Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Chang‐Yun Liu"'
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:
2023 24th International Symposium on Quality Electronic Design (ISQED).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88464ba7f07f1f1fa47aa042d027c7b3
https://doi.org/10.1109/isqed57927.2023.10129288
https://doi.org/10.1109/isqed57927.2023.10129288
Autor:
CHANG-YUN LIU1 13365910778@189.cn, ZHEN-HUA ZHAO2, ZHI-TING CHEN1, CHUN-HUI CHE1, ZHANG-YU ZOU1, XIAO-MIN WU1, SHENG-GEN CHEN1, YUAN-XIAO LI1, HAN-BIN LIN1, XIAO-FAN WEI1, JIE YOU3, HUA-PIN HUANG1
Publikováno v:
Experimental & Therapeutic Medicine. Sep2017, Vol. 14 Issue 3, p2241-2248. 8p.
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:
Xiao-Huan Zou, Dong-Ping Chen, Bing-Cong Hong, Yao-Bin Liu, Lu-Lu Lai, Xin-Xin Guo, Chang-Yun Liu, Ji-Dong Peng, Jing-Hui Lai, Hui-Zhen Su, Qing-Yang Yao, Hua-Song Lin, Yu-Ying Zhao, Xiao-Pei Lu, Hong-Xia Fu, Yao Xiangping, Dan-Qin Huang, Wan-Jin Chen, Pan Lin, Chong Wang, Yu-Chun Deng, Xiao-Qun Zhu, Hai-Liang Lin, Yan-Fang Niu, Xue-Jiao Chen, Yong-Kun Li, Ning Wang, Hai-Ting Chen, Gen-Bin Huang
Publikováno v:
Human Mutation. 40:392-403
Primary familial brain calcification (PFBC) is a rare neurodegenerative disorder with four causative genes (SLC20A2, PDGFRB, PDGFB, and XPR1) that have been identified. Here, we aim to describe the mutational spectrum of four causative genes in a ser
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fccdfb0beac5e5a9cbbc297b7be489ad
https://doi.org/10.1002/humu.23703
https://doi.org/10.1002/humu.23703
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
Autor:
Yu-Xian Duan, Chang-Yun Liu
Publikováno v:
2021 4th International Conference on Advanced Electronic Materials, Computers and Software Engineering (AEMCSE).
Harris Hawk algorithm has received a lot of attention due to its few control parameters, simplicity and practicality. However, there are still some shortcomings, such as the problem of slow convergence, and hard to maintain the balance between explor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10628730a6255c5e553133adb071b705
https://doi.org/10.1109/aemcse51986.2021.00107
https://doi.org/10.1109/aemcse51986.2021.00107