W Tong

发表

Derivation of a pharmacophore model for anandamide using constrained conformational searching and comparative molecular field analysis.

W. Welsh, W. Tong, A. Howlett, 1998, Journal of medicinal chemistry.

Use of moment of inertia in comparative molecular field analysis to model chromatographic retention of nonpolar solutes.

W. Tong, W. Zielinski, E. Collantes, 1996, Analytical chemistry.

The estrogen receptor relative binding affinities of 188 natural and xenochemicals: structural diversity of ligands.

H Fang, W S Branham, D M Sheehan, 2000, Toxicological sciences : an official journal of the Society of Toxicology.

A comparative molecular field analysis study of N-benzylpiperidines as acetylcholinesterase inhibitors.

W. Welsh, W. Tong, W J Welsh, 1996, Journal of medicinal chemistry.

Genomic indicators in the blood predict drug-induced liver injury

H Fang, T. Nikolskaya, Y. Nikolsky, 2010, The Pharmacogenomics Journal.

Comparison of estrogen receptor alpha and beta subtypes based on comparative molecular field analysis (CoMFA).

D M Sheehan, R. Perkins, W. Welsh, 1999, SAR and QSAR in environmental research.

Functional analysis of multiple genomic signatures demonstrates that classification algorithms choose phenotype-related genes

C. Furlanello, Giuseppe Jurman, T. Nikolskaya, 2010, The Pharmacogenomics Journal.

QSAR models for binding of estrogenic compounds to estrogen receptor alpha and beta subtypes.

D M Sheehan, R. Perkins, W. Welsh, 1997, Endocrinology.

Quantitative comparisons of in vitro assays for estrogenic activities.

H Fang, D M Sheehan, H. Fang, 2000, Environmental health perspectives.

Quantitative structure-activity relationships (QSARs) for estrogen binding to the estrogen receptor: predictions across species.

W S Branham, D M Sheehan, R. Perkins, 1997, Environmental health perspectives.

Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens.

Q Xie, H Fang, D M Sheehan, 2001, Chemical research in toxicology.