Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

B Tobin

Showing results (231-240 of 292) with videos related to

Pageof 30
Sort By:
Molecular Pharmacology|August 28, 2013
The pharmacology of TUG-891, a potent and selective agonist of the free fatty acid receptor 4 (FFA4/GPR120), demonstrates both potential opportunity and possible challenges to therapeutic agonismBrian D Hudson, Bharat Shimpukade, Amanda E Mackenzie, et al.
The Journal of Biological Chemistry|September 3, 2023
G protein-receptor kinases 5/6 are the key regulators of G protein-coupled receptor 35-arrestin interactionsAmlan Ganguly, Tezz Quon, Laura Jenkins, et al.
ACS Chemical Neuroscience|November 16, 2020
Restoring Agonist Function at a Chemogenetically Modified M<sub>1</sub> Muscarinic Acetylcholine ReceptorElham Khajehali, Sophie Bradley, Emma T van der Westhuizen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 3, 2019
Receptor selectivity between the G proteins Gα<sub>12</sub> and Gα<sub>13</sub> is defined by a single leucine-to-isoleucine variationAmanda E Mackenzie, Tezz Quon, Li-Chiung Lin, et al.
Scientific Reports|March 4, 2016
Distinct phosphorylation sites on the ghrelin receptor, GHSR1a, establish a code that determines the functions of ß-arrestinsMonica Bouzo-Lorenzo, Icía Santo-Zas, Maria Lodeiro, 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.
Journal of Medicinal Chemistry|January 31, 2026
Shaping Antimalarials: A Geometry-First Approach to <i>Pf</i>CLK3 Covalent InhibitorsSkye B Brettell, Carla Fuentes-Guerra Bustos, Saumya Sharma, 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.
Proceedings of the National Academy of Sciences of the United States of America|October 20, 2025
Museum genomics suggests long-term population decline in a putatively extinct bumble beeRena M Schweizer, Jared A Grummer, Kerrigan B Tobin, et al.
Pageof 30

Showing results (231-240 of 292) with videos related to

Sort By:
Pageof 30
Molecular Pharmacology|August 28, 2013
The pharmacology of TUG-891, a potent and selective agonist of the free fatty acid receptor 4 (FFA4/GPR120), demonstrates both potential opportunity and possible challenges to therapeutic agonismBrian D Hudson, Bharat Shimpukade, Amanda E Mackenzie, et al.
The Journal of Biological Chemistry|September 3, 2023
G protein-receptor kinases 5/6 are the key regulators of G protein-coupled receptor 35-arrestin interactionsAmlan Ganguly, Tezz Quon, Laura Jenkins, et al.
ACS Chemical Neuroscience|November 16, 2020
Restoring Agonist Function at a Chemogenetically Modified M<sub>1</sub> Muscarinic Acetylcholine ReceptorElham Khajehali, Sophie Bradley, Emma T van der Westhuizen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 3, 2019
Receptor selectivity between the G proteins Gα<sub>12</sub> and Gα<sub>13</sub> is defined by a single leucine-to-isoleucine variationAmanda E Mackenzie, Tezz Quon, Li-Chiung Lin, et al.
Scientific Reports|March 4, 2016
Distinct phosphorylation sites on the ghrelin receptor, GHSR1a, establish a code that determines the functions of ß-arrestinsMonica Bouzo-Lorenzo, Icía Santo-Zas, Maria Lodeiro, 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.
Journal of Medicinal Chemistry|January 31, 2026
Shaping Antimalarials: A Geometry-First Approach to <i>Pf</i>CLK3 Covalent InhibitorsSkye B Brettell, Carla Fuentes-Guerra Bustos, Saumya Sharma, 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.
Proceedings of the National Academy of Sciences of the United States of America|October 20, 2025
Museum genomics suggests long-term population decline in a putatively extinct bumble beeRena M Schweizer, Jared A Grummer, Kerrigan B Tobin, et al.
Pageof 30