Electrophysiology of the neuromuscular junction of the laminin-2 (merosin) deficient C57 BL/6J dy2J/dy2J dystrophic mouse
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Neurology (clinical),Molecular Biology,General Neuroscience
Reference38 articles.
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3. Neural abnormalities in the dystrophic mouse;Bradley;J. Neurol. Sci.,1975
4. The nodes of Ranvier in the nerves of mice with muscular dystrophy;Bradley;J. Neuropathol. Exp. Neurol.,1977
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1. Enhancement of neuromuscular dynamics and strength behavior using extremely low magnitude mechanical signals in mice;Journal of Biomechanics;2014-01
2. A Biologically Active Sequence of the Laminin α2 Large Globular 1 Domain Promotes Cell Adhesion through Syndecan-1 by Inducing Phosphorylation and Membrane Localization of Protein Kinase Cδ;Journal of Biological Chemistry;2009-11
3. Synaptic plasticity in the dy2J mouse model of laminin α2-deficient congenital muscular dystrophy;Brain Research;2005-04
4. Increased quantal size in transmission at slow but not fast neuromuscular synapses of apolipoprotein E deficient mice;Experimental Neurology;2004-02
5. Sternohyoid Muscle Fatigue Properties of dy/dy Dystrophic Mice, an Animal Model of Merosin-Deficient Congenital Muscular Dystrophy;Pediatric Research;2003-10
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