Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Shu-Ping Tsai"'
Autor:
Shu-Ping Tsai, 蔡淑萍
97
With the changes of life style, people spend daily lives in buildings, have weak relationships increasingly with society, cities and environment, and don’t take them seriously. On the other hand, with the changes of communicative ways, we g
With the changes of life style, people spend daily lives in buildings, have weak relationships increasingly with society, cities and environment, and don’t take them seriously. On the other hand, with the changes of communicative ways, we g
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/51620848978322402208
Autor:
Gunn-Guang Liou, Sue-Ping Lee, Shu-Yun Tung, Hsiao-Hsuian Shen, Jia-Yang Hong, Shu-Ping Tsai, Sue-Hong Wang, Kuan-Chung Su, Ming-Shiun Tsai
Publikováno v:
Genes
Volume 10
Issue 8
Genes, Vol 10, Iss 8, p 577 (2019)
Volume 10
Issue 8
Genes, Vol 10, Iss 8, p 577 (2019)
O-acetyl-ADP-ribose (AAR) is a metabolic small molecule relevant in epigenetics that is generated by NAD-dependent histone deacetylases, such as Sir2. The formation of silent heterochromatin in yeast requires histone deacetylation by Sir2, structural
Autor:
Shu-Ping Tsai, Sue-Ping Lee, Jia-Yang Hong, Feng-Jung Chen, Hsieh-Chin Tsai, Hsiao-Hsuian Shen, Bang-Hung Liu, Yu-Yi Wu, Shu-Yun Tung, Sheng-Pin Hsiao, Sue-Hong Wang, Gunn-Guang Liou, Kuan-Chung Su, Ming-Shiun Tsai
Publikováno v:
Archives of biochemistry and biophysics. 671
In Saccharomyces cerevisiae, Sir proteins mediate heterochromatin epigenetic gene silencing. The assembly of silent heterochromatin requires histone deacetylation by Sir2, conformational change of SIR complexes, and followed by spreading of SIR compl
Autor:
Feng-Jung Chen, Chun-Chieh Lai, Ling-Mei Wang, Gunn-Guang Liou, Sue-Ping Lee, Kuan-Wei Lee, Hsiao-Hsuian Shen, Bang-Hung Liu, Shu-Ping Tsai
Publikováno v:
Biochemical and Biophysical Research Communications. 439:351-356
Receptor tyrosine kinases (RTKs) regulate many cellular processes, and Sprouty2 (Spry2) is known as an important regulator of RTK signaling pathways. Therefore, it is worth investigating the properties of Spry2 in more detail. In this study, we found
Autor:
Hung Li, Chun Yu Lin, Yuan Yow Chiou, Hua Hui Ho, Yi Lin Chien, Ellian Wang, Fang Ju Tsai, Shu Ping Tsai, Si Tse Jiang
Publikováno v:
Human Molecular Genetics. 18:1566-1577
Nephrocystin mutations account for the vast majority of juvenile nephronophthisis, the most common inherited cause of renal failure in children. Nephrocystin has been localized to the ciliary transition zone of epithelial cells or its analogous struc
Publikováno v:
Biochemical Journal. 343:87-93
Cytosolic glutathione S-transferases (GSTs) were isolated from 1-day-old Leghorn chick livers by glutathione (GSH)-affinity chromatography. After sample loading and extensive washing with 0.2 M NaCl, the column was sequentially eluted with 5 mM GSH a
Publikováno v:
Biochemical Journal. 333:735-739
Glutathione S-transferase rGSTM5* was isolated from rat testis with a combination of glutathione affinity column and reverse-phase column chromatography. The protein was digested with Achromobacter protease I or endoproteinase Arg-C. The peptide frag
Publikováno v:
Biochemical Journal. 323:503-510
Cytosolic glutathione S-transferases (GSTs) from rat ovaries and testis were purified by a combination of GSH and S-hexylglutathione affinity chromatography. The isolated GSTs were subjected to reverse-phase HPLC, electrospray MS and N-terminal pepti
Publikováno v:
Biochemical Journal. 314:1017-1025
Cytosolic glutathione S-transferases (GSTs) from rat kidneys were purified by a combination of glutathione and S-hexylglutathione affinity columns. The isolated GSTs were subjected to reverse-phase HPLC and electrospray MS analysis. The major GST iso
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1292:289-292
An unidentified 30 kDa protein was co-purified with chick liver glutathione S-transferases from S-hexylglutathione affinity column. The protein was isolated to apparent homogeneity with chromatofocusing. The molecular mass of the protein was determin