Structures of the E46K mutant-type α-synuclein protein and impact of E46K mutation on the structures of the wild-type α-synuclein proteinMolecular determinants of α-synuclein mutants' oligomerization and membrane interactionsClinically employed opioid analgesics produce antinociception via μ-δ opioid receptor heteromers in Rhesus monkeysAnandamide externally added to lipid vesicles containing trapped fatty acid amide hydrolase (FAAH) is readily hydrolyzed in a sterol-modulated fashionEndocannabinoid signaling in female reproductionSingle-Vesicle Fusion Assay Reveals Munc18-1 Binding to the SNARE Core Is Sufficient for Stimulating Membrane FusionThe δ opioid receptor agonist SNC80 selectively activates heteromeric μ-δ opioid receptorsStandard opioid agonists activate heteromeric opioid receptors: evidence for morphine and [d-Ala(2)-MePhe(4)-Glyol(5)]enkephalin as selective μ-δ agonistsDiscovery, Synthesis, and Structure–Activity Relationship of a Series of N -Aryl-bicyclo[2.2.1]heptane-2-carboxamides: Characterization of ML213 as a Novel KCNQ2 and KCNQ4 Potassium Channel OpenerDrug abuse and the simplest neurotransmitterNeuroprotective properties and mechanisms of resveratrol in in vitro and in vivo experimental cerebral stroke modelsDendrimer advances for the central nervous system delivery of therapeuticsLithium and the other mood stabilizers effective in bipolar disorder target the rat brain arachidonic acid cascadeACS chemical neuroscience molecule spotlight on Potiga (Ezogabine)Dye-binding assays for evaluation of the effects of small molecule inhibitors on amyloid (aβ) self-assemblyHydrogels in spinal cord injury repair strategiesACS chemical neuroscience molecule spotlight on viibryd (Vilazodone)ACS chemical neuroscience molecule spotlight on STX209 (arbaclofen)Lithium and autophagyRegulation of G protein-coupled receptors by allosteric ligandsClassification of H₂O₂as a neuromodulator that regulates striatal dopamine release on a subsecond time scaleThe molecular basis of memory. Part 2: chemistry of the tripartite mechanismEye movements as a probe of corollary discharge function in schizophreniaRecent advances in the medicinal chemistry of the metabotropic glutamate receptor 1 (mGlu₁)Interoception and learning: import to understanding and treating diseases and psychopathologiesInteraction between prion protein and Aβ amyloid fibrils revisited"Redundancy" of endocannabinoid inactivation: new challenges and opportunities for pain controlModulation of thermoreceptor TRPM8 by cooling compoundsNeurons and tumor suppressorsImaging mass spectrometry in neuroscience.ACS chemical neuroscience molecule spotlight on Suvorexant5-HT1A Receptor-Mediated Autoinhibition and the Control of Serotonergic Cell FiringEpigenetic Mechanisms of Serotonin Signaling.Spontaneous inward opening of the dopamine transporter is triggered by PIP2-regulated dynamics of the N-terminusImpaired Brain Dopamine and Serotonin Release and Uptake in Wistar Rats Following Treatment with CarboplatinBinding mode of an α-amino acid-linked quinoxaline-2,3-dione analogue at glutamate receptor subtype GluK1Synthesis and Pharmacology of Mono-, Di-, and Trialkyl-Substituted 7-Chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-Dioxides Combined with X-ray Structure Analysis to Understand the Unexpected Structure-Activity Relationship at AMPA ReceptorsPalonosetron-5-HT3 Receptor Interactions As Shown by a Binding Protein Cocrystal StructureHigh affinity radiopharmaceuticals based upon lansoprazole for PET imaging of aggregated tau in Alzheimer's disease and progressive supranuclear palsy: synthesis, preclinical evaluation, and lead selectionDiscovery of the first small-molecule opioid pan antagonist with nanomolar affinity at mu, delta, kappa, and nociceptin opioid receptors
P1433
Q22061749-A8ADA67B-97D4-4B9F-9412-5A611F543BBBQ24312185-5104F6B8-3B5D-42A8-A0AE-A17FB64DC014Q24597777-92C86BE2-1C48-405D-A52D-4642336C478AQ24598965-2B4AD205-2887-4C17-B29C-B94A6B886CDAQ24599033-9AF06633-308F-4162-8F5C-9AB45C19CEEEQ24622854-A861F19A-D96E-4A49-BD67-3E8D2D9146A2Q24630886-F6404245-B3B2-410D-B51F-A7A703F496F9Q24631212-24ED131C-8241-41A4-B9B8-7FF75DB19EE9Q24634116-1757FD68-6BEB-4CDC-9109-5BDEF8C12152Q26823063-C9F4C20D-758A-4702-8288-17B2E439E722Q26824390-F0AB63E5-2A26-4D4F-AFDD-A4C0F6C3B825Q26828423-56E4626D-8757-4CF5-AAF5-B6E9DECA880DQ26850084-43FF0FCD-37A7-4DD3-BE69-39353458B163Q26851224-86A0A39C-BC7F-4917-9234-1EABDE0DAC27Q26852205-45E9778C-D4FD-4ECE-BC16-A83EC8FE197BQ26852732-B74559BB-5659-4889-8F57-FACBE7E92D5DQ26860359-993F02AC-844C-40F0-A4AC-650349951BD0Q26861783-33553FE8-A376-4380-B0AB-43368DC3D3DCQ26863513-2C118E20-8F1D-4562-8F13-D43B04BA8558Q26864384-D277BB06-66E7-455C-A27C-A6B895C66B16Q26865538-B5481892-D7E7-4EC4-9351-281CD39DFC16Q26998797-3CB2F73B-EA85-464D-AC62-65A2AA763F97Q26999690-60A6859B-0F54-4A22-942A-8801869E0D19Q27000190-688904A2-54D7-4BED-A240-E5632A55B232Q27013751-4FFC8AD7-598A-4F64-A02F-99F9D77C4911Q27013909-1BF7D2D6-980D-4A3A-8DBC-31FE92E976BBQ27015753-8BC343A3-E7C5-40BD-BA53-9EA018F4ED07Q27021645-9D4F9D1B-CE06-454B-8140-38B05E41B46DQ27021969-AF1DDAB0-AC70-4C76-9EAF-C0A5A8005267Q27024594-4F951A67-F50F-4362-8E7E-39585641C2FCQ27026233-F22E6974-72AC-4BBC-9158-828C5983F808Q27027416-EEC4FC81-A703-4114-BAEC-476AD5C822F8Q27027985-AB2BF5FF-F7EB-498A-9F46-872A5D62A5A7Q27300323-AB90DB05-D037-4F9B-ACCE-3795A28EB84FQ27300384-CE092EB9-AC8C-4EDD-95B8-658604A5254FQ27700165-E61FCD95-F390-493F-8B56-88EA994A2F43Q27703617-6060CE6A-EE10-4DF8-A0F2-33EA9ED7BAE2Q27728102-1FFF4989-F173-4653-B24B-B842BFCA79E3Q28241366-A40AAE5E-A6BE-4A71-BC11-0A97C80E64E8Q28256196-EB1B08DC-FC19-4638-937C-CC4D007630E6
P1433
description
begutachtete wissenschaftliche Zeitschrift
@de
peer-reviewed scientific journal
@en
revista científica
@es
rivista scientifica
@it
videnskabeligt tidsskrift
@da
vědecký časopis
@cs
wetenschappelijk tijdschrift van American Chemical Society
@nl
рецензований науковий журнал
@uk
वैज्ञानिक पत्रिका
@hi
英语期刊
@zh
name
ACS Chemical Neuroscience
@ast
ACS Chemical Neuroscience
@da
ACS Chemical Neuroscience
@de
ACS Chemical Neuroscience
@en
ACS Chemical Neuroscience
@es
ACS Chemical Neuroscience
@fo
ACS Chemical Neuroscience
@fr
ACS Chemical Neuroscience
@is
ACS Chemical Neuroscience
@it
ACS Chemical Neuroscience
@kl
type
label
ACS Chemical Neuroscience
@ast
ACS Chemical Neuroscience
@da
ACS Chemical Neuroscience
@de
ACS Chemical Neuroscience
@en
ACS Chemical Neuroscience
@es
ACS Chemical Neuroscience
@fo
ACS Chemical Neuroscience
@fr
ACS Chemical Neuroscience
@is
ACS Chemical Neuroscience
@it
ACS Chemical Neuroscience
@kl
prefLabel
ACS Chemical Neuroscience
@ast
ACS Chemical Neuroscience
@da
ACS Chemical Neuroscience
@de
ACS Chemical Neuroscience
@en
ACS Chemical Neuroscience
@es
ACS Chemical Neuroscience
@fo
ACS Chemical Neuroscience
@fr
ACS Chemical Neuroscience
@is
ACS Chemical Neuroscience
@it
ACS Chemical Neuroscience
@kl
P1042
P3181
P4616
P1042
P1055
P1058
P1156
19700172804
P1159
P1160
ACS Chem. Neurosci.
P1277
P1476
ACS Chemical Neuroscience
@en
P1813
ACS Chem Neurosci
@en
P236
P407
P571
2010-01-01T00:00:00Z