The sigma-1 receptor binds to the Nav1.5 voltage-gated Na+ channel with 4-fold symmetry. - Wikidata - wikimedia - TriplyDB

The sigma-1 receptor binds to the Nav1.5 voltage-gated Na+ channel with 4-fold symmetry.

The sigma-1 receptor binds to the Nav1.5 voltage-gated Na+ channel with 4-fold symmetry.

http://www.wikidata.org/entity/Q36347732

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Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison Crystal Structure and Molecular Imaging of the Nav Channel 3 Subunit Indicates a Trimeric Assembly A Review of the Human Sigma-1 Receptor Structure.The oligomeric states of the purified sigma-1 receptor are stabilized by ligands.The Sigma-1 Receptor as a Pluripotent Modulator in Living Systems.Role of the Sigma-1 receptor in Amyotrophic Lateral Sclerosis (ALS)The sigma-1 receptors are present in monomeric and oligomeric forms in living cells in the presence and absence of ligands Sigma1 receptors inhibit store-operated Ca2+ entry by attenuating coupling of STIM1 to Orai1 Proliferation of embryonic cardiomyocytes in zebrafish requires the sodium channel scn5Lab The sigma-1 receptor: a regulator of cancer cell electrical plasticity?Structural domains underlying the activation of acid-sensing ion channel 2a.Involvement of ion channels and transporters in carcinoma angiogenesis and metastasis.Sigma-1 receptors modulate neonatal Nav1.5 ion channels in breast cancer cell lines.Pharmacological Modulation of the Sigma 1 Receptor and the Treatment of Pain.Sigma 1 Receptor and Ion Channel Dynamics in Cancer.The σ-1 receptor interacts directly with GluN1 but not GluN2A in the GluN1/GluN2A NMDA receptor.The SigmaR1 chaperone drives breast and colorectal cancer cell migration by tuning SK3-dependent Ca2+ homeostasis.A direct interaction between the sigma-1 receptor and the hERG voltage-gated K+ channel revealed by atomic force microscopy and homogeneous time-resolved fluorescence (HTRF®).Improved expression and purification of sigma 1 receptor fused to maltose binding protein by alteration of linker sequence Solution NMR studies reveal the location of the second transmembrane domain of the human sigma-1 receptor.The sigma-1 receptor modulates dopamine transporter conformation and cocaine binding and may thereby potentiate cocaine self-administration in rats.TRPV1 channels and the progesterone receptor Sig-1R interact to regulate pain.Sigma-1 Receptor and Neuronal Excitability.The Sigma-1 Receptor-A Therapeutic Target for the Treatment of ALS?Aberrant Subcellular Dynamics of Sigma-1 Receptor Mutants Underlying Neuromuscular Diseases.Sigma-1 Receptor and Pain.Sigma-1 receptor: a new player in neuroprotection against chemotherapy-induced peripheral neuropathy.

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The sigma-1 receptor binds to the Nav1.5 voltage-gated Na+ channel with 4-fold symmetry.

http://www.wikidata.org/entity/Q36347732

description

2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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2012年學術文章

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2012年學術文章

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name

The sigma-1 receptor binds to the Nav1.5 voltage-gated Na+ channel with 4-fold symmetry.

@ast

The sigma-1 receptor binds to the Nav1.5 voltage-gated Na+ channel with 4-fold symmetry.

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type

label

The sigma-1 receptor binds to the Nav1.5 voltage-gated Na+ channel with 4-fold symmetry.

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The sigma-1 receptor binds to the Nav1.5 voltage-gated Na+ channel with 4-fold symmetry.

@en

prefLabel

The sigma-1 receptor binds to the Nav1.5 voltage-gated Na+ channel with 4-fold symmetry.

@ast

The sigma-1 receptor binds to the Nav1.5 voltage-gated Na+ channel with 4-fold symmetry.

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JBC.M112.382077

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Journal of Biological Chemistry

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The sigma-1 receptor binds to the Nav1.5 voltage-gated Na+ channel with 4-fold symmetry.

@en

P2093

Andrew P Stewart

http://www.w3.org/2001/XMLSchema#string

David Crottès

http://www.w3.org/2001/XMLSchema#string

Dilshan Balasuriya

http://www.w3.org/2001/XMLSchema#string

J Michael Edwardson

http://www.w3.org/2001/XMLSchema#string

Olivier Soriani

http://www.w3.org/2001/XMLSchema#string

P2860

The hallucinogen N,N-dimethyltryptamine (DMT) is an endogenous sigma-1 receptor regulator

Antagonist action of progesterone at σ-receptors in the modulation of voltage-gated sodium channels

Purification, molecular cloning, and expression of the mammalian sigma1-binding site

Membrane-delimited coupling between sigma receptors and K+ channels in rat neurohypophysial terminals requires neither G-protein nor ATP

Structure of acid-sensing ion channel 1 at 1.9 A resolution and low pH

Differential recruitment of Kv1.4 and Kv4.2 to lipid rafts by PSD-95

Antagonism of NMDA receptors by sigma receptor ligands attenuates chemical ischemia-induced neuronal death in vitro

sigma Receptor activation blocks potassium channels and depresses neuroexcitability in rat intracardiac neurons

Sigma-1 receptor chaperones at the ER-mitochondrion interface regulate Ca(2+) signaling and cell survival

International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels

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37021-37029

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scholarly article

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10.1074/JBC.M112.382077

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3481303

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