Guangju Ji

Biography

1978-1983     The Forth Military Medical University，M.D. 1988-1991　 The Forth Military Medical University，M.S. (Pharmacology) 1994-1999　 University of Cologne, Germany, Ph.D., (physiology) 1999-2001　 University of Pennsylvania US, Postdoctoral Fellow 2001-2004　 Cornell University, Dept. of Biomedical Sciences, Research Assistant Prof. 2004-2006　 Cornell University, Dept. of Biomedical Sciences, Research Associate Prof 2006-　　 　Investigator, Institute of Biophysics, Chinese Academy of Sciences Editorial boards Journal of Physiology and Biophysics, Frontier in physiology, Archives of Biochemistry and Biophysics, Molecular and Cellular Biochemistry, ISRN Physiology, Frontiers in Skeletal Muscle Physioloogy, Journal of Geriatric Cardiology, Chinese Circulation Research. 1978-1983     The Forth Military Medical University，M.D. 1988-1991　 The Forth Military Medical University，M.S. (Pharmacology) 1994-1999　 University of Cologne, Germany, Ph.D., (physiology) 1999-2001　 University of Pennsylvania US, Postdoctoral Fellow 2001-2004　 Cornell University, Dept. of Biomedical Sciences, Research Assistant Prof. 2004-2006　 Cornell University, Dept. of Biomedical Sciences, Research Associate Prof 2006-　　 　Investigator, Institute of Biophysics, Chinese Academy of Sciences Editorial boards Journal of Physiology and Biophysics, Frontier in physiology, Archives of Biochemistry and Biophysics, Molecular and Cellular Biochemistry, ISRN Physiology, Frontiers in Skeletal Muscle Physioloogy, Journal of Geriatric Cardiology, Chinese Circulation Research.

Research Interest

My laboratory focuses on the molecular processes underlying excitation-contraction coupling, integration /modulation of Ca2+ signaling in vivo, as well as the roles and mechanisms of Ca2+ homeostasis disturbance-caused diseases. Current studies seek to understand the role of the specific sarcoplasmic/endoplasmic reticular calcium release channels, the sarcolemmal ion channels and their regulatory proteins in cellular excitation-contraction coupling. A major goal of the laboratory is to understand the processes of intercellular communication and the generation of spontaneous Ca2+ signal activity and the mechanisms of Ca2+ signaling disturbance causing diseases related. Projects in the laboratory include the study of the molecular mechanism of the Ca2+ signaling disturbance, the development and progress of related diseases induced by intracellular Ca2+ homeostasis disturbance, identification of genes encoding channel regulatory proteins and relating signaling molecules involved in muscle biology and determination of the extent to which these genes are altered in specific disease processes, and the development of genetically encoded sensors of cell signaling. An additional effort in the laboratory is to combine molecular design, electrophysiology and advanced optical imaging technologies to advance the understanding of path- physiological processes, destination, functions, integration with host tissues /organs of implanted ESC derived cells for treatment of injured organ function