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Nucleic Acids Research
|
January 10, 2023
canSAR: update to the cancer translational research and drug discovery knowledgebase
Patrizio di Micco, Albert A Antolin, Costas Mitsopoulos, et al.
Cancer Research
|
October 12, 2010
MGMT-independent temozolomide resistance in pediatric glioblastoma cells associated with a PI3-kinase-mediated HOX/stem cell gene signature
Nathalie Gaspar, Lynley Marshall, Lara Perryman, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
October 18, 2008
Phase I pharmacokinetic and pharmacodynamic study of LAQ824, a hydroxamate histone deacetylase inhibitor with a heat shock protein-90 inhibitory profile, in patients with advanced solid tumors
Johann S de Bono, Rebecca Kristeleit, Anthony Tolcher, et al.
Molecular Cancer Therapeutics
|
June 24, 2026
Anti-Tumor Activity of Cdk2/9 Inhibitor Fadraciclib in an In Vivo Model of Temozolomide Refractory Neuroblastoma
Evon Poon, Tong Liang, Qiong Gao, et al.
Cancer Research
|
August 4, 2006
In vivo biological activity of the histone deacetylase inhibitor LAQ824 is detectable with 3'-deoxy-3'-[18F]fluorothymidine positron emission tomography
Julius Leyton, John P Alao, Marco Da Costa, et al.
Molecular Cancer Therapeutics
|
December 20, 2007
Mechanism of action of the Aurora kinase inhibitor CCT129202 and in vivo quantification of biological activity
Florence Chan, Chongbo Sun, Meg Perumal, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 16, 2005
The identification, synthesis, protein crystal structure and in vitro biochemical evaluation of a new 3,4-diarylpyrazole class of Hsp90 inhibitors
Kwai-Ming J Cheung, Thomas P Matthews, Karen James, et al.
Chemistry & Biology
|
June 26, 2004
Structure-activity relationships in purine-based inhibitor binding to HSP90 isoforms
Lisa Wright, Xavier Barril, Brian Dymock, et al.
Journal of Medicinal Chemistry
|
March 19, 2008
Identification of 4-(4-aminopiperidin-1-yl)-7H-pyrrolo[2,3-d]pyrimidines as selective inhibitors of protein kinase B through fragment elaboration
John J Caldwell, Thomas G Davies, Alastair Donald, et al.
Molecular & Cellular Proteomics : MCP
|
December 22, 2022
Native Size-Exclusion Chromatography-Based Mass Spectrometry Reveals New Components of the Early Heat Shock Protein 90 Inhibition Response Among Limited Global Changes
Rahul S Samant, Silvia Batista, Mark Larance, et al.
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of 32
Search research articles
Search
Showing results (231-240 of 315) with videos related to
Sort By:
Page
of 32
Nucleic Acids Research
|
January 10, 2023
canSAR: update to the cancer translational research and drug discovery knowledgebase
Patrizio di Micco, Albert A Antolin, Costas Mitsopoulos, et al.
Cancer Research
|
October 12, 2010
MGMT-independent temozolomide resistance in pediatric glioblastoma cells associated with a PI3-kinase-mediated HOX/stem cell gene signature
Nathalie Gaspar, Lynley Marshall, Lara Perryman, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
October 18, 2008
Phase I pharmacokinetic and pharmacodynamic study of LAQ824, a hydroxamate histone deacetylase inhibitor with a heat shock protein-90 inhibitory profile, in patients with advanced solid tumors
Johann S de Bono, Rebecca Kristeleit, Anthony Tolcher, et al.
Molecular Cancer Therapeutics
|
June 24, 2026
Anti-Tumor Activity of Cdk2/9 Inhibitor Fadraciclib in an In Vivo Model of Temozolomide Refractory Neuroblastoma
Evon Poon, Tong Liang, Qiong Gao, et al.
Cancer Research
|
August 4, 2006
In vivo biological activity of the histone deacetylase inhibitor LAQ824 is detectable with 3'-deoxy-3'-[18F]fluorothymidine positron emission tomography
Julius Leyton, John P Alao, Marco Da Costa, et al.
Molecular Cancer Therapeutics
|
December 20, 2007
Mechanism of action of the Aurora kinase inhibitor CCT129202 and in vivo quantification of biological activity
Florence Chan, Chongbo Sun, Meg Perumal, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 16, 2005
The identification, synthesis, protein crystal structure and in vitro biochemical evaluation of a new 3,4-diarylpyrazole class of Hsp90 inhibitors
Kwai-Ming J Cheung, Thomas P Matthews, Karen James, et al.
Chemistry & Biology
|
June 26, 2004
Structure-activity relationships in purine-based inhibitor binding to HSP90 isoforms
Lisa Wright, Xavier Barril, Brian Dymock, et al.
Journal of Medicinal Chemistry
|
March 19, 2008
Identification of 4-(4-aminopiperidin-1-yl)-7H-pyrrolo[2,3-d]pyrimidines as selective inhibitors of protein kinase B through fragment elaboration
John J Caldwell, Thomas G Davies, Alastair Donald, et al.
Molecular & Cellular Proteomics : MCP
|
December 22, 2022
Native Size-Exclusion Chromatography-Based Mass Spectrometry Reveals New Components of the Early Heat Shock Protein 90 Inhibition Response Among Limited Global Changes
Rahul S Samant, Silvia Batista, Mark Larance, et al.
Page
of 32