Pages that link to "Q22011028"
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The following pages link to Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels (Q22011028):
Displaying 50 items.
- Contactin associated protein 2 (Q21102466) (← links)
- Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1 (Q21261497) (← links)
- Advances in autism genetics: on the threshold of a new neurobiology (Q22251023) (← links)
- The local differentiation of myelinated axons at nodes of Ranvier (Q22337224) (← links)
- The human contactin-associated protein-like 2 gene (CNTNAP2) spans over 2 Mb of DNA at chromosome 7q35 (Q24291227) (← links)
- Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues (Q24291372) (← links)
- The Role of the Ankyrin-Binding Protein NrCAM in Node of Ranvier Formation (Q24299302) (← links)
- Caspr3 and caspr4, two novel members of the caspr family are expressed in the nervous system and interact with PDZ domains (Q24300668) (← links)
- CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila (Q24315560) (← links)
- Contactin-associated protein (Caspr) 2 interacts with carboxypeptidase E in the CNS (Q24320519) (← links)
- Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1 (Q24321543) (← links)
- Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan's syndrome and acquired neuromyotonia (Q24623766) (← links)
- A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism (Q24643479) (← links)
- Nogo-A at CNS paranodes is a ligand of Caspr: possible regulation of K(+) channel localization (Q24644741) (← links)
- [Beta]IV-spectrin regulates sodium channel clustering through ankyrin-G at axon initial segments and nodes of Ranvier (Q24652657) (← links)
- Sodium channel Na(v)1.6 is localized at nodes of ranvier, dendrites, and synapses (Q24653551) (← links)
- Caspr regulates the processing of contactin and inhibits its binding to neurofascin (Q24672003) (← links)
- Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cells (Q24674840) (← links)
- Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers (Q24675297) (← links)
- Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development (Q26269870) (← links)
- Pediatric Autoimmune Disorders Associated with Streptococcal Infections and Tourette's Syndrome in Preclinical Studies. (Q26738436) (← links)
- Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders (Q26748761) (← links)
- Mouse Genetic Models of Human Brain Disorders (Q26752246) (← links)
- Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder (Q26768144) (← links)
- Striatal Circuits as a Common Node for Autism Pathophysiology (Q26768226) (← links)
- Behavioral phenotypes of genetic mouse models of autism (Q26781456) (← links)
- New insights into the pathogenesis and therapeutics of episodic ataxia type 1 (Q26782897) (← links)
- Myelin damage and repair in pathologic CNS: challenges and prospects (Q26797407) (← links)
- Autoimmune encephalitis in psychiatric institutions: current perspectives (Q28079666) (← links)
- Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders (Q28086930) (← links)
- Structure and evolution of neurexin genes: insight into the mechanism of alternative splicing (Q28201310) (← links)
- Protein 4.1B associates with both Caspr/paranodin and Caspr2 at paranodes and juxtaparanodes of myelinated fibres (Q28204655) (← links)
- alpha-Latrotoxin and its receptors: neurexins and CIRL/latrophilins (Q28214351) (← links)
- ADAM22, a Kv1 channel-interacting protein, recruits membrane-associated guanylate kinases to juxtaparanodes of myelinated axons (Q28505131) (← links)
- Opalin, a transmembrane sialylglycoprotein located in the central nervous system myelin paranodal loop membrane (Q28505219) (← links)
- A glial signal consisting of gliomedin and NrCAM clusters axonal Na+ channels during the formation of nodes of Ranvier (Q28507204) (← links)
- Multiple molecular interactions determine the clustering of Caspr2 and Kv1 channels in myelinated axons (Q28507978) (← links)
- Contactin associated protein 1 (Q28558809) (← links)
- Potassium voltage-gated channel subfamily A regulatory beta subunit 2 (Q28561951) (← links)
- Potassium voltage-gated channel subfamily A member 2 (Q28562552) (← links)
- Two heteromeric Kv1 potassium channels differentially regulate action potential firing (Q28569793) (← links)
- Type II brain 4.1 (4.1B/KIAA0987), a member of the protein 4.1 family, is localized to neuronal paranodes (Q28579926) (← links)
- Spectrins and ankyrinB constitute a specialized paranodal cytoskeleton (Q28581257) (← links)
- Localization of Caspr2 in myelinated nerves depends on axon-glia interactions and the generation of barriers along the axon (Q28595021) (← links)
- Using Gene Ontology to describe the role of the neurexin-neuroligin-SHANK complex in human, mouse and rat and its relevance to autism (Q28645671) (← links)
- Shining a light on CNTNAP2: complex functions to complex disorders (Q28660523) (← links)
- Distribution of language-related Cntnap2 protein in neural circuits critical for vocal learning (Q28660821) (← links)
- Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments (Q28672682) (← links)
- What does CNTNAP2 reveal about autism spectrum disorder? (Q28708820) (← links)
- Recent advances in the genetics of language impairment (Q28748712) (← links)