J. Tsay

发表

THE DESIGN AND SYNTHESIS OF PURINE INHIBITORS OF CDK2. III

A. Bitonti, J. Dumont, P. Wright, 2001 .

Overproduction of beta-ketoacyl-acyl carrier protein synthase I imparts thiolactomycin resistance to Escherichia coli K-12

C. Rock, S. Jackowski, J. Tsay, 1992, Journal of bacteriology.

Isolation and characterization of the beta-ketoacyl-acyl carrier protein synthase III gene (fabH) from Escherichia coli K-12.

C. Rock, T. Larson, S. Jackowski, 1992, The Journal of biological chemistry.

Thiolactomycin resistance in Escherichia coli is associated with the multidrug resistance efflux pump encoded by emrAB

C. Rock, S. Jackowski, J. Tsay, 1993, Journal of bacteriology.

Approaches to Drug Sample Differentiation. III: A Comparative Study of the Use of Chiral and Achiral Capillary Column Gas Chromatography/Mass Spectrometry for the Determination of Methamphetamine Enantiomers and Possible Impurities

M. Fitzgerald, W. Ku, J. Tsay, 1982 .

Approaches to Drug Sample Differentiation. II: Nuclear Magnetic Resonance Spectrometric Determination of Methamphetamine Enantiomers

M. Fitzgerald, W. Ku, J. Tsay, 1981 .

A probe of the active site acidity of carboxypeptidase A.

W. L. Mock, J. Tsay, 1986, Biochemistry.

Strategies for optimal synthesis and secretion of heterologous proteins in the methylotrophic yeast Pichia pastoris.

A. Subramaniam, P L Smith, K Sreekrishna, 1997, Gene.

Sulfoximine and sulfodiimine transition state analog inhibitors for carboxypeptidase A

W. L. Mock, J. Tsay, 1989 .

Use of chiral lanthanide shift reagents for the nuclear magnetic resonance spectrometric determination of amphetamine enantiomers

J. Tsay, Juei-Ho. Liu, 1982 .

Kinetic investigation of the functional role of phenylalanine-31 of recombinant human dihydrofolate reductase.

W. Beard, Raymond L. Blakley, J. Freisheim, 1990, Biochemistry.

pK values for active site residues of carboxypeptidase A.

W. L. Mock, J T Tsay, W L Mock, 1988, The Journal of biological chemistry.

Crystal structure of human cyclin-dependent kinase 2 in complex with the adenine-derived inhibitor H717.

A. Bitonti, J. Dumont, P. Wright, 2001, Journal of medicinal chemistry.