Results 1-15 of 15 (Search time: 0.003 seconds).
| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link | |
|---|---|---|---|---|---|---|---|
| 1 | 2012 | 1H, 13C and 15N resonance assignments of the pyrin domain from human PYNOD | Su, MY; Chang, CI ; Chang, CF | Biomolecular NMR assignments 7, 141-143 | |||
| 2 | 2004 | A Drosophila pattern recognition receptor contains a peptidoglycan docking groove and unusual L,D-carboxypeptidase activity. | Chang, CI ; Pili-Floury, S; Herve, M; Parquet, C; Chelliah, Y; Lemaitre, B; Mengin-Lecreulx, D; Deisenhofer, J | PLOS Biology 2(9), 1293-1302 | |||
| 3 | 2012 | A Lon-Like Protease with No ATP-Powered Unfolding Activity | Jiahn-Haur Liao; Chiao-I Kuo; Ya-Yi Huang; Yu-Ching Lin; Yen-Chen Lin; Chen-Yui Yang; Wan-Ling Wu; Wei-Hau Chang; Yen-Chywan Liaw ; Li-Hua Lin; Chung-I Chang ; Shih-Hsiung Wu | PloS one 7(7), e40226 | |||
| 4 | 2002 | Another twist in helix C and a missing pocket. | Goldsmith, EJ; Chang, CI | Structure 10(7), 888-889 | |||
| 5 | 2002 | Crystal structures of MAP kinase p38 complexed to the docking sites on its nuclear substrate MEF2A and activator MKK3b. | Chang, CI ; Xu, BE; Akella, R; Cobb, MH; Goldsmith, EJ | Molecular Cell 9(6), 1241-1249 | |||
| 6 | 2007 | Structural basis for conserved complement factor-like function in the antimalarial protein TEP1. | Baxter, RH; Chang, CI ; Chelliah, Y; Blandin, S; Levashina, EA; Deisenhofer, J | Proceedings of the National Academy of Sciences of the United States of America 104, 11615-11620 | |||
| 7 | 2016 | Structural Basis for the Magnesium-Dependent Activation and Hexamerization of the Lon AAA+ Protease | Su, SC; Lin, CC; Tai, HC; Chang, MY; Ho, MR ; Babu, CS; Liao, JH; Wu, SH ; Chang, YC ; Lim, C ; Chang, CI | Structure 24(5), 676-686 | |||
| 8 | 2004 | Structure of MAPKs | Goldsmith, EJ; Cobb, MH; Chang, CI | Methods in Molecular Biology 250, 127-144 | |||
| 9 | 2005 | Structure of the ectodomain of Drosophila peptidoglycan-recognition protein LCa suggests a molecular mechanism for pattern recognition. | Chang, CI ; Ihara, K; Chelliah, Y; Mengin-Lecreulx, D; Wakatsuki, S; Deisenhofer, J | Proceedings of the National Academy of Sciences of the United States of America 102, 10279-10284 | |||
| 10 | 2006 | Structure of tracheal cytotoxin in complex with a heterodimeric pattern-recognition receptor. | Chang, CI ; Chelliah, Y; Borek, D; Mengin-Lecreulx, D; Deisenhofer, J | Science 311, 1761-1764 | |||
| 11 | 2013 | Structures of an ATP-independent Lon-like protease and its complexes with covalent inhibitors | Liao, JH; Ihara, K; Kuo, CI; Huang, KF ; Wakatsuki, S; Wu, SH ; Chang, CI | Acta Crystallographica Section D Biological Crystallography D69, 1395-1402 | |||
| 12 | 2012 | Synthesis and Biological Evaluation of ortho-Aryl N-Hydroxycinnamides as Potent Histone Deacetylase (HDAC) 8 Isoform-Selective Inhibitors | Huang, WJ; Wang, YC; Chao, SW; Yang, CY; Chen, LC; Lin, MH; Hou, WC; Chen, MY; Lee, TL; Yang, P; Chang, CI | ChemMedChem 7(10), 1815-1824 | |||
| 13 | 2011 | Synthesis and evaluation of aliphatic-chain hydroxamates capped with osthole derivatives as histone deacetylase inhibitors | Huang, WJ; Chen, CC; Chao, SW; Yu, CC; Yang, CY; Guh, JH; Lin, YC; Kuo, CI; Yang, P; Chang, CI | EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 46(9), 4042-4049 | |||
| 14 | 2010 | Synthesis of N-Hydroxycinnamides Capped with a Naturally Occurring Moiety as Inhibitors of Histone Deacetylase. | Huang, WJ; Chen, CC; Chao, SW; Lee, SS; Hsu, FL; Lu, YL; Hung, MF; Chang, CI | ChemMedChem 5(4), 598-607 | |||
| 15 | 2007 | The peptidoglycan recognition proteins LCa and LCx. | Chang, CI ; Deisenhofer, J | Cellular and Molecular Life Sciences 64, 1395-1402 |
