about
Identification of a serotonin/glutamate receptor complex implicated in psychosisPreferred supramolecular organization and dimer interfaces of opioid receptors from simulated self-associationClosed headpiece of integrin IIb 3 and its complex with an IIb 3-specific antagonist that does not induce openingInward-facing conformation of the zinc transporter YiiP revealed by cryoelectron microscopyStructure-Guided Design of a High-Affinity Platelet Integrin IIb 3 Receptor Antagonist That Disrupts Mg2+ Binding to the MIDASSynthetic and Receptor Signaling Explorations of the Mitragyna Alkaloids: Mitragynine as an Atypical Molecular Framework for Opioid Receptor ModulatorsLigand-Based Discovery of a New Scaffold for Allosteric Modulation of the μ-Opioid Receptor.Discovery, synthesis, and molecular pharmacology of selective positive allosteric modulators of the δ-opioid receptor.Showcasing modern molecular dynamics simulations of membrane proteins through G protein-coupled receptors.Structural and therapeutic insights from the species specificity and in vivo antithrombotic activity of a novel alphaIIb-specific alphaIIbbeta3 antagonist.Membrane driven spatial organization of GPCRs.Requirements and ontology for a G protein-coupled receptor oligomerization knowledge base.αIIbβ3 variants defined by next-generation sequencing: predicting variants likely to cause Glanzmann thrombasthenia.Modeling activated states of GPCRs: the rhodopsin template.Increasingly accurate dynamic molecular models of G-protein coupled receptor oligomers: Panacea or Pandora's box for novel drug discovery?Dynamic models of G-protein coupled receptor dimers: indications of asymmetry in the rhodopsin dimer from molecular dynamics simulations in a POPC bilayer.Putative active states of a prototypic g-protein-coupled receptor from biased molecular dynamics.Effects of limiting extension at the alphaIIb genu on ligand binding to integrin alphaIIbbeta3.GPCR-OKB: the G Protein Coupled Receptor Oligomer Knowledge Base.Mechanistic insights into the allosteric modulation of opioid receptors by sodium ions.Ligand-induced modulation of the free-energy landscape of G protein-coupled receptors explored by adaptive biasing techniquesMaking structural sense of dimerization interfaces of delta opioid receptor homodimers.Decoding the signaling of a GPCR heteromeric complex reveals a unifying mechanism of action of antipsychotic drugs.RUC-4: a novel αIIbβ3 antagonist for prehospital therapy of myocardial infarctionAssessing the relative stability of dimer interfaces in g protein-coupled receptors.Discovery of a novel selective kappa-opioid receptor agonist using crystal structure-based virtual screening.Identification of a μ-δ opioid receptor heteromer-biased agonist with antinociceptive activity.Structure-based virtual screening of small-molecule antagonists of platelet integrin αIIbβ3 that do not prime the receptor to bind ligandThe Dynamic Process of Drug-GPCR Binding at Either Orthosteric or Allosteric Sites Evaluated by MetadynamicsSynthetic Studies of Neoclerodane Diterpenes from Salvia divinorum: Identification of a Potent and Centrally Acting μ Opioid Analgesic with Reduced Abuse Liability.Differential response to morphine of the oligomeric state of μ-opioid in the presence of δ-opioid receptorsMolecular determinants and thermodynamics of the amyloid precursor protein transmembrane domain implicated in Alzheimer's disease.Exploring molecular mechanisms of ligand recognition by opioid receptors with metadynamics.Differential stability of the crystallographic interfaces of mu- and kappa-opioid receptorsIdentification of a small-molecule ligand that activates the neuropeptide receptor GPR171 and increases food intake.Opioid receptors: Structural and mechanistic insights into pharmacology and signaling.The study of G-protein coupled receptor oligomerization with computational modeling and bioinformatics.Impact of Lipid Composition and Receptor Conformation on the Spatio-temporal Organization of μ-Opioid Receptors in a Multi-component Plasma Membrane Model.Mutations affecting the oligomerization interface of G-protein-coupled receptors revealed by a novel de novo protein design frameworkInternational Union of Basic and Clinical Pharmacology. LXVII. Recommendations for the recognition and nomenclature of G protein-coupled receptor heteromultimers.
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P50
description
hulumtuese
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researcher
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ricercatrice
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wetenschapper
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հետազոտող
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name
Marta Filizola
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Marta Filizola
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Marta Filizola
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Marta Filizola
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Marta Filizola
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type
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Marta Filizola
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Marta Filizola
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Marta Filizola
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Marta Filizola
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Marta Filizola
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prefLabel
Marta Filizola
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Marta Filizola
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Marta Filizola
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Marta Filizola
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Marta Filizola
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P1006
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P244
P1006
P106
P1153
7004102565
P21
P213
0000 0004 2343 862X
P214
P244
nb2014002175
P2456
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0000-0002-4382-8276
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lccn-nb2014002175