J. A. Ribeiro

Crystal structures of the closed form of Mycobacterium tuberculosis dihydrofolate reductase in complex with dihydrofolate and antifolates.

M. Dias, G. de Oliveira, S. M. Chavez-Pacheco, 2019, Acta crystallographica. Section D, Structural biology.

Design, synthesis and biological activity of novel substituted 3-benzoic acid derivatives as MtDHFR inhibitors.

G. M. Ferreira, A. Poso, T. Kronenberger, 2020, Bioorganic & medicinal chemistry.

Using a fragment-based approach to identify alternative chemical scaffolds targeting dihydrofolate reductase from Mycobacterium tuberculosis.

T. Blundell, C. Abell, Roberto Parise-Filho, 2020, ACS infectious diseases.

Crystal structures of the closed form of Mycobacterium tuberculosis dihydrofolate reductase in complex with dihydrofolate and antifolates.

M. Dias, G. de Oliveira, G. Oliveira, 2019, Acta crystallographica. Section D, Structural biology.

The molecular structure of an epoxide hydrolase from Trichoderma reesei in complex with urea or amide-based inhibitors.

B. Hammock, C. Morisseau, F. Chambergo, 2019, International journal of biological macromolecules.

EFFECTS OF PURINES AND FORSKOLIN ON HAEMOLYSIS

J. A. Ribeiro, M. L. Gonçalves, 1987, Fundamental & clinical pharmacology.

Folate biosynthesis pathway: mechanisms and insights into drug design for infectious diseases.

M. V. Bertacine Dias, S. M. Chavez-Pacheco, G. Libreros-Zúñiga, 2018, Future medicinal chemistry.

Using a fragment-based approach to identify novel chemical scaffolds targeting the dihydrofolate reductase (DHFR) from Mycobacterium tuberculosis

T. Blundell, C. Abell, A. Coyne, 2020, bioRxiv.

Relation of three genetic traits to venous thrombosis in an African-American population.

N. Wenger, H. Austin, W. Hooper, 1998, American journal of epidemiology.