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Research (Washington, D.C.)|May 22, 2023
Discovery of Partial Differential Equations from Highly Noisy and Sparse Data with Physics-Informed Information CriterionHao Xu, Junsheng Zeng, Dongxiao ZhangZhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 8, 2015
[Transglutaminase and neurodegenerative diseases]Zhen Liu, Junsheng Zeng, Sheng Zeng, et al.Dementia and Geriatric Cognitive Disorders|December 6, 2023
Differentially Expressed miR-511-3p in Stroke Patients Predicts the Presence of Post-Stroke Cognitive ImpairmentTe Wang, Wei Zhao, Yan Liu, et al.Neuroscience|May 14, 2025
A novel predictive model constructed based on the combination of SIX3OS1, miR-511-3p and RBP4 for stroke-prost cognitive impairmentTe Wang, Rui Wang, Junsheng Zeng, et al.BMC Neurology|December 25, 2024
lncRNA six3os1 diagnoses acute stroke, predicts disease severity, and predicts post-stroke cognitive impairmentYan Liu, Rui Wang, Junsheng Zeng, et al.General Physiology and Biophysics|November 25, 2024
Silencing lncRNA SIX3OS1 mitigates inflammation and apoptosis in post-stroke cognitive impairment via miR-511-3pJunsheng Zeng, Fen Yang, Hui Xiao, et al.Journal of the Neurological Sciences|October 5, 2015
SCA38 is rare in Mainland ChinaZhen Liu, Sheng Zeng, Junsheng Zeng, et al.Journal of Human Genetics|January 9, 2015
Chinese homozygous Machado-Joseph disease (MJD)/SCA3: a case reportSheng Zeng, Junsheng Zeng, Miao He, et al.Journal of the Neurological Sciences|March 14, 2015
Friedreich's Ataxia (FRDA) is an extremely rare cause of autosomal recessive ataxia in Chinese Han populationJunsheng Zeng, Junling Wang, Sheng Zeng, et al.Biochemical and Biophysical Research Communications|December 2, 2019
PRRT2 frameshift mutation reduces its mRNA stability resulting loss of function in paroxysmal kinesigenic dyskinesiaYongcheng Pan, Qiong Liu, Jennifer Zhang, et al.Pageof 2