Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy. - sprookjes - yvandenbroek - TriplyDB

Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy.

Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy.

http://www.wikidata.org/entity/Q37100287

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The role of genetics in IBS.Channelopathies Pain as a channelopathy Experimental and Automated Analysis Techniques for High-resolution Electrical Mapping of Small Intestine Slow Wave Activity Electrophysiological Mechanisms of Gastrointestinal Arrhythmogenesis: Lessons from the Heart Mechanisms of Electrical Activation and Conduction in the Gastrointestinal System: Lessons from Cardiac Electrophysiology Irritable bowel syndrome: methods, mechanisms, and pathophysiology. Genetic epidemiology and pharmacogenetics in irritable bowel syndrome The role of the SCN5A-encoded channelopathy in irritable bowel syndrome and other gastrointestinal disorders SCN5A variant that blocks fibroblast growth factor homologous factor regulation causes human arrhythmia Loss-of-Function of the Voltage-Gated Sodium Channel NaV1.5 (Channelopathies) in Patients With Irritable Bowel Syndrome Detection of anticonductive tissue autoantibodies in a patient with chronic intestinal pseudo-obstruction and sick sinus syndrome.Beyond the Electrocardiogram: Mutations in Cardiac Ion Channel Genes Underlie Nonarrhythmic Phenotypes.Identifying the Ion Channels Responsible for Signaling Gastro-Intestinal Based Pain Genetics and irritable bowel syndrome: from genomics to intermediate phenotype and pharmacogenetics Physiology, injury, and recovery of interstitial cells of Cajal: basic and clinical science A quantitative model of human jejunal smooth muscle cell electrophysiology.Ion channelopathies in functional GI disorders.MAPKs represent novel therapeutic targets for gastrointestinal motility disorders.Inhibitory effect of TongXie-YaoFang formula on colonic contraction in rats Recent progress in gastric arrhythmia: pathophysiology, clinical significance and future horizons Evidence-based clinical practice guidelines for irritable bowel syndrome.The Relationship Between Gastric Myoelectric Activity and SCN5A Mutation Suggesting Sodium Channelopathy in Patients With Brugada Syndrome and Functional Dyspepsia - A Pilot Study.Ranolazine inhibits voltage-gated mechanosensitive sodium channels in human colon circular smooth muscle cells.Recent advances in small bowel diseases: Part I.Targeting Ion Channels: An Important Therapeutic Implication in Gastrointestinal Dysmotility in Patients With Spinal Cord Injury Expression and function of the Scn5a-encoded voltage-gated sodium channel NaV 1.5 in the rat jejunum.Quantification of gastrointestinal sodium channelopathy.Mapping and modeling gastrointestinal bioelectricity: from engineering bench to bedside Genetic approaches to functional gastrointestinal disorders.Green light from the FDA for new drug development in irritable bowel syndrome and functional dyspepsia.Pain channelopathies.Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart.Multiscale modeling of gastrointestinal electrophysiology and experimental validation.Biophysically based modeling of the interstitial cells of cajal: current status and future perspectives.Targeting ion channels for the treatment of gastrointestinal motility disorders Genetics of human gastrointestinal sensation.Therapeutic strategies for functional dyspepsia and irritable bowel syndrome based on pathophysiology.Lessons learned--resolving the enigma of genetic factors in IBS.Mechanosensitive ion channel Piezo2 is inhibited by D-GsMTx4.Mechanosensitive Piezo Channels in the Gastrointestinal Tract.

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Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy.

http://www.wikidata.org/entity/Q37100287

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 04 December 2008

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy.

@en

Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy.

@nl

type

label

Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy.

@en

Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy.

@nl

prefLabel

Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy.

@en

Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy.

@nl

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AJPGI.90571.2008

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American Journal of Physiology - Gastrointestinal and Liver Physiology

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Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy.

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Cheryl E Bernard

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David J Tester

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G Richard Locke

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Gianrico Farrugia

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James L Rae

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Jonathan C Makielski

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Michael J Ackerman

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Nicholas J Talley

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Peter R Strege

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Yuri A Saito

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P2860

A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

Functional bowel disorders and functional abdominal pain

SCN5A is expressed in human jejunal circular smooth muscle cells.

Syntrophin gamma 2 regulates SCN5A gating by a PDZ domain-mediated interaction.

Vagal afferent innervation of the rat fundic stomach: morphological characterization of the gastric tension receptor.

Neuroimaging of the brain-gut axis: from basic understanding to treatment of functional GI disorders.

Irritable bowel syndrome aggregates strongly in families: a family-based case-control study.

Irritable bowel syndrome in twins: genes and environment.

Familial aggregation of irritable bowel syndrome: a prospective study

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