zhu's research interests include many aspects of cell signaling, especially those that involve heterotrimeric G proteins and ion channels that affect Ca2+ signaling. Dr. Zhu's main contributions include identification and characterization of multiple TRPC channels in mammalian species and determination of the molecular identity of endolysosomal Ca2+ release channels activated by the Ca2+ mobilizing messenger, nicotinic acid adenine dinucleotide phosphate. He has published more than 200 research papers, reviews, and book chapters and delivered lectures at many international conferences and symposia. Dr. Zhu has served on the editorial boards of Journal of Cellular Physiology, Pflügers Archiv, Biophysics Reports, Cells, and Molecular Pharmacology. He has been serving as a series editor of the CRC Methods in Signal Transduction book series since 2013. Dr. Zhu has chaired or co-chaired many international conferences, including the 17th International Symposium on Ca2+-Binding Proteins and Ca2+ Function in Health and Disease, Beijing, 2011, and the 2nd Gordon Research Conference on Organellar Channels and Transporters, Vermont, 2017.
Texte du rabat
The field of Transient Receptor Potential (TRP) channels has gained momentum in recent years partially because of the growing appreciation of the diverse and important physiological and pathophysiological functions of this diverse family of cation channels.
Contenu
Chapter 1. Recent advances in the structural pharmacology of TRPC channels. Chapter 2. Characterizing the structures and regulation of TRPV channels using Cryo-EM. Chapter 3. Role of the TRPM2 channel as a ROS sensing and signaling mechanism in ischemia-reperfusion brain damage. Chapter 4. Investigating TRP channel function with tools for high-precision manipulation of gating mechanism by light. Chapter 5. Pathophysiological role of TRPC1 in cell function. Chapter 6. TRPM4 and TRPM5 Channels as Chemical-to-Electrical Signal Converter. Chapter 7. Physiological and pathological functions of TRPML1. Chapter 8. TRP Channels in Cardiac Diseases. Chapter 9. Vascular Function Mediators: TRP Channels in Endothelial and Smooth Muscle Cells. Chapter 10. Study of TRP Channels in Stroke. Chapter 11. Evolution of thermosensitive TRP channels as a source of sensory diversification and environmental adaptation.