| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
| 2006 | Aminopeptidase p mediated detoxification of organophosphonate analogues of sarin: mechanistic and stereochemical study at the phosphorus atom of the substrate. | Huang, LF; Su, B; Jao, SC; Liu, KT; Li, WS | Chembiochem : a European journal of chemical biology 7(3), 506-14 | | | |
| 2002 | Characterization of the role of the N-loop of MIP-1 beta in CCR5 binding. | Bondue, A; Jao, SC; Blanpain, C; Parmentier, M; LiWang, PJ | Biochemistry 41(46), 13548-55 | | | |
| 2006 | Computational and mutational analysis of human glutaredoxin (thioltransferase): probing the molecular basis of the low pKa of cysteine 22 and its role in catalysis. | Jao, SC; English Ospina, SM; Berdis, AJ; Starke, DW; Post, CB; Mieyal, JJ | Biochemistry 45(15), 4785-96 | | | |
| 2006 | Design of potent inhibitors for <i>Schistosoma japonica</i> glutathione S-transferase. | Jao, SC; Chen, J; Yang, K; Li, WS | Bioorganic & Medicinal Chemistry 14, 304-318 | | | |
| 2006 | Design of potent inhibitors for Schistosoma japonica glutathione S-transferase. | Jao, SC; Chen, J; Yang, K; Li, WS | Bioorganic & medicinal chemistry 14(2), 304-18 | | | |
| 2007 | Enzymatic and Nonenzymatic Synthesis of Glutathione Conjugates: Application to the Understanding of Parasite's Defense System and Alternative to the Discovery of Potent Glutathione S-Transferase Inhibitors. | Lo, WJ; Chiou, YC; Hsu, YT; Lam, WS; Chang, MY; Jao, SC; Li, WS | Bioconjugate Chemistry 18, 109-120 | | | |
| 2008 | Evaluation of organophosphorus chemicals-degrading enzymes: a comparison of Escherichia coli and human cytosolic aminopeptidase P. | Hsu, YT; Su, CY; Du, HC; Jao, SC; Li, WS | Chemistry & biodiversity 5(7), 1401-11 | | | |
| 2011 | Inhibition of Glutathione S-Transferase M1 by New Gabosine Analogues Is Essential for Overcoming Cisplatin Resistance in Lung Cancer Cells. | Wang, CH; Wu, HT; Cheng, HM; Yen, TJ; Lu, IH; Chang, HC; Jao, SC; Shing, TK; Li, WS | Journal of medicinal chemistry 54(24), 8574-81 | | | |
| 2010 | Overcoming the drug resistance in breast cancer cells by rational design of efficient glutathione S-transferase inhibitors. | Li, WS; Lam, WS; Liu, KC; Wang, CH; Chang, HC; Jen, YC; Hsu, YT; Shivatare, SS; Jao, SC | Organic letters 12(1), 20-3 | | | |
| 2011 | Polyfluorinated bipyridine cisplatins manipulate cytotoxicity through the induction of S-G(2)/M arrest and partial intercalation mechanism. | Chang, TT; More, SV; Lu, N; Jhuo, JW; Chen, YC; Jao, SC; Li, WS | Bioorganic & medicinal chemistry 19(16), 4887-94 | | | |
| 1998 | Reactivity of the human thioltransferase (glutaredoxin) C7S, C25S, C78S, C82S mutant and NMR solution structure of its glutathionyl mixed disulfide intermediate reflect catalytic specificity. | Yang, Y; Jao, SC; Nanduri, S; Starke, DW; Mieyal, JJ; Qin, J | Biochemistry 37(49), 17145-56 | | | |
| 2006 | Selective inactivation of glutaredoxin by sporidesmin and other epidithiopiperazinediones. | Srinivasan, U; Bala, A; Jao, SC; Starke, DW; Jordan, TW; Mieyal, JJ | Biochemistry 45(29), 8978-87 | | | |
| 2006 | Solution structure of the complex between poxvirus-encoded CC chemokine inhibitor vCCI and human MIP-1beta. | Zhang, L; Derider, M; McCornack, MA; Jao, SC; Isern, N; Ness, T; Moyer, R; LiWang, PJ | Proceedings of the National Academy of Sciences of the United States of America 103(38), 13985-90 | | | |
| 1999 | Solution structures of micelle-bound amyloid β-(1-40) and β-(1-42) peptides of Alzheimer's disease. | Shao, H; Jao, SC; Ma, K; Zagorski, MG | J. Mol. Biol. 285, 755-773 | | | |
| 2001 | Structural comparison of monomeric variants of the chemokine MIP-1β having differing ability to bind the receptor CCR5. | Kim, S; Jao, SC; Laurence, JS; LiWang, PJ | Biochemistry 40, 10782-10791 | | | |
| 2006 | Structural elucidation of phosphoglycolipids from strains of the bacterial thermophiles Thermus and Meiothermus. | Yang, YL; Yang, FL; Jao, SC; Chen, MY; Tsay, SS; Zou, W; Wu, SH | Journal of lipid research 47(8), 1823-32 | | | |
| 2010 | Synthesis and structure-activity relationships of novel furazan-3,4-diamide analogs as potent anti-cancer agents. | Li, WS; More, SV; Wang, CH; Jen, YC; Yao, CF; Wang, TF; Hung, CC; Jao, SC | Bioorganic & medicinal chemistry letters 20(3), 1148-52 | | | |
| 2011 | The calcium-chelating capability of tetrahydrofuranic moieties modulates the cytotoxicity of annonaceous acetogenins. | Liaw, CC; Liao, WY; Chen, CS; Jao, SC; Wu, YC; Shen, CN; Wu, SH | Angewandte Chemie-International edition 50(34), 7885-7891 | | | |
| 2011 | The calcium-chelating capability of tetrahydrofuranic moieties modulates the cytotoxicity of annonaceous acetogenins. | Liaw, CC; Liao, WY; Chen, CS; Jao, SC; Wu, YC; Shen, CN; Wu, SH | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 50(34), 7885-7891 | | | |
| 1997 | Trifluoroacetic acid pretreatment reproducibly disaggregates the amyloid β-peptide. | Jao, SC; Ma, K; Talafous, J; Orlando, R; Zagorski, MG | Amyloid-International Journal of Experimental and Clinical Investigation 4, 240-252 | | | |
