Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins
about
Blood pressure is regulated by an alpha1D-adrenergic receptor/dystrophin signalosomeDephosphorylation of beta2-syntrophin and Ca2+/mu-calpain-mediated cleavage of ICA512 upon stimulation of insulin secretionSarcospan-deficient mice maintain normal muscle functionSyntrophin-dependent expression and localization of Aquaporin-4 water channel proteinDiacylglycerol kinase-zeta localization in skeletal muscle is regulated by phosphorylation and interaction with syntrophinsalpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruptionThe neuregulin receptor ErbB-4 interacts with PDZ-containing proteins at neuronal synapsesAnkyrinG is required for clustering of voltage-gated Na channels at axon initial segments and for normal action potential firingDifferent dystrophin-like complexes are expressed in neurons and gliaIn vivo requirement of the alpha-syntrophin PDZ domain for the sarcolemmal localization of nNOS and aquaporin-4Absence of alpha-syntrophin leads to structurally aberrant neuromuscular synapses deficient in utrophinDystrophins and dystrobrevins.The biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal musclePhysiological and Pathophysiological Insights of Nav1.4 and Nav1.5 ComparisonDefective interactions of protein partner with ion channels and transporters as alternative mechanisms of membrane channelopathiesProteomic profiling of the dystrophin-deficient mdx phenocopy of dystrophinopathy-associated cardiomyopathyβ2-Syntrophin is a Cdk5 substrate that restrains the motility of insulin secretory granulesα1-Syntrophin Variant Identified in Drug-Induced Long QT Syndrome Increases Late Sodium CurrentLearning from Heterogeneous Data Sources: An Application in Spatial ProteomicsConsensus substrate sequence for protein-tyrosine phosphatase receptor type ZDistribution of proteins implicated in excitation-contraction coupling in rat ventricular myocytesCharacterization of human alpha-dystrobrevin isoforms in HL-60 human promyelocytic leukemia cells undergoing granulocytic differentiation.Profound human/mouse differences in alpha-dystrobrevin isoforms: a novel syntrophin-binding site and promoter missing in mouse and rat.Chronic hypoxia impairs muscle function in the Drosophila model of Duchenne's muscular dystrophy (DMD).Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome.Role of mental retardation-associated dystrophin-gene product Dp71 in excitatory synapse organization, synaptic plasticity and behavioral functions.β1-syntrophin modulation by miR-222 in mdx mice.Therapeutic targeting of signaling pathways in muscular dystrophy.Α-syntrophin modulates myogenin expression in differentiating myoblasts.Mechanical and electrophysiological properties of the sarcolemma of muscle fibers in two murine models of muscle dystrophy: col6a1-/- and mdxGene expression changes in areas of focal loss of retinal ganglion cells in the retina of DBA/2J mice.From Fifth Business to Protagonist: the complex roles of ion channel anchors in cardiac arrhythmia.The ZZ domain of dystrophin in DMD: making sense of missense mutations.Defining a new paradigm for human arrhythmia syndromes: phenotypic manifestations of gene mutations in ion channel- and transporter-associated proteins.The alpha-syntrophin PH and PDZ domains scaffold acetylcholine receptors, utrophin, and neuronal nitric oxide synthase at the neuromuscular junction.Membrane stretch affects gating modes of a skeletal muscle sodium channelVoltage-dependent sodium channel function is regulated through membrane mechanics.Structure of the split PH domain and distinct lipid-binding properties of the PH-PDZ supramodule of alpha-syntrophin.Lack of dystrophin protein Dp71 results in progressive cataract formation due to loss of fiber cell organization.The light chains of microtubule-associated proteins MAP1A and MAP1B interact with α1-syntrophin in the central and peripheral nervous system.
P2860
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P2860
Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Interaction of muscle and brai ...... dystrophin-associated proteins
@ast
Interaction of muscle and brai ...... dystrophin-associated proteins
@en
Interaction of muscle and brai ...... dystrophin-associated proteins
@nl
type
label
Interaction of muscle and brai ...... dystrophin-associated proteins
@ast
Interaction of muscle and brai ...... dystrophin-associated proteins
@en
Interaction of muscle and brai ...... dystrophin-associated proteins
@nl
prefLabel
Interaction of muscle and brai ...... dystrophin-associated proteins
@ast
Interaction of muscle and brai ...... dystrophin-associated proteins
@en
Interaction of muscle and brai ...... dystrophin-associated proteins
@nl
P2093
P3181
P1476
Interaction of muscle and brai ...... dystrophin-associated proteins
@en
P2093
J H Caldwell
R Madhavan
S C Froehner
S R Levinson
P304
P3181
P356
10.1523/JNEUROSCI.18-01-00128.1998
P407
P577
1998-01-01T00:00:00Z