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W Lindsley

Showing results (411-420 of 570) with videos related to

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ACS Medicinal Chemistry Letters|September 28, 2018
VU6007477, a Novel M<sub>1</sub> PAM Based on a Pyrrolo[2,3-<i>b</i>]pyridine Carboxamide Core Devoid of Cholinergic Adverse EventsJulie L Engers, Elizabeth S Childress, Madeline F Long, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|March 28, 2018
M<sub>1</sub>-positive allosteric modulators lacking agonist activity provide the optimal profile for enhancing cognitionSean P Moran, Jonathan W Dickerson, Hyekyung P Cho, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 2, 2014
Specific activin receptor-like kinase 3 inhibitors enhance liver regenerationDaisuke Tsugawa, Yuki Oya, Ryota Masuzaki, et al.
Journal of Medicinal Chemistry|November 26, 2014
Discovery of (S)-2-cyclopentyl-N-((1-isopropylpyrrolidin2-yl)-9-methyl-1-oxo-2,9-dihydro-1H-pyrrido[3,4-b]indole-4-carboxamide (VU0453379): a novel, CNS penetrant glucagon-like peptide 1 receptor (GLP-1R) positive allosteric modulator (PAM)Lindsey C Morris, Kellie D Nance, Patrick R Gentry, et al.
Human Molecular Genetics|March 4, 2016
mGlu5 positive allosteric modulation normalizes synaptic plasticity defects and motor phenotypes in a mouse model of Rett syndromeRocco G Gogliotti, Rebecca K Senter, Jerri M Rook, et al.
Bioorganic & Medicinal Chemistry Letters|September 2, 2014
Substituted indoles as selective protease activated receptor 4 (PAR-4) antagonists: Discovery and SAR of ML354Wandong Wen, Summer E Young, Matthew T Duvernay, et al.
Neuropharmacology|July 22, 2017
Cognitive enhancement and antipsychotic-like activity following repeated dosing with the selective M<sub>4</sub> PAM VU0467154Robert W Gould, Michael D Grannan, Barak W Gunter, et al.
Journal of Medicinal Chemistry|January 5, 2019
Discovery of an Orally Bioavailable and Central Nervous System (CNS) Penetrant mGlu<sub>7</sub> Negative Allosteric Modulator (NAM) in Vivo Tool Compound: N-(2-(1 H-1,2,4-triazol-1-yl)-5-(trifluoromethoxy)phenyl)-4-(cyclopropylmethoxy)-3-methoxybenzamide (VU6012962)Carson W Reed, Samantha E Yohn, Jordan P Washecheck, et al.
Plos One|October 5, 2011
Impaired striatal Akt signaling disrupts dopamine homeostasis and increases feedingNicole Speed, Christine Saunders, Adeola R Davis, et al.
ACS Chemical Biology|August 20, 2014
Chemical modulation of mutant mGlu1 receptors derived from deleterious GRM1 mutations found in schizophrenicsHyekyung P Cho, Pedro M Garcia-Barrantes, John T Brogan, et al.
Pageof 57

Showing results (411-420 of 570) with videos related to

Sort By:
Pageof 57
ACS Medicinal Chemistry Letters|September 28, 2018
VU6007477, a Novel M<sub>1</sub> PAM Based on a Pyrrolo[2,3-<i>b</i>]pyridine Carboxamide Core Devoid of Cholinergic Adverse EventsJulie L Engers, Elizabeth S Childress, Madeline F Long, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|March 28, 2018
M<sub>1</sub>-positive allosteric modulators lacking agonist activity provide the optimal profile for enhancing cognitionSean P Moran, Jonathan W Dickerson, Hyekyung P Cho, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 2, 2014
Specific activin receptor-like kinase 3 inhibitors enhance liver regenerationDaisuke Tsugawa, Yuki Oya, Ryota Masuzaki, et al.
Journal of Medicinal Chemistry|November 26, 2014
Discovery of (S)-2-cyclopentyl-N-((1-isopropylpyrrolidin2-yl)-9-methyl-1-oxo-2,9-dihydro-1H-pyrrido[3,4-b]indole-4-carboxamide (VU0453379): a novel, CNS penetrant glucagon-like peptide 1 receptor (GLP-1R) positive allosteric modulator (PAM)Lindsey C Morris, Kellie D Nance, Patrick R Gentry, et al.
Human Molecular Genetics|March 4, 2016
mGlu5 positive allosteric modulation normalizes synaptic plasticity defects and motor phenotypes in a mouse model of Rett syndromeRocco G Gogliotti, Rebecca K Senter, Jerri M Rook, et al.
Bioorganic & Medicinal Chemistry Letters|September 2, 2014
Substituted indoles as selective protease activated receptor 4 (PAR-4) antagonists: Discovery and SAR of ML354Wandong Wen, Summer E Young, Matthew T Duvernay, et al.
Neuropharmacology|July 22, 2017
Cognitive enhancement and antipsychotic-like activity following repeated dosing with the selective M<sub>4</sub> PAM VU0467154Robert W Gould, Michael D Grannan, Barak W Gunter, et al.
Journal of Medicinal Chemistry|January 5, 2019
Discovery of an Orally Bioavailable and Central Nervous System (CNS) Penetrant mGlu<sub>7</sub> Negative Allosteric Modulator (NAM) in Vivo Tool Compound: N-(2-(1 H-1,2,4-triazol-1-yl)-5-(trifluoromethoxy)phenyl)-4-(cyclopropylmethoxy)-3-methoxybenzamide (VU6012962)Carson W Reed, Samantha E Yohn, Jordan P Washecheck, et al.
Plos One|October 5, 2011
Impaired striatal Akt signaling disrupts dopamine homeostasis and increases feedingNicole Speed, Christine Saunders, Adeola R Davis, et al.
ACS Chemical Biology|August 20, 2014
Chemical modulation of mutant mGlu1 receptors derived from deleterious GRM1 mutations found in schizophrenicsHyekyung P Cho, Pedro M Garcia-Barrantes, John T Brogan, et al.
Pageof 57