Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Chuanman Zhou"'
Autor:
Chuanman Zhou, Qian Zhou, Xiaohui He, Yunxia He, Xiaoqin Wang, Xiaowei Zhu, Yujia Zhang, Long Ma
Publikováno v:
PLoS Genetics, Vol 18, Iss 4, p e1010126 (2022)
Two-pore domain potassium channels (K2P) are a large family of "background" channels that allow outward "leak" of potassium ions. The NALCN/UNC80/UNC79 complex is a non-selective channel that allows inward flow of sodium and other cations. It is uncl
Externí odkaz:
https://doaj.org/article/0a9feefb005c48879839246ff108bc3a
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 10, Iss 1, Pp 199-210 (2020)
Externí odkaz:
https://doaj.org/article/6aad13ece9704790a1604ee438c7ddb8
Autor:
Zhiping Tan, Hui Zeng, Zhaofa Xu, Qi Tian, Xiaoyang Gao, Chuanman Zhou, Yu Zheng, Jian Wang, Guanghui Ling, Bing Wang, Yifeng Yang, Long Ma
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-9 (2018)
Abstract Background Ankylosing spondylitis (AS) is a debilitating autoimmune disease affecting tens of millions of people in the world. The genetics of AS is unclear. Analysis of rare AS pedigrees might facilitate our understanding of AS pathogenesis
Externí odkaz:
https://doaj.org/article/d554e726c88d4e1d99501c947fc5101f
Autor:
Xiaoyang Gao, Jing Xu, Hao Chen, Dingwu Xue, Wenju Pan, Chuanman Zhou, Yongchao C. Ma, Long Ma
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Spinal muscular atrophy (SMA) is a severe motor neuron degenerative disease caused by loss-of-function mutations in the survival motor neuron gene SMN1. It is widely posited that defective gene expression underlies SMA. However, the identities of the
Externí odkaz:
https://doaj.org/article/671c0ee67e3d4e7cb5fde4113f042186
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 10, Iss 1, Pp 199-210 (2020)
NALCN (Na+ leak channel, non-selective) is a conserved, voltage-insensitive cation channel that regulates resting membrane potential and neuronal excitability. UNC79 and UNC80 are key regulators of the channel function. However, the behavioral effect
Differential modulation of C. elegans motor behavior by NALCN and two-pore domain potassium channels
Autor:
Chuanman Zhou, Qian Zhou, Xiaohui He, Yunxia He, Xiaoqin Wang, Xiaowei Zhu, Yujia Zhang, Long Ma
Publikováno v:
PLoS genetics. 18(4)
Two-pore domain potassium channels (K2P) are a large family of “background” channels that allow outward “leak” of potassium ions. The NALCN/UNC80/UNC79 complex is a non-selective channel that allows inward flow of sodium and other cations. It
NALCN (Na+leakchannel,non-selective), UNC80 and UNC79 form a non-selective, voltage-independent cation channel complex that affects a broad array of neuronal activities. The molecular and neuronal mechanisms underlying the functions of the NALCN comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd45b9f28867cfab1558e657a5c70ca6
Publikováno v:
RNA Biology
A key step in pre-mRNA splicing is the recognition of 3’ splicing sites by the U2AF large and small subunits, a process regulated by numeroustrans-acting splicing factors. How thesetrans-acting factors interact with U2AFin vivois unclear. From a sc
Autor:
Jian Wang, Qi Tian, Long Ma, Zhaofa Xu, Chuanman Zhou, Xiaoyang Gao, Guanghui Ling, Yifeng Yang, Hui Zeng, Bing Wang, Yu Zheng, Zhi-Ping Tan
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-9 (2018)
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-9 (2018)
Background Ankylosing spondylitis (AS) is a debilitating autoimmune disease affecting tens of millions of people in the world. The genetics of AS is unclear. Analysis of rare AS pedigrees might facilitate our understanding of AS pathogenesis. Methods
Autor:
Zhiping Tan, Zeng, Hui, Zhaofa Xu, Tian, Qi, Xiaoyang Gao, Chuanman Zhou, Zheng, Yu, Wang, Jian, Guanghui Ling, Wang, Bing, Yifeng Yang, Ma, Long
Table S5. ANKDD1B PCR and sequencing primers. (PPTX 40 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::155fdfc1e634ac2047425486dfcfd800