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BAY is a potent (IC50 = μM) and selective antagonist at mGlu1 receptors and inhibits >60% of mGlu1a receptor constitutive activity (IC50 = μM). , McGrane, V.
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This module is connected to a heptahelical domain that activates G proteins. , Gomeza, J. , Haldeman, B. Our goal is to instill essential life skills, including health. Recently, the structure of the dimer of mGlu1 VFTMs revealed two important.
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Here, using molecular modeling and site-directed mutagenesis, we have identified residues in the GABAB1 subunit that are critical for agonist. A.
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