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Neuron
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June 20, 2014
Triad3A regulates synaptic strength by ubiquitination of Arc
Angela M Mabb, H Shawn Je, Mark J Wall, et al.
Neuropharmacology
|
February 13, 2022
The comparative effects of mGlu5 receptor positive allosteric modulators VU0409551 and VU0360172 on cognitive deficits and signalling in the sub-chronic PCP rat model for schizophrenia
Jessica Brown, Luisa Iacovelli, Gabriele Di Cicco, et al.
Neuropharmacology
|
August 10, 2020
Pharmacological activation of mGlu5 receptors with the positive allosteric modulator VU0360172, modulates thalamic GABAergic transmission
Roberta Celli, Mark J Wall, Ines Santolini, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 20, 2018
Discovery and optimization of a novel series of pyrazolyltetrahydropyran N-type calcium channel (Ca<sub>v</sub> 2.2) blockers for the treatment of pain
Mark J Wall, Nalin L Subasinghe, Michael P Winters, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 22, 2012
A novel series of pyrazolylpiperidine N-type calcium channel blockers
Nalin L Subasinghe, Mark J Wall, Michael P Winters, et al.
Neuron
|
June 5, 2018
The Temporal Dynamics of Arc Expression Regulate Cognitive Flexibility
Mark J Wall, Dawn R Collins, Samantha L Chery, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 23, 2008
Structure-based optimization of a potent class of arylamide FMS inhibitors
Sanath K Meegalla, Mark J Wall, Jinsheng Chen, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 5, 2008
Discovery of novel FMS kinase inhibitors as anti-inflammatory agents
Carl R Illig, Jinsheng Chen, Mark J Wall, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 24, 2010
Reducing ion channel activity in a series of 4-heterocyclic arylamide FMS inhibitors
Kenneth J Wilson, Carl R Illig, Jinsheng Chen, et al.
Journal of Medicinal Chemistry
|
November 2, 2011
Optimization of a potent class of arylamide colony-stimulating factor-1 receptor inhibitors leading to anti-inflammatory clinical candidate 4-cyano-N-[2-(1-cyclohexen-1-yl)-4-[1-[(dimethylamino)acetyl]-4-piperidinyl]phenyl]-1H-imidazole-2-carboxamide (JNJ-28312141)
Carl R Illig, Carl L Manthey, Mark J Wall, et al.
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of 8
Search research articles
Search
Showing results (61-70 of 75) with videos related to
Sort By:
Page
of 8
Neuron
|
June 20, 2014
Triad3A regulates synaptic strength by ubiquitination of Arc
Angela M Mabb, H Shawn Je, Mark J Wall, et al.
Neuropharmacology
|
February 13, 2022
The comparative effects of mGlu5 receptor positive allosteric modulators VU0409551 and VU0360172 on cognitive deficits and signalling in the sub-chronic PCP rat model for schizophrenia
Jessica Brown, Luisa Iacovelli, Gabriele Di Cicco, et al.
Neuropharmacology
|
August 10, 2020
Pharmacological activation of mGlu5 receptors with the positive allosteric modulator VU0360172, modulates thalamic GABAergic transmission
Roberta Celli, Mark J Wall, Ines Santolini, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 20, 2018
Discovery and optimization of a novel series of pyrazolyltetrahydropyran N-type calcium channel (Ca<sub>v</sub> 2.2) blockers for the treatment of pain
Mark J Wall, Nalin L Subasinghe, Michael P Winters, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 22, 2012
A novel series of pyrazolylpiperidine N-type calcium channel blockers
Nalin L Subasinghe, Mark J Wall, Michael P Winters, et al.
Neuron
|
June 5, 2018
The Temporal Dynamics of Arc Expression Regulate Cognitive Flexibility
Mark J Wall, Dawn R Collins, Samantha L Chery, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 23, 2008
Structure-based optimization of a potent class of arylamide FMS inhibitors
Sanath K Meegalla, Mark J Wall, Jinsheng Chen, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 5, 2008
Discovery of novel FMS kinase inhibitors as anti-inflammatory agents
Carl R Illig, Jinsheng Chen, Mark J Wall, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 24, 2010
Reducing ion channel activity in a series of 4-heterocyclic arylamide FMS inhibitors
Kenneth J Wilson, Carl R Illig, Jinsheng Chen, et al.
Journal of Medicinal Chemistry
|
November 2, 2011
Optimization of a potent class of arylamide colony-stimulating factor-1 receptor inhibitors leading to anti-inflammatory clinical candidate 4-cyano-N-[2-(1-cyclohexen-1-yl)-4-[1-[(dimethylamino)acetyl]-4-piperidinyl]phenyl]-1H-imidazole-2-carboxamide (JNJ-28312141)
Carl R Illig, Carl L Manthey, Mark J Wall, et al.
Page
of 8