Molecular bilayer graphene von Zhao, Xin-Jing, Hou, Hao, Fan, Xue-Ting, Wang, Yu, Liu, Yu-Min, Tang, Chun, Liu, Shun-He, Ding, Peng-Peng, Cheng, Jun, Lin, Dong-Hai, Wang, Cheng, Yang, Ye, Tan, Yuan-Zhi

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Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy von Dong, Hai-Lin, Ma, Yin, Yu, Hao, Wei, Qiao, Li, Jia-Qi, Liu, Gong-Lu, Li, Hong-Fu, Chen, Lei, Chen, Dian-Fu, Bai, Ge, Wu, Zhi-Ying

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Genetic spectrum and clinical features in a cohort of Chinese patients with autosomal recessive cerebellar ataxias von Cheng, Hao-Ling, Shao, Ya-Ru, Dong, Yi, Dong, Hai-Lin, Yang, Lu, Ma, Yin, Shen, Ying, Wu, Zhi-Ying

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A novel frameshift ACTN2 variant causes a rare adult‐onset distal myopathy with multi‐minicores von Chen, Lei, Chen, Dian‐Fu, Dong, Hai‐Lin, Liu, Gong‐Lu, Wu, Zhi‐Ying

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A de novo variant of POLR3B causes demyelinating Charcot-Marie-Tooth disease in a Chinese patient: a case report von Xue, Yan-Yan, Cheng, Hao-Ling, Dong, Hai-Lin, Yin, Hou-Min, Yuan, Yun, Meng, Ling-Chao, Wu, Zhi-Ying, Yu, Hao

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Targeted next-generation sequencing improves diagnosis of hereditary spastic paraplegia in Chinese patients von Lu, Cong, Li, Li-Xi, Dong, Hai-Lin, Wei, Qiao, Liu, Zhi-Jun, Ni, Wang, Gitler, Aaron D., Wu, Zhi-Ying

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Metabolic profiling of cold adaptation of a deep-sea psychrotolerant Microbacterium sediminis to prolonged low temperature under high hydrostatic pressure von Xia, Jin-Mei, Hu, Xiao-Min, Huang, Cai-Hua, Yu, Li-Bo, Xu, Ru-Fang, Tang, Xi-Xiang, Lin, Dong-Hai

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Targeting cancer cachexia: Molecular mechanisms and clinical study von Wang, Yong‐Fei, An, Zi‐Yi, Lin, Dong‐Hai, Jin, Wei‐Lin

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Functional study and pathogenicity classification of PRRT2 missense variants in PRRT2‐related disorders von Zhao, Shao‐Yun, Li, Li‐Xi, Chen, Yu‐Lan, Chen, Yi‐Jun, Liu, Gong‐Lu, Dong, Hai‐Lin, Chen, Dian‐Fu, Li, Hong‐Fu, Wu, Zhi‐Ying

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Identified novel heterozygous HTRA1 pathogenic variants in Chinese patients with HTRA1-associated dominant cerebral small vessel disease von Chen, Mei-Jiao, Zhang, Yi, Luo, Wen-Jiao, Dong, Hai-Lin, Wei, Qiao, Zhang, Juan, Ruan, Qi-Qi, Ni, Wang, Li, Hong-Fu

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Construction of a novel electrochemical biosensor based on a mesoporous silica/oriented graphene oxide planar electrode for detecting hydrogen peroxide von Lu, Kun-Chao, Wang, Ji-Kui, Lin, Dong-Hai, Chen, Xue, Yin, Shi-Yu, Chen, Guo-Song

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A Novel Missense Mutation in Peripheral Myelin Protein-22 Causes Charcot-Marie-Tooth Disease von Li, Li-Xi, Dong, Hai-Lin, Xiao, Bao-Guo, Wu, Zhi-Ying

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Underlying action mechanism of a novel antioxidant peptide derived from Allium tuberosum Rottler protein hydrolysates and its protective effects on hydrogen peroxide induced cell i... von Chen, Taotao, Chen, Zheng, Wang, Huimin, Chen, Xiaodong, Yang, Juanjuan, Han, Aidong, Lin, Dong-Hai, Hong, Jing

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Metabolomic Investigations on Nesterenkonia flava Revealed Significant Differences between Marine and Terrestrial Actinomycetes von Xie, Chun-Lan, Xia, Jin-Mei, Wang, Jun-Song, Lin, Dong-Hai, Yang, Xian-Wen

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Facile Hydrothermal Synthesis of Highly Efficient and Durable Ternary PtPdCu Electrocatalysts for the Methanol Oxidation Reaction von Tian, Gui-Xian, Yang, Yi, Zhang, Rong-Hua, Yan, Luo-Yi, Cheng, Zheng, Lin, Dong-Hai, Zhou, Xin-Wen

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A novel de novo SPTAN1 nonsense variant causes hereditary motor neuropathy in a Chinese family von Dong, Hai-Lin, Chen, Lei, Wu, Zhi-Ying

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Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy von Luo, Wen‐Jiao, Wei, Qiao, Dong, Hai‐Lin, Yan, Yang‐Tian, Chen, Mei‐Jiao, Li, Hong‐Fu

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Structural transformation of the tandem ubiquitin-interacting motifs in ataxin-3 and their cooperative interactions with ubiquitin chains von Song, Ai-Xin, Zhou, Chen-Jie, Peng, Yu, Gao, Xue-Chao, Zhou, Zi-Ren, Fu, Qing-Shan, Hong, Jing, Lin, Dong-Hai, Hu, Hong-Yu

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A Metabonomic Comparison of Urinary Changes in Zucker and GK Rats von Zhao, Liang-Cai, Zhang, Xiao-Dong, Liao, Shi-Xian, Gao, Hong-Chang, Wang, He-Yao, Lin, Dong-Hai

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A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia von Wei, Qiao, Wang, Pei‐Shan, Dong, Hai‐Lin, Luo, Wen‐Jiao, Wu, Zhi‐Ying, Li, Hong‐Fu

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