Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Hua-pin Huang"'
Autor:
Ling⁃xiao CAO, Yue HUANG, Zhi⁃you CAI, Piu CHAN, Sheng⁃di CHEN, Dong⁃sheng FAN, Bo⁃ yan FANG, Yan⁃jun GUO, Ying HAN, Hua⁃pin HUANG, Wen⁃jun JI, Hong⁃yan LI, Kun LIU, Zhong PEI, Dan⁃tao PENG, Fu⁃dong SHI, Yi SUI, Bei⁃sha TANG, Feng WANG, Wen WANG, Zhao⁃ xia WANG, An⁃hua WU, Yun XU, Dong⁃dong YANG, Guo⁃fu ZHANG, Li⁃wei ZHANG, Zhen⁃tao ZHANG, Wei ZHAO, Xing⁃quan ZHAO, Yong⁃jun WANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 20, Iss 10, Pp 914-923 (2020)
Human brain bank is the foundation for neurology and neuroscience, which provides research materials for medical scientists to explore what happen in human brains. Through voluntary postmortem brain tissue donation, brain bank collects, classifies, s
Externí odkaz:
https://doaj.org/article/fc35d37f43e94164aebe3f7aa53e1f61
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:
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
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
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 88:540-549
Background Genetic studies have shown that C9orf72 , SOD1 , TARDBP and FUS are the most common mutated genes in amyotrophic lateral sclerosis (ALS). Here, we performed a meta-analysis to determine the mutation frequencies of these major ALS-related g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::626fbde3c3ba556c31e167785859c182
https://doi.org/10.1136/jnnp-2016-315018
https://doi.org/10.1136/jnnp-2016-315018
Autor:
Zhi‑Ting Chen, Chun Hui Che, Chang Yun Liu, Sheng‑Gen Chen, Jie You, Zhang-Yu Zou, Han‑Bin Lin, Hua Pin Huang, Zhen‑Hua Zhao, Xiao‑Fan Wei, Yuan‑Xiao Li, Xiao‑Min Wu
Endothelial dysfunction, regarded as a key step in the pathophysiological course of diabetic vascular complications, is initiated and deteriorated by advanced glycation end products (AGEs). DL-3-n-butylphthalide (DL-NBP) has been proven to have prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::461d9213b659332ca23a882c94cf9950
https://europepmc.org/articles/PMC5609149/
https://europepmc.org/articles/PMC5609149/
Autor:
Zhen-hua Zhao, Xiaodong Pan, Hua-pin Huang, Zhi-ting Chen, Qinyong Ye, Bin Sun, Ying Chen, An Zheng
Publikováno v:
Molecular Medicine Reports. 11:1956-1962
The Leigh syndrome (LS), characterized by psychomotor retardation, seizures, nystagmus, ophthalmoparesis, optic atrophy, ataxia, dystonia, or respiratory failure, is one of the most severe mitochondrial diseases. In the majority of cases, the disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd10326e3683f3ec3d20dac35354f6ec
https://doi.org/10.3892/mmr.2014.2911
https://doi.org/10.3892/mmr.2014.2911