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Journal of Neuroscience Research
|
March 3, 2004
Elevated expression of a regulator of the G2/M phase of the cell cycle, neuronal CIP-1-associated regulator of cyclin B, in Alzheimer's disease
Xiongwei Zhu, Andrew McShea, Peggy L R Harris, et al.
Molecular Cancer Therapeutics
|
October 6, 2017
The Irreversible Covalent Fibroblast Growth Factor Receptor Inhibitor PRN1371 Exhibits Sustained Inhibition of FGFR after Drug Clearance
Eleni Venetsanakos, Ken A Brameld, Vernon T Phan, et al.
Journal of Medicinal Chemistry
|
July 1, 2017
Discovery of the Irreversible Covalent FGFR Inhibitor 8-(3-(4-Acryloylpiperazin-1-yl)propyl)-6-(2,6-dichloro-3,5-dimethoxyphenyl)-2-(methylamino)pyrido[2,3-d]pyrimidin-7(8H)-one (PRN1371) for the Treatment of Solid Tumors
Ken A Brameld, Timothy D Owens, Erik Verner, et al.
The Journal of Biological Chemistry
|
January 17, 2015
Targeting interleukin-2-inducible T-cell kinase (ITK) and resting lymphocyte kinase (RLK) using a novel covalent inhibitor PRN694
Yiming Zhong, Shuai Dong, Ethan Strattan, et al.
Nature Chemical Biology
|
May 26, 2015
Prolonged and tunable residence time using reversible covalent kinase inhibitors
J Michael Bradshaw, Jesse M McFarland, Ville O Paavilainen, et al.
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Search research articles
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Showing results (11-20 of 15) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 15 results.
Journal of Neuroscience Research
|
March 3, 2004
Elevated expression of a regulator of the G2/M phase of the cell cycle, neuronal CIP-1-associated regulator of cyclin B, in Alzheimer's disease
Xiongwei Zhu, Andrew McShea, Peggy L R Harris, et al.
Molecular Cancer Therapeutics
|
October 6, 2017
The Irreversible Covalent Fibroblast Growth Factor Receptor Inhibitor PRN1371 Exhibits Sustained Inhibition of FGFR after Drug Clearance
Eleni Venetsanakos, Ken A Brameld, Vernon T Phan, et al.
Journal of Medicinal Chemistry
|
July 1, 2017
Discovery of the Irreversible Covalent FGFR Inhibitor 8-(3-(4-Acryloylpiperazin-1-yl)propyl)-6-(2,6-dichloro-3,5-dimethoxyphenyl)-2-(methylamino)pyrido[2,3-d]pyrimidin-7(8H)-one (PRN1371) for the Treatment of Solid Tumors
Ken A Brameld, Timothy D Owens, Erik Verner, et al.
The Journal of Biological Chemistry
|
January 17, 2015
Targeting interleukin-2-inducible T-cell kinase (ITK) and resting lymphocyte kinase (RLK) using a novel covalent inhibitor PRN694
Yiming Zhong, Shuai Dong, Ethan Strattan, et al.
Nature Chemical Biology
|
May 26, 2015
Prolonged and tunable residence time using reversible covalent kinase inhibitors
J Michael Bradshaw, Jesse M McFarland, Ville O Paavilainen, et al.
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of 2