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A mutation in telethonin alters Nav1.5 function

A mutation in telethonin alters Nav1.5 function

http://www.wikidata.org/entity/Q28276372

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The role of late I Na in development of cardiac arrhythmias Channelopathies from mutations in the cardiac sodium channel protein complex The role of the SCN5A-encoded channelopathy in irritable bowel syndrome and other gastrointestinal disorders Telethonin deficiency is associated with maladaptation to biomechanical stress in the mammalian heart 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.Mechano-signaling in heart failure Physiology, injury, and recovery of interstitial cells of Cajal: basic and clinical science Loss of function of hNav1.5 by a ZASP1 mutation associated with intraventricular conduction disturbances in left ventricular noncompaction A quantitative model of human jejunal smooth muscle cell electrophysiology.Diseases caused by mutations in Nav1.5 interacting proteins Ion channelopathies in functional GI disorders.The sarcomeric Z-disc and Z-discopathies.A novel frequency analysis method for assessing K(ir)2.1 and Na (v)1.5 currents.Diabetes-related alterations in the enteric nervous system and its microenvironment.Expression and function of the Scn5a-encoded voltage-gated sodium channel NaV 1.5 in the rat jejunum.Quantification of gastrointestinal sodium channelopathy.Z-disc transcriptional coupling, sarcomeroptosis and mechanoptosis [corrected].Toward the virtual stomach: progress in multiscale modeling of gastric electrophysiology and motility.Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient Biology of cardiac sodium channel Nav1.5 expression.Voltage-gated sodium channels: biophysics, pharmacology, and related channelopathies.Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects.Ranolazine inhibits shear sensitivity of endogenous Na+ current and spontaneous action potentials in HL-1 cells.Ranolazine decreases mechanosensitivity of the voltage-gated sodium ion channel Na(v)1.5: a novel mechanism of drug action.Mechanosensitivity of Nav1.5, a voltage-sensitive sodium channel.A muscle-specific MuRF1-E2 network requires stabilization of MuRF1-E2 complexes by telethonin, a newly identified substrate.Cardiac Arrhythmias Related to Sodium Channel Dysfunction.

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P2860

A mutation in telethonin alters Nav1.5 function

http://www.wikidata.org/entity/Q28276372

description

2008 nî lūn-bûn

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2008 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2008 թվականի հունիսին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

A mutation in telethonin alters Nav1.5 function

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A mutation in telethonin alters Nav1.5 function

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A mutation in telethonin alters Nav1.5 function

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A mutation in telethonin alters Nav1.5 function

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A mutation in telethonin alters Nav1.5 function

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A mutation in telethonin alters Nav1.5 function

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A mutation in telethonin alters Nav1.5 function

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A mutation in telethonin alters Nav1.5 function

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A mutation in telethonin alters Nav1.5 function

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Journal of Biological Chemistry

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A mutation in telethonin alters Nav1.5 function

@en

P2093

Amelia Mazzone

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

Cheryl E Bernard

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

David J Tester

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Georgine Faulkner

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Gianrico Farrugia

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Jonathan C Makielski

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Michael J Ackerman

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Peter R Strege

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Roberto De Giorgio

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Simon J Gibbons

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P2860

Structural basis for activation of the titin kinase domain during myofibrillogenesis

FATZ, a filamin-, actinin-, and telethonin-binding protein of the Z-disc of skeletal muscle

Specific interaction of the potassium channel beta-subunit minK with the sarcomeric protein T-cap suggests a T-tubule-myofibril linking system

The muscle ankyrin repeat proteins: CARP, ankrd2/Arpp and DARP as a family of titin filament-based stress response molecules

Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes

The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel

Telethonin, a novel sarcomeric protein of heart and skeletal muscle

Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin

Titin-cap associates with, and regulates secretion of, Myostatin

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16537-44

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scholarly article

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10.1074/JBC.M801744200

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24

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283

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18408010

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