Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Wen- Jun Bian"'
Autor:
Wang Song, Wen- Jun Bian, Hua Li, Qing- Hui Guo, Jie Wang, Bin Tang, Jia- Yuan Zhang, Wei Wei, Xiao- Rong Liu, Wei- Ping Liao, Bin Li, Na He
Publikováno v:
Journal of Medical Genetics; Sep2024, Vol. 61 Issue 9, p895-903, 9p
Autor:
Xue-Lian Li, Zong-Jun Li, Xiao-Yu Liang, De-Tian Liu, Mi Jiang, Liang-Di Gao, Huan Li, Xue-Qing Tang, Yi-Wu Shi, Bing-Mei Li, Na He, Bin Li, Wen-Jun Bian, Yong-Hong Yi, Chuan-Fang Cheng, Jie Wang
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
PurposePreviously, mutations in the voltage-gated calcium channel subunit alpha1 A (CACNA1A) gene have been reported to be associated with paroxysmal disorders, typically as episodic ataxia type 2. To determine the relationship between CACNA1A and ep
Externí odkaz:
https://doaj.org/article/981aa0573eed479999bed5b81e0a9a97
Autor:
Wen-Jun Bian, Zong-Jun Li, Jie Wang, Sheng Luo, Bing-Mei Li, Liang-Di Gao, Na He, Yong-Hong Yi
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
ObjectiveSHROOM4 gene encodes an actin-binding proteins, which plays an important role in cytoskeletal architecture, synaptogenesis, and maintaining gamma-aminobutyric acid receptors-mediated inhibition. SHROOM4 mutations were reported in patients wi
Externí odkaz:
https://doaj.org/article/98690529f89c4e06af34756e553f88ca
Autor:
Yi-Wu Shi, Jie Wang, Fu-Li Min, Wen-Jun Bian, Bi-Jun Mao, Yong Mao, Bing Qin, Bing-Mei Li, Yang-Mei Ou, Yun-Qi Hou, Xin Zou, Bao-Zhu Guan, Na He, Yong-Jun Chen, Xue-Lian Li, Juan Wang, Wei-Yi Deng, Han-Kui Liu, Nan-Xiang Shen, Xiao-Rong Liu, Yong-Hong Yi, Lie-Min Zhou, Dong Zhou, Patrick Kwan, Wei-Ping Liao
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
To characterize human leukocyte antigen (HLA) loci as risk factors in aromatic antiepileptic drug-induced maculopapular exanthema (AED-MPE). A case-control study was performed to investigate HLA loci involved in AED-MPE in a southern Han Chinese popu
Externí odkaz:
https://doaj.org/article/b2d52788d724455490d24acdd1a03ac9
Autor:
Xiao-Rong Liu, Wen-Jun Bian, Jie Wang, Ting-Ting Ye, Bing-Mei Li, De-Tian Liu, Bin Tang, Wei-Wen Deng, Yi-Wu Shi, Tao Su, Yong-Hong Yi, Wei-Ping Liao
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
IntroductionIdiopathic focal epilepsy (IFE) is a group of self-limited epilepsies. The etiology for the majority of the patients with IFE remains elusive. We thus screened disease-causing variants in the patients with IFE.MethodsWhole-exome sequencin
Externí odkaz:
https://doaj.org/article/da75918c6dff4a3c8196714c29215396
Autor:
Na He, Bing-Mei Li, Zhao-Xia Li, Jie Wang, Xiao-Rong Liu, Heng Meng, Bin Tang, Wen-Jun Bian, Yi-Wu Shi, Wei-Ping Liao
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 10, Iss 1, Pp 1-8 (2018)
Abstract Background Autism spectrum disorder (ASD) in epilepsy has been a topic of increasing interest, which in general occurs in 15–35% of the patients with epilepsy, more frequently in those with intellectual disability (ID). Lennox-Gastaut synd
Externí odkaz:
https://doaj.org/article/0266287b00834141a41a5c633b20bde7
Autor:
Zheng, Chen, Sheng, Luo, Zhi-Gang, Liu, Yan-Chun, Deng, Su-Li, He, Xiao-Rong, Liu, Yong-Hong, Yi, Jie, Wang, Liang-Di, Gao, Bing-Mei, Li, Zhi-Jun, Wu, Zi-Long, Ye, De-Hai, Liang, Wen-Jun, Bian, Wei-Ping, Liao
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 189:247-256
CELSR1 gene, encoding cadherin EGF LAG seven-pass G-type receptor 1, is mainly expressed in neural stem cells during the embryonic period. It plays an important role in neurodevelopment. However, the relationship between CELSR1 and disease of the cen
Publikováno v:
Molecular Neurobiology. 58:2046-2060
The Shaker-related potassium channel Kv1.1 subunit has important implications for controlling neuronal excitabilities. A particular recoding by A-to-I RNA editing at I400 of Kv1.1 mRNA is an underestimated mechanism for fine-tuning the properties of
Autor:
Bin Li, Wen-jun Bian, Peng Zhou, Jie Wang, Cui-xia Fan, Hai-qing Xu, Lu Yu, Na He, Yi-wu Shi, Tao Su, Yong-hong Yi, Wei-Ping Liao
Publikováno v:
SSRN Electronic Journal.
Autor:
Xiang Li, Wen-Jun Bian, Xiao-Rong Liu, Jie Wang, Sheng Luo, Bing-Mei Li, Yong-Hong Yi, Qian-Yi Wu, Qiong-Xiang Zhai, Liang-Di Gao, Hai-Feng Zhang, Na He, Wei-Ping Liao
Publikováno v:
Epilepsy Research. 187:107036
BCOR gene, encoding a corepressor of BCL6, plays an important role in fetal development. BCOR mutations were previously associated with oculofaciocardiodental syndrome (OFCD or MCOPS2, OMIM# 300166). The BCOR protein is ubiquitously expressed in mult