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Neuroscience Letters|October 18, 2002
Mutation screen of the GABA(A) receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsyJianjun Lu, Yucai Chen, Yuehua Zhang, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|February 7, 2018
Dopa-Responsive Dystonia in Han Chinese Patients: One Novel Heterozygous Mutation in GTP Cyclohydrolase 1 (GCH1) and Three Known Mutations in THKunfang Yang, Rongrong Yin, Xiaoping Lan, et al.
Plos One|June 15, 2016
Mitochondrial DNA Rearrangement Spectrum in Brain Tissue of Alzheimer's Disease: Analysis of 13 CasesYucai Chen, Changsheng Liu, William Davis Parker, et al.
Environmental Science & Technology|July 4, 2024
Enhanced Intrusion of Exogenous Airborne Fine Particles toward Eyes in Humans and Animals: Where Damaged Blood-Ocular Barrier Plays a Crucial RoleYu Qi, Xiaoxue Liu, Yucai Chen, et al.
Cell Death and Differentiation|August 11, 2023
FBXL4 mutations cause excessive mitophagy via BNIP3/BNIP3L accumulation leading to mitochondrial DNA depletion syndromeYingji Chen, Dongyue Jiao, Yang Liu, et al.
Neuroscience Letters|April 5, 2003
T-type calcium channel gene alpha (1G) is not associated with childhood absence epilepsy in the Chinese Han populationYucai Chen, Jianjun Lu, Yuehua Zhang, et al.
Internal Medicine (Tokyo, Japan)|June 21, 2021
Novel Mutations of the ALMS1 Gene in Patients with Alström SyndromeChunmei Wang, Xiaona Luo, Yilin Wang, et al.
Child and Adolescent Psychiatry and Mental Health|July 18, 2024
Randomized, double-blind, placebo-controlled trial of aripiprazole oral solution in children and adolescents with Tourette's disorderFan He, Jie Luo, Yi Huang, et al.
Frontiers in Cell and Developmental Biology|April 7, 2022
Clinical Study of 8 Cases of <i>CHD2</i> Gene Mutation-Related Neurological Diseases and Their MechanismsXiaona Luo, Xiaoang Sun, Yilin Wang, et al.
Stem Cell Research|May 17, 2020
Generation of an induced pluripotent stem cell line SHCDNi001-A from a one-year-old Chinese girl with mitochondrial DNA depletion syndrome 13Fang Yuan, Chunmei Wang, Jiaming Xi, et al.
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