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The International Journal of Neuroscience|September 14, 2016
A novel tyrosine hydroxylase variant in a group of Chinese patients with dopa-responsive dystoniaYa-Ping Yan, Bo Zhang, Yan-Fang Mao, et al.
Molecular Genetics & Genomic Medicine|August 15, 2020
Analysis of rare variants of autosomal-dominant genes in a Chinese population with sporadic Parkinson's diseaseRan Zheng, Chong-Yao Jin, Ying Chen, et al.
Neural Regeneration Research|October 18, 2022
Impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in Parkinson's diseaseTing Shen, Jia-Li Pu, Ya-Si Jiang, et al.
International Journal of Molecular Sciences|May 27, 2023
Nuclear DJ-1 Regulates DNA Damage Repair via the Regulation of PARP1 ActivityZhong-Xuan Wang, Yi Liu, Yao-Lin Li, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|December 3, 2005
[Genetic linkage analysis in localizing a gene of autosomal dominant familial dilated cardiomyopathy with conduction defect]Wei Xu, Bao-Rong Zhang, Zheng-Mao Hu, et al.
International Journal of Biological Sciences|January 12, 2026
Parkin Deficiency Impairs ER-Mitochondria Associations and calcium homeostasis via IP3R-Grp75-VDAC1 ComplexNai-Jia Xue, Yi Liu, Zhi-Hao Lin, et al.
CNS Neuroscience & Therapeutics|March 21, 2020
Genetic testing of FUS, HTRA2, and TENM4 genes in Chinese patients with essential tremorYa-Ping Yan, Cong-Ying Xu, Lu-Yan Gu, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences|December 7, 2005
[Clinical, pathological and genetic studies in a Chinese Charcot-Marie-Tooth disease type 2 family]Wei Luo, Ye-Lei Tang, Bei-sha Tang, et al.
Neuroscience Letters|September 30, 2022
Mitochondrial morphology and synaptic structure altered in the retina of parkin-deficient miceZheng-Xiang Hu, Jia-Li Pu, Rong Zheng, et al.
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