Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Qiu-bo Li"'
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Rett syndrome (RTT) is a rare neurodevelopmental disorder characterized by severe cognitive, social, and physical impairments resulting from de novo mutations in the X-chromosomal methyl-CpG binding protein gene 2 (MECP2). While there is still no cur
Externí odkaz:
https://doaj.org/article/91e2240779de427997139777911e262f
Autor:
Yuan-Yuan Dong, Min Xia, Lin Wang, Shuai Cui, Qiu-Bo Li, Jun-Chen Zhang, Shu-Shu Meng, Yan-Ke Zhang, Qing-Xia Kong
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Temporal lobe epilepsy (TLE) is a severe chronic neurological disease caused by abnormal discharge of neurons in the brain and seriously affect the long-term life quality of patients. Currently, new insights into the pathogenesis of TLE are urgently
Externí odkaz:
https://doaj.org/article/30b2aae7289c45638ed5f226c8381972
Autor:
Yi-Dan Liu, Meng-Yu Ma, Xi-Bin Hu, Huan Yan, Yan-Ke Zhang, Hao-Xiang Yang, Jing-Hui Feng, Lin Wang, Hao Zhang, Bin Zhang, Qiu-Bo Li, Jun-Chen Zhang, Qing-Xia Kong
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Tuberous sclerosis complex (TSC) is a genetic disease characterized by seizures, mental deficiency, and abnormalities of the skin, brain, kidney, heart, and lungs. TSC is inherited in an autosomal dominant manner and is caused by variations in either
Externí odkaz:
https://doaj.org/article/ca781d439f5242a0a8c7f681dcd1fa24
Autor:
Can Liu, Rui-Hua Liu, Guang-Fei Sun, Lin Yang, Qin-Liang Zheng, Shan-Ying Wei, Qing-Xia Kong, Qiu-Bo Li
Publikováno v:
Biomedical Reports. 16
Autor:
Meng-Yu Ma, Qing-Xia Kong, Ying Sun, Hong-Juan Lin, Xi-Bin Hu, Yi-Dan Liu, Chunyan Li, Qiu-Bo Li, Guangfei Sun, Bang-Zhe Feng
Publikováno v:
International Journal of Neuroscience. 130:1156-1160
Purpose: Sjogren-Larsson syndrome is a rare, autosomal, recessive neurocutaneous disorder caused by mutations in the ALDH3A2 gene, which encodes the fatty aldehyde dehydrogenase enzyme. Deficiency ...
Publikováno v:
Frontiers in neurology. 13
Rett syndrome (RTT) is a rare neurodevelopmental disorder characterized by severe cognitive, social, and physical impairments resulting from
Autor:
Jun-Chen Zhang, Min Xia, Yan-Ke Zhang, Shu-Shu Meng, Shuai Cui, Qiu-Bo Li, Lin Wang, Qing-Xia Kong, Yuan-Yuan Dong
Publikováno v:
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Temporal lobe epilepsy (TLE) is a severe chronic neurological disease caused by abnormal discharge of neurons in the brain and seriously affect the long-term life quality of patients. Currently, new insights into the pathogenesis of TLE are urgently
Autor:
Yi-Dan, Liu, Hong-Juan, Lin, Chun-Yan, Li, Guang-Fei, Sun, Xi-Bin, Hu, Meng-Yu, Ma, Ying, Sun, Bang-Zhe, Feng, Qiu-Bo, Li, Qing-Xia, Kong
Publikováno v:
The International journal of neuroscience. 130(11)
Publikováno v:
International Journal of Neuroscience. 128:881-885
Baraitser-Winter cerebrofrontofacial syndrome (BWCFF) is a rare autosomal dominant genetic disorder involving multiple organ systems and primarily characterized by structural brain abnormalities and a distinctive facial appearance.To study the clinic
Autor:
Qiu-bo Li, Ya Guo, Yuan-yuan Wang, Peipei Liu, Hongfang He, Fei Li, Yedan Liu, Chengqing Yang, Shihai Liu, Zongbo Chen, Yuxia Tan
Publikováno v:
Archives of Virology. 162:1717-1723
Enterovirus 71 (EV71) infection has become one of the major threats to children globally in recent years. Toll-like receptor 3 (TLR3) plays an essential role in host defense against EV71 infection. This study was designed to assess the possible assoc