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A E Eakin

Showing results (21-30 of 27) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 1, 1989
Serine proteases from nematode and protozoan parasites: isolation of sequence homologs using generic molecular probesJ A Sakanari, C E Staunton, A E Eakin, et al.
Biochemistry|October 28, 1998
A 1.4 A crystal structure for the hypoxanthine phosphoribosyltransferase of Trypanosoma cruziP J Focia, S P Craig, R Nieves-Alicea, et al.
Journal of Molecular Biology|March 24, 1995
The crystal structure of cruzain: a therapeutic target for Chagas' diseaseM E McGrath, A E Eakin, J C Engel, et al.
Antimicrobial Agents and Chemotherapy|March 1, 1995
Comparative complement selection in bacteria enables screening for lead compounds targeted to a purine salvage enzyme of parasitesA E Eakin, R Nieves-Alicea, R Tosado-Acevedo, et al.
Chemistry & Biology|January 4, 2001
Efficient identification of inhibitors targeting the closed active site conformation of the HPRT from Trypanosoma cruziD M Freymann, M A Wenck, J C Engel, et al.
Protein Science : a Publication of the Protein Society|May 25, 1999
Ternary complex structure of human HGPRTase, PRPP, Mg2+, and the inhibitor HPP reveals the involvement of the flexible loop in substrate bindingG K Balendiran, J A Molina, Y Xu, et al.
Antimicrobial Agents and Chemotherapy|March 6, 2019
Considerations for Dose Selection and Clinical Pharmacokinetics/Pharmacodynamics for the Development of Antibacterial AgentsM L Rizk, S M Bhavnani, G Drusano, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1989
Serine proteases from nematode and protozoan parasites: isolation of sequence homologs using generic molecular probesJ A Sakanari, C E Staunton, A E Eakin, et al.
Biochemistry|October 28, 1998
A 1.4 A crystal structure for the hypoxanthine phosphoribosyltransferase of Trypanosoma cruziP J Focia, S P Craig, R Nieves-Alicea, et al.
Journal of Molecular Biology|March 24, 1995
The crystal structure of cruzain: a therapeutic target for Chagas' diseaseM E McGrath, A E Eakin, J C Engel, et al.
Antimicrobial Agents and Chemotherapy|March 1, 1995
Comparative complement selection in bacteria enables screening for lead compounds targeted to a purine salvage enzyme of parasitesA E Eakin, R Nieves-Alicea, R Tosado-Acevedo, et al.
Chemistry & Biology|January 4, 2001
Efficient identification of inhibitors targeting the closed active site conformation of the HPRT from Trypanosoma cruziD M Freymann, M A Wenck, J C Engel, et al.
Protein Science : a Publication of the Protein Society|May 25, 1999
Ternary complex structure of human HGPRTase, PRPP, Mg2+, and the inhibitor HPP reveals the involvement of the flexible loop in substrate bindingG K Balendiran, J A Molina, Y Xu, et al.
Antimicrobial Agents and Chemotherapy|March 6, 2019
Considerations for Dose Selection and Clinical Pharmacokinetics/Pharmacodynamics for the Development of Antibacterial AgentsM L Rizk, S M Bhavnani, G Drusano, et al.
Pageof 3