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2008, Progress in brain research, ISBN 0444532358, Volume 172., xv, 665 p. [6] p. of plates
This book provides a unique and timely multidisciplinary synthesis of our current knowledge of the anatomy, pharmacology, physiology and behavioral data of the... 
Neurochemistry | Neurotransmitters | Dopamine | Serotonin | Neurochimie
Book
1997, Lung biology in health and disease, ISBN 9780824794965, Volume 106, xvi, 443
Book
Journal of Pharmacology and Experimental Therapeutics, ISSN 0022-3565, 04/2007, Volume 321, Issue 1, pp. 308 - 317
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 08/2014, Volume 289, Issue 31, pp. 21795 - 21806
The α4β2 nicotinic acetylcholine receptor (nAChR) is the most abundant nAChR type in the brain, and this receptor type exists in alternate (α4β2)2α4 and... 
Ligands | Receptors, Nicotinic - metabolism | Animals | Receptors, Nicotinic - genetics | Xenopus laevis | Nicotinic Agonists - pharmacology | Nicotinic Acetylcholine Receptor (nAChR) | Electrophysiology | Ligand-binding Protein | Receptor Structure-Function | Cys-loop Receptor | Neurobiology
Journal Article
NATURE, ISSN 0028-0836, 01/2011, Volume 469, Issue 7329, pp. 241 - 244
beta-adrenergic receptors (beta ARs) are G-protein-coupled receptors (GPCRs) that activate intracellular G proteins upon binding catecholamine agonist ligands... 
CRYSTALLIZATION | AMINO-ACID | ACTIVATION | LIGAND-BINDING | BETA-ADRENERGIC-RECEPTORS | PROTEIN-COUPLED RECEPTOR | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | CRYSTALLOGRAPHY | HIGH-AFFINITY BINDING | BETA-ADRENERGIC RECEPTOR | Dobutamine - metabolism | Hydroxyquinolines - chemistry | Catecholamines - metabolism | Albuterol - pharmacology | Amphetamines - pharmacology | Adrenergic beta-1 Receptor Antagonists - pharmacology | Crystallography, X-Ray | Adrenergic beta-1 Receptor Agonists - chemistry | Structure-Activity Relationship | Receptors, Adrenergic, beta-1 - chemistry | Adrenergic beta-1 Receptor Agonists - pharmacology | Turkeys | Adrenergic beta-1 Receptor Antagonists - chemistry | Drug Design | Adrenergic beta-1 Receptor Antagonists - metabolism | Dobutamine - chemistry | Isoproterenol - chemistry | Binding Sites | Hydroxyquinolines - pharmacology | Amphetamines - chemistry | Drug Partial Agonism | Albuterol - metabolism | Hydroxyquinolines - metabolism | Isoproterenol - metabolism | Models, Molecular | Receptors, Adrenergic, beta-1 - metabolism | Serine - chemistry | Serine - metabolism | Dobutamine - pharmacology | Animals | Hydrogen Bonding | Amphetamines - metabolism | Isoproterenol - pharmacology | Protein Stability - drug effects | Albuterol - chemistry | Ligands | Protein Conformation | Adrenergic beta-1 Receptor Agonists - metabolism
Journal Article
Journal Article
Journal Article
British Journal of Pharmacology, ISSN 0007-1188, 02/1999, Volume 126, Issue 3, pp. 665 - 672
We have tested our prediction that AM630 is a CB2 cannabinoid receptor ligand and also investigated whether L759633 and L759656, are CB2 receptor agonists.... 
AM630 | CB2‐selective ligands | L759656 | CB2‐selective inverse agonist | [35S]‐GTPγS | CB2‐selective agonist | cyclic AMP | Cannabinoid CB1 and CB2 receptors | L759633 | Cannabinoid CB | selective agonist | receptors | Cyclic AMP | selective ligands | and CB | selective inverse agonist | S]-GTPγS | ANTAGONIST | cannabinoid CB1 and CB2 receptors | [S-35]-GTP gamma S | CB2-selective agonist | CB2-selective ligands | CB2-selective inverse agonist | PHARMACOLOGY | PHARMACOLOGY & PHARMACY | BINDING | BRAIN | Guanosine 5'-O-(3-Thiotriphosphate) - pharmacology | Cannabinoids - antagonists & inhibitors | Humans | Bornanes - pharmacology | Tritium | Benzoxazines | Receptors, Drug - agonists | Cyclohexanols - metabolism | Chromans - pharmacology | Indoles - pharmacology | Cyclohexanols - pharmacology | Radioligand Assay | Naphthalenes - metabolism | Cannabinoids - metabolism | Cyclic AMP - metabolism | CHO Cells | Pyrazoles - pharmacology | Cricetinae | Colforsin - pharmacology | Morpholines - pharmacology | Morpholines - metabolism | Pyrazoles - metabolism | Receptors, Drug - metabolism | Naphthalenes - pharmacology | Binding, Competitive - drug effects | Guanosine 5'-O-(3-Thiotriphosphate) - metabolism | Animals | Bornanes - metabolism | Receptors, Cannabinoid | Receptors, Drug - antagonists & inhibitors | Papers | [35S]-GTPγS
Journal Article
Journal Article
NeuroImage, ISSN 1053-8119, 04/2016, Volume 130, pp. 167 - 174
[11C]Cimbi-36 is a recently developed serotonin 2A (5-HT2A) receptor agonist positron emission tomography (PET) radioligand that has been successfully applied... 
Neuroimaging | Agonist | 5-HT | Positron emission tomography | Radiotracer evaluation | Test–retest variability | Test-retest variability | SURFACE-BASED ANALYSIS | SYSTEM | LOCALIZATION | BOLUS/INFUSION APPROACH | QUANTIFICATION | BEHAVIOR | 5-HT2A RECEPTOR | RATS | NEUROSCIENCES | POSITRON-EMISSION-TOMOGRAPHY | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | PET RADIOLIGAND | Serotonin 5-HT2 Receptor Agonists - pharmacokinetics | Humans | Ketanserin - analogs & derivatives | Male | Benzylamines - metabolism | Brain - metabolism | Young Adult | Radiopharmaceuticals - metabolism | Fluorine Radioisotopes - pharmacokinetics | Phenethylamines - pharmacokinetics | Female | Serotonin 5-HT2 Receptor Agonists - metabolism | Neuroimaging - methods | Reproducibility of Results | Radiopharmaceuticals - pharmacokinetics | Carbon Radioisotopes - pharmacokinetics | Phenethylamines - metabolism | Positron-Emission Tomography - methods | Serotonin 5-HT2 Receptor Antagonists - pharmacokinetics | Ketanserin - metabolism | Ketanserin - pharmacokinetics | Serotonin 5-HT2 Receptor Antagonists - metabolism | Fluorine Radioisotopes - metabolism | Carbon Radioisotopes - metabolism | Benzylamines - pharmacokinetics | Phenols | Brain | Serotonin | Analysis | Choroid plexus | Medical imaging | Lysergic acid diethylamide--LSD | Cortex | Radioisotopes | Serotonin S2 receptors | Tomography | Receptor density | Agonists | Hippocampus
Journal Article