scholarly article | Q13442814 |
P356 | DOI | 10.1002/CNE.20321 |
P698 | PubMed publication ID | 15514980 |
P50 | author | Steven S. Scherer | Q109937193 |
P2093 | author name string | Rohan Chitale | |
Edgardo J Arroyo | |||
Erich E Sirkowski | |||
P2860 | cites work | Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels | Q22011028 |
The local differentiation of myelinated axons at nodes of Ranvier | Q22337224 | ||
Subunit composition and novel localization of K+ channels in spinal cord | Q24290543 | ||
Identification of a novel contactin-associated transmembrane receptor with multiple domains implicated in protein-protein interactions | Q24316000 | ||
[Beta]IV-spectrin regulates sodium channel clustering through ankyrin-G at axon initial segments and nodes of Ranvier | Q24652657 | ||
Connexin29 expression, immunocytochemistry and freeze-fracture replica immunogold labelling (FRIL) in sciatic nerve | Q24670178 | ||
Syndecan-3 and syndecan-4 are enriched in Schwann cell perinodal processes | Q24799049 | ||
Protein 4.1B associates with both Caspr/paranodin and Caspr2 at paranodes and juxtaparanodes of myelinated fibres | Q28204655 | ||
Ezrin, radixin, and moesin are components of Schwann cell microvilli | Q28565637 | ||
Paranodin, a glycoprotein of neuronal paranodal membranes | Q28572513 | ||
Kv3.1b is a novel component of CNS nodes | Q28575189 | ||
Type II brain 4.1 (4.1B/KIAA0987), a member of the protein 4.1 family, is localized to neuronal paranodes | Q28579926 | ||
Paranodal junction formation and spermatogenesis require sulfoglycolipids | Q28588514 | ||
Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination | Q28588768 | ||
The node of Ranvier in experimental allergic neuritis: An electron microscope study | Q30640240 | ||
Axon-glia interactions and the domain organization of myelinated axons requires neurexin IV/Caspr/Paranodin | Q31923923 | ||
Myelin galactolipids: mediators of axon-glial interactions? | Q33811074 | ||
Structural alterations of nerve during cuff compression | Q33926539 | ||
Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems. | Q34142186 | ||
The effect of myelinating Schwann cells on axons. | Q34194525 | ||
Organizing principles of the axoglial apparatus | Q34275361 | ||
Morphogenesis of the Node of Ranvier: Co-Clusters of Ankyrin and Ankyrin-Binding Integral Proteins Define Early Developmental Intermediates | Q34437511 | ||
Nodes of Ranvier form in association with ezrin-radixin-moesin (ERM)-positive Schwann cell processes | Q34657208 | ||
Development of nodes of Ranvier | Q34942239 | ||
Molecular constituents of the node of Ranvier | Q34995041 | ||
Disease mechanisms in inherited neuropathies | Q35209953 | ||
Monoclonal antibodies recognize individual neurofilament triplet proteins | Q36315036 | ||
An oligodendrocyte cell adhesion molecule at the site of assembly of the paranodal axo-glial junction | Q36328448 | ||
Electron microscope observations on demyelination and remyelination in experimental allergic neuritis. I. Demyelination | Q36574232 | ||
Repair of segmental dehyelination in peripheral nerves: an electron microscope study | Q36574858 | ||
Molecular and functional characterization of protein 4.1B, a novel member of the protein 4.1 family with high level, focal expression in brain | Q41716768 | ||
M Channel KCNQ2 Subunits Are Localized to Key Sites for Control of Neuronal Network Oscillations and Synchronization in Mouse Brain | Q42513993 | ||
Schwann cell proliferation and migration during paranodal demyelination | Q42522418 | ||
Role of glial cells in the differentiation and function of myelinated axons | Q43973240 | ||
KCNQ2 is a nodal K+ channel. | Q44755361 | ||
Axonal Swellings and Degeneration in Mice Lacking the Major Proteolipid of Myelin | Q48004959 | ||
Monoclonal antibodies distinguish several differentially phosphorylated states of the two largest rat neurofilament subunits (NF-H and NF-M) and demonstrate their existence in the normal nervous system of adult rats | Q48190050 | ||
Contactin orchestrates assembly of the septate-like junctions at the paranode in myelinated peripheral nerve | Q52134357 | ||
Ion channel sequestration in central nervous system axons | Q52168360 | ||
Myelinating Schwann cells determine the internodal localization of Kv1.1, Kv1.2, Kvbeta2, and Caspr | Q52538564 | ||
Clustering of Na+ channels and node of Ranvier formation in remyelinating axons. | Q55065290 | ||
Genetic dysmyelination alters the molecular architecture of the nodal region | Q58107241 | ||
‘Intercalated’ Internodes in Nerve Fibres | Q58946208 | ||
Phosphorylation-dependent neurofilament epitopes are reduced at the node of Ranvier | Q67533964 | ||
Distortions of the nodes of Ranvier from axonal distension by filamentous masses in hexacarbon intoxication | Q71233615 | ||
Remodelling during remyelination in the peripheral nervous system | Q71311361 | ||
Clusters of axonal Na+ channels adjacent to remyelinating Schwann cells | Q71603568 | ||
Reorganization of the Axon Membrane in Demyelinated Peripheral Nerve Fibers: Morphological Evidence | Q72621440 | ||
Nerve conduction during peripheral demyelination and remyelination | Q72869138 | ||
Clustering of neuronal sodium channels requires contact with myelinating Schwann cells | Q73598232 | ||
Matrix metalloproteinase-dependent shedding of syndecan-3, a transmembrane heparan sulfate proteoglycan, in Schwann cells | Q73829253 | ||
Sodium channel distribution in axons of hypomyelinated and MAG null mutant mice | Q73886556 | ||
Potassium channel distribution, clustering, and function in remyelinating rat axons | Q73977270 | ||
Molecular organization of the nodal region is not altered in spontaneously diabetic BB-Wistar rats | Q74140651 | ||
Paranodal demyelination by gradual nerve stretch can be repaired by elongation of internodes | Q78457878 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | nervous system | Q9404 |
P304 | page(s) | 424-434 | |
P577 | publication date | 2004-11-01 | |
P1433 | published in | The Journal of Comparative Neurology | Q3186907 |
P1476 | title | Acute demyelination disrupts the molecular organization of peripheral nervous system nodes | |
P478 | volume | 479 |
Q28507204 | A glial signal consisting of gliomedin and NrCAM clusters axonal Na+ channels during the formation of nodes of Ranvier |
Q39505613 | A-kinase anchoring protein 150 expression in a specific subset of TRPV1- and CaV 1.2-positive nociceptive rat dorsal root ganglion neurons. |
Q38267815 | Accumulation of Kv7.2 channels in putative ectopic transduction zones of mice nerve-end neuromas |
Q47681711 | Altered distribution of juxtaparanodal kv1.2 subunits mediates peripheral nerve hyperexcitability in type 2 diabetes mellitus. |
Q36827564 | Altered potassium channel distribution and composition in myelinated axons suppresses hyperexcitability following injury. |
Q34538348 | An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations |
Q52578365 | Anti-GM1 antibodies cause complement-mediated disruption of sodium channel clusters in peripheral motor nerve fibers |
Q36930794 | Canadian Association of Neurosciences review: regulation of myelination by trophic factors and neuron-glial signaling. |
Q50321873 | Cell transplantation strategies for acquired and inherited disorders of peripheral myelin |
Q21144936 | Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels |
Q39554858 | Chronic peripheral nerve compression disrupts paranodal axoglial junctions. |
Q27335500 | Delayed nerve stimulation promotes axon-protective neurofilament phosphorylation, accelerates immune cell clearance and enhances remyelination in vivo in focally demyelinated nerves |
Q90436707 | Detecting Demyelination by PET: The Lesion as Imaging Target |
Q44424031 | Disruption of nodal architecture in skin biopsies of patients with demyelinating neuropathies |
Q24323237 | Early events in node of Ranvier formation during myelination and remyelination in the PNS |
Q36484556 | Evaluating dermal myelinated nerve fibers in skin biopsy |
Q36957751 | Evaluation of dermal myelinated nerve fibers in diabetes mellitus |
Q64970137 | Immunostaining in whole-mount lipid-cleared peripheral nerves and dorsal root ganglia after neuropathy in mice. |
Q88716863 | Internode length is reduced during myelination and remyelination by neurofilament medium phosphorylation in motor axons |
Q52572278 | Major myelin protein gene (P0) mutation causes a novel form of axonal degeneration. |
Q102389012 | Mechanisms of node of Ranvier assembly |
Q30474717 | Molecular disruptions of the panglial syncytium block potassium siphoning and axonal saltatory conduction: pertinence to neuromyelitis optica and other demyelinating diseases of the central nervous system |
Q33329730 | Nav1.7 expression is increased in painful human dental pulp |
Q36228999 | Neurofascin as a novel target for autoantibody-mediated axonal injury |
Q27009974 | Node of Ranvier Disruption as a Cause of Neurological Diseases |
Q33720640 | Organization of myelinated axons by Caspr and Caspr2 requires the cytoskeletal adapter protein 4.1B |
Q81651287 | Peripheral nerve hyperexcitability and the neuromuscular junction |
Q46614637 | Regulation and dysregulation of axon infrastructure by myelinating glia. |
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 |
Q52663506 | Stimulation-induced Ca(2+) influx at nodes of Ranvier in mouse peripheral motor axons. |
Q92527444 | Structure-activity relationship studies of four novel 4-aminopyridine K+ channel blockers |
Q58095242 | The conceptual introduction of the "demyelinating Schwann cell" in peripheral demyelinating neuropathies |
Q35744538 | The cytoskeletal adapter protein 4.1G organizes the internodes in peripheral myelinated nerves |
Q34555983 | The relationship of nerve fibre pathology to sensory function in entrapment neuropathy. |
Search more.