Pharmacological evaluation of the long-term effects of xanomeline on the M(1) muscarinic acetylcholine receptor - Wikidata - awgldk - TriplyDB

Pharmacological evaluation of the long-term effects of xanomeline on the M(1) muscarinic acetylcholine receptor

Pharmacological evaluation of the long-term effects of xanomeline on the M(1) muscarinic acetylcholine receptor

http://www.wikidata.org/entity/Q33784371

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Xanomeline suppresses excessive pro-inflammatory cytokine responses through neural signal-mediated pathways and improves survival in lethal inflammation.Long-term activation upon brief exposure to xanomleline is unique to M1 and M4 subtypes of muscarinic acetylcholine receptors.

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P2860

Pharmacological evaluation of the long-term effects of xanomeline on the M(1) muscarinic acetylcholine receptor

http://www.wikidata.org/entity/Q33784371

description

2010 nî lūn-bûn

@nan

2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Pharmacological evaluation of ...... carinic acetylcholine receptor

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Pharmacological evaluation of ...... carinic acetylcholine receptor

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Pharmacological evaluation of ...... carinic acetylcholine receptor

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Esam E El-Fakahany

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Kayla C De Lorme

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Marianne K O Grant

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Meredith J Noetzel

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Vladimír Doležal

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P2860

On the unique binding and activating properties of xanomeline at the M1 muscarinic acetylcholine receptor

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Selective muscarinic receptor agonist xanomeline as a novel treatment approach for schizophrenia

Functional comparison of muscarinic partial agonists at muscarinic receptor subtypes hM1, hM2, hM3, hM4 and hM5 using microphysiometry

Evolving concepts in G protein-coupled receptor endocytosis: the role in receptor desensitization and signaling

Differential regulation of muscarinic M1 receptors by orthosteric and allosteric ligands.

Seven-transmembrane receptors: crystals clarify.

Agonist-selective mechanisms of GPCR desensitization

G protein-coupled receptor kinases.

Pharmacology of a constitutively active muscarinic receptor generated by random mutagenesis.

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10.1371/JOURNAL.PONE.0015722

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