Inhibition of neuronal voltage-gated sodium channels by brilliant blue G - Wikidata - awgldk - TriplyDB

Inhibition of neuronal voltage-gated sodium channels by brilliant blue G

Inhibition of neuronal voltage-gated sodium channels by brilliant blue G

http://www.wikidata.org/entity/Q35122828

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Brilliant Blue Dyes in Daily Food: How Could Purinergic System Be Affected?Inhibition of Inactive States of Tetrodotoxin-Sensitive Sodium Channels Reduces Spontaneous Firing of C-Fiber Nociceptors and Produces Analgesia in Formalin and Complete Freund's Adjuvant Models of Pain P2X7 blockade attenuates murine lupus nephritis by inhibiting activation of the NLRP3/ASC/caspase 1 pathway.Effect of genetic deletion and pharmacological antagonism of P2X7 receptors in a mouse animal model of migraine.P2X7 receptor antagonism in amyotrophic lateral sclerosis.Modulation of neuronal sodium channels by the sea anemone peptide BDS-I.Characterization of Endogenous Sodium Channels in the ND7-23 Neuroblastoma Cell Line: Implications for Use as a Heterologous Ion Channel Expression System Suitable for Automated Patch Clamp Screening P2X7 Receptor Mediates Spinal Microglia Activation of Visceral Hyperalgesia in a Rat Model of Chronic Pancreatitis.Block of human cardiac sodium channels by lacosamide: evidence for slow drug binding along the activation pathway.Recent developments regarding voltage-gated sodium channel blockers for the treatment of inherited and acquired neuropathic pain syndromes.P2X receptor antagonists for pain management: examination of binding and physicochemical properties.P2X receptors as drug targets.The role of slow and persistent TTX-resistant sodium currents in acute tumor necrosis factor-α-mediated increase in nociceptors excitability.Effects of Brilliant Blue G on Serum Tumor Necrosis Factor-α Levels and Depression-like Behavior in Mice after Lipopolysaccharide Administration.Flow Synthesis and Biological Studies of an Analgesic Adamantane Derivative That Inhibits P2X7-Evoked Glutamate Release.The food dye FD&C Blue No. 1 is a selective inhibitor of the ATP release channel Panx1.Left-shifted nav channels in injured bilayer: primary targets for neuroprotective nav antagonists?Reduction of cytotoxicity of benzalkonium chloride and octenidine by Brilliant Blue G The P2X7 receptor is not essential for development of imiquimod-induced psoriasis-like inflammation in mice.The Selective Nav1.7 Inhibitor, PF-05089771, Interacts Equivalently with Fast and Slow Inactivated Nav1.7 Channels.The P2X7 Receptor in Inflammatory Diseases: Angel or Demon?Diverse effects of Brilliant Blue G administration in models of trigeminal activation in the rat.ATP-P2X7 Receptor Modulates Axon Initial Segment Composition and Function in Physiological Conditions and Brain Injury.Lacosamide Inhibition of Nav1.7 Voltage-Gated Sodium Channels: Slow Binding to Fast-Inactivated States.

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P2860

Inhibition of neuronal voltage-gated sodium channels by brilliant blue G

http://www.wikidata.org/entity/Q35122828

description

2011 nî lūn-bûn

@nan

2011 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի մայիսին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Inhibition of neuronal voltage-gated sodium channels by brilliant blue G

@ast

Inhibition of neuronal voltage-gated sodium channels by brilliant blue G

@en

type

label

Inhibition of neuronal voltage-gated sodium channels by brilliant blue G

@ast

Inhibition of neuronal voltage-gated sodium channels by brilliant blue G

@en

prefLabel

Inhibition of neuronal voltage-gated sodium channels by brilliant blue G

@ast

Inhibition of neuronal voltage-gated sodium channels by brilliant blue G

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Molecular Pharmacology

P1476

Inhibition of neuronal voltage-gated sodium channels by brilliant blue G

@en

P2093

Bruce P Bean

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

Sooyeon Jo

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P2860

Systemic administration of an antagonist of the ATP-sensitive receptor P2X7 improves recovery after spinal cord injury

Common molecular determinants of local anesthetic, antiarrhythmic, and anticonvulsant block of voltage-gated Na+ channels

Fast- or slow-inactivated state preference of Na+ channel inhibitors: a simulation and experimental study

Voltage-gated sodium channels in taste bud cells.

Sodium channels and pain.

Molecular model of anticonvulsant drug binding to the voltage-gated sodium channel inner pore.

Voltage-gated sodium channels and pain pathways.

Synergistic interactions between commonly used food additives in a developmental neurotoxicity test.

Slow inactivation in voltage-gated sodium channels: molecular substrates and contributions to channelopathies.

The roles of sodium channels in nociception: Implications for mechanisms of pain

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247-257

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scholarly article

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10.1124/MOL.110.070276

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2

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80

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2011-05-02T00:00:00Z

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51092787

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21536754

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3141889

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