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Brian D Hudson

Showing results (31-40 of 60) with videos related to

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Molecular Pharmacology|February 14, 2016
Distinct Phosphorylation Clusters Determine the Signaling Outcome of Free Fatty Acid Receptor 4/G Protein-Coupled Receptor 120Rudi Prihandoko, Elisa Alvarez-Curto, Brian D Hudson, et al.
The Journal of Biological Chemistry|February 1, 2022
Agonist-induced phosphorylation of orthologues of the orphan receptor GPR35 functions as an activation sensorNina Divorty, Laura Jenkins, Amlan Ganguly, et al.
Plos One|January 19, 2012
Mechanism and function of Drosophila capa GPCR: a desiccation stress-responsive receptor with functional homology to human neuromedinU receptorSelim Terhzaz, Pablo Cabrero, Joris H Robben, et al.
Scientific Reports|October 25, 2017
A single extracellular amino acid in Free Fatty Acid Receptor 2 defines antagonist species selectivity and G protein selection biasEugenia Sergeev, Anders Højgaard Hansen, Daniele Bolognini, et al.
Scientific Reports|December 22, 2017
Three classes of ligands each bind to distinct sites on the orphan G protein-coupled receptor GPR84Zobaer Al Mahmud, Laura Jenkins, Trond Ulven, et al.
The Biochemical Journal|October 6, 2010
Identification of novel species-selective agonists of the G-protein-coupled receptor GPR35 that promote recruitment of β-arrestin-2 and activate Gα13Laura Jenkins, Jose Brea, Nicola J Smith, et al.
Journal of Chemical Information and Computer Sciences|March 26, 2003
A consensus neural network-based technique for discriminating soluble and poorly soluble compoundsDavid T Manallack, Benjamin G Tehan, Emanuela Gancia, et al.
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|January 12, 2011
Selective orthosteric free fatty acid receptor 2 (FFA2) agonists: identification of the structural and chemical requirements for selective activation of FFA2 versus FFA3Johannes Schmidt, Nicola J Smith, Elisabeth Christiansen, 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.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Molecular Pharmacology|February 14, 2016
Distinct Phosphorylation Clusters Determine the Signaling Outcome of Free Fatty Acid Receptor 4/G Protein-Coupled Receptor 120Rudi Prihandoko, Elisa Alvarez-Curto, Brian D Hudson, et al.
The Journal of Biological Chemistry|February 1, 2022
Agonist-induced phosphorylation of orthologues of the orphan receptor GPR35 functions as an activation sensorNina Divorty, Laura Jenkins, Amlan Ganguly, et al.
Plos One|January 19, 2012
Mechanism and function of Drosophila capa GPCR: a desiccation stress-responsive receptor with functional homology to human neuromedinU receptorSelim Terhzaz, Pablo Cabrero, Joris H Robben, et al.
Scientific Reports|October 25, 2017
A single extracellular amino acid in Free Fatty Acid Receptor 2 defines antagonist species selectivity and G protein selection biasEugenia Sergeev, Anders Højgaard Hansen, Daniele Bolognini, et al.
Scientific Reports|December 22, 2017
Three classes of ligands each bind to distinct sites on the orphan G protein-coupled receptor GPR84Zobaer Al Mahmud, Laura Jenkins, Trond Ulven, et al.
The Biochemical Journal|October 6, 2010
Identification of novel species-selective agonists of the G-protein-coupled receptor GPR35 that promote recruitment of β-arrestin-2 and activate Gα13Laura Jenkins, Jose Brea, Nicola J Smith, et al.
Journal of Chemical Information and Computer Sciences|March 26, 2003
A consensus neural network-based technique for discriminating soluble and poorly soluble compoundsDavid T Manallack, Benjamin G Tehan, Emanuela Gancia, et al.
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|January 12, 2011
Selective orthosteric free fatty acid receptor 2 (FFA2) agonists: identification of the structural and chemical requirements for selective activation of FFA2 versus FFA3Johannes Schmidt, Nicola J Smith, Elisabeth Christiansen, 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.
Pageof 6