Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Chun Hui Che"'
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Mutations in the valosin-containing protein (VCP) gene have been linked to amyotrophic lateral sclerosis (ALS) in the Caucasian populations. However, the phenotype of VCP mutations in Chinese patients with (ALS) remains unclear. Targeted next-generat
Externí odkaz:
https://doaj.org/article/b9443d60e5f84199a1324602f37081fc
Autor:
Ying-Qian Lu, Jian-Min Chen, Han Lin, Shu-Yan Feng, Chun-Hui Che, Chang-Yun Liu, Hua-Pin Huang, Zhang-Yu Zou
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
TANK-binding kinase 1 (TBK1) has been identified as a causative gene of amyotrophic lateral sclerosis (ALS) in the Caucasian population in 2015. Here, we sequenced for TBK1 variants in a cohort of 15 familial ALS (fALS) and 275 sporadic ALS (sALS) of
Externí odkaz:
https://doaj.org/article/84fe27d9a7f048a6aaeeb571bfa6e91d
Autor:
Shu‐Man Feng, Chun‐Hui Che, Shu‐Yan Feng, Chang‐Yun Liu, Liu‐Yi Li, Yuan‐Xiao Li, Hua‐Pin Huang, Zhang‐Yu Zou
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 12, Pp 2377-2383 (2019)
Abstract Objective Mutations in optineurin (OPTN) have been identified in familial and sporadic amyotrophic lateral sclerosis (ALS). We screened a cohort of Chinese patients for mutations in optineurin. We also performed an extensive literatures revi
Externí odkaz:
https://doaj.org/article/6a46c934631e4159b210d9f09ff77220
Publikováno v:
Frontiers in Neuroanatomy, Vol 12 (2018)
Purpose: The aim of this study was to evaluate microstructural changes of major white matter (WM) tracts in patients with vascular cognitive impairment (VCI).Method: Diffusion tensor imaging (DTI) data were obtained from 24 subjects with subcortical
Externí odkaz:
https://doaj.org/article/e234ac9710b042b7bc0c6fda40e8c790
Publikováno v:
Computational intelligence and neuroscience. 2022
Current epidemiological and experimental studies have indicated the overlapping genetic foundation of epilepsy and depression. However, the detailed pleiotropic genetic etiology and neurobiological pathways have not been well understood, and there ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49da265f1e3358b4d99302f6a2a24f52
https://pubmed.ncbi.nlm.nih.gov/35463244
https://pubmed.ncbi.nlm.nih.gov/35463244
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Mutations in the valosin-containing protein (VCP) gene have been linked to amyotrophic lateral sclerosis (ALS) in the Caucasian populations. However, the phenotype of VCP mutations in Chinese patients with (ALS) remains unclear. Targeted next-generat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79dad9348ab8d68f1204a53d0952d153
https://pubmed.ncbi.nlm.nih.gov/35197922
https://pubmed.ncbi.nlm.nih.gov/35197922
Autor:
Chang-Yun Liu, Rui-Ling Zhou, Chun-Hui Che, Shu-Yan Feng, Zhang-Yu Zou, Huapin Huang, Sheng Chen, Wei Zhang
Publikováno v:
Neurobiology of aging. 107
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder that predominately involves the motor neurons in the brain and spinal cord. The TARDBP gene, encoding TAR DNA-binding protein 43 (TDP-43) protein, has been identified as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5d788d24dfc594bc37d414ccb99614d
https://pubmed.ncbi.nlm.nih.gov/34175147
https://pubmed.ncbi.nlm.nih.gov/34175147
Publikováno v:
IEEE Access, Vol 12, Pp 95846-95856 (2024)
Blockchain technology is widely used in the field of e-commerce, but with the increasing variety of blockchains, there is a problem of how to interact with different blockchain assets. To address this issue, a new e-commerce transaction model based o
Externí odkaz:
https://doaj.org/article/753bd2e6692044a09cd05aaa455acde6
Publikováno v:
Amyotrophic lateral sclerosisfrontotemporal degeneration. 22(1-2)
FUS gene is one of the most common mutated genes in amyotrophic lateral sclerosis (ALS). We sequenced for FUS mutations in a cohort of 15 familial ALS and 275 sporadic ALS of Chinese origin. All 15 exons of the FUS gene were sequenced by targeted nex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4005b5551414ade565309363e72cc013
https://pubmed.ncbi.nlm.nih.gov/32720527
https://pubmed.ncbi.nlm.nih.gov/32720527
Publikováno v:
Journal of Clinical Neurology (Seoul, Korea)
Background and Purpose Mutations in the FIG4 gene have been linked to amyotrophic lateral sclerosis (ALS) type 11 in Caucasian populations. The purpose of this study was to identify FIG4 variants in a cohort of 15 familial ALS (FALS) indexes and 275
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5718db20fba1c642aede4de7d9183995
https://doi.org/10.3988/jcn.2022.18.1.41
https://doi.org/10.3988/jcn.2022.18.1.41