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Journal of Medicinal Chemistry|December 20, 1996
Synthesis, biotransformation, and pharmacokinetic studies of 9-(beta-D-arabinofuranosyl)-6-azidopurine: a prodrug for ara-A designed to utilize the azide reduction pathwayL P Kotra, K K Manouilov, E Cretton-Scott, et al.
Biochemistry|July 28, 1999
X-ray structure of the Asn276Asp variant of the Escherichia coli TEM-1 beta-lactamase: direct observation of electrostatic modulation in resistance to inactivation by clavulanic acidP Swarén, D Golemi, S Cabantous, et al.
The Journal of Biological Chemistry|August 7, 1999
Effects on substrate profile by mutational substitutions at positions 164 and 179 of the class A TEM(pUC19) beta-lactamase from Escherichia coliS B Vakulenko, P Taibi-Tronche, M Tóth, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Templates for design of inhibitors for serine proteases: application of the program DOCK to the discovery of novel inhibitors for thrombinI Massova, P Martin, A Bulychev, et al.
Journal of Medicinal Chemistry|November 8, 1996
In vitro and in vivo evaluation of 6-azido-2',3'-dideoxy-2'-fluoro-beta-D-arabinofuranosylpurine and N6-methyl-2',3'-dideoxy-2'-fluoro-beta-D-arabinofuranosyladenine as prodrugs of the anti-HIV nucleosides 2'-F-ara-ddA and 2'-F-ara-ddIT Koudriakova, K K Manouilov, K Shanmuganathan, et al.
Chemical Research in Toxicology|September 18, 2001
Identification of colchicine in placental blood from patients using herbal medicinesH R Petty, M Fernando, A L Kindzelskii, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 2001
A 1.2-A snapshot of the final step of bacterial cell wall biosynthesisW Lee, M A McDonough, L Kotra, et al.
The Journal of Antibiotics|January 2, 2001
6-(hydroxyalkyl)penicillanates as probes for mechanisms of beta-lactamasesD Golemi, L Maveyraud, A Ishiwata, et al.
The Journal of Biological Chemistry|September 22, 2000
Tissue inhibitor of metalloproteinase (TIMP)-2 acts synergistically with synthetic matrix metalloproteinase (MMP) inhibitors but not with TIMP-4 to enhance the (Membrane type 1)-MMP-dependent activation of pro-MMP-2M Toth, M M Bernardo, D C Gervasi, et al.
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