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Ying Chen
yingchen@xmu.edu.cn
English, Chinese
Fujian
Xiamen University
Life Sciences
  • 1996 - B.S. in Biochemistry: Fudan University
  • 1999 - M.S. in Pathogenic Organisms: Chinese Academy of Preventive Medicine
  • 2006 - Ph.D. in Immunology and Microbiology: Rush University
  • 2007-2012 - UTSW Medical Center - Postdoctoral Fellow
  • 2013-Present - Xiamen University, School of Life Sciences - Professor
Molecular mechanisms of myelinating glial cell development and disease
Epigenetic and chromatin remodeling control of myelinating cell differentiation and disease
Signaling mechanisms in glial differentiation and regeneration
  • A GPR17-cAMP-Lactate Signaling Axis in Oligodendrocytes Regulates Whole-Body Metabolism., Ou Z, Ma Y, Sun Y, Zheng G, Wang S, Xing R, Chen X, Han Y, Wang J, Lu QR, Zhao TJ, Chen Y., 2019
  • Olig2-Targeted G-Protein-Coupled Receptor Gpr17 Regulates Oligodendrocyte Survival in Response to Lysolecithin-Induced Demyelination., Ou Z, Sun Y, Lin L, You N, Liu X, Li H, Ma Y, Cao L, Han Y, Liu M, Deng Y, Yao L, Lu QR, Chen Y., 2016
  • Olig2 Targets Chromatin Remodelers To Enhancers To Initiate Oligodendrocyte Differentiation., Yu Y, Y. Chen, B. Kim, H. Wang, C. Zhao, X. He, L. Liu, W. Liu, L. M. N. Wu, M. Mao, J. R. Chan, J. Wu and Q. R. Lu, 2013
  • HDAC-mediated Deacetylation of NF-κB is Critical for Schwann cell Myelination., Ying Chen, Haibo Wang, Sung Ok Yoon, Xiaomei Xu, Michael Hottiger, Haesun Kim, Eric N. Olson, and Q. Richard Lu., 2011
  • The oligodendrocyte-specific G-protein coupled receptor GPR17 is a cell intrinsic timer of myelination., Chen, Y. H. Wu, S. Wang, H. Koito, J. Li, J. Hoang, F. Ye, S. S. Escobar, A. Gow, H. A. Arnett, B. D. Trapp, N. J. Karandikar, J. Hsieh and Q. R. Lu., 2009
  • The basic helix-loop-helix transcription factor olig2 is critical for reactive astrocyte proliferation after cortical injury., Chen Y, Miles DK, Hoang T, Shi J, Hurlock E, Kernie SG, Lu QR., 2008
Myelination Glial Cells Molecular Mechanisms Epigenetics Chromatin Remodeling Differentiation Disease Signaling Pathways Gpcr Regeneration

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