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Cerebellum (London, England)|July 15, 2021
Identification of the Largest SCA36 Pedigree in Asia: with Multimodel Neuroimaging Evaluation for the First TimeYue Xie, Zhao Chen, Zhe Long, et al.Biomaterials|September 5, 2024
A dendritic cell-recruiting, antimicrobial blood clot hydrogel for melanoma recurrence prevention and infected wound managementWen-Shang Liu, Zheng-Mao Lu, Xiao-Hui Pu, et al.Drug Resistance Updates : Reviews and Commentaries in Antimicrobial and Anticancer Chemotherapy|May 21, 2025
CSDE1 enhances genotoxic drug resistance in cancer by modulating RPA2 through CSDE1-eIF3a regulatory complexJia-Jia Cui, Cheng-Xian Guo, Jun Li, et al.Brain : a Journal of Neurology|November 26, 2010
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencingJun Ling Wang, Xu Yang, Kun Xia, et al.Bulletin of the World Health Organization|August 1, 2006
Trend and disease burden of bacillary dysentery in China (1991-2000)Xuan-yi Wang, Fangbiao Tao, Donglou Xiao, et al.The Journal of Clinical Investigation|May 2, 2022
Loss of the collagen IV modifier prolyl 3-hydroxylase 2 causes thin basement membrane nephropathyHande Aypek, Christoph Krisp, Shun Lu, et al.Journal of Medical Genetics|September 9, 2018
Long-read sequencing identified intronic repeat expansions in SAMD12 from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsySheng Zeng, Mei-Yun Zhang, Xue-Jing Wang, et al.Brain : a Journal of Neurology|November 29, 2011
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesiasJun-Ling Wang, Li Cao, Xun-Hua Li, et al.Brain : a Journal of Neurology|December 11, 2019
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremorQi-Ying Sun, Qian Xu, Yun Tian, et al.Human Molecular Genetics|January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.Pageof 21