Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kuei-Ming Lin"'
Autor:
Fan-Ya Chou, Te-Fa Chiu, Fen-Wei Huang, Tai-Yi Hsu, Chien-Yu Liu, Chin-Han Lin, Po-Yao Huang, Kuei-Ming Lin, Shih-Hao Wu
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
IntroductionSleep disturbance and insufficient sleep have been linked to metabolic syndrome, increasing cardiovascular disease and mortality risk. However, few studies investigate the joint effect of sleep and exercise on metabolic syndrome. We hypot
Externí odkaz:
https://doaj.org/article/bd273c20f1354ceca3b8c1a8f57875d8
Autor:
Kuei-Ming Lin1, Chen-En Wang2, Hong-Ji Liao3, Wei-Laing Chen4, Sheng-Ta Tsai2,5,6, Shih-Hao Wu1, Jia-Lun Huang1,7, Chia-Wei Lin1,7 d16690@mail.cmuh.org.tw
Publikováno v:
Neurology Asia. 2024, Vol. 29 Issue 1, p19-25. 7p.
Autor:
Kuei-Ming Lin, 藺奎銘
104
Transmissible Spongiform Encephalopathies (TSE), also known as prion diseases, are fatal and infectious neurodegenerative diseases. The conformational change of prion protein from α to β is considered to be the main cause of the disease. H
Transmissible Spongiform Encephalopathies (TSE), also known as prion diseases, are fatal and infectious neurodegenerative diseases. The conformational change of prion protein from α to β is considered to be the main cause of the disease. H
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/88738313444372462036
Autor:
Orion Shih, Chih-Hsuan Lee, U-Ser Jeng, Eric H.-L. Chen, Kuei-Ming Lin, Meng-Ru Ho, Yi-Qi Yeh, Rita P.-Y. Chen, Chun-Jen Su, Jason C. Sang
Publikováno v:
IUBMB Life. 74:780-793
Prion protein is composed of a structure-unsolved N-terminal domain and a globular C-terminal domain. Under limited trypsin digestion, mouse recombinant prion protein can be cleaved into two parts at residue Lys105. Here, we termed these two fragment