Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Jinfan, Zheng"'
Clinical and diagnostic features of anti‐neurofascin‐155 antibody‐positive neuropathy in Han Chinese
Autor:
Wenqing Wang, Chang Liu, Wei Li, Dong Zhang, Yi Shan, Jinfan Zheng, Jingli Shan, Yuying Zhao, Chuanzhu Yan, Qinzhou Wang
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 9, Iss 5, Pp 695-706 (2022)
Abstract Objective To investigate the clinical features of Han Chinese patients with anti‐neurofascin‐155 (NF155) antibody‐positive neuropathy. Methods We screened 194 patients with peripheral neuropathy for NF155 antibodies using a cell‐base
Externí odkaz:
https://doaj.org/article/01df2d992b134a81b561bc4ee9a02673
Publikováno v:
Molecules, Vol 28, Iss 14, p 5526 (2023)
Heteroatom doping, particularly with nonmetallic atoms such as N, P, and S, has proven to be an effective strategy for modulating the fluorescent properties of carbon dots (CDs). However, there are few reports on the regulation of the photoluminescen
Externí odkaz:
https://doaj.org/article/84818b4af86f4304983460864e23f1a3
Publikováno v:
IEEE Access, Vol 6, Pp 57814-57825 (2018)
The success of robotic, such as UGV systems, largely benefits from the fundamental capability of autonomously finding collision-free path(s) to commit mobile tasks in routinely rough and complicated environments. Optimization of navigation under such
Externí odkaz:
https://doaj.org/article/9393e6310a3c43ea91b28528e93b3efc
Autor:
Jingwen Xu, Heng Liu, Yan Yun, Zonglai Liang, Xiao Yu, Jinfan Zheng, Yun Zhang, Juan Zhao, Weihong Song, Xiulian Sun, Fuchen Liu, Qianwen Sun
Publikováno v:
Molecular Psychiatry. 23:1542-1554
Potassium channel Kv2.1 regulates potassium current in cortical neurons and potassium efflux is necessary for cell apoptosis. As a major component of delayed rectifier current potassium channels, Kv2.1 forms clusters in the membrane of hippocampal ne
Publikováno v:
Journal of Muscle Research and Cell Motility. 32:411-419
Studies on comparing the effect of lengthening, isometric and shortening contractions on dystrophin-deficient muscles are unavailable. We hypothesized that different types of contractions lead to different extents to which dystrophin-deficient muscle
Publikováno v:
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 127(6)
Background and objective Mutations in KCNJ18 , which encodes the inwardly rectifying potassium channel Kir2.6, have rarely been reported in hypokalemic periodic paralysis. We describe the clinical phenotype of a novel KCNJ18 gene mutation and perform
Publikováno v:
Neurological Sciences. 34:561-563
Pantothenate kinase-associated neurodegeneration (PKAN) is an autosomal-recessive disorder characterized by neurodegeneration and iron accumulation in the brain. Classic and atypical PKAN are distinguished on the basis of age at onset and disease pro
Autor:
Jingwei Lv, Yue-Bei Luo, Yuying Zhao, Xinbo Ji, Chuanzhu Yan, Wei Li, Jinfan Zheng, Jingwen Xu, Kunqian Ji
Publikováno v:
Free radical biologymedicine. 84
Fibroblast growth factor 21 (FGF21) is a growth factor with pleiotropic effects on regulating lipid and glucose metabolism. Its expression is increased in skeletal muscle of mice and humans with mitochondrial disorders. However, the effects of FGF21
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 31(3)
Mutations of presenilin 1 (PSEN1) gene are the most frequent cause for familial Alzheimers disease (AD). This study was set to explore potential mutation of PSEN1 gene in a Chinese family featuring early-onset Alzheimers disease (FAD).DNA was isolate
Autor:
Pengfei Lin, Yun Yuan, Jingli Shan, Chuanzhu Yan, Bin Chen, Yue-Bei Luo, Duoling Li, Kunqian Ji, Jinfan Zheng
Publikováno v:
Neuromolecular medicine. 16(4)
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant late-onset neuromuscular degenerative disease characterized by ptosis, dysphagia, and proximal muscle weakness. The genetic basis has been identified as an abnormal (GCN) expansion en