Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Qijiang Yan"'
Autor:
Yuhuan Xue, Xiaoyan Zhu, Wenyong Yan, Zhihan Zhang, Enhui Cui, Yongji Wu, Cixia Li, Jiarong Pan, Qijiang Yan, Xuejun Chai, Shanting Zhao
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
BackgroundMultiple sclerosis is a chronic demyelinating disease of uncertain etiology. Traditional treatment methods produce more adverse effects. Epidemiological and clinical treatment findings showed that unknown environmental factors contribute to
Externí odkaz:
https://doaj.org/article/cc5f5f44135543baa3d9aaba2b8fb60e
Publikováno v:
Wednesday, April 26.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a80a9ccf9696ff455fa5f1dc7aa79790
https://doi.org/10.1212/wnl.0000000000202604
https://doi.org/10.1212/wnl.0000000000202604
Autor:
Yuhuan, Xue, Xiaoyan, Zhu, Wenyong, Yan, Zhihan, Zhang, Enhui, Cui, Yongji, Wu, Cixia, Li, Jiarong, Pan, Qijiang, Yan, Xuejun, Chai, Shanting, Zhao
Publikováno v:
Frontiers in neuroscience. 16
Multiple sclerosis is a chronic demyelinating disease of uncertain etiology. Traditional treatment methods produce more adverse effects. Epidemiological and clinical treatment findings showed that unknown environmental factors contribute to the etiol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::16515222f074899392df022a66fd3a3e
https://pubmed.ncbi.nlm.nih.gov/35585921
https://pubmed.ncbi.nlm.nih.gov/35585921
Autor:
Hualei Luo, Reem N Hassan, Liwei Sun, Weiying Jiang, Qijiang Yan, Li Liu, Peng Du, Yonghua Wang
Publikováno v:
Hematology. 23:501-509
Prenatal diagnosis (PND) procedure is urgent to be established for timely management and fatal consequence prevention of factor XIII deficiency (FXIIID), and variations data among Chinese are very scanty. We aimed to find a novel mutation among Chine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3cd263403e7dedd0543b506c680a08d
https://doi.org/10.1080/10245332.2017.1422315
https://doi.org/10.1080/10245332.2017.1422315
Publikováno v:
Molecular Medicine Reports
Neural stem cells (NSCs) are important pluripotent stem cells, which have potential applications in cell replacement therapy. Brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) have been demonstrated to exert a marked impact on th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fc649c0cc0b7219351fe2e6f0484ac5
https://doi.org/10.3892/mmr.2014.2393
https://doi.org/10.3892/mmr.2014.2393
Publikováno v:
Neuropharmacology. 49:1053-1066
Fragile X Syndrome is the most common form of inherited mental retardation worldwide. A Fragile X mouse model, fmr1(tm1Cgr), with a disruption in the X-linked Fmr1 gene, has three substantial deficits observed in several strains: (1) sensitivity to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::465143ca90acd0851ff5c7c44d13ba4a
https://doi.org/10.1016/j.neuropharm.2005.06.004
https://doi.org/10.1016/j.neuropharm.2005.06.004
Autor:
Wangfa Zhao, Robert K. S. Wong, Qijiang Yan, Shih-Chieh Chuang, Robert Bauchwitz, Riccardo Bianchi
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 25(35)
Mutations inFMR1, which encodes the fragile X mental retardation protein (FMRP), are the cause of fragile X syndrome (FXS), an X-linked mental retardation disorder. Inactivation of the mouse geneFmr1confers a number of FXS-like phenotypes including a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09a30bf1f246211ce31a0d4b662f6227
https://pubmed.ncbi.nlm.nih.gov/16135762
https://pubmed.ncbi.nlm.nih.gov/16135762
Autor:
Shih-Chieh Chuang, Wangfa Zhao, Bauchwitz, Robert, Qijiang Yan, Bianchi, Riccardo, Wong, Robert K. S.
Publikováno v:
Journal of Neuroscience; 8/31/2005, Vol. 25 Issue 35, p8048-8055, 8p, 1 Diagram, 4 Graphs