M. J. Huang

发表

The Role of Computational Techniques in Retrometabolic Drug Design Strategies

Nicholas Bodor, Peter Buchwald, N. Bodor, 1999 .

Theoretical studies on the structures of natural and alkylated cyclodextrins.

N. Bodor, J. Watts, M. J. Huang, 1995, Journal of pharmaceutical sciences.

Computer-assisted design of new drugs based on retrometabolic concepts.

P Buchwald, N. Bodor, P. Buchwald, 1998, SAR and QSAR in environmental research.

Soft drugs. 17: Quantitative structure-activity relationships of soft anticholinergics based on methatropine and methscopolamine.

N. Bodor, G. Kumar, N Bodor, 1994, Journal of pharmaceutical sciences.

A new method for the estimation of the aqueous solubility of organic compounds.

N. Bodor, N Bodor, M J Huang, 1992, Journal of pharmaceutical sciences.

An extended version of a novel method for the estimation of partition coefficients.

N. Bodor, N Bodor, M J Huang, 1992, Journal of pharmaceutical sciences.

Diverse point mutations result in glucose-6-phosphate dehydrogenase (G6PD) polymorphism in Taiwan.

C. Tang, T. Tang, C. S. Huang, 1992, Blood.

Expression and biochemical characterization of human glucose-6-phosphate dehydrogenase in Escherichia coli: a system to analyze normal and mutant enzymes.

T. Tang, C. S. Huang, M. J. Huang, 1994, Blood.

Efficacy of a 3-substituted versus 17-substituted chemical delivery system for estradiol brain targeting.

N. Bodor, M. Brewster, P. Druzgala, 1995, Journal of pharmaceutical sciences.