T. Carr

发表

Studies on acyl pyrrolidine inhibitors of HCV RNA-dependent RNA polymerase to identify a molecule with replicon antiviral activity.

G. Hofmann, G. Burton, R. Sarisky, 2007, Bioorganic & medicinal chemistry letters.

Identification of small molecule inhibitors of the hepatitis C virus RNA-dependent RNA polymerase from a pyrrolidine combinatorial mixture.

George Burton, Dashyant Dhanak, G. Hofmann, 2005, Bioorganic & medicinal chemistry letters.

Peptide Aldehyde Inhibitors of Cathepsin K Inhibit Bone Resorption Both In Vitro and In Vivo

D. Veber, A. Badger, I. James, 1997, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Structure and Design of Potent and Selective Cathepsin K Inhibitors

S. Carr, R. DesJarlais, Baoguang Zhao, 1997 .

Procede d'inhibition de la cathepsine k

Baoguang Zhao, Y. Ru, D. Veber, 1996 .

Drosophila Muller F Elements Maintain a Distinct Set of Genomic Properties Over 40 Million Years of Evolution

Jimmy Ma, Jeremy Buhler, Matt J. Kusner, 2015, G3: Genes, Genomes, Genetics.

Hydroxyethylene isostere inhibitors of human immunodeficiency virus-1 protease: structure-activity analysis using enzyme kinetics, X-ray crystallography, and infected T-cell assays.

A M Hassell, M. Minnich, D. Lambert, 1992, Biochemistry.

Inhibition of HIV-1 protease in infected T-lymphocytes by synthetic peptide analogues

Brian W. Metcalf, Michael L. Moore, C. Debouck, 1990, Nature.

Inhibition of human immunodeficiency virus 1 protease in vitro: rational design of substrate analogue inhibitors.

C. Debouck, J. Strickler, T. Meek, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Expanding the avian micro RNA repertoire of domesticated poultry and investigating the NLRP3 inflammasome messenger RNA and micro RNA transcriptomes in Anas platyrhynchos (ducks)

T. Carr, 2017 .

Use of papain as a model for the structure-based design of cathepsin K inhibitors: crystal structures of two papain-inhibitor complexes demonstrate binding to S'-subsites.

R. DesJarlais, D. Veber, S. Abdel-Meguid, 1999, Journal of medicinal chemistry.

Aggressive treatment for postcardiac transplant lymphoproliferation.

R. Fisher, L. Swinnen, M. Costanzo, 1995, Blood.

BCL-2 but not its Epstein-Barr virus-encoded homologue, BHRF1, is commonly expressed in posttransplantation lymphoproliferative disorders.

P. Murray, L. Swinnen, R. Ambinder, 1996, Blood.

An orally bioavailable HIV-1 protease inhibitor containing an imidazole-derived peptide bond replacement: crystallographic and pharmacokinetic analysis.

R. DesJarlais, Baoguang Zhao, K. Murthy, 1994, Biochemistry.