Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Shin-Cheng Chang"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract The most common mutation in southern Chinese individuals with late-onset multiple acyl-coenzyme A dehydrogenase deficiency (MADD; a fatty acid metabolism disorder) is c.250G > A (p.Ala84Thr) in the electron transfer flavoprotein dehydrogenas
Externí odkaz:
https://doaj.org/article/58102a6b95644f00bd0f9a7d77eab7a4
Autor:
Shin-Cheng Chang, 張仕正
91
Titanium oxide is a semi-conducting photocatalyst. It can decompose the pollutants by irradiation of UV light. This study attempted to decrease the band-gap of TiO2 in order to improve the optical absorption properties in visible region. Phot
Titanium oxide is a semi-conducting photocatalyst. It can decompose the pollutants by irradiation of UV light. This study attempted to decrease the band-gap of TiO2 in order to improve the optical absorption properties in visible region. Phot
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/45204185664916474868
Autor:
Shin-Cheng Chang, 張欣城
91
Berberine (BE) is an alkaoid which is derived from berberis aristata. It is a antiseptic medicine which has inhibitive effects for the streptococcus, staphylococcus and shigella and is widely used as a stomach and bowel medicine. BE is an ant
Berberine (BE) is an alkaoid which is derived from berberis aristata. It is a antiseptic medicine which has inhibitive effects for the streptococcus, staphylococcus and shigella and is widely used as a stomach and bowel medicine. BE is an ant
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/03854847966742593329
Autor:
Yen-Fong Lin, Bai-Hsiun Chen, Ting-Yuan Liu, Yuh-Jyh Jong, Ichizo Nishino, Shin-Cheng Chang, Wen-Chen Liang
Publikováno v:
Muscle & Nerve. 56:479-485
INTRODUCTION c.250G>A (p.Ala84Thr) in ETFDH is the most common mutation that causes later-onset multiple acyl-coenzyme A dehydrogenase deficiency (MADD) in the southern Chinese population. No functional study has targeted this mutation. METHODS Using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2371b40c9b33a03fe683eb34c43b04ee
https://doi.org/10.1002/mus.25501
https://doi.org/10.1002/mus.25501
Autor:
Wen-Chen, Liang, Yen-Fong, Lin, Ting-Yuan, Liu, Shin-Cheng, Chang, Bai-Hsiun, Chen, Ichizo, Nishino, Yuh-Jyh, Jong
Publikováno v:
Musclenerve. 56(3)
c.250GA (p.Ala84Thr) in ETFDH is the most common mutation that causes later-onset multiple acyl-coenzyme A dehydrogenase deficiency (MADD) in the southern Chinese population. No functional study has targeted this mutation.Using cells expressing ETFDH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e8746ea86153918bc597ac9c1bc23a69
https://pubmed.ncbi.nlm.nih.gov/27935074
https://pubmed.ncbi.nlm.nih.gov/27935074