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Sara Marsango

Showing results (11-20 of 30) with videos related to

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The Journal of Biological Chemistry|April 16, 2016
Dynamic Regulation of Quaternary Organization of the M1 Muscarinic Receptor by Subtype-selective Antagonist DrugsJohn D Pediani, Richard J Ward, Antoine G Godin, et al.
Springerplus|July 8, 2016
Defining the organizational structure of dopamine and muscarninic acetylcholine receptorsGraeme Milligan, María José Varela Liste, Gianluigi Caltabiano Caltabiano, et al.
Molecular Pharmacology|March 15, 2015
The molecular basis of oligomeric organization of the human M3 muscarinic acetylcholine receptorMaría José Varela Liste, Gianluigi Caltabiano, Richard J Ward, et al.
Scientific Reports|May 20, 2017
A Molecular Basis for Selective Antagonist Destabilization of Dopamine D<sub>3</sub> Receptor Quaternary OrganizationSara Marsango, Gianluigi Caltabiano, Mireia Jiménez-Rosés, et al.
The Journal of Biological Chemistry|December 3, 2020
Chemokine receptor CXCR4 oligomerization is disrupted selectively by the antagonist ligand IT1tRichard J Ward, John D Pediani, Sara Marsango, et al.
Nature|June 18, 2025
Allosteric modulation and biased signalling at free fatty acid receptor 2Xuan Zhang, Abdul-Akim Guseinov, Laura Jenkins, et al.
ACS Pharmacology & Translational Science|October 18, 2021
Discovery and Characterization of Novel Antagonists of the Proinflammatory Orphan Receptor GPR84Laura Jenkins, Sara Marsango, Sarah Mancini, et al.
The Journal of Biological Chemistry|April 15, 2022
Selective phosphorylation of threonine residues defines GPR84-arrestin interactions of biased ligandsSara Marsango, Richard J Ward, Laura Jenkins, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 7, 2022
The M<sub>1</sub> muscarinic receptor is present in situ as a ligand-regulated mixture of monomers and oligomeric complexesSara Marsango, Laura Jenkins, John D Pediani, et al.
Journal of Medicinal Chemistry|August 10, 2022
Investigating the Structure-Activity Relationship of 1,2,4-Triazine G-Protein-Coupled Receptor 84 (GPR84) AntagonistsAmit Mahindra, Laura Jenkins, Sara Marsango, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
The Journal of Biological Chemistry|April 16, 2016
Dynamic Regulation of Quaternary Organization of the M1 Muscarinic Receptor by Subtype-selective Antagonist DrugsJohn D Pediani, Richard J Ward, Antoine G Godin, et al.
Springerplus|July 8, 2016
Defining the organizational structure of dopamine and muscarninic acetylcholine receptorsGraeme Milligan, María José Varela Liste, Gianluigi Caltabiano Caltabiano, et al.
Molecular Pharmacology|March 15, 2015
The molecular basis of oligomeric organization of the human M3 muscarinic acetylcholine receptorMaría José Varela Liste, Gianluigi Caltabiano, Richard J Ward, et al.
Scientific Reports|May 20, 2017
A Molecular Basis for Selective Antagonist Destabilization of Dopamine D<sub>3</sub> Receptor Quaternary OrganizationSara Marsango, Gianluigi Caltabiano, Mireia Jiménez-Rosés, et al.
The Journal of Biological Chemistry|December 3, 2020
Chemokine receptor CXCR4 oligomerization is disrupted selectively by the antagonist ligand IT1tRichard J Ward, John D Pediani, Sara Marsango, et al.
Nature|June 18, 2025
Allosteric modulation and biased signalling at free fatty acid receptor 2Xuan Zhang, Abdul-Akim Guseinov, Laura Jenkins, et al.
ACS Pharmacology & Translational Science|October 18, 2021
Discovery and Characterization of Novel Antagonists of the Proinflammatory Orphan Receptor GPR84Laura Jenkins, Sara Marsango, Sarah Mancini, et al.
The Journal of Biological Chemistry|April 15, 2022
Selective phosphorylation of threonine residues defines GPR84-arrestin interactions of biased ligandsSara Marsango, Richard J Ward, Laura Jenkins, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 7, 2022
The M<sub>1</sub> muscarinic receptor is present in situ as a ligand-regulated mixture of monomers and oligomeric complexesSara Marsango, Laura Jenkins, John D Pediani, et al.
Journal of Medicinal Chemistry|August 10, 2022
Investigating the Structure-Activity Relationship of 1,2,4-Triazine G-Protein-Coupled Receptor 84 (GPR84) AntagonistsAmit Mahindra, Laura Jenkins, Sara Marsango, et al.
Pageof 3