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Jiada Li
lijiada@csu.edu.cn
Chinese, English
Hunan
Central South University
Life Sciences
  • 1989-1993 Bachelor of Science in Biochemistry, Lanzhou University
  • 1996-2001 Doctor of Science in Biochemistry and Cell Biology, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences
  • 1993-1996 Assistant, Biochemistry Teaching and Research Department, Hengyang Medical College, Nanhua University
  • 2001-2009 Postdoctoral Researcher, University of California, Irvine, USA
  • 2009-present Professor, School of Life Sciences, Central South University
  • 2010 Furong Scholar Distinguished Professor, Hunan Province
  • 2011 New Century Excellent Talents in University, Ministry of Education
  • 2016 Outstanding Scientific and Technological Worker of Hunan Province
  • 2016 First Prize of Natural Science, Hunan Province (Ranked fourth)
  • 2021 Outstanding Graduate Supervisor, Hunan Province
Genetic regulation mechanisms of neurodevelopmental disorders
  • Cry1Δ11 mutation induces ADHD-like symptoms through hyperactive dopamine D1 receptor signaling, Liu D, Xie Z, Gu P, Li X, Zhang Y, Wang X, Chen Z, Deng S, Shu Y, Li JD*, 2023
  • CNTNAP2 intracellular domain (CICD) generated by γ-secretase cleavage improves autism-related behaviors, Zhang J, Cai F, Lu R, Xing X, Xu L, Wu K, Gong Z, Zhang Q, Zhang Y, Xing M, Song W*, Li JD*, 2023
  • RNF216 regulates meiosis and PKA stability in the testes, Li D, Li F, Meng L, Wei H, Zhang Q, Jiang F, Chen DN, Li W*, Tan YQ*, Li JD*, 2021
  • Necdin regulates BMAL1 stability and circadian clock through SGT1-HSP90 chaperone machinery, Lu R, Dong Y, Li JD*, 2020
  • Prevalence and associated phenotypes of DUSP6, IL17RD and SPRY4 variants in a large Chinese cohort with isolated hypogonadotropic hypogonadism, Men M, Wang X, Wu J, Zeng W, Jiang F, Zheng R*, Li JD*, 2020
  • Phenotypic spectrum of idiopathic hypogonadotropic hypogonadism patients with CHD7 variants from a large Chinese cohort, Li JD, Wu J, Zhao Y, Wang X, Jiang F, Hou Q, Chen DN, Zheng R, Yu R, Zhou W, Men M*, 2019
  • PROKR2 mutations in idiopathic hypogonadotropic hypogonadism: selective disruption of the binding to a Gα-protein leads to biased signaling, Zhao Y, Wu J, Jia H, Wang X, Zheng R, Jiang F, Chen DN, Chen Z*, Li JD*, 2019
  • CirGRDB: a database for the genome-wide deciphering circadian genes and regulators, Li X, Shi L, Zhang K, Wei W, Liu Q, Mao F, Li J, Cai W, Chen H, Teng H*, Li J*, Sun Z*, 2018
  • Functional Rescue of Kallmann Syndrome-associated Prokineticin Receptor 2 (PKR2) Mutants Deficient in Trafficking, Chen DN, Ma YT, Liu H, Zhou QY, Li JD*, 2014
  • Disease-causing Mutation in PKR2 Receptor Reveals a Critical Role of Positive Charges in the Second Intracellular Loop for G-protein Coupling and Receptor Trafficking, Peng Z, Tang Y, Luo H, Jiang F, Yang J, Sun L, Li JD*, 2011
  • Disruption of the circadian output molecule prokineticin 2 results in anxiolytic and antidepressant-like effects in mice, Li JD, Hu WP, Zhou QY*, 2009
  • Attenuated Circadian Rhythms in Mice Lacking the Prokineticin 2 Gene, Li JD, Hu WP, Boehmer L, Cheng MY, Lee AG, Jilek A, Siegel JM, Zhou QY*, 2006
  • Dependence of olfactory bulb neurogenesis on prokineticin 2 signaling, Ng KL, Li JD, Cheng MY, Leslie FM, Lee AG, Zhou QY*, 2005
Genetics Biochemistry Molecular Biology Electrophysiology Behavioral Science Autism Adhd Gnrh Deficiency Molecular Pathology Therapeutic Targets

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