Keshi Chen
chen_keshi@gibh.ac.cn
Chinese, English
Guangdong
University of Chinese Academy of Sciences
Medical School
  • 2008-09--2013-07 PhD: University of Chinese Academy of Sciences
  • 2004-09--2008-07 Bachelor: University of Science and Technology of China
  • 2023-01~Present - Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences - Researcher
  • 2017-01~2022-12 - Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences - Associate Researcher
  • 2013-07~2016-12 - Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences - Assistant Researcher
  • Outstanding Member of the Youth Innovation Promotion Association, Chinese Academy of Sciences (2022)
  • First Prize for Research on Mitochondrial Signaling Regulation of Cell Fate (2020)
  • Collective Research on Mechanisms of Stem Cell Pluripotency and Reprogramming (2017)
Regulation of pluripotent stem cell fate based on epigenetics and metabolism
  • MAP2K6 remodels chromatin and facilitates reprogramming by activating Gatad2b-phosphorylation dependent heterochromatin loosening, Corresponding Author, 2022
  • Plin2-mediated lipid droplet mobilization accelerates exit from pluripotency by lipidomic remodeling and histone acetylation, Second Author, 2022
  • Glis1 facilitates induction of pluripotency via an epigenome-metabolome-epigenome signalling cascade, Second Author, 2020
  • Topology-dependent, bifurcated mitochondrial quality control under starvation, Tenth Author, 2020
  • Heterochromatin loosening by the Oct4 linker region facilitates Klf4 binding and iPSC reprogramming, First Author, 2020
  • Phospholipid remodeling is critical for stem cell pluripotency by facilitating mesenchymal-to-epithelial transition, Second Author, 2019
  • Short-term mitochondrial permeability transition pore opening modulates histone lysine methylation at the early phase of somatic cell reprogramming, Eighth Author, 2018
  • Polybrene induces neural degeneration by bidirectional Ca2+ influx-dependent mitochondrial and ER-mitochondrial dynamics, Eighth Author, 2018
  • BNIP3L-dependent mitophagy accounts for mitochondrial clearance during 3 factors-induced somatic cell reprogramming, Fourth Author, 2017
  • Gadd45a opens up the promoter regions of miR-295 facilitating pluripotency induction, Second Author, 2017
  • Srebp-1 Interacts with c-Myc to Enhance Somatic Cell Reprogramming, Second Author, 2016
  • Transient Activation of Mitoflashes Modulates Nanog at the Early Phase of Somatic Cell Reprogramming, Second Author, 2016
  • Gadd45a is a heterochromatin relaxer that enhances iPS cell generation, First Author, 2016
  • Valproic Acid-Induced Hepatotoxicity in Alpers Syndrome Is Associated With Mitochondrial Permeability Transition Pore Opening-Dependent Apoptotic Sensitivity in an Induced Pluripotent Stem Cell Model, Sixth Author, 2015
  • Tbx3 isoforms are involved in pluripotency maintaining through distinct regulation of Nanog transcriptional activity, Corresponding Author, 2014
  • The Histone Demethylases Jhdm1a/1b Enhance Somatic Cell Reprogramming in a Vitamin-C-Dependent Manner, Second Author, 2011
  • Vitamin C Enhances the Generation of Mouse and Human Induced Pluripotent Stem Cells, Eleventh Author, 2010
Epigenetics Metabolism Pluripotent Stem Cells Cell Fate Embryonic Stem Cells Somatic Cell Reprogramming Mitochondrial Metabolism Chromatin Remodeling Gene Expression Cellular Signaling

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