Published in J Neurosci on December 24, 2008
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits. Cell (2011) 4.58
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Caspr regulates the processing of contactin and inhibits its binding to neurofascin. J Cell Biol (2003) 1.45
Protein trafficking and anchoring complexes revealed by proteomic analysis of inward rectifier potassium channel (Kir2.x)-associated proteins. J Biol Chem (2004) 1.43
Protein 4.1B associates with both Caspr/paranodin and Caspr2 at paranodes and juxtaparanodes of myelinated fibres. Eur J Neurosci (2003) 1.43
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Retention of a cell adhesion complex at the paranodal junction requires the cytoplasmic region of Caspr. J Cell Biol (2002) 1.35
PSD-93 knock-out mice reveal that neuronal MAGUKs are not required for development or function of parallel fiber synapses in cerebellum. J Neurosci (2001) 1.34
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Caspr3 and caspr4, two novel members of the caspr family are expressed in the nervous system and interact with PDZ domains. Mol Cell Neurosci (2002) 1.22
The MAGUK protein MPP7 binds to the polarity protein hDlg1 and facilitates epithelial tight junction formation. Mol Biol Cell (2007) 1.12
Regulation of protein 4.1R, p55, and glycophorin C ternary complex in human erythrocyte membrane. J Biol Chem (2000) 1.08
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Type II brain 4.1 (4.1B/KIAA0987), a member of the protein 4.1 family, is localized to neuronal paranodes. Brain Res Mol Brain Res (2000) 1.04
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p55 protein is a member of PSD scaffold proteins in the rat brain and interacts with various PSD proteins. Brain Res Mol Brain Res (2005) 0.82
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits. Cell (2011) 4.58
The local differentiation of myelinated axons at nodes of Ranvier. Nat Rev Neurosci (2003) 4.14
Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1. J Cell Biol (2003) 3.80
Investigations of caspr2, an autoantigen of encephalitis and neuromyotonia. Ann Neurol (2011) 2.99
Gliomedin mediates Schwann cell-axon interaction and the molecular assembly of the nodes of Ranvier. Neuron (2005) 2.63
AnkyrinG is required for maintenance of the axon initial segment and neuronal polarity. J Cell Biol (2008) 2.59
betaIV spectrin is recruited to axon initial segments and nodes of Ranvier by ankyrinG. J Cell Biol (2007) 2.25
A distal axonal cytoskeleton forms an intra-axonal boundary that controls axon initial segment assembly. Cell (2012) 2.21
Neurofascin assembles a specialized extracellular matrix at the axon initial segment. J Cell Biol (2007) 2.20
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Spectrins and ankyrinB constitute a specialized paranodal cytoskeleton. J Neurosci (2006) 1.90
Neurofascin as a novel target for autoantibody-mediated axonal injury. J Exp Med (2007) 1.77
A central role for Necl4 (SynCAM4) in Schwann cell-axon interaction and myelination. Nat Neurosci (2007) 1.72
BetaIV spectrins are essential for membrane stability and the molecular organization of nodes of Ranvier. J Neurosci (2004) 1.69
Three mechanisms assemble central nervous system nodes of Ranvier. Neuron (2013) 1.68
A glial signal consisting of gliomedin and NrCAM clusters axonal Na+ channels during the formation of nodes of Ranvier. Neuron (2010) 1.67
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A myelin galactolipid, sulfatide, is essential for maintenance of ion channels on myelinated axon but not essential for initial cluster formation. J Neurosci (2002) 1.51
ADAM22, a Kv1 channel-interacting protein, recruits membrane-associated guanylate kinases to juxtaparanodes of myelinated axons. J Neurosci (2010) 1.47
Anti-GM1 antibodies cause complement-mediated disruption of sodium channel clusters in peripheral motor nerve fibers. J Neurosci (2007) 1.46
Caspr regulates the processing of contactin and inhibits its binding to neurofascin. J Cell Biol (2003) 1.45
Molecular domains of myelinated axons in the peripheral nervous system. Glia (2008) 1.44
Postsynaptic density-93 clusters Kv1 channels at axon initial segments independently of Caspr2. J Neurosci (2008) 1.41
Gangliosides contribute to stability of paranodal junctions and ion channel clusters in myelinated nerve fibers. Glia (2007) 1.36
BetaIVSigma1 spectrin stabilizes the nodes of Ranvier and axon initial segments. J Cell Biol (2004) 1.36
Molecular mechanisms of node of Ranvier formation. Curr Opin Cell Biol (2008) 1.35
Retention of a cell adhesion complex at the paranodal junction requires the cytoplasmic region of Caspr. J Cell Biol (2002) 1.35
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Glial regulation of the axonal membrane at nodes of Ranvier. Curr Opin Neurobiol (2006) 1.30
Where is the spike generator of the cochlear nerve? Voltage-gated sodium channels in the mouse cochlea. J Neurosci (2005) 1.28
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Organization of myelinated axons by Caspr and Caspr2 requires the cytoskeletal adapter protein 4.1B. J Neurosci (2010) 1.24
Caspr3 and caspr4, two novel members of the caspr family are expressed in the nervous system and interact with PDZ domains. Mol Cell Neurosci (2002) 1.22
Spectrin and ankyrin-based cytoskeletons at polarized domains in myelinated axons. Exp Biol Med (Maywood) (2008) 1.22
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Mechanisms and roles of axon-Schwann cell interactions. J Neurosci (2004) 1.21
WAVE1 is required for oligodendrocyte morphogenesis and normal CNS myelination. J Neurosci (2006) 1.21
alphaII-spectrin is essential for assembly of the nodes of Ranvier in myelinated axons. Curr Biol (2007) 1.20
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Genetic dysmyelination alters the molecular architecture of the nodal region. J Neurosci (2002) 1.19
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Short- and long-term plasticity at the axon initial segment. J Neurosci (2011) 1.19
Proteomic mapping provides powerful insights into functional myelin biology. Proc Natl Acad Sci U S A (2004) 1.17
Early events in node of Ranvier formation during myelination and remyelination in the PNS. Neuron Glia Biol (2006) 1.14
An ankyrinG-binding motif is necessary and sufficient for targeting Nav1.6 sodium channels to axon initial segments and nodes of Ranvier. J Neurosci (2012) 1.13
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