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2007, 1, Frontiers in neuroscience, ISBN 9780849339776, 206
A number of developments spanning a multitude of techniques makes this an exciting time for research in serotonin receptors. A comprehensive review of the... 
Receptors, Serotonin | Receptors | Serotonin | Signal Transduction | Serotoninergic mechanisms | Anatomy | Neuroscience | Biochemistry
Book
Journal of Biological Chemistry, ISSN 0021-9258, 11/2012, Volume 287, Issue 48, pp. 40239 - 40245
Journal Article
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, Handbook of experimental pharmacology, ISBN 9783540626664, Volume 129., xxx, 767
Book
Brain Research Reviews, ISSN 0165-0173, 2007, Volume 58, Issue 2, pp. 415 - 452
Journal Article
Journal Article
1988, ISBN 9780471911548, xii, 555
Book
2006, 1. Aufl., The receptors, ISBN 9781588295682, xvii, 618 p., [4] p. of plates
A comprehensive, state-of-the-art review of our current understanding of the molecular and structural biology of 5-HT receptors and their potential use for... 
Serotonin | Other branches of medicine | Receptors | Physiological effect | Serotoninergic mechanisms | Pharmacy
Book
Journal Article
British Journal of Pharmacology, ISSN 0007-1188, 07/2013, Volume 169, Issue 6, pp. 1252 - 1262
Background and Purpose The 5‐HT3 receptor antagonist palonosetron is an important treatment for emesis and nausea during cancer therapy. Its clinical efficacy... 
cancer therapy | irreversible antagonism | down‐regulation | receptor trafficking | emesis | endocytosis | 5‐HT3 receptor | palonosetron | allosterism | receptor | down-regulation | 5-HT | 5-HYDROXYTRYPTAMINE TYPE-3 RECEPTORS | PROTEIN-KINASE-C | CHEMOTHERAPY-INDUCED NAUSEA | HUMAN PLASMA | PHASE-III | ONDANSETRON | IN-VITRO | MODERATELY EMETOGENIC CHEMOTHERAPY | DOUBLE-BLIND | PHARMACOLOGY & PHARMACY | EXPRESSION | 5-HT3 receptor | Receptors, Serotonin, 5-HT3 - chemistry | Allosteric Regulation | Humans | Serotonin 5-HT3 Receptor Antagonists - metabolism | Cercopithecus aethiops | Protein Transport - drug effects | Isoquinolines - pharmacology | Nystatin - pharmacology | Cell Membrane - metabolism | Radioligand Assay | Granisetron - pharmacology | Cell Membrane - drug effects | Isoquinolines - metabolism | Recombinant Proteins - metabolism | Receptors, Serotonin, 5-HT3 - genetics | Endocytosis - drug effects | Quinuclidines - pharmacology | Recombinant Proteins - chemistry | Down-Regulation - drug effects | Hydrazones - pharmacology | Animals | Antiemetics - metabolism | Receptors, Serotonin, 5-HT3 - metabolism | Granisetron - metabolism | Kinetics | Serotonin 5-HT3 Receptor Antagonists - pharmacology | COS Cells | Quinuclidines - metabolism | Antiemetics - pharmacology | Health aspects | Nausea | Enzyme-linked immunosorbent assay | Binding sites | Research Papers
Journal Article
Naunyn-Schmiedeberg's Archives of Pharmacology, ISSN 0028-1298, 8/2015, Volume 388, Issue 8, pp. 883 - 903
G-protein coupled receptors (GPCRs) are the targets of over half of all prescribed drugs today. The UniProt database has records for about 800 proteins... 
Neurosciences | CXCR 1 , CXCR 2 , CCR 4 and CCR 5 , chemokine receptors | TM, trans-membrane helix | β 2 AR, β 2 -adrenergic receptor | ProS, pairwise protein similarity method | CRF1, corticotropin releasing factor receptor 1 | T4L, T4-lysozyme | ECL, extracellular loop | GLP-1, Glucagon-like peptide-1 receptor | hM 3 R, human muscarinic M3 receptor | α1B Adrenergic receptor | Pharmacology/Toxicology | 7TM, seven-transmembrane domain | HGMP, hierarchical GPCR modelling protocol | PDB, Protein Data Bank | XFELs, x-ray free electron lasers | 5-HT 2B and 5-HT 2C , human 5-hydroxytryptamine receptors 2B and 2C, respectively | GLAS, GPCR-likeness assessment score | H 1 , histamine receptor 1 | 3D, three-dimensional | Biomedicine | CCK 2 R, cholecystokinin receptor-2 | MD, molecular dynamic simulations | GPCRs, G-protein coupled receptors | Dopamine D 2 receptor | BRIL, apocytochrome b 562 RIL | δ-OR, delta-opioid receptor | SDM, site-directed mutagenesis | CCK2R, cholecystokinin receptor-2 | PEPTIDE-1 RECEPTOR | DESIGN | CXCR1, CXCR2, CCR4, and CCR5, chemokine receptors | beta 2AR, beta 2-adrenergic receptor | hMR, human muscarinic M3 receptor | HUMAN OREXIN-1 | PHARMACOLOGY & PHARMACY | ANTAGONISTS | Dopamine D-2 receptor | PROTEIN-COUPLED RECEPTORS | SITE-DIRECTED MUTAGENESIS | alpha 1B Adrenergic receptor | LIPIDIC CUBIC PHASE | delta-OR, delta-opioid receptor | 5-HT2B and 5-HT2C, human 5-hydroxytryptamine receptors 2B and 2C, respectively | H-1, histamine receptor 1 | SERIAL FEMTOSECOND CRYSTALLOGRAPHY | BINDING | SELECTIVITY | BRIL, apocytochrome bRIL | Animals | Receptors, G-Protein-Coupled - metabolism | Computer Simulation | Drug Industry | Humans | Cooperative Behavior | Models, Molecular | Crystallography | Drug Discovery | Universities | Drug discovery | BRIL, apocytochrome b562RIL | Meeting Report | H1, histamine receptor 1 | β2AR, β2-adrenergic receptor | CXCR1, CXCR2, CCR4 and CCR5, chemokine receptors | hM3R, human muscarinic M3 receptor | Dopamine D2 receptor
Journal Article