| Year |
Citation |
Score |
| 2013 |
Tian S, Li Y, Li D, Xu X, Wang J, Zhang Q, Hou T. Modeling compound-target interaction network of traditional Chinese medicines for type II diabetes mellitus: insight for polypharmacology and drug design. Journal of Chemical Information and Modeling. 53: 1787-803. PMID 23768230 DOI: 10.1021/Ci400146U |
0.409 |
|
| 2013 |
Tian S, Li Y, Wang J, Xu X, Xu L, Wang X, Chen L, Hou T. Drug-likeness analysis of traditional Chinese medicines: 2. Characterization of scaffold architectures for drug-like compounds, non-drug-like compounds, and natural compounds from traditional Chinese medicines. Journal of Cheminformatics. 5: 5. PMID 23336706 DOI: 10.1186/1758-2946-5-5 |
0.416 |
|
| 2012 |
Shen M, Tian S, Li Y, Li Q, Xu X, Wang J, Hou T. Drug-likeness analysis of traditional Chinese medicines: 1. property distributions of drug-like compounds, non-drug-like compounds and natural compounds from traditional Chinese medicines. Journal of Cheminformatics. 4: 31. PMID 23181938 DOI: 10.1186/1758-2946-4-31 |
0.421 |
|
| 2012 |
Tian S, Wang J, Li Y, Xu X, Hou T. Drug-likeness analysis of traditional Chinese medicines: prediction of drug-likeness using machine learning approaches. Molecular Pharmaceutics. 9: 2875-86. PMID 22738405 DOI: 10.1021/Mp300198D |
0.419 |
|
| 2009 |
Wang J, Hou T, Xu X. Aqueous solubility prediction based on weighted atom type counts and solvent accessible surface areas. Journal of Chemical Information and Modeling. 49: 571-81. PMID 19226181 DOI: 10.1021/ci800406y |
0.411 |
|
| 2007 |
Wang J, Krudy G, Hou T, Zhang W, Holland G, Xu X. Development of reliable aqueous solubility models and their application in druglike analysis. Journal of Chemical Information and Modeling. 47: 1395-404. PMID 17569522 DOI: 10.1021/Ci700096R |
0.427 |
|
| 2007 |
Wang J, Xie XQ, Hou T, Xu X. Fast approaches for molecular polarizability calculations. The Journal of Physical Chemistry. A. 111: 4443-8. PMID 17461556 DOI: 10.1021/jp068423w |
0.432 |
|
| 2007 |
Hou T, Wang J, Zhang W, Xu X. ADME evaluation in drug discovery. 6. Can oral bioavailability in humans be effectively predicted by simple molecular property-based rules? Journal of Chemical Information and Modeling. 47: 460-3. PMID 17381169 DOI: 10.1021/ci6003515 |
0.425 |
|
| 2007 |
Hou T, Wang J, Zhang W, Xu X. ADME evaluation in drug discovery. 7. Prediction of oral absorption by correlation and classification. Journal of Chemical Information and Modeling. 47: 208-18. PMID 17238266 DOI: 10.1021/ci600343x |
0.433 |
|
| 2006 |
Hou T, Wang J, Zhang W, Wang W, Xu X. Recent advances in computational prediction of drug absorption and permeability in drug discovery. Current Medicinal Chemistry. 13: 2653-67. PMID 17017917 DOI: 10.2174/092986706778201558 |
0.414 |
|
| 2005 |
Yandeau-Nelson MD, Zhou Q, Yao H, Xu X, Nikolau BJ, Schnable PS. MuDR transposase increases the frequency of meiotic crossovers in the vicinity of a Mu insertion in the maize a1 gene. Genetics. 169: 917-29. PMID 15489518 DOI: 10.1534/Genetics.104.035089 |
0.677 |
|
| 2002 |
Xu X, Dietrich CR, Lessire R, Nikolau BJ, Schnable PS. The Endoplasmic reticulum-associated maize GL8 protein is a component of the acyl-coenzyme A elongase ivolved in the production of cuticular waxes. Plant Physiology. 128: 924-34. PMID 11891248 DOI: 10.1104/Pp.010621 |
0.517 |
|
| 1997 |
Xu X, Dietrich CR, Delledonne M, Xia Y, Wen TJ, Robertson DS, Nikolau BJ, Schnable PS. Sequence analysis of the cloned glossy8 gene of maize suggests that it may code for a beta-ketoacyl reductase required for the biosynthesis of cuticular waxes. Plant Physiology. 115: 501-10. PMID 9342868 DOI: 10.1104/Pp.115.2.501 |
0.645 |
|
| 1995 |
Xu X, Hsia AP, Zhang L, Nikolau BJ, Schnable PS. Meictic recombination break points resolve at high rates at the 5′ end of a maize coding sequence Plant Cell. 7: 2151-2161. PMID 8718625 DOI: 10.1105/Tpc.7.12.2151 |
0.683 |
|
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