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Craig J Thomas

Showing results (51-60 of 237) with videos related to

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Current Protocols in Chemical Biology|January 7, 2014
Multiplexing high-content flow (HCF) and quantitative high-throughput screening (qHTS) to identify compounds capable of decreasing cell viability, activating caspase 3/7, expressing annexin V, and changing mitochondrial membrane integrityLesley A Mathews, Jonathan M Keller, Crystal McKnight, et al.
Acta Crystallographica. Section C, Crystal Structure Communications|July 3, 2002
Structural properties of a series of photochromic fluorinated indolylfulgidesMason A Wolak, Robert C Finn, Randy S Rarig, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2016
Selective small molecule inhibitor of the Mycobacterium tuberculosis fumarate hydratase reveals an allosteric regulatory siteMonica Kasbekar, Gerhard Fischer, Bryan T Mott, et al.
Journal of the American Chemical Society|March 25, 2008
A virtual screen for diverse ligands: discovery of selective G protein-coupled receptor antagonistsStanislav Engel, Amanda P Skoumbourdis, John Childress, et al.
Plos Neglected Tropical Diseases|February 1, 2008
Quantitative high-throughput screen identifies inhibitors of the Schistosoma mansoni redox cascadeAnton Simeonov, Ajit Jadhav, Ahmed A Sayed, et al.
Breast Cancer Research : BCR|June 26, 2014
Drug repurposing screen identifies lestaurtinib amplifies the ability of the poly (ADP-ribose) polymerase 1 inhibitor AG14361 to kill breast cancer associated gene-1 mutant and wild type breast cancer cellsGuelaguetza Vazquez-Ortiz, Cristine Chisholm, Xiaoling Xu, et al.
Glycobiology|October 3, 2024
Compromised CDK12 activity causes dependency on the high activity of O-GlcNAc transferaseSatu Pallasaho, Aishwarya Gondane, Julia Kutz, et al.
Journal of the American Chemical Society|July 3, 2003
Solid-phase synthesis of bleomycin group antibiotics. Construction of a 108-member deglycobleomycin libraryChristopher J Leitheiser, Kenneth L Smith, Michael J Rishel, et al.
Bioorganic & Medicinal Chemistry|June 7, 2011
Exploratory analysis of kinetic solubility measurements of a small molecule libraryRajarshi Guha, Thomas S Dexheimer, Aimee N Kestranek, et al.
Bioorganic & Medicinal Chemistry Letters|May 7, 2013
Small-molecule pyrimidine inhibitors of the cdc2-like (Clk) and dual specificity tyrosine phosphorylation-regulated (Dyrk) kinases: development of chemical probe ML315Thomas C Coombs, Cordelle Tanega, Min Shen, et al.
Pageof 24

Showing results (51-60 of 237) with videos related to

Sort By:
Pageof 24
Current Protocols in Chemical Biology|January 7, 2014
Multiplexing high-content flow (HCF) and quantitative high-throughput screening (qHTS) to identify compounds capable of decreasing cell viability, activating caspase 3/7, expressing annexin V, and changing mitochondrial membrane integrityLesley A Mathews, Jonathan M Keller, Crystal McKnight, et al.
Acta Crystallographica. Section C, Crystal Structure Communications|July 3, 2002
Structural properties of a series of photochromic fluorinated indolylfulgidesMason A Wolak, Robert C Finn, Randy S Rarig, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2016
Selective small molecule inhibitor of the Mycobacterium tuberculosis fumarate hydratase reveals an allosteric regulatory siteMonica Kasbekar, Gerhard Fischer, Bryan T Mott, et al.
Journal of the American Chemical Society|March 25, 2008
A virtual screen for diverse ligands: discovery of selective G protein-coupled receptor antagonistsStanislav Engel, Amanda P Skoumbourdis, John Childress, et al.
Plos Neglected Tropical Diseases|February 1, 2008
Quantitative high-throughput screen identifies inhibitors of the Schistosoma mansoni redox cascadeAnton Simeonov, Ajit Jadhav, Ahmed A Sayed, et al.
Breast Cancer Research : BCR|June 26, 2014
Drug repurposing screen identifies lestaurtinib amplifies the ability of the poly (ADP-ribose) polymerase 1 inhibitor AG14361 to kill breast cancer associated gene-1 mutant and wild type breast cancer cellsGuelaguetza Vazquez-Ortiz, Cristine Chisholm, Xiaoling Xu, et al.
Glycobiology|October 3, 2024
Compromised CDK12 activity causes dependency on the high activity of O-GlcNAc transferaseSatu Pallasaho, Aishwarya Gondane, Julia Kutz, et al.
Journal of the American Chemical Society|July 3, 2003
Solid-phase synthesis of bleomycin group antibiotics. Construction of a 108-member deglycobleomycin libraryChristopher J Leitheiser, Kenneth L Smith, Michael J Rishel, et al.
Bioorganic & Medicinal Chemistry|June 7, 2011
Exploratory analysis of kinetic solubility measurements of a small molecule libraryRajarshi Guha, Thomas S Dexheimer, Aimee N Kestranek, et al.
Bioorganic & Medicinal Chemistry Letters|May 7, 2013
Small-molecule pyrimidine inhibitors of the cdc2-like (Clk) and dual specificity tyrosine phosphorylation-regulated (Dyrk) kinases: development of chemical probe ML315Thomas C Coombs, Cordelle Tanega, Min Shen, et al.
Pageof 24