| scholarly article | Q13442814 |
| P50 | author | Elior Peles | Q38642146 |
| James L Salzer | Q46611651 | ||
| P2093 | author name string | R Martinez | |
| J S Trimmer | |||
| S Poliak | |||
| S Einheber | |||
| P Shrager | |||
| A Custer | |||
| L Gollan | |||
| P2860 | cites work | AnkyrinG. A new ankyrin gene with neural-specific isoforms localized at the axonal initial segment and node of Ranvier | Q24311821 |
| Identification of a novel contactin-associated transmembrane receptor with multiple domains implicated in protein-protein interactions | Q24316000 | ||
| A tripartite protein complex with the potential to couple synaptic vesicle exocytosis to cell adhesion in brain | Q24317295 | ||
| Neurexins: synaptic cell surface proteins related to the alpha-latrotoxin receptor and laminin | Q24337780 | ||
| Neurexin III alpha: extensive alternative splicing generates membrane-bound and soluble forms | Q26269980 | ||
| Binding of neuroligins to PSD-95 | Q28247782 | ||
| Neurexins: three genes and 1001 products | Q28260363 | ||
| Structure and evolution of neurexophilin | Q28284061 | ||
| The carbonic anhydrase domain of receptor tyrosine phosphatase beta is a functional ligand for the axonal cell recognition molecule contactin | Q28294756 | ||
| Heteromultimeric K+ channels in terminal and juxtaparanodal regions of neurons | Q28505460 | ||
| Molecular composition of the node of Ranvier: identification of ankyrin-binding cell adhesion molecules neurofascin (mucin+/third FNIII domain-) and NrCAM at nodal axon segments | Q28566036 | ||
| Paranodin, a glycoprotein of neuronal paranodal membranes | Q28572513 | ||
| Association and colocalization of the Kvbeta1 and Kvbeta2 beta-subunits with Kv1 alpha-subunits in mammalian brain K+ channel complexes | Q28573970 | ||
| Regional and ultrastructural distribution of the alpha 8 integrin subunit in developing and adult rat brain suggests a role in synaptic function | Q28583637 | ||
| Generation and characterization of subtype-specific monoclonal antibodies to K+ channel alpha- and beta-subunit polypeptides | Q28583840 | ||
| Temperature-sensitive neuromuscular transmission in Kv1.1 null mice: role of potassium channels under the myelin sheath in young nerves | Q28584818 | ||
| Neuroligin 1: a splice site-specific ligand for beta-neurexins | Q29614429 | ||
| The PDZ domain of human erythrocyte p55 mediates its binding to the cytoplasmic carboxyl terminus of glycophorin C. Analysis of the binding interface by in vitro mutagenesis. | Q33292135 | ||
| Molecular dissection of the myelinated axon | Q34305770 | ||
| Clustering sodium channels at the node of Ranvier: close encounters of the axon-glia kind | Q34431218 | ||
| Morphogenesis of the node of Ranvier: co-clusters of ankyrin and ankyrin-binding integral proteins define early developmental intermediates. | Q34437511 | ||
| Myelinated nerve fibres in the CNS. | Q34730523 | ||
| The axonal membrane protein Caspr, a homologue of neurexin IV, is a component of the septate-like paranodal junctions that assemble during myelination | Q36254979 | ||
| A conserved functional domain of Drosophila coracle is required for localization at the septate junction and has membrane-organizing activity | Q36255151 | ||
| Hippocampal alpha2a-adrenergic receptors are located predominantly presynaptically but are also found postsynaptically and in selective astrocytes | Q39758463 | ||
| Molecular specializations at nodes and paranodes in peripheral nerve | Q41135988 | ||
| Node-paranode regions as local degradative centres in alpha-motor axons | Q41140026 | ||
| PDZs and receptor/channel clustering: rounding up the latest suspects | Q41189268 | ||
| Deciphering the function of neurexins at cellular junctions | Q41470748 | ||
| Axon-glia interactions: Building a smart nerve fiber | Q41520600 | ||
| Synaptic clustering of Fascilin II and Shaker: essential targeting sequences and role of Dlg. | Q46097977 | ||
| Induction of sodium channel clustering by oligodendrocytes | Q46198260 | ||
| A glial-neuronal signaling pathway revealed by mutations in a neurexin-related protein | Q47070174 | ||
| A Drosophila neurexin is required for septate junction and blood-nerve barrier formation and function | Q47071954 | ||
| Discs Lost, a novel multi-PDZ domain protein, establishes and maintains epithelial polarity. | Q47975688 | ||
| Neurexin IV, caspr and paranodin--novel members of the neurexin family: encounters of axons and glia | Q48368271 | ||
| Extranodal particle accumulations in the axolemma of myelinated frog optic axons | Q48634489 | ||
| Development of nodal and paranodal membrane specializations in amphibian peripheral nerves. | Q48960405 | ||
| Clustering of Na+ channels and node of Ranvier formation in remyelinating axons. | Q55065290 | ||
| Clustering of voltage-dependent sodium channels on axons depends on Schwann cell contact | Q59095459 | ||
| The clustering of axonal sodium channels during development of the peripheral nervous system | Q71394719 | ||
| Hypomyelination alters K+ channel expression in mouse mutants shiverer and Trembler | Q71623681 | ||
| Multifocal pattern of postnatal development of the macroglial framework of the rat fimbria | Q71680806 | ||
| Potassium channel distribution, clustering, and function in remyelinating rat axons | Q73977270 | ||
| Neurexins are functional alpha-latrotoxin receptors | Q77303735 | ||
| Dynamic potassium channel distributions during axonal development prevent aberrant firing patterns | Q77765616 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | myelination | Q14876135 |
| juxtaparanode region of axon | Q14905631 | ||
| Contactin associated protein 2 | Q21102466 | ||
| P304 | page(s) | 1037-1047 | |
| P577 | publication date | 1999-12-01 | |
| P1433 | published in | Neuron | Q3338676 |
| P1476 | title | Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels | |
| P478 | volume | 24 |
| Q35960033 | A Chinese female Morvan patient with LGI1 and CASPR2 antibodies: a case report |
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| Q39505613 | A-kinase anchoring protein 150 expression in a specific subset of TRPV1- and CaV 1.2-positive nociceptive rat dorsal root ganglion neurons. |
| Q28505131 | ADAM22, a Kv1 channel-interacting protein, recruits membrane-associated guanylate kinases to juxtaparanodes of myelinated axons |
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| Q80932207 | Acute demyelination disrupts the molecular organization of peripheral nervous system nodes |
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| Q36328448 | An oligodendrocyte cell adhesion molecule at the site of assembly of the paranodal axo-glial junction |
| Q38678076 | Anatomy and Cell Biology of Autism Spectrum Disorder: Lessons from Human Genetics |
| Q24623766 | 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 |
| Q92404698 | Antigenic Targets of Patient and Maternal Autoantibodies in Autism Spectrum Disorder |
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| Q92851636 | Association of GDNF and CNTNAP2 gene variants with gambling |
| Q24675297 | Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers |
| Q37235447 | Association of the Kv1 family of K+ channels and their functional blueprint in the properties of auditory neurons as revealed by genetic and functional analyses |
| Q38031004 | Autism genetics: searching for specificity and convergence |
| Q37068738 | Autism spectrum disorder causes, mechanisms, and treatments: focus on neuronal synapses |
| Q55021064 | Autoantibodies Against the Node of Ranvier in Seropositive Chronic Inflammatory Demyelinating Polyneuropathy: Diagnostic, Pathogenic, and Therapeutic Relevance. |
| Q37903490 | Autoantibodies associated with diseases of the CNS: new developments and future challenges |
| Q30446880 | Autoantibodies to epilepsy-related LGI1 in limbic encephalitis neutralize LGI1-ADAM22 interaction and reduce synaptic AMPA receptors |
| Q28079666 | Autoimmune encephalitis in psychiatric institutions: current perspectives |
| Q31923923 | Axon-glia interactions and the domain organization of myelinated axons requires neurexin IV/Caspr/Paranodin |
| Q26781456 | Behavioral phenotypes of genetic mouse models of autism |
| Q44222897 | Bidirectional relation between schizophrenia and epilepsy: a population-based retrospective cohort study |
| Q35207611 | C-peptide and diabetic neuropathy |
| Q48176109 | CASPR2 forms a complex with GPR37 via MUPP1 but not with GPR37(R558Q), an autism spectrum disorder-related mutation |
| Q24315560 | CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila |
| Q51901247 | CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy. |
| Q38794873 | CNTNAP2 is a direct FoxP2 target in vitro and in vivo in zebra finches: complex regulation by age and activity |
| Q34206301 | CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder |
| Q37191646 | CNTNAP2 polymorphisms and structural brain connectivity: a diffusion-tensor imaging study |
| Q26269870 | Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development |
| Q30176395 | Caspr and caspr2 are required for both radial and longitudinal organization of myelinated axons. |
| Q24672003 | Caspr regulates the processing of contactin and inhibits its binding to neurofascin |
| Q30376831 | Caspr2 autoantibodies target multiple epitopes. |
| Q41609524 | Caspr2-reactive antibody cloned from a mother of an ASD child mediates an ASD-like phenotype in mice |
| Q24300668 | Caspr3 and caspr4, two novel members of the caspr family are expressed in the nervous system and interact with PDZ domains |
| Q35850065 | Caspr4 interaction with LNX2 modulates the proliferation and neuronal differentiation of mouse neural progenitor cells |
| Q42482654 | Cell adhesion molecule contactin-associated protein 3 is expressed in the mouse basal ganglia during early postnatal stages. |
| Q35914130 | Characterisation of CASPR2 deficiency disorder--a syndrome involving autism, epilepsy and language impairment. |
| Q26748761 | Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders |
| Q34343185 | Clustered K+ channel complexes in axons |
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| Q55098524 | Common Ribs of Inhibitory Synaptic Dysfunction in the Umbrella of Neurodevelopmental Disorders. |
| Q37785806 | Comparing peripheral glial cell differentiation in Drosophila and vertebrates |
| Q28086930 | Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders |
| Q34142186 | Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems. |
| Q48333335 | Contactin-2/TAG-1, active on the front line for three decades |
| Q24320519 | Contactin-associated protein (Caspr) 2 interacts with carboxypeptidase E in the CNS |
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| Q38226805 | Convergent synaptic and circuit substrates underlying autism genetic risks |
| Q35013000 | Copy number variations in a population-based study of Charcot-Marie-Tooth disease |
| Q58106959 | Cross-species models of attention-deficit/hyperactivity disorder and autism spectrum disorder: lessons from CNTNAP2, ADGRL3, and PARK2 |
| Q36087830 | Crucial role of Drosophila neurexin in proper active zone apposition to postsynaptic densities, synaptic growth, and synaptic transmission |
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| Q34182374 | Differences and similarities in the transcriptional profile of peripheral whole blood in early and late-onset preeclampsia: insights into the molecular basis of the phenotype of preeclampsiaa |
| Q90272970 | Different protein expression patterns in rat spinal nerves during Wallerian degeneration assessed using isobaric tags for relative and absolute quantitation proteomics profiling |
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| Q34613441 | Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome. |
| Q24674840 | Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cells |
| Q28660821 | Distribution of language-related Cntnap2 protein in neural circuits critical for vocal learning |
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| Q33546654 | Downregulation of genes with a function in axon outgrowth and synapse formation in motor neurones of the VEGFdelta/delta mouse model of amyotrophic lateral sclerosis |
| Q47970219 | Drosophila Studies on Autism Spectrum Disorders |
| Q58803428 | Dysregulation of Parvalbumin Expression in the Mouse Model of Autism Spectrum Disorder |
| Q50497151 | Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum. |
| Q47650807 | Enhanced Transmission at the Calyx of Held Synapse in a Mouse Model for Angelman Syndrome |
| Q91750862 | Essential genetic findings in neurodevelopmental disorders |
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| Q47188113 | Expanding spectrum of contactin-associated protein 2 (CASPR2) autoimmunity-syndrome of parkinsonism and ataxia. |
| Q36370798 | Expanding the Ig superfamily code for laminar specificity in retina: expression and role of contactins |
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| Q40432935 | Expression of three gene families encoding cell-cell communication molecules in the prepubertal nonhuman primate hypothalamus |
| Q35168433 | First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes |
| Q30466258 | Function and mechanism of axonal targeting of voltage-sensitive potassium channels |
| Q26768144 | Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder |
| Q47140291 | Fundamental Elements in Autism: From Neurogenesis and Neurite Growth to Synaptic Plasticity. |
| Q34989614 | Galactolipids are molecular determinants of myelin development and axo-glial organization |
| Q28751380 | Genes and vocal learning |
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| Q58107241 | Genetic dysmyelination alters the molecular architecture of the nodal region |
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| Q35051968 | Genome-wide approach to identify second gene targets for malignant rhabdoid tumors using high-density oligonucleotide microarrays |
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| Q36159247 | Gilles de la Tourette syndrome is not linked to contactin-associated protein receptor 2 antibodies |
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| Q42013569 | Gliotactin, a novel marker of tricellular junctions, is necessary for septate junction development in Drosophila |
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| Q38108556 | Molecular basis for prospective pharmacological treatment strategies in intellectual disability syndromes |
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| Q26752246 | Mouse Genetic Models of Human Brain Disorders |
| Q28507978 | Multiple molecular interactions determine the clustering of Caspr2 and Kv1 channels in myelinated axons |
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| Q33329730 | Nav1.7 expression is increased in painful human dental pulp |
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| Q38178068 | Neurobiology of autism gene products: towards pathogenesis and drug targets. |
| Q30444060 | Neuronal Ig/Caspr recognition promotes the formation of axoaxonic synapses in mouse spinal cord |
| Q26782897 | New insights into the pathogenesis and therapeutics of episodic ataxia type 1 |
| Q48086006 | New members of the neurexin superfamily: multiple rodent homologues of the human CASPR5 gene |
| Q24644741 | Nogo-A at CNS paranodes is a ligand of Caspr: possible regulation of K(+) channel localization |
| Q34100081 | Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2 |
| Q33385599 | Novel leptin-regulated genes revealed by transcriptional profiling of the hypothalamic paraventricular nucleus |
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| Q28505219 | Opalin, a transmembrane sialylglycoprotein located in the central nervous system myelin paranodal loop membrane |
| Q33726825 | Organization and maintenance of molecular domains in myelinated axons |
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| Q55618045 | PECONPI: a novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders. |
| Q37287991 | Paraneoplastic Morvan's syndrome following surgical treatment of recurrent thymoma: A case report |
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| Q26738436 | Pediatric Autoimmune Disorders Associated with Streptococcal Infections and Tourette's Syndrome in Preclinical Studies. |
| Q35189801 | Periaxin is required for hexagonal geometry and membrane organization of mature lens fibers |
| Q40227033 | Peroxisomal dysfunctions cause lysosomal storage and axonal Kv1 channel redistribution in peripheral neuropathy |
| Q52049502 | Physiological maturation of photoreceptors depends on the voltage-gated sodium channel NaV1.6 (Scn8a). |
| Q35558428 | Polarized domains of myelinated axons. |
| Q37311277 | Postsynaptic density-93 clusters Kv1 channels at axon initial segments independently of Caspr2. |
| Q37503310 | Potential Autoepitope within the Extracellular Region of Contactin-Associated Protein-like 2 in Mice |
| Q48294517 | Presynaptic rat Kv1.2 channels suppress synaptic terminal hyperexcitability following action potential invasion |
| Q92524935 | Probing disrupted neurodevelopment in autism using human stem cell-derived neurons and organoids: An outlook into future diagnostics and drug development |
| Q28204655 | Protein 4.1B associates with both Caspr/paranodin and Caspr2 at paranodes and juxtaparanodes of myelinated fibres |
| Q39314105 | Psychiatric behaviors associated with cytoskeletal defects in radial neuronal migration |
| Q44473516 | RA175, which is the mouse ortholog of TSLC1, a tumor suppressor gene in human lung cancer, is a cell adhesion molecule |
| Q28748712 | Recent advances in the genetics of language impairment |
| Q42519872 | Recent progress on the molecular organization of myelinated axons |
| Q92375089 | Reduced Prefrontal Synaptic Connectivity and Disturbed Oscillatory Population Dynamics in the CNTNAP2 Model of Autism |
| Q38612196 | Regulation of neuronal migration, an emerging topic in autism spectrum disorders |
| Q33796083 | Relatively frequent switching of transcription start sites during cerebellar development. |
| Q36324587 | Retention of a cell adhesion complex at the paranodal junction requires the cytoplasmic region of Caspr |
| Q43908029 | Reversal of neuronal polarity characterized by conversion of dendrites into axons in neonatal rat cortical neurons in vitro. |
| Q33887392 | Role of transverse bands in maintaining paranodal structure and axolemmal domain organization in myelinated nerve fibers: effect on longevity in dysmyelinated mutant mice |
| Q28660523 | Shining a light on CNTNAP2: complex functions to complex disorders |
| Q35883077 | Significance of transcytosis in Alzheimer's disease: BACE1 takes the scenic route to axons |
| Q48460269 | Sodium channel Na(v)1.6 is expressed along nonmyelinated axons and it contributes to conduction |
| Q24653551 | Sodium channel Na(v)1.6 is localized at nodes of ranvier, dendrites, and synapses |
| Q33292270 | Sodium channel Nav1.6 accumulates at the site of infraorbital nerve injury |
| Q33475316 | Sodium channel expression and localization at demyelinated sites in painful human dental pulp |
| Q24291372 | Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues |
| Q28581257 | Spectrins and ankyrinB constitute a specialized paranodal cytoskeleton |
| Q37238305 | Sphingosine-1-phosphate can promote mast cell hyper-reactivity through regulation of contactin-4 expression |
| Q26768226 | Striatal Circuits as a Common Node for Autism Pathophysiology |
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| Q93013702 | Temporal Profile of Brain Gene Expression After Prey Catching Conditioning in an Anuran Amphibian |
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| Q83629652 | The genetics of Tourette syndrome |
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| Q34361263 | The pleiotropin/midkine family of cytokines: role in glial-neuronal signalling |
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| Q37776425 | The spectrin-ankyrin-4.1-adducin membrane skeleton: adapting eukaryotic cells to the demands of animal life |
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