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J F MacDonald

Showing results (171-180 of 210) with videos related to

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ACS Medicinal Chemistry Letters|February 21, 2015
Relative binding affinities of integrin antagonists by equilibrium dialysis and liquid chromatography-mass spectrometryWilliam J Tipping, Nkazimulo Tshuma, James Adams, et al.
Nature|August 14, 1997
Recruitment of functional GABA(A) receptors to postsynaptic domains by insulinQ Wan, Z G Xiong, H Y Man, et al.
The Journal of Biological Chemistry|July 5, 1996
Platelet-derived growth factor induces a long-term inhibition of N-methyl-D-aspartate receptor functionC F Valenzuela, Z Xiong, J F MacDonald, et al.
Journal of Neurochemistry|July 1, 1993
A comparison of two alternatively spliced forms of a metabotropic glutamate receptor coupled to phosphoinositide turnoverD S Pickering, C Thomsen, P D Suzdak, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 5, 2020
Late-Stage Functionalization by Chan-Lam Amination: Rapid Access to Potent and Selective Integrin InhibitorsHenry Robinson, Steven A Oatley, James E Rowedder, et al.
Journal of Chemical Information and Modeling|May 13, 2009
Analysis of neighborhood behavior in lead optimization and array designGeorge Papadatos, Anthony W J Cooper, Visakan Kadirkamanathan, et al.
Organic & Biomolecular Chemistry|May 27, 2016
Synthesis and determination of absolute configuration of a non-peptidic αvβ6 integrin antagonist for the treatment of idiopathic pulmonary fibrosisNiall A Anderson, Ian B Campbell, Brendan J Fallon, et al.
Neuron|March 10, 2001
CAKbeta/Pyk2 kinase is a signaling link for induction of long-term potentiation in CA1 hippocampusY Huang, W Lu, D W Ali, et al.
Journal of Medicinal Chemistry|January 28, 2017
Design and Elaboration of a Tractable Tricyclic Scaffold To Synthesize Druglike Inhibitors of Dipeptidyl Peptidase-4 (DPP-4), Antagonists of the C-C Chemokine Receptor Type 5 (CCR5), and Highly Potent and Selective Phosphoinositol-3 Kinase δ (PI3Kδ) InhibitorsCarolin Schwehm, Barrie Kellam, Aimie E Garces, et al.
Chemmedchem|June 18, 2019
The Design of Potent, Selective and Drug-Like RGD αvβ1 Small-Molecule Inhibitors Derived from non-RGD α4β1 AntagonistsRichard J D Hatley, Tim N Barrett, Robert J Slack, et al.
Pageof 21

Showing results (171-180 of 210) with videos related to

Sort By:
Pageof 21
ACS Medicinal Chemistry Letters|February 21, 2015
Relative binding affinities of integrin antagonists by equilibrium dialysis and liquid chromatography-mass spectrometryWilliam J Tipping, Nkazimulo Tshuma, James Adams, et al.
Nature|August 14, 1997
Recruitment of functional GABA(A) receptors to postsynaptic domains by insulinQ Wan, Z G Xiong, H Y Man, et al.
The Journal of Biological Chemistry|July 5, 1996
Platelet-derived growth factor induces a long-term inhibition of N-methyl-D-aspartate receptor functionC F Valenzuela, Z Xiong, J F MacDonald, et al.
Journal of Neurochemistry|July 1, 1993
A comparison of two alternatively spliced forms of a metabotropic glutamate receptor coupled to phosphoinositide turnoverD S Pickering, C Thomsen, P D Suzdak, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 5, 2020
Late-Stage Functionalization by Chan-Lam Amination: Rapid Access to Potent and Selective Integrin InhibitorsHenry Robinson, Steven A Oatley, James E Rowedder, et al.
Journal of Chemical Information and Modeling|May 13, 2009
Analysis of neighborhood behavior in lead optimization and array designGeorge Papadatos, Anthony W J Cooper, Visakan Kadirkamanathan, et al.
Organic & Biomolecular Chemistry|May 27, 2016
Synthesis and determination of absolute configuration of a non-peptidic αvβ6 integrin antagonist for the treatment of idiopathic pulmonary fibrosisNiall A Anderson, Ian B Campbell, Brendan J Fallon, et al.
Neuron|March 10, 2001
CAKbeta/Pyk2 kinase is a signaling link for induction of long-term potentiation in CA1 hippocampusY Huang, W Lu, D W Ali, et al.
Journal of Medicinal Chemistry|January 28, 2017
Design and Elaboration of a Tractable Tricyclic Scaffold To Synthesize Druglike Inhibitors of Dipeptidyl Peptidase-4 (DPP-4), Antagonists of the C-C Chemokine Receptor Type 5 (CCR5), and Highly Potent and Selective Phosphoinositol-3 Kinase δ (PI3Kδ) InhibitorsCarolin Schwehm, Barrie Kellam, Aimie E Garces, et al.
Chemmedchem|June 18, 2019
The Design of Potent, Selective and Drug-Like RGD αvβ1 Small-Molecule Inhibitors Derived from non-RGD α4β1 AntagonistsRichard J D Hatley, Tim N Barrett, Robert J Slack, et al.
Pageof 21