Showing results (81-90 of 107) with videos related to
Sort By:
Pageof 11
Scientific Data|February 12, 2025
OHID-1: A New Large Hyperspectral Image Dataset for Multi-ClassificationAshish Mani, Sergey Gorbachev, Jun Yan, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 12, 2022
Diagnostic Value of Salivary Real-Time Quaking-Induced Conversion in Parkinson's Disease and Multiple System AtrophyMingyue Luan, Yunchuang Sun, Jing Chen, et al.Molecular Neurobiology|September 28, 2022
FUS Mutation Causes Disordered Lipid Metabolism in Skeletal Muscle Associated with ALSBinbin Zhou, Yilei Zheng, Xiaobing Li, et al.Frontiers in Pharmacology|March 13, 2023
Effect of Dl-3-n-butylphthalide on mitochondrial Cox7c in models of cerebral ischemia/reperfusion injuryJingjing Jia, Jianwen Deng, Haiqiang Jin, et al.Nature Communications|November 18, 2022
A Myb enhancer-guided analysis of basophil and mast cell differentiationTakayoshi Matsumura, Haruhito Totani, Yoshitaka Gunji, et al.Plos Genetics|September 4, 2015
FUS Interacts with HSP60 to Promote Mitochondrial DamageJianwen Deng, Mengxue Yang, Yanbo Chen, et al.Muscle & Nerve|July 24, 2024
Clinical and pathological characteristics of OPDM4 patients in advanced diseaseHaixia Tang, Ying Xiong, Kaiyan Jiang, et al.Neuromuscular Disorders : NMD|September 16, 2023
Clinical, pathological, and genetic characterization in a large Chinese cohort with female dystrophinopathyChang Liu, Jiajian Ma, Yanyu Lu, et al.Frontiers in Pediatrics|July 11, 2022
First Identification of Rare Exonic and Deep Intronic Splice-Altering Variants in Patients With Beta-SarcoglycanopathyZhiying Xie, Chengyue Sun, Chang Liu, et al.Molecular Genetics & Genomic Medicine|March 31, 2023
Novel variants, muscle imaging, and myopathological changes in Chinese patients with VCP-related multisystem proteinopathyYalan Wan, Qi Wang, Yiming Zheng, et al.Pageof 11