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Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
May 15, 2009
Rapid gynogenetic mapping of Xenopus tropicalis mutations to chromosomes
Mustafa K Khokha, Vladimir Krylov, Michael J Reilly, et al.
Science Advances
|
January 4, 2020
Blocking FcRn in humans reduces circulating IgG levels and inhibits IgG immune complex-mediated immune responses
L J Blumberg, J E Humphries, S D Jones, et al.
Journal of Medicinal Chemistry
|
September 11, 2018
Introduction of a Methyl Group Curbs Metabolism of Pyrido[3,4- d]pyrimidine Monopolar Spindle 1 (MPS1) Inhibitors and Enables the Discovery of the Phase 1 Clinical Candidate N<sup>2</sup>-(2-Ethoxy-4-(4-methyl-4 H-1,2,4-triazol-3-yl)phenyl)-6-methyl- N<sup>8</sup>-neopentylpyrido[3,4- d]pyrimidine-2,8-diamine (BOS172722)
Hannah L Woodward, Paolo Innocenti, Kwai-Ming J Cheung, et al.
Molecular Cancer Therapeutics
|
April 14, 2007
Inhibition of the heat shock protein 90 molecular chaperone in vitro and in vivo by novel, synthetic, potent resorcinylic pyrazole/isoxazole amide analogues
Swee Y Sharp, Chrisostomos Prodromou, Kathy Boxall, et al.
Journal of Medicinal Chemistry
|
November 22, 2013
Structure-based design of orally bioavailable 1H-pyrrolo[3,2-c]pyridine inhibitors of mitotic kinase monopolar spindle 1 (MPS1)
Sébastien Naud, Isaac M Westwood, Amir Faisal, et al.
Journal of Medicinal Chemistry
|
November 30, 2021
Into Deep Water: Optimizing BCL6 Inhibitors by Growing into a Solvated Pocket
Matthew G Lloyd, Rosemary Huckvale, Kwai-Ming J Cheung, et al.
Journal of Medicinal Chemistry
|
June 3, 2022
Optimizing Shape Complementarity Enables the Discovery of Potent Tricyclic BCL6 Inhibitors
Owen A Davis, Kwai-Ming J Cheung, Alfie Brennan, et al.
Perspectives on Medical Education
|
March 25, 2024
Competence By Design: a transformational national model of time-variable competency-based postgraduate medical education
Jason R Frank, Jolanta Karpinski, Jonathan Sherbino, et al.
Journal of Medicinal Chemistry
|
November 25, 2011
Structure-guided evolution of potent and selective CHK1 inhibitors through scaffold morphing
John C Reader, Thomas P Matthews, Suki Klair, et al.
Journal of Medicinal Chemistry
|
April 7, 2023
Discovery of an <i>In Vivo</i> Chemical Probe for BCL6 Inhibition by Optimization of Tricyclic Quinolinones
Alice C Harnden, Owen A Davis, Gary M Box, et al.
Page
of 30
Search research articles
Search
Showing results (281-290 of 298) with videos related to
Sort By:
Page
of 30
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
May 15, 2009
Rapid gynogenetic mapping of Xenopus tropicalis mutations to chromosomes
Mustafa K Khokha, Vladimir Krylov, Michael J Reilly, et al.
Science Advances
|
January 4, 2020
Blocking FcRn in humans reduces circulating IgG levels and inhibits IgG immune complex-mediated immune responses
L J Blumberg, J E Humphries, S D Jones, et al.
Journal of Medicinal Chemistry
|
September 11, 2018
Introduction of a Methyl Group Curbs Metabolism of Pyrido[3,4- d]pyrimidine Monopolar Spindle 1 (MPS1) Inhibitors and Enables the Discovery of the Phase 1 Clinical Candidate N<sup>2</sup>-(2-Ethoxy-4-(4-methyl-4 H-1,2,4-triazol-3-yl)phenyl)-6-methyl- N<sup>8</sup>-neopentylpyrido[3,4- d]pyrimidine-2,8-diamine (BOS172722)
Hannah L Woodward, Paolo Innocenti, Kwai-Ming J Cheung, et al.
Molecular Cancer Therapeutics
|
April 14, 2007
Inhibition of the heat shock protein 90 molecular chaperone in vitro and in vivo by novel, synthetic, potent resorcinylic pyrazole/isoxazole amide analogues
Swee Y Sharp, Chrisostomos Prodromou, Kathy Boxall, et al.
Journal of Medicinal Chemistry
|
November 22, 2013
Structure-based design of orally bioavailable 1H-pyrrolo[3,2-c]pyridine inhibitors of mitotic kinase monopolar spindle 1 (MPS1)
Sébastien Naud, Isaac M Westwood, Amir Faisal, et al.
Journal of Medicinal Chemistry
|
November 30, 2021
Into Deep Water: Optimizing BCL6 Inhibitors by Growing into a Solvated Pocket
Matthew G Lloyd, Rosemary Huckvale, Kwai-Ming J Cheung, et al.
Journal of Medicinal Chemistry
|
June 3, 2022
Optimizing Shape Complementarity Enables the Discovery of Potent Tricyclic BCL6 Inhibitors
Owen A Davis, Kwai-Ming J Cheung, Alfie Brennan, et al.
Perspectives on Medical Education
|
March 25, 2024
Competence By Design: a transformational national model of time-variable competency-based postgraduate medical education
Jason R Frank, Jolanta Karpinski, Jonathan Sherbino, et al.
Journal of Medicinal Chemistry
|
November 25, 2011
Structure-guided evolution of potent and selective CHK1 inhibitors through scaffold morphing
John C Reader, Thomas P Matthews, Suki Klair, et al.
Journal of Medicinal Chemistry
|
April 7, 2023
Discovery of an <i>In Vivo</i> Chemical Probe for BCL6 Inhibition by Optimization of Tricyclic Quinolinones
Alice C Harnden, Owen A Davis, Gary M Box, et al.
Page
of 30