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Jingyu Liu
Life Science
University of Chinese Academy of Sciences
Shanghai
Language: Chinese, English
Genetic Diseases
Neurology
Pathogenic Mechanisms
Drug Development
Neuroscience
Genetics
Brain
Disease Prevention
Therapeutics
Research
Areas of Focus
- Pathogenic mechanisms of genetic neurological diseases and corresponding drug development
Work Experience
- 2007-01~2019-12 - Huazhong University of Science and Technology - Professor
- 2005-01~2007-12 - Huazhong University of Science and Technology - Associate Professor
- 2002-01~2005-12 - Wuhan University - Postdoctoral Researcher
Academic Background & Achievements
- 1998-09--2001-06 PhD: Northeast Normal University
- 1989-09--1992-06 Master's: Northeast Normal University
- 1983-09--1987-06 Bachelor's: Central China Normal University
Publications
- Functional characterization of novel NPRL3 mutations identified in three families with focal epilepsy, Jingyu Liu, 2023
- Mechanisms of PiT2-loop7 Missense Mutations Induced Pi Dyshomeostasis, Jingyu Liu, 2023
- The Pathology of Primary Familial Brain Calcification: Implications for Treatment, Jingyu Liu, 2023
- PRMT7 modulates neuronal excitability by interacting with NaV1.9, Jingyu Liu, 2022
- A Novel SPAST Mutation Results in Spastin Accumulation and Defects in Microtubule Dynamics, Jingyu Liu, 2022
- Norbisabolane-type sesquiterpenoid derivatives, benzofuran lignans and a phenolic glycoside from the roots of Glochidion wilsonii Hutch, Jingyu Liu, 2022
- Severe brain calcification and migraine headache caused by SLC20A2 and PDGFRB heterozygous mutations in a five-year-old Chinese girl, Jingyu Liu, 2021
- Germline Mutation of PLCD1 Contributes to Human Multiple Pilomatricomas through Protein Kinase D/Extracellular Signal-Regulated Kinase1/2 Cascade and TRPV6, Jingyu Liu, 2021
- Novel SCN9A missense mutations contribute to congenital insensitivity to pain: Unexpected correlation between electrophysiological characterization and clinical phenotype, Jingyu Liu, 2020
- Alcohol-aggravated episodic pain in humans with SCN11A mutation and ALDH2 polymorphism, Jingyu Liu, 2020
- Spider venom-derived peptide induces hyperalgesia in Na v 1.7 knockout mice by activating Na v 1.9 channels, Jingyu Liu, 2020
- p.His16Arg of STXBP1 (MUNC18-1) Associated With Syntaxin 3B Causes Autosomal Dominant Congenital Nystagmus, Jingyu Liu, 2020
- A Novel CDH1 Mutation Causing Reduced E-Cadherin Dimerization Is Associated with Nonsyndromic Cleft Lip With or Without Cleft Palate, Jingyu Liu, 2019
- A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B, Jingyu Liu, 2018
- PiT2 regulates neuronal outgrowth through interaction with microtubule-associated protein 1B, Jingyu Liu, 2017
- Gain-of-Function Mutations in SCN11A cause familial episodic pain, Jingyu Liu, 2013
- Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis, Jingyu Liu, 2012
