scholarly article | Q13442814 |
P2093 | author name string | V. Bennett | |
S. Lambert | |||
J. Q. Davis | |||
P2860 | cites work | Brain spectrin. Isolation of subunits and formation of hybrids with erythrocyte spectrin subunits. | Q48793742 |
Identification of O-linked N-acetylglucosamine modification of ankyrinG isoforms targeted to nodes of Ranvier | Q48831078 | ||
Sodium channels in single demyelinated mammalian axons | Q51755545 | ||
Clustering of Na+ channels and node of Ranvier formation in remyelinating axons. | Q55065290 | ||
Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A | Q55671003 | ||
Ankyrin binding to (Na+ + K+)ATPase and implications for the organization of membrane domains in polarized cells | Q57253842 | ||
Clustering of voltage-dependent sodium channels on axons depends on Schwann cell contact | Q59095459 | ||
Ankyrin and spectrin associate with voltage-dependent sodium channels in brain | Q59095499 | ||
Long lives for homozygous trembler mutant mice despite virtual absence of peripheral nerve myelin | Q68425029 | ||
Co-localization of the myelin-associated glycoprotein and the microfilament components, F-actin and spectrin, in Schwann cells of myelinated nerve fibres | Q69061419 | ||
Mechanism for binding site diversity on ankyrin. Comparison of binding sites on ankyrin for neurofascin and the Cl-/HCO3- anion exchanger | Q70825986 | ||
Development of axonal membrane specializations defines nodes of Ranvier and precedes Schwann cell myelin elaboration | Q71360196 | ||
The clustering of axonal sodium channels during development of the peripheral nervous system | Q71394719 | ||
Aggregation of sodium channels induced by a postnatally upregulated isoform of agrin | Q71574134 | ||
Hypomyelination alters K+ channel expression in mouse mutants shiverer and Trembler | Q71623681 | ||
The ANK Repeats of Erythrocyte Ankyrin Form Two Distinct but Cooperative Binding Sites for the Erythrocyte Anion Exchanger | Q72036870 | ||
Asymmetry currents in the mammalian myelinated nerve | Q72899292 | ||
AnkyrinG. A new ankyrin gene with neural-specific isoforms localized at the axonal initial segment and node of Ranvier | Q24311821 | ||
A theory of the effects of fibre size in medullated nerve | Q24543926 | ||
Bravo/Nr-CAM is closely related to the cell adhesion molecules L1 and Ng-CAM and has a similar heterodimer structure | Q27485693 | ||
Ankyrin-independent membrane protein-binding sites for brain and erythrocyte spectrin | Q28285943 | ||
The L1 family of neural cell adhesion molecules: old proteins performing new tricks | Q28294788 | ||
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 | ||
Existence of distinct sodium channel messenger RNAs in rat brain | Q28566276 | ||
An isoform of ankyrin is localized at nodes of Ranvier in myelinated axons of central and peripheral nerves | Q28579175 | ||
Structure and function of the beta 2 subunit of brain sodium channels, a transmembrane glycoprotein with a CAM motif | Q28579493 | ||
The agrin gene codes for a family of basal lamina proteins that differ in function and distribution | Q34234963 | ||
Tyrosine phosphorylation at a site highly conserved in the L1 family of cell adhesion molecules abolishes ankyrin binding and increases lateral mobility of neurofascin | Q34426198 | ||
Agrin-like molecules at synaptic sites in normal, denervated, and damaged skeletal muscles | Q36217250 | ||
Neuroglian-mediated cell adhesion induces assembly of the membrane skeleton at cell contact sites | Q36236826 | ||
Immunocytochemical localization of sodium channel distributions in the excitable membranes of Electrophorus electricus | Q36319331 | ||
A new 440-kD isoform is the major ankyrin in neonatal rat brain | Q36530617 | ||
440-kD ankyrinB: structure of the major developmentally regulated domain and selective localization in unmyelinated axons | Q36534838 | ||
Density of sodium channels in mammalian myelinated nerve fibers and nature of the axonal membrane under the myelin sheath | Q37598575 | ||
The spectrin-based membrane skeleton and micron-scale organization of the plasma membrane | Q40800564 | ||
From anemia to cerebellar dysfunction. A review of the ankyrin gene family | Q40871566 | ||
Expression of four immunoglobulin superfamily adhesion molecules (L1, Nr-CAM/Bravo, neurofascin/ABGP, and N-CAM) in the developing mouse spinal cord | Q41370103 | ||
Immunoelectron microscopic localization of neural cell adhesion molecules (L1, N-CAM, and MAG) and their shared carbohydrate epitope and myelin basic protein in developing sciatic nerve | Q41522607 | ||
Development of the axon membrane during differentiation of myelinated fibres in spinal nerve roots | Q41539234 | ||
Ankyrin-binding proteins related to nervous system cell adhesion molecules: candidates to provide transmembrane and intercellular connections in adult brain | Q42259093 | ||
Ankyrin binding activity shared by the neurofascin/L1/NrCAM family of nervous system cell adhesion molecules | Q42695486 | ||
Ultrastructural features of the immature peripheral nerve | Q43016266 | ||
The node of Ranvier in the central nervous system | Q43653035 | ||
Induction of sodium channel clustering by oligodendrocytes | Q46198260 | ||
Three-dimensional fine structure of cytoskeletal-membrane interactions at nodes of Ranvier | Q46593782 | ||
Clustering of voltage-sensitive sodium channels on axons is independent of direct Schwann cell contact in the dystrophic mouse. | Q46875791 | ||
P433 | issue | 18 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | morphogenesis | Q815547 |
avian proteins | Q75833037 | ||
P304 | page(s) | 7025-7036 | |
P577 | publication date | 1997-09-01 | |
1997-09-15 | |||
P1433 | published in | Journal of Neuroscience | Q1709864 |
P1476 | title | Morphogenesis of the node of Ranvier: co-clusters of ankyrin and ankyrin-binding integral proteins define early developmental intermediates | |
Morphogenesis of the Node of Ranvier: Co-Clusters of Ankyrin and Ankyrin-Binding Integral Proteins Define Early Developmental Intermediates | |||
P478 | volume | 17 |
Q28507204 | A glial signal consisting of gliomedin and NrCAM clusters axonal Na+ channels during the formation of nodes of Ranvier |
Q34738298 | A hierarchy of ankyrin-spectrin complexes clusters sodium channels at nodes of Ranvier |
Q80932207 | Acute demyelination disrupts the molecular organization of peripheral nervous system nodes |
Q51237153 | Altered ion channels in an animal model of Charcot-Marie-Tooth disease type IA. |
Q36328448 | An oligodendrocyte cell adhesion molecule at the site of assembly of the paranodal axo-glial junction |
Q41391566 | Ankyrin 3: genetic association with bipolar disorder and relevance to disease pathophysiology |
Q31048324 | Ankyrin G and voltage gated sodium channels colocalize in human neuroma--key proteins of membrane remodeling after axonal injury |
Q51565790 | Ankyrin G expression is associated with androgen receptor stability, invasiveness, and lethal outcome in prostate cancer patients |
Q37617545 | Ankyrin protein networks in membrane formation and stabilization |
Q24685343 | Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments |
Q24682474 | AnkyrinG is required for clustering of voltage-gated Na channels at axon initial segments and for normal action potential firing |
Q34132769 | Ankyrins and cellular targeting of diverse membrane proteins to physiological sites |
Q36251703 | Assembly and maintenance of nodes of ranvier rely on distinct sources of proteins and targeting mechanisms |
Q37743241 | Axo-glial antigens as targets in multiple sclerosis: implications for axonal and grey matter injury. |
Q36313415 | Axo-glial interactions regulate the localization of axonal paranodal proteins |
Q36328416 | Axo-glial septate junctions. The maestro of nodal formation and myelination? |
Q33650497 | Axonal Membranes and Their Domains: Assembly and Function of the Axon Initial Segment and Node of Ranvier |
Q45966072 | Axons and astrocytes release ATP and glutamate to evoke calcium signals in NG2-glia. |
Q80467956 | BetaIV spectrins are essential for membrane stability and the molecular organization of nodes of Ranvier |
Q41866964 | Both laminin and Schwann cell dystroglycan are necessary for proper clustering of sodium channels at nodes of Ranvier. |
Q22011028 | Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels |
Q33290469 | Cloning and expression of a zebrafish SCN1B ortholog and identification of a species-specific splice variant |
Q36323794 | Clustering of neuronal potassium channels is independent of their interaction with PSD-95. |
Q33945987 | Compact myelin dictates the differential targeting of two sodium channel isoforms in the same axon. |
Q30447603 | Compartmentalizing the neuronal plasma membrane from axon initial segments to synapses |
Q28188411 | Contactin associates with Na+ channels and increases their functional expression |
Q52134357 | Contactin orchestrates assembly of the septate-like junctions at the paranode in myelinated peripheral nerve |
Q52174918 | Dependence of nodal sodium channel clustering on paranodal axoglial contact in the developing CNS. |
Q42510977 | Deposition of the NG2 proteoglycan at nodes of Ranvier in the peripheral nervous system. |
Q34013147 | Developing nodes of Ranvier are defined by ankyrin-G clustering and are independent of paranodal axoglial adhesion |
Q44746062 | Development of a model for microphysiological simulations: small nodes of ranvier from peripheral nerves of mice reconstructed by electron tomography |
Q34942239 | Development of nodes of Ranvier |
Q46951133 | Differential expression and functions of neuronal and glial neurofascin isoforms and splice variants during PNS development |
Q34389405 | Disrupted synaptic development in the hypoxic newborn brain |
Q42010808 | Early and Late Loss of the Cytoskeletal Scaffolding Protein, Ankyrin G Reveals Its Role in Maturation and Maintenance of Nodes of Ranvier in Myelinated Axons. |
Q24323237 | Early events in node of Ranvier formation during myelination and remyelination in the PNS |
Q28207269 | FIGQY phosphorylation defines discrete populations of L1 cell adhesion molecules at sites of cell-cell contact and in migrating neurons |
Q44376585 | Functional specialization of the axon initial segment by isoform-specific sodium channel targeting. |
Q58107241 | Genetic dysmyelination alters the molecular architecture of the nodal region |
Q39644189 | Glial and neuronal isoforms of Neurofascin have distinct roles in the assembly of nodes of Ranvier in the central nervous system |
Q37231051 | Guided exploration of genomic risk for gray matter abnormalities in schizophrenia using parallel independent component analysis with reference |
Q34193048 | Identification of a Conserved Ankyrin-binding Motif in the Family of Sodium Channel α Subunits |
Q33244434 | Identification of novel cell-adhesion molecules in peripheral nerves using a signal-sequence trap |
Q73002671 | Initiation of sodium channel clustering at the node of Ranvier in the mouse optic nerve |
Q52168360 | Ion channel sequestration in central nervous system axons |
Q34560911 | Ion transport proteins anchor and regulate the cytoskeleton |
Q36323012 | Local ERM activation and dynamic growth cones at Schwann cell tips implicated in efficient formation of nodes of Ranvier |
Q37698145 | Long-term maintenance of Na+ channels at nodes of Ranvier depends on glial contact mediated by gliomedin and NrCAM. |
Q35924084 | Mechanisms and roles of axon-Schwann cell interactions. |
Q102389012 | Mechanisms of node of Ranvier assembly |
Q34995041 | Molecular constituents of the node of Ranvier |
Q34085479 | Molecular domains of myelinated axons |
Q37273627 | Molecular domains of myelinated axons in the peripheral nervous system |
Q37302001 | Molecular mechanisms of node of Ranvier formation. |
Q33666278 | Myelination and regional domain differentiation of the axon |
Q36256346 | Nervous system defects of AnkyrinB (-/-) mice suggest functional overlap between the cell adhesion molecule L1 and 440-kD AnkyrinB in premyelinated axons |
Q41755566 | Neural cell recognition molecule L1: from cell biology to human hereditary brain malformations |
Q35044841 | Neurofascin 140 is an embryonic neuronal neurofascin isoform that promotes the assembly of the node of Ranvier |
Q57362501 | Neurofascin interactions play a critical role in clustering sodium channels, ankyrinG and βIV spectrin at peripheral nodes of Ranvier |
Q78795197 | Nodal sodium channel domain integrity depends on the conformation of the paranodal junction, not on the presence of transverse bands |
Q34558317 | Nodes of Ranvier act as barriers to restrict invasion of flanking paranodal domains in myelinated axons. |
Q28582251 | Nodes of Ranvier and axon initial segments are ankyrin G-dependent domains that assemble by distinct mechanisms |
Q34500816 | Nodes of Ranvier come of age. |
Q34657208 | Nodes of Ranvier form in association with ezrin-radixin-moesin (ERM)-positive Schwann cell processes |
Q77307241 | Nr-CAM and neurofascin interactions regulate ankyrin G and sodium channel clustering at the node of Ranvier |
Q48895120 | Nr-CAM expression in the developing mouse nervous system: ventral midline structures, specific fiber tracts, and neuropilar regions |
Q33726825 | Organization and maintenance of molecular domains in myelinated axons |
Q34275361 | Organizing principles of the axoglial apparatus |
Q35510088 | Paranodal myelin retraction in relapsing experimental autoimmune encephalomyelitis visualized by coherent anti-Stokes Raman scattering microscopy |
Q38020957 | Pathogenic and physiological autoantibodies in the central nervous system |
Q35042867 | Perlecan is recruited by dystroglycan to nodes of Ranvier and binds the clustering molecule gliomedin. |
Q35558428 | Polarized domains of myelinated axons. |
Q30837291 | Postnatal Loss of Neuronal and Glial Neurofascins Differentially Affects Node of Ranvier Maintenance and Myelinated Axon Function |
Q37010706 | Protein kinase CK2 contributes to the organization of sodium channels in axonal membranes by regulating their interactions with ankyrin G. |
Q26766627 | Reciprocal Interactions between Cell Adhesion Molecules of the Immunoglobulin Superfamily and the Cytoskeleton in Neurons |
Q34321652 | Regulation of Na+ channel distribution in the nervous system |
Q89120913 | Reorganization of Destabilized Nodes of Ranvier in βIV Spectrin Mutants Uncovers Critical Timelines for Nodal Restoration and Prevention of Motor Paresis |
Q28566467 | Restriction of 480/270-kD Ankyrin G to Axon Proximal Segments Requires Multiple Ankyrin G-specific Domains |
Q36324587 | Retention of a cell adhesion complex at the paranodal junction requires the cytoplasmic region of Caspr |
Q33707595 | Schwann cells and their precursors emerge as major regulators of nerve development |
Q36119690 | Secreted gliomedin is a perinodal matrix component of peripheral nerves |
Q55360507 | Simultaneous Ablation of Neuronal Neurofascin and Ankyrin G in Young and Adult Mice Reveals Age-Dependent Increase in Nodal Stability in Myelinated Axons and Differential Effects on the Lifespan. |
Q24685559 | Sodium channel beta1 and beta3 subunits associate with neurofascin through their extracellular immunoglobulin-like domain |
Q24291372 | Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues |
Q38364754 | Subcellular patterning: axonal domains with specialized structure and function. |
Q24669523 | Targeted ablation of NrCAM or ankyrin-B results in disorganized lens fibers leading to cataract formation |
Q28594823 | The Effect of the Mouse MutationClaw Pawon Myelination and Nodal Frequency in Sciatic Nerves |
Q52167693 | The L1-type cell adhesion molecule neuroglian influences the stability of neural ankyrin in the Drosophila embryo but not its axonal localization. |
Q38583864 | The Nodes of Ranvier: Molecular Assembly and Maintenance |
Q24299302 | The Role of the Ankyrin-Binding Protein NrCAM in Node of Ranvier Formation |
Q37333152 | The actin cytoskeleton in endothelial cell phenotypes |
Q21560854 | The cognitive impact of the ANK3 risk variant for bipolar disorder: initial evidence of selectivity to signal detection during sustained attention |
Q36514764 | The distribution and targeting of neuronal voltage-gated ion channels |
Q36328347 | The glycosylphosphatidyl inositol-anchored adhesion molecule F3/contactin is required for surface transport of paranodin/contactin-associated protein (caspr) |
Q37288431 | The interaction between L1-type proteins and ankyrins--a master switch for L1-type CAM function |
Q22337224 | The local differentiation of myelinated axons at nodes of Ranvier |
Q38119786 | The making of a node: a co-production of neurons and glia |
Q24290724 | The neural cell recognition molecule neurofascin interacts with syntenin-1 but not with syntenin-2, both of which reveal self-associating activity |
Q33851812 | The peripheral myelin protein 22 and epithelial membrane protein family |
Q37969855 | The role of NrCAM in neural development and disorders—Beyond a simple glue in the brain |
Q37776425 | The spectrin-ankyrin-4.1-adducin membrane skeleton: adapting eukaryotic cells to the demands of animal life |
Q28579926 | Type II brain 4.1 (4.1B/KIAA0987), a member of the protein 4.1 family, is localized to neuronal paranodes |
Q46503296 | Vesicular apparatus, including functional calcium channels, are present in developing rodent optic nerve axons and are required for normal node of Ranvier formation. |
Q34479857 | Voltage-gated ion channels in the axon initial segment of human cortical pyramidal cells and their relationship with chandelier cells |
Q28574440 | Voltage-gated sodium channels and ankyrinG occupy a different postsynaptic domain from acetylcholine receptors from an early stage of neuromuscular junction maturation in rats |
Q24652657 | [Beta]IV-spectrin regulates sodium channel clustering through ankyrin-G at axon initial segments and nodes of Ranvier |
Q36117801 | betaIV spectrin is recruited to axon initial segments and nodes of Ranvier by ankyrinG. |
Q24290541 | betaIV spectrin, a new spectrin localized at axon initial segments and nodes of ranvier in the central and peripheral nervous system |
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