Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies.
about
Altered social behavior and ultrasonic communication in the dystrophin-deficient mdx mouse model of Duchenne muscular dystrophy.Evaluation of neural damage in Duchenne muscular dystrophy patients.Understanding the molecular diversity of GABAergic synapses.New dystrophin/dystroglycan interactors control neuron behavior in Drosophila eye.Rescue of a dystrophin-like protein by exon skipping in vivo restores GABAA-receptor clustering in the hippocampus of the mdx mouse.Fine mapping of complex traits in non-model species: using next generation sequencing and advanced intercross lines in Japanese quail.Orai1 mediates exacerbated Ca(2+) entry in dystrophic skeletal muscleGenome-wide association study of retinopathy in individuals without diabetes.Nonmechanical Roles of Dystrophin and Associated Proteins in Exercise, Neuromuscular Junctions, and Brains.A case report: Becker muscular dystrophy presenting with epilepsy and dysgnosia induced by duplication mutation of Dystrophin gene.Autonomic Modulation in Duchenne Muscular Dystrophy during a Computer Task: A Prospective Control Trial.Label-free mass spectrometric analysis reveals complex changes in the brain proteome from the mdx-4cv mouse model of Duchenne muscular dystrophy.The dystrophin gene and cognitive function in the general population.Characterization of a Dmd (EGFP) reporter mouse as a tool to investigate dystrophin expression.Dystrophin Distribution and Expression in Human and Experimental Temporal Lobe Epilepsy.A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy.Cognitive dysfunction in Duchenne muscular dystrophy: a possible role for neuromodulatory immune molecules.Tissue expression and actin binding of a novel N-terminal utrophin isoformIntellectual ability in the duchenne muscular dystrophy and dystrophin gene mutation location.Utrophin regulates modal gating of mechanosensitive ion channels in dystrophic skeletal muscle.Distinct mechanisms regulate GABAA receptor and gephyrin clustering at perisomatic and axo-axonic synapses on CA1 pyramidal cells.Dystrophic Cardiomyopathy: Complex Pathobiological Processes to Generate Clinical Phenotype.Influence of full-length dystrophin on brain volumes in mouse models of Duchenne muscular dystrophy.
P2860
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P2860
Dystrophins, utrophins, and associated scaffolding complexes: role in mammalian brain and implications for therapeutic strategies.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Dystrophins, utrophins, and as ...... ns for therapeutic strategies.
@ast
Dystrophins, utrophins, and as ...... ns for therapeutic strategies.
@en
type
label
Dystrophins, utrophins, and as ...... ns for therapeutic strategies.
@ast
Dystrophins, utrophins, and as ...... ns for therapeutic strategies.
@en
prefLabel
Dystrophins, utrophins, and as ...... ns for therapeutic strategies.
@ast
Dystrophins, utrophins, and as ...... ns for therapeutic strategies.
@en
P2860
P921
P356
P1476
Dystrophins, utrophins, and as ...... ns for therapeutic strategies.
@en
P2093
Caroline Perronnet
Cyrille Vaillend
P2860
P304
P356
10.1155/2010/849426
P577
2010-06-17T00:00:00Z