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Craig J Thomas

Showing results (41-50 of 237) with videos related to

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Chemmedchem|March 16, 2010
A highly potent and selective caspase 1 inhibitor that utilizes a key 3-cyanopropanoic acid moietyMatthew B Boxer, Amy M Quinn, Min Shen, et al.
Molecular Cancer Therapeutics|May 22, 2023
Schlafen 11 (SLFN11) Kills Cancer Cells Undergoing Unscheduled Re-replicationJunko Murai, Michele Ceribelli, Haiqing Fu, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 27, 2012
TCR signaling via Tec kinase ITK and interferon regulatory factor 4 (IRF4) regulates CD8+ T-cell differentiationRibhu Nayar, Megan Enos, Amanda Prince, et al.
Journal of Medicinal Chemistry|July 22, 2005
"Reversine" and its 2-substituted adenine derivatives as potent and selective A3 adenosine receptor antagonistsMelissa Perreira, Jian-Kang Jiang, Athena M Klutz, et al.
Cancer Research|October 1, 2020
Targeting the PI3K/mTOR Pathway Augments CHK1 Inhibitor-Induced Replication Stress and Antitumor Activity in High-Grade Serous Ovarian CancerTzu-Ting Huang, Ethan Brill, Jayakumar R Nair, et al.
Endocrinology|August 2, 2008
A low-molecular-weight antagonist for the human thyrotropin receptor with therapeutic potential for hyperthyroidismSusanne Neumann, Gunnar Kleinau, Stefano Costanzi, et al.
Cell Reports Methods|July 23, 2021
KiRNet: Kinase-centered network propagation of pharmacological screen resultsThomas Bello, Marina Chan, Martin Golkowski, et al.
Journal of the American Chemical Society|April 11, 2002
Alteration of the selectivity of DNA cleavage by a deglycobleomycin analogue containing a trithiazole moietyCraig J Thomas, Michael M McCormick, Corine Vialas, et al.
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.
Biochimica Et Biophysica Acta|July 1, 2008
Inhibition of erythroblast growth and fetal hemoglobin production by ribofuranose-substituted adenosine derivativesNatarajan V Bhanu, Y Terry Lee, Patricia A Oneal, et al.
Pageof 24

Showing results (41-50 of 237) with videos related to

Sort By:
Pageof 24
Chemmedchem|March 16, 2010
A highly potent and selective caspase 1 inhibitor that utilizes a key 3-cyanopropanoic acid moietyMatthew B Boxer, Amy M Quinn, Min Shen, et al.
Molecular Cancer Therapeutics|May 22, 2023
Schlafen 11 (SLFN11) Kills Cancer Cells Undergoing Unscheduled Re-replicationJunko Murai, Michele Ceribelli, Haiqing Fu, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 27, 2012
TCR signaling via Tec kinase ITK and interferon regulatory factor 4 (IRF4) regulates CD8+ T-cell differentiationRibhu Nayar, Megan Enos, Amanda Prince, et al.
Journal of Medicinal Chemistry|July 22, 2005
"Reversine" and its 2-substituted adenine derivatives as potent and selective A3 adenosine receptor antagonistsMelissa Perreira, Jian-Kang Jiang, Athena M Klutz, et al.
Cancer Research|October 1, 2020
Targeting the PI3K/mTOR Pathway Augments CHK1 Inhibitor-Induced Replication Stress and Antitumor Activity in High-Grade Serous Ovarian CancerTzu-Ting Huang, Ethan Brill, Jayakumar R Nair, et al.
Endocrinology|August 2, 2008
A low-molecular-weight antagonist for the human thyrotropin receptor with therapeutic potential for hyperthyroidismSusanne Neumann, Gunnar Kleinau, Stefano Costanzi, et al.
Cell Reports Methods|July 23, 2021
KiRNet: Kinase-centered network propagation of pharmacological screen resultsThomas Bello, Marina Chan, Martin Golkowski, et al.
Journal of the American Chemical Society|April 11, 2002
Alteration of the selectivity of DNA cleavage by a deglycobleomycin analogue containing a trithiazole moietyCraig J Thomas, Michael M McCormick, Corine Vialas, et al.
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.
Biochimica Et Biophysica Acta|July 1, 2008
Inhibition of erythroblast growth and fetal hemoglobin production by ribofuranose-substituted adenosine derivativesNatarajan V Bhanu, Y Terry Lee, Patricia A Oneal, et al.
Pageof 24