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Frontiers in Aging Neuroscience|December 26, 2022
Association between NOTCH3 gene and Parkinson's disease based on whole-exome sequencingQian Zeng, Hongxu Pan, Yuwen Zhao, et al.Epilepsy Research|February 6, 2008
A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsionsHaiyan Li, Nan Li, Lu Shen, et al.Scientific Reports|July 7, 2016
Genome-wide analysis of DNA methylation during antagonism of DMOG to MnCl2-induced cytotoxicity in the mouse substantia nigraNannan Yang, Yang Wei, Tan Wang, et al.Journal of the Neurological Sciences|July 18, 2016
The rs3756063 polymorphism is associated with SNCA methylation in the Chinese Han populationYang Wei, Nannan Yang, Qian Xu, et al.Biochemical and Biophysical Research Communications|January 3, 2014
The BAG2 protein stabilises PINK1 by decreasing its ubiquitinationXiangqian Che, Beisha Tang, Xuejing Wang, et al.Materials (Basel, Switzerland)|June 27, 2025
Dual-Band Resonant Acoustic Metasurfaces from Nested Negative Effective Parameter UnitLimei Hao, Dongan Liu, Xiaole Yan, et al.Parkinsonism & Related Disorders|March 11, 2022
Evaluation of common and rare variants of Alzheimer's disease-causal genes in Parkinson's diseaseQian Zeng, Hongxu Pan, Yuwen Zhao, et al.Cellular and Molecular Life Sciences : CMLS|April 7, 2025
Loss of NgBR causes neuronal damage through decreasing KAT7-mediated RFX1 acetylation and FGF1 expressionYuwei Hu, Yanni Ma, Lele Liu, et al.Journal of the Peripheral Nervous System : JPNS|September 14, 2013
Two novel MPZ mutations in Chinese CMT patientsLei Liu, Xiaobo Li, Xiaohong Zi, et al.Frontiers in Aging Neuroscience|November 3, 2022
The effect of regional white matter hyperintensities on essential tremor subtypes and severityRuncheng He, Yan Qin, Xun Zhou, et al.Pageof 2,468