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Jian-Nong Ma

Showing results (1-10 of 26) with videos related to

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The Journal of Pharmacology and Experimental Therapeutics|October 1, 2013
The protease activated receptor 2 (PAR2) polymorphic variant F240S constitutively activates PAR2 receptors and potentiates responses to small-molecule PAR2 agonistsJian-Nong Ma, Ethan S Burstein
ACS Chemical Neuroscience|July 27, 2016
Estrogen Receptor Beta Selective Agonists as Agents to Treat Chemotherapeutic-Induced Neuropathic PainJian-Nong Ma, Krista McFarland, Roger Olsson, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 9, 2013
Identification of the antiarrhythmic drugs amiodarone and lorcainide as potent H3 histamine receptor inverse agonistsAndria L Del Tredici, Jian-Nong Ma, Fabrice Piu, et al.
Oncogene|January 9, 2004
G-protein-coupled receptor-mediated activation of rap GTPases: characterization of a novel Galphai regulated pathwayJacques T Weissman, Jian-Nong Ma, Anthony Essex, et al.
ACS Chemical Neuroscience|October 15, 2013
Low dose bexarotene treatment rescues dopamine neurons and restores behavioral function in models of Parkinson's diseaseKrista McFarland, Tracy A Spalding, David Hubbard, et al.
Chemmedchem|June 21, 2013
Design of a highly selective and potent class of non-planar estrogen receptor β agonistsHenrik Sundén, Jian-Nong Ma, Lars K Hansen, et al.
Bioorganic & Medicinal Chemistry Letters|February 24, 2009
Discovery of non-peptidergic MrgX1 and MrgX2 receptor agonists and exploration of an initial SAR using solid-phase synthesisLeila Malik, Nicholas M Kelly, Jian-Nong Ma, et al.
Bioorganic & Medicinal Chemistry|June 24, 2010
Optimization of isochromanone based urotensin II receptor agonistsFredrik Lehmann, Erika A Currier, Roger Olsson, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|August 26, 2011
II. In vitro evidence that (-)-OSU6162 and (+)-OSU6162 produce their behavioral effects through 5-HT2A serotonin and D2 dopamine receptorsEthan S Burstein, Maria L Carlsson, Michelle Owens, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 18, 2011
Characterization of highly efficacious allosteric agonists of the human calcium-sensing receptorJian-Nong Ma, Michelle Owens, Magnus Gustafsson, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
The Journal of Pharmacology and Experimental Therapeutics|October 1, 2013
The protease activated receptor 2 (PAR2) polymorphic variant F240S constitutively activates PAR2 receptors and potentiates responses to small-molecule PAR2 agonistsJian-Nong Ma, Ethan S Burstein
ACS Chemical Neuroscience|July 27, 2016
Estrogen Receptor Beta Selective Agonists as Agents to Treat Chemotherapeutic-Induced Neuropathic PainJian-Nong Ma, Krista McFarland, Roger Olsson, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 9, 2013
Identification of the antiarrhythmic drugs amiodarone and lorcainide as potent H3 histamine receptor inverse agonistsAndria L Del Tredici, Jian-Nong Ma, Fabrice Piu, et al.
Oncogene|January 9, 2004
G-protein-coupled receptor-mediated activation of rap GTPases: characterization of a novel Galphai regulated pathwayJacques T Weissman, Jian-Nong Ma, Anthony Essex, et al.
ACS Chemical Neuroscience|October 15, 2013
Low dose bexarotene treatment rescues dopamine neurons and restores behavioral function in models of Parkinson's diseaseKrista McFarland, Tracy A Spalding, David Hubbard, et al.
Chemmedchem|June 21, 2013
Design of a highly selective and potent class of non-planar estrogen receptor β agonistsHenrik Sundén, Jian-Nong Ma, Lars K Hansen, et al.
Bioorganic & Medicinal Chemistry Letters|February 24, 2009
Discovery of non-peptidergic MrgX1 and MrgX2 receptor agonists and exploration of an initial SAR using solid-phase synthesisLeila Malik, Nicholas M Kelly, Jian-Nong Ma, et al.
Bioorganic & Medicinal Chemistry|June 24, 2010
Optimization of isochromanone based urotensin II receptor agonistsFredrik Lehmann, Erika A Currier, Roger Olsson, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|August 26, 2011
II. In vitro evidence that (-)-OSU6162 and (+)-OSU6162 produce their behavioral effects through 5-HT2A serotonin and D2 dopamine receptorsEthan S Burstein, Maria L Carlsson, Michelle Owens, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 18, 2011
Characterization of highly efficacious allosteric agonists of the human calcium-sensing receptorJian-Nong Ma, Michelle Owens, Magnus Gustafsson, et al.
Pageof 3