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L Trainor

Showing results (41-50 of 104) with videos related to

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Journal of Medicinal Chemistry|May 14, 2025
XPO1-Targeting Selective Inhibitors of Transcriptional Activation Suppress Graft-versus-Host DiseaseYanqiu Shen, Yi Fan Chen, David F Yan, et al.
Academic Emergency Medicine : Official Journal of the Society for Academic Emergency Medicine|July 14, 2000
Setting-based practice variation in the management of simple febrile seizureL C Hampers, J L Trainor, R Listernick, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|June 25, 2009
Development and evaluation of a simulation-based pediatric emergency medicine curriculumMark D Adler, John A Vozenilek, Jennifer L Trainor, et al.
Bioorganic & Medicinal Chemistry Letters|October 16, 1999
Synthesis and evaluation of analogs of Efavirenz (SUSTIVA) as HIV-1 reverse transcriptase inhibitorsM Patel, S S Ko, R J McHugh, et al.
Bioorganic & Medicinal Chemistry Letters|August 21, 2012
Modulation of cofilin phosphorylation by inhibition of the Lim family kinasesLiqi He, Steven P Seitz, George L Trainor, et al.
Simulation in Healthcare : Journal of the Society for Simulation in Healthcare|February 19, 2011
Comparison of checklist and anchored global rating instruments for performance rating of simulated pediatric emergenciesMark D Adler, John A Vozenilek, Jennifer L Trainor, et al.
Antimicrobial Agents and Chemotherapy|October 18, 2002
Regulated expression of the Escherichia coli lepB gene as a tool for cellular testing of antimicrobial compounds that inhibit signal peptidase I in vitroMaria D F S Barbosa, Siqi Lin, Jay A Markwalder, et al.
Journal of Medicinal Chemistry|September 3, 2004
Design, synthesis, and biological evaluation of 1,2,3,7-tetrahydro-6h-purin-6-one and 3,7-dihydro-1h-purine-2,6-dione derivatives as corticotropin-releasing factor(1) receptor antagonistsRichard A Hartz, Kausik K Nanda, Charles L Ingalls, et al.
Journal of Medicinal Chemistry|August 9, 2002
Discovery and structure-activity relationship of N-(ureidoalkyl)-benzyl-piperidines as potent small molecule CC chemokine receptor-3 (CCR3) antagonistsGeorge V De Lucca, Ui T Kim, Curt Johnson, et al.
Bioorganic & Medicinal Chemistry Letters|January 12, 2010
Discovery of matrix metalloproteases selective and activated peptide-doxorubicin prodrugs as anti-tumor agentsZilun Hu, Xiangjun Jiang, Charles F Albright, et al.
Pageof 11

Showing results (41-50 of 104) with videos related to

Sort By:
Pageof 11
Journal of Medicinal Chemistry|May 14, 2025
XPO1-Targeting Selective Inhibitors of Transcriptional Activation Suppress Graft-versus-Host DiseaseYanqiu Shen, Yi Fan Chen, David F Yan, et al.
Academic Emergency Medicine : Official Journal of the Society for Academic Emergency Medicine|July 14, 2000
Setting-based practice variation in the management of simple febrile seizureL C Hampers, J L Trainor, R Listernick, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|June 25, 2009
Development and evaluation of a simulation-based pediatric emergency medicine curriculumMark D Adler, John A Vozenilek, Jennifer L Trainor, et al.
Bioorganic & Medicinal Chemistry Letters|October 16, 1999
Synthesis and evaluation of analogs of Efavirenz (SUSTIVA) as HIV-1 reverse transcriptase inhibitorsM Patel, S S Ko, R J McHugh, et al.
Bioorganic & Medicinal Chemistry Letters|August 21, 2012
Modulation of cofilin phosphorylation by inhibition of the Lim family kinasesLiqi He, Steven P Seitz, George L Trainor, et al.
Simulation in Healthcare : Journal of the Society for Simulation in Healthcare|February 19, 2011
Comparison of checklist and anchored global rating instruments for performance rating of simulated pediatric emergenciesMark D Adler, John A Vozenilek, Jennifer L Trainor, et al.
Antimicrobial Agents and Chemotherapy|October 18, 2002
Regulated expression of the Escherichia coli lepB gene as a tool for cellular testing of antimicrobial compounds that inhibit signal peptidase I in vitroMaria D F S Barbosa, Siqi Lin, Jay A Markwalder, et al.
Journal of Medicinal Chemistry|September 3, 2004
Design, synthesis, and biological evaluation of 1,2,3,7-tetrahydro-6h-purin-6-one and 3,7-dihydro-1h-purine-2,6-dione derivatives as corticotropin-releasing factor(1) receptor antagonistsRichard A Hartz, Kausik K Nanda, Charles L Ingalls, et al.
Journal of Medicinal Chemistry|August 9, 2002
Discovery and structure-activity relationship of N-(ureidoalkyl)-benzyl-piperidines as potent small molecule CC chemokine receptor-3 (CCR3) antagonistsGeorge V De Lucca, Ui T Kim, Curt Johnson, et al.
Bioorganic & Medicinal Chemistry Letters|January 12, 2010
Discovery of matrix metalloproteases selective and activated peptide-doxorubicin prodrugs as anti-tumor agentsZilun Hu, Xiangjun Jiang, Charles F Albright, et al.
Pageof 11