Defining the Molecular Basis for the First Potent and Selective Orthosteric Agonists of the FFA2 Free Fatty Acid Receptor-Reference-Cited by-同舟云学术

Defining the Molecular Basis for the First Potent and Selective Orthosteric Agonists of the FFA2 Free Fatty Acid Receptor

Published:2013-06 Issue:24 Volume:288 Page:17296-17312
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Hudson Brian D.,Due-Hansen Maria E.,Christiansen Elisabeth,Hansen Anna Mette,Mackenzie Amanda E.,Murdoch Hannah,Pandey Sunil K.,Ward Richard J.,Marquez Rudi,Tikhonova Irina G.,Ulven Trond,Milligan Graeme

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

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4. Experimental challenges to targeting poorly characterized GPCRs. Uncovering the therapeutic potential for free fatty acid receptors;Hudson;Adv. Pharmacol,2011

5. The orphan G Protein-coupled Receptors GPR41 and GPR43 are activated by propionate and other short chain carboxylic acids;Brown;J. Biol. Chem,2003

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