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Amy C Anderson

Showing results (31-40 of 71) with videos related to

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Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 21, 2012
Acetylenic linkers in lead compounds: a study of the stability of the propargyl-linked antifolatesWangda Zhou, Kishore Viswanathan, Dennis Hill, et al.
Acta Crystallographica. Section D, Biological Crystallography|May 26, 2004
A subgroup algorithm to identify cross-rotation peaks consistent with non-crystallographic symmetryRyan H Lilien, Chris Bailey-Kellogg, Amy C Anderson, et al.
Biochemistry|March 28, 2009
The solution structure of Bacillus anthracis dihydrofolate reductase yields insight into the analysis of structure-activity relationships for novel inhibitorsJennifer M Beierlein, Lalit Deshmukh, Kathleen M Frey, et al.
Biochemistry|December 21, 2006
Redesigning the PheA domain of gramicidin synthetase leads to a new understanding of the enzyme's mechanism and selectivityBrian W Stevens, Ryan H Lilien, Ivelin Georgiev, et al.
Bioorganic & Medicinal Chemistry|March 12, 2014
Studies on the antiproliferative effects of tropolone derivatives in Jurkat T-lymphocyte cellsSophia N Ononye, Michael D Vanheyst, Charles Giardina, et al.
Pharmaceutical Patent Analyst|October 29, 2013
Toward isozyme-selective inhibitors of histone deacetylase as therapeutic agents for the treatment of cancerSophia N Ononye, Michael van Heyst, Eric M Falcone, et al.
The Journal of Eukaryotic Microbiology|January 23, 2004
The crystal structure of dihydrofolate reductase-thymidylate synthase from Cryptosporidium hominis reveals a novel architecture for the bifunctional enzymeRobert H O'Neil, Ryan H Lilien, Bruce R Donald, et al.
The Journal of Biological Chemistry|October 14, 2003
Phylogenetic classification of protozoa based on the structure of the linker domain in the bifunctional enzyme, dihydrofolate reductase-thymidylate synthaseRobert H O'Neil, Ryan H Lilien, Bruce R Donald, et al.
Eukaryotic Cell|January 27, 2009
Towards new antifolates targeting eukaryotic opportunistic infectionsJieying Liu, David B Bolstad, Erin S D Bolstad, et al.
Journal of Medicinal Chemistry|October 7, 2008
Structure-based approach to the development of potent and selective inhibitors of dihydrofolate reductase from cryptosporidiumDavid B Bolstad, Erin S D Bolstad, Kathleen M Frey, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 21, 2012
Acetylenic linkers in lead compounds: a study of the stability of the propargyl-linked antifolatesWangda Zhou, Kishore Viswanathan, Dennis Hill, et al.
Acta Crystallographica. Section D, Biological Crystallography|May 26, 2004
A subgroup algorithm to identify cross-rotation peaks consistent with non-crystallographic symmetryRyan H Lilien, Chris Bailey-Kellogg, Amy C Anderson, et al.
Biochemistry|March 28, 2009
The solution structure of Bacillus anthracis dihydrofolate reductase yields insight into the analysis of structure-activity relationships for novel inhibitorsJennifer M Beierlein, Lalit Deshmukh, Kathleen M Frey, et al.
Biochemistry|December 21, 2006
Redesigning the PheA domain of gramicidin synthetase leads to a new understanding of the enzyme's mechanism and selectivityBrian W Stevens, Ryan H Lilien, Ivelin Georgiev, et al.
Bioorganic & Medicinal Chemistry|March 12, 2014
Studies on the antiproliferative effects of tropolone derivatives in Jurkat T-lymphocyte cellsSophia N Ononye, Michael D Vanheyst, Charles Giardina, et al.
Pharmaceutical Patent Analyst|October 29, 2013
Toward isozyme-selective inhibitors of histone deacetylase as therapeutic agents for the treatment of cancerSophia N Ononye, Michael van Heyst, Eric M Falcone, et al.
The Journal of Eukaryotic Microbiology|January 23, 2004
The crystal structure of dihydrofolate reductase-thymidylate synthase from Cryptosporidium hominis reveals a novel architecture for the bifunctional enzymeRobert H O'Neil, Ryan H Lilien, Bruce R Donald, et al.
The Journal of Biological Chemistry|October 14, 2003
Phylogenetic classification of protozoa based on the structure of the linker domain in the bifunctional enzyme, dihydrofolate reductase-thymidylate synthaseRobert H O'Neil, Ryan H Lilien, Bruce R Donald, et al.
Eukaryotic Cell|January 27, 2009
Towards new antifolates targeting eukaryotic opportunistic infectionsJieying Liu, David B Bolstad, Erin S D Bolstad, et al.
Journal of Medicinal Chemistry|October 7, 2008
Structure-based approach to the development of potent and selective inhibitors of dihydrofolate reductase from cryptosporidiumDavid B Bolstad, Erin S D Bolstad, Kathleen M Frey, et al.
Pageof 8