Search Results - "Zhou, Ya Fang"

Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders by Tian, Yun, Wang, Jun-Ling, Huang, Wen, Zeng, Sheng, Jiao, Bin, Liu, Zhen, Chen, Zhao, Li, Yujing, Wang, Ying, Min, Hao-Xuan, Wang, Xue-Jing, You, Yong, Zhang, Ru-Xu, Chen, Xiao-Yu, Yi, Fang, Zhou, Ya-Fang, Long, Hong-Yu, Zhou, Chao-Jun, Hou, Xuan, Wang, Jun-Pu, Xie, Bin, Liang, Fan, Yang, Zhuan-Yi, Sun, Qi-Ying, Allen, Emily G., Shafik, Andrew Mark, Kong, Ha Eun, Guo, Ji-Feng, Yan, Xin-Xiang, Hu, Zheng-Mao, Xia, Kun, Jiang, Hong, Xu, Hong-Wei, Duan, Ran-Hui, Jin, Peng, Tang, Bei-Sha, Shen, Lu

“…Neuronal intranuclear inclusion disease (NIID) is a slowly progressing neurodegenerative disease characterized by eosinophilic intranuclear inclusions in the…”
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The Protective Effects of Osteocyte‐Derived Extracellular Vesicles Against Alzheimer's Disease Diminished with Aging by Jiang, Ya‐Ling, Wang, Zhen‐Xing, Liu, Xi‐Xi, Wan, Mei‐Dan, Liu, Yi‐Wei, Jiao, Bin, Liao, Xin‐Xin, Luo, Zhong‐Wei, Wang, Yi‐Yi, Hong, Chun‐Gu, Tan, Yi‐Juan, Weng, Ling, Zhou, Ya‐Fang, Rao, Shan‐Shan, Cao, Jia, Liu, Zheng‐Zhao, Wan, Teng‐Fei, Zhu, Yuan, Xie, Hui, Shen, Lu

“…Both Alzheimer's disease (AD) and osteoporosis (OP) are common age‐associated degenerative diseases and are strongly correlated with clinical epidemiology…”
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Mutations in GBA, SNCA, and VPS35 are not associated with Alzheimer's disease in a Chinese population: a case-control study by Wen, Ya-Fei, Xiao, Xue-Wen, Zhou, Lu, Jiang, Ya-Ling, Zhu, Yuan, Guo, Li-Na, Wang, Xin, Liu, Hui, Zhou, Ya-Fang, Wang, Jun-Ling, Liao, Xin-Xin, Shen, Lu, Jiao, Bin

“…SNCA, GBA, and VPS35 are three common genes associated with Parkinson's disease. Previous studies have shown that these three genes may be associated with…”
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SUMO-1 modification on K166 of polyQ-expanded ataxin-3 strengthens its stability and increases its cytotoxicity by Zhou, Ya-Fang, Liao, Shu-Sheng, Luo, Ying-Ying, Tang, Jian-Guang, Wang, Jun-Ling, Lei, Li-Fang, Chi, Jing-Wei, Du, Juan, Jiang, Hong, Xia, Kun, Tang, Bei-Sha, Shen, Lu

“…Post-translational modification by SUMO was proposed to modulate the pathogenesis of several neurodegenerative diseases. Spinocerebellar ataxia type…”
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Associations of multiple visual rating scales based on structural magnetic resonance imaging with disease severity and cerebrospinal fluid biomarkers in patients with Alzheimer’s disease by Wan, Mei-dan, Liu, Hui, Liu, Xi-xi, Zhang, Wei-wei, Xiao, Xue-wen, Zhang, Si-zhe, Jiang, Ya-ling, Zhou, Hui, Liao, Xin-xin, Zhou, Ya-fang, Tang, Bei-sha, Wang, Jun-Ling, Guo, Ji-feng, Jiao, Bin, Shen, Lu

“…The relationships between multiple visual rating scales based on structural magnetic resonance imaging (sMRI) with disease severity and cerebrospinal fluid…”
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Effectiveness of Combined Immunoglobulin and Glucocorticoid Treatments in a Patient With Stiff Limb Syndrome: Case Report and Review of the Literature by Huang, Juan, Meng, Huan-yu, Duan, Xian, Li, Wen-wen, Xu, Hong-Wei, Zhou, Ya-fang, Zhou, Lin

“…Stiff limb syndrome (SLS) is a rare autoimmune-related central nervous system disorder, resulting in stiffness and spasms of limbs since onset with rare…”
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Multinodule abnormalities of the tracheobronchus: bronchoscopy findings and clinical diagnosis by An, Jian, Yang, Hua-Ping, Hu, Cheng-Ping, Cao, Li-Ming, Zhou, Ya-Fang, Xiao, Qi-Ming, Pan, Pin-Hua, Luo, Bai-Ling, Meng, Jie, Zheng, Zhi-Yuan, Su, Xiao-Li, Li, Yuan-Yuan

“…Bronchoscopy is an important method for diagnosing respiratory disease. Multiple tracheobronchial nodules are rarely reported and their causes remain unclear…”
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Inclusion interaction of chloramphenicol and heptakis (2,6-di- O-methyl)-β-cyclodextrin: Phase solubility and spectroscopic methods by Shi, Jie-Hua, Zhou, Ya-fang

“…There is interaction between chloramphenicol and DMBCD leading to producing 1:1 complex and increasing solubility of chloramphenicol in water. The results…”
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ABCC2 rs2273697 is associated with valproic acid concentrations in patients with epilepsy on valproic acid monotherapy by Chen, Juan, Su, Qi-Biao, Tao, Yu-Qian, Qin, Jia-Ming, Zhou, Yi, Zhou, Shan, Li, Hong-Liang, Chen, Zhuo-Jia, Zhou, Ya-Fang, Zhou, Lie-Min, Wang, Xue-Ding, Huang, Min

“…Valproic acid (VPA), a widely used antiepileptic drug, is characterized by intensive inter-individual variability in concentration. Both efflux and influx…”
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C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China by Jiao, Bin, Guo, Ji-Feng, Wang, Ya-Qin, Yan, Xin-Xiang, Zhou, Lin, Liu, Xiao-Yan, Zhang, Fu-Feng, Zhou, Ya-Fang, Xia, Kun, Tang, Bei-Sha, Shen, Lu

“…GGGGCC repeat expansions in the C9orf72 gene have been identified as a major contributing factor in patients with amyotrophic lateral sclerosis (ALS) and…”
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TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing by Wang, Jun Ling, Yang, Xu, Xia, Kun, Hu, Zheng Mao, Weng, Ling, Jin, Xin, Jiang, Hong, Zhang, Peng, Shen, Lu, Feng Guo, Ji, li, Nan, Li, Ying Rui, Lei, Li Fang, Zhou, Jie, Du, Juan, Zhou, Ya Fang, Pan, Qian, Wang, Jian, Wang, Jun, Li, Rui Qiang, Tang, Bei Sha

“…Autosomal-dominant spinocerebellar ataxias constitute a large, heterogeneous group of progressive neurodegenerative diseases with multiple types. To date,…”
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Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum by Liao, Shu-sheng, Shen, Lu, Du, Juan, Zhao, Guo-huan, Wang, Xiao-yi, Yang, Yi, Xiao, Zi-quan, Yuan, Yi, Jiang, Hong, Li, Nan, Sun, He-dong, Wang, Jun-ling, Wang, Chun-yu, Zhou, Ya-fang, Mo, Xiao-yun, Xia, Kun, Tang, Bei-sha

“…Abstract Background Hereditary spastic paraplegia with thin corpus callosum (HSP–TCC) is a clinically and genetically heterogeneous neurodegenerative disorder…”
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Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population by Wang, Jun-ling, Wu, Yun-qin, Lei, Li-fang, Shen, Lu, Jiang, Hong, Zhou, Ya-fang, Yi, Ji-ping, Zhou, Jie, Yan, Xin-xiang, Pan, Qian, Xia, Kun, Tang, Bei-sha

“…To assist the establishment of platform and provide the reference standard for mutation detection in spinocerebellar ataxia (SCA) subtypes 1, 2, 3, 6, 7, 8,…”
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Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han by Wang, Jun-Ling, Jiang, Hong, Zhang, Shen, Xu, Qian, Zhou, Ya-Fang, Liao, Shu-Sheng, Shen, Lu, Yan, Xin-Xiang, Zhu, Huai-Xu, Pan, Qian, Xia, Kun, Tang, Bei-Sha

“…A study used fluorescence-PCR, capillary electrophoresis and Southern blot to analyze ATTCT repeat in a series of unassigned spinaocerebellar ataxias (SCA) SCA…”
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The advances in research on phosphorylation of polyglutamine disease by Zhou, Ya-fang, Jiang, Hong, Tang, Jian-guang, Tang, Bei-sha

“…Polyglutamine (polyQ) diseases are a group of hereditary neurodegenerative disorders caused by expansion of a glutamine repeat in responsible gene products. To…”
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Mutations in GBA, SNCA, and VPS35 are not associated with Alzheimer 's disease in a Chinese population: a case-control study by Ya-Fei Wen, Xue-Wen Xiao, Lu Zhou, Ya-Ling Jiang, Yuan Zhu, Li-Na Guo, Xin Wang, Hui Liu, Ya-Fang Zhou, Jun-Ling Wang, Xin-Xin Liao, Lu Shen, Bin Jiao

“…SNCA, GBA, and VPS35 are three common genes associated with Parkinson's disease. Previous studies have shown that these three genes may be associated with…”
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Serum inducible kinase is a positive regulator of cortical dendrite development and is required for BDNF-promoted dendritic arborization by Guo, Shun-Ling, Tan, Guo-He, Li, Shuai, Cheng, Xue-Wen, Zhou, Ya, Jia, Yun-Fang, Xiong, Hui, Tao, Jiong, Xiong, Zhi-Qi

“…Serum inducible kinase （SNK）, also known as polo-like kinase 2 （PLK2）, is a known regulator of mitosis, synapto- genesis and synaptic homeostasis. However, its…”
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Roles of axonal transport affected by K141N mutant HSP22 in the pathogenesis of CMT2L by Zhang, Fu-Feng, Lu, Xiao-Qin, Zhou, Ya-Fang, Shen, Lu, Jiang, Hong, Yan, Xin-Xiang, Tang, Bei-Sha

“…To compare the axonal transport of wild-type (WT) and K141N mutant HSP22 in transfected primary cultured cortical neurons. The plasmid (pCAGGS-HA-wtHSP22 or…”
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Effectiveness of Combined Immunoglobulin and Glucocorticoid Treatments in a Patient With Stiff Limb Syndrome: Case Report and Review of the Literature by Huang, Juan, Meng, Huan-Yu, Duan, Xian, Li, Wen-Wen, Xu, Hong-Wei, Zhou, Ya-Fang, Zhou, Lin

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Study on the single-nucleotide substitution (c.-16C to T) of the PURATROPHIN-1 gene in Chinese patients with spinocerebellar ataxia by Zhou, Yafang, Song, Xingwang, Yi, Jiping, Jiang, Hong, Wang, Junling, Liao, Shusheng, Tang, Beisha

“…To study the single-nucleotide substitution (c.-16C to T) of the PURATROPHIN-1 gene in spinocerebellar ataxia (SCA) patients in China. The single-nucleotide…”
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