Zobrazeno 1 - 8
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pro vyhledávání: '"Meng-Syuan Lin"'
Autor:
Meng-Syuan Lin, 林孟璇
107
Huntington’s disease (HD) is an autosomal neurodegenerative disease caused by the expansion of CAG repeat in the huntingtin (HTT) gene. Photoreceptors and intrinsically photosensitive retinal ganglion cells (ipRGCs), which express the phot
Huntington’s disease (HD) is an autosomal neurodegenerative disease caused by the expansion of CAG repeat in the huntingtin (HTT) gene. Photoreceptors and intrinsically photosensitive retinal ganglion cells (ipRGCs), which express the phot
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/587ur6
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 39(8)
Intrinsically photosensitive retinal ganglion cells (ipRGCs), which express the photopigment melanopsin, are photosensitive neurons in the retina and are essential for non-image-forming functions, circadian photoentrainment, and pupillary light refle
Autor:
Chen Chang, Ching-Pang Chang, Yu-Shuo Wu, Meng-Syuan Lin, Chun-Kuei Su, Huei-Mei Chen, Yijuang Chern, Hsing-Lin Lai, Chen-Li Chien
Publikováno v:
Experimental Neurology. 248:10-15
Visceral functions are regulated by a basal sympathetic nerve discharge (SND), also known as ‘sympathetic tone’. We demonstrate herein that AC6 existed in tyrosine hydroxylase-positive rostral ventrolateral medulla neurons in the brainstem. Adeny
Autor:
Hsing Lin Lai, Chen Chang, Wen Hsien Hou, Pei-Lin Cheng, Chen Li Chien, Yijuang Chern, Cheng Chang Lien, Ching Pang Chang, Cheng Ta Lee, Meng Syuan Lin
Publikováno v:
Scientific Reports
The calcium-sensitive type VI adenylyl cyclase (AC6) is a membrane-bound adenylyl cyclase (AC) that converts ATP to cAMP under stimulation. It is a calcium-inhibited AC and integrates negative inputs from Ca2+ and multiple other signals to regulate t
Publikováno v:
Journal of Neuroscience; 2/20/2019, Vol. 39 Issue 8, p1505-1524, 20p
Autor:
Chiung-Mei Chen, Hui-Mei Chen, Yijuang Chern, Yu-Han Kao, Chun-Jung Lin, Meng-Syuan Lin, Yih-Ru Wu, Hsing-Lin Lai
Publikováno v:
Human Molecular Genetics. :ddw402
Huntington's disease (HD) is caused by an abnormal CAG expansion in the exon 1 of huntingtin gene. The treatment of HD is an unmet medical need. Given the important role of adenosine in modulating brain activity, in this study, levels of adenosine an
Autor:
Yu-Han Kao, Meng-Syuan Lin, Chiung-Mei Chen, Yih-Ru Wu, Hui-Mei Chen, Hsing-Lin Lai, Yijuang Chern, Chun-Jung Lin
Publikováno v:
Human Molecular Genetics; Feb2017, Vol. 26 Issue 3, p467-478, 12p