Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Xiang Qian Che"'
Altered immune pathways in patients of temporal lobe epilepsy with and without hippocampal sclerosis
Autor:
Xiang-Qian Che, Shi-Kun Zhan, Jiao-Jiao Song, Yu-Lei Deng, Wei-Liu, Peng-Huang, Jing-Zhang, Zhan-Fang Sun, Zai-Qian Che, Jun Liu
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Over the past decades, the immune responses have been suspected of participating in the mechanisms for epilepsy. To assess the immune related pathway in temporal lobe epilepsy (TLE), we explored the altered immune pathways in TLE patients wi
Externí odkaz:
https://doaj.org/article/c700ce449b284c50b7177294fd5e19ac
Autor:
Qiang Huang, Yong-Fang Zhang, Lin-Jie Li, Eric B. Dammer, Yong-Bo Hu, Xin-Yi Xie, Ran Tang, Jian-Ping Li, Jin-Tao Wang, Xiang-Qian Che, Gang Wang, Ru-Jing Ren
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
Neuronal ceroid lipofuscinosis (NCL) is composed of a group of inherited neurodegenerative diseases, with the hallmark of lipofuscin deposit (a mixture of lipids and proteins with metal materials) inside the lysosomal lumen, which typically emits aut
Externí odkaz:
https://doaj.org/article/2a657fe4c0e64d5ab16f9cd57231b87e
Autor:
Qiang, Huang, Yong-Fang, Zhang, Lin-Jie, Li, Eric B, Dammer, Yong-Bo, Hu, Xin-Yi, Xie, Ran, Tang, Jian-Ping, Li, Jin-Tao, Wang, Xiang-Qian, Che, Gang, Wang, Ru-Jing, Ren
Publikováno v:
Frontiers in aging neuroscience. 14
Neuronal ceroid lipofuscinosis (NCL) is composed of a group of inherited neurodegenerative diseases, with the hallmark of lipofuscin deposit (a mixture of lipids and proteins with metal materials) inside the lysosomal lumen, which typically emits aut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3e6687b42f2569af82c04c7adf430ac2
https://pubmed.ncbi.nlm.nih.gov/35462699
https://pubmed.ncbi.nlm.nih.gov/35462699
Publikováno v:
Frontiers in Bioscience. 23:1144-1165
Frontotemporal dementia (FTD) is the second most common neurodegenerative cause of early-onset dementia. FTD has an important genetic component contributing to its pathogenic mechanisms. Currently, extensive research on neuroimaging biomarkers and ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46997a992ab24aadc708b459f401fd42
https://doi.org/10.2741/4637
https://doi.org/10.2741/4637
Autor:
Ying Gao, Xiang-Qian Che, Xiao-Hong Liu, Gang Wang, Ru-Jing Ren, Qianhua Zhao, Qihao Guo, Xia Li
Background: In addition to the increasing evidence for a molecular mechanism of rho kinase 1 ( ROCK1 ) in Alzheimer’s disease (AD), there are several published studies regarding the relationship between ROCK1 gene polymorphisms and neurological dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaffa48a5a07f454852c4b14d9945433
https://europepmc.org/articles/PMC6281534/
https://europepmc.org/articles/PMC6281534/
Autor:
Mei Zhang, Li Cao, Xiao-Jun Huang, Xiao Mao, Sheng-Di Chen, Jin Li, Yu Zhang, Beisha Tang, Li Wu, Jing-yi Wang, Xiao-Li Liu, Junling Wang, Jun-Yi Shen, Guang-Hui Bi, Tian Wang, Xiang-Qian Che
Publikováno v:
Neurology. 85:1546-1553
Objective: We aimed to investigate the clinical and genetic features of paroxysmal kinesigenic dyskinesia (PKD) in a large population and to analyze the genotype–phenotype correlation of PKD. Methods: We analyzed clinical manifestations and conduct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ae66f8456075bbad639217ba85b3d0f
https://doi.org/10.1212/wnl.0000000000002079
https://doi.org/10.1212/wnl.0000000000002079
Autor:
Gang Wang, Yue Huang, Qianhua Zhao, Qihao Guo, Xiang-Qian Che, Xia Li, Sheng-Di Chen, Ru-Jing Ren
Publikováno v:
Journal of Alzheimer's disease : JAD. 61(4)
As an important multifunctional protein involved in regulation of mitochondrial metabolism, CHCHD2 was identified as a causative gene for Parkinson's disease (PD), yet the relationship between CHCHD2 and neurodegenerative dementia is not well underst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac143e5290c1c9dd06b6cb03da91a44b
https://pubmed.ncbi.nlm.nih.gov/29376860
https://pubmed.ncbi.nlm.nih.gov/29376860
Publikováno v:
Applied Mechanics and Materials. :1016-1020
Circular features are one of the most widely used shapes for camera calibration, due to several advantages: easy to make and recognize, not sensitive to image noise, symmetry, analytic formulation is simple. However, perspective projection is general
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e6cb19520fcb4bbc2a0a4d7b95714b8
https://doi.org/10.4028/www.scientific.net/amm.397-400.1016
https://doi.org/10.4028/www.scientific.net/amm.397-400.1016
Autor:
Sheng-Di Chen, Ru-Jing Ren, Qian-Hua Zhao, Xiang-Qian Che, Yue Huang, Qihao Guo, Xia Li, Gang Wang
Publikováno v:
Current Alzheimer research. 14(10)
Background Mutations in microtubule associated protein tau (MAPT), progranulin (GRN), chromosome 9 open-reading frame 72 (C9orf72) and CHCHD10 genes have been reported causing frontotemporal dementia (FTD) in different populations. However, collectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28ee83d44961aeceab657be4ce32e573
https://pubmed.ncbi.nlm.nih.gov/28462717
https://pubmed.ncbi.nlm.nih.gov/28462717
Autor:
Xinxiang Yan, Hong Jiang, Beisha Tang, Zhanfang Sun, Nan Li, Lu Shen, Xiang-Qian Che, Xiao Mao, Kun Xia
Publikováno v:
The International journal of neuroscience. 127(1)
Proline-rich transmembrane protein 2 gene (PRRT2) mutations are reported to cause common paroxysmal neurological disorders and show a remarkable pleiotropy. Benign epilepsy with centrotemporal spikes (BECTS) is considered to be the most common epilep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ee0de6b945208fbcef3af052b9e3e66
https://pubmed.ncbi.nlm.nih.gov/26954261
https://pubmed.ncbi.nlm.nih.gov/26954261