Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Xia-Nan Guo"'
Autor:
Ning Yang, Long‐kai Li, Hui He, Xia‐nan Guo, Xue‐feng Yuan, Zhi‐tong Li, Wei‐dong Wang, Biao‐jie Qin, Xiang‐ning Du, Xu Zhang, Shu‐ni Chen, Hong‐li Lin
Publikováno v:
Immunity, Inflammation and Disease, Vol 10, Iss 9, Pp n/a-n/a (2022)
Abstract Background α‐1,6 Fucosyltransferase (FUT8) appears to play an essential role in the pathogenesis of renal fibrosis. However, it remained unknown whether FUT8 also contributed to renal fibrosis in immunoglobulin A nephropathy (IgAN). In th
Externí odkaz:
https://doaj.org/article/3882a85ddc704a289c5223184957c340
Autor:
Xiao-Li Liu, Xiao-Rong Liu, Yang-Qi Xu, Hui-Dong Tang, Xiao-Jun Huang, Xiao-Meng Yin, Xia-Nan Guo, Qing Liu, Sheng Zeng, Mei Zhang, Wo-Tu Tian, Sheng-Di Chen, Li Cao, Xiao Mao, Jun-Yi Shen, Beisha Tang, Wei-Guo Tang
Publikováno v:
Movement Disorders. 33:459-467
Background Paroxysmal kinesigenic dyskinesia is the most common type of paroxysmal dyskinesia. Approximately half of the cases of paroxysmal kinesigenic dyskinesia worldwide are attributable to proline-rich transmembrane protein 2 mutations. Objectiv
Autor:
Tian-Yi Rong, Sheng-Di Chen, Xia-Nan Guo, Zhenguo Liu, Li Wu, Qing Liu, Hua Li, Hai-Yan Zhou, Ruxu Zhang, Lan Zheng, Wang Yan, Yan-Yan Song, Chunyu Wang, Ze-Yu Zhu, Xun-Hua Li, Xiaoli Liu, Xiao-Rong Liu, Yu Zhang, Shi-Ge Wang, Li Cao, Xiao-Meng Yin, Guang-Hui Bi, Ping Zhong, Wei-Guo Tang, Mei Zhang, Lu Wei, Tian Wang, Xiao-Jun Huang, Tao Chen, Hui-Dong Tang, Kai-Li Yin, Xiao-Guang Luo, Hai-Yan Li, Wo-Tu Tian, Beisha Tang, Fei-Xia Zhan, Xing-Hua Luan, Guohua Zhao, Chao Zhang, Jianguang Tang
Publikováno v:
Movement disorders : official journal of the Movement Disorder SocietyReferences. 35(8)
BACKGROUND Paroxysmal kinesigenic dyskinesia is a spectrum of involuntary dyskinetic disorders with high clinical and genetic heterogeneity. Mutations in proline-rich transmembrane protein 2 have been identified as the major pathogenic factor. OBJECT
Publikováno v:
Annals of Translational Medicine. 8:7-7
Background: The genetic mechanisms of binge eating (BE) as a disease identity remain obscure. BE is usually viewed as a part of the behavioral variant of frontotemporal dementia (bvFTD) features. We encountered a family with hereditary diffuse leukoe
Autor:
Wo-Tu, Tian, Xiao-Jun, Huang, Xiao, Mao, Qing, Liu, Xiao-Li, Liu, Sheng, Zeng, Xia-Nan, Guo, Jun-Yi, Shen, Yang-Qi, Xu, Hui-Dong, Tang, Xiao-Meng, Yin, Mei, Zhang, Wei-Guo, Tang, Xiao-Rong, Liu, Bei-Sha, Tang, Sheng-Di, Chen, Li, Cao
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 33(3)
Paroxysmal kinesigenic dyskinesia is the most common type of paroxysmal dyskinesia. Approximately half of the cases of paroxysmal kinesigenic dyskinesia worldwide are attributable to proline-rich transmembrane protein 2 mutations.The objective of thi
Autor:
Xiang Qin Zhou, Zhan Qi, Xia Nan Guo, Nuo Si, Mingrong Zhang, Liying Cui, Yan Huang, Qing Liu, Lian Qing Wang
Publikováno v:
Journal of Child Neurology. 30:610-614
Tuberous sclerosis complex is an autosomal dominant disorder characterized by hamartomas in multiple organ systems. Mutations in the 2 large genes TSC1 and TSC2 have been demonstrated to be associated with tuberous sclerosis complex by various mutati
Autor:
Xiaoguang Li, Fang Liu, Bo Cui, Rong Rong Wang, Liying Cui, Qing Liu, Xia Nan Guo, Mingsheng Liu, Chao Xia Lu, Xue Zhang
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry. 87(11)
Amyotrophic lateral sclerosis (ALS) is a fatal neurological disorder characterised by motor neuron degeneration in the primary motor cortex, brainstem and spinal cord. In two studies, >20 genes were associated with ALS and a number of patients carrie
Autor:
Mingsheng Liu, Bin Peng, Qing Liu, Rong Rong Wang, Xue Zhang, Fang Liu, Bo Cui, Xiaoguang Li, Shi Shu, Chao Xia Lu, Xia Nan Guo, Liying Cui
Publikováno v:
Neurology. 87(17)
Objective: To identify the disease-causing gene of a family with upper limb predominant, slowly progressive amyotrophic lateral sclerosis (ALS), which was diagnosed as flail arm syndrome (FAS). Methods: After causation of 24 known ALS genes was exclu
Autor:
Xue Zhang, Mingsheng Liu, Bo Cui, Rong Rong Wang, Xiaoguang Li, Fang Liu, Chao Xia Lu, Liying Cui, Xia Nan Guo, Qing Liu
Publikováno v:
Neurobiology of Aging. 47:219.e1-219.e5
Abnormal expansion of a hexanucleotide GGGGCC repeat in the C9orf72 gene is the most common cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia in Caucasians. However, the underlying pathologic mechanisms remain controversial, an
Autor:
Qing Liu, Fang Liu, Bo Cui, Chao Xia Lu, Xia Nan Guo, Rong Rong Wang, Ming Sheng Liu, Xiao Guang Li, Li-ying Cui, Xue Zhang, Liu, Qing, Liu, Fang, Cui, Bo, Lu, Chao Xia, Guo, Xia Nan, Wang, Rong Rong, Liu, Ming Sheng, Li, Xiao Guang, Cui, Li-Ying, Zhang, Xue
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry; Nov2016, Vol. 87 Issue 11, p1272-1274, 3p, 1 Diagram