Gliomedin mediates Schwann cell-axon interaction and the molecular assembly of the nodes of Ranvier

Identification of a Gene That Causes Primary Open Angle Glaucoma

Stone, E. M., Fingert, J. H., Alward, W. L. M., Nguyen, T. D., Polansky, J. R., Sunden, S. L. F., Nishimura, D. Y., Clark, A. F., Nystuen, A., Nichols, B. E., et al. (1997) · Science · doi:10.1126/science.275.5300.668 · Cited by 1,432 · see citing works

Collagens, modifying enzymes and their mutations in humans, flies and worms

Myllyharju, J. (2003) · Trends in Genetics · doi:10.1016/j.tig.2003.11.004 · Cited by 1,179 · see citing works

Stable suppression of tumorigenicity by virus-mediated RNA interference

Brummelkamp, T. R., Bernards, R., & Agami, R. (2002) · Cancer Cell · doi:10.1016/s1535-6108(02)00122-8 · Cited by 1,137 · see citing works

Neurexins Induce Differentiation of GABA and Glutamate Postsynaptic Specializations via Neuroligins

Graf, E. R., Zhang, X., Jin, S., Linhoff, M. W., & Craig, A. M. (2004) · Cell · doi:10.1016/j.cell.2004.11.035 · Cited by 989 · see citing works

The local differentiation of myelinated axons at nodes of Ranvier

Poliak, S., & Peles, E. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1253 · Cited by 673 · see citing works

Axon-glia interactions and the domain organization of myelinated axons requires neurexin IV/Caspr/Paranodin.

Bhat, M., Rios, J. C., Lu, Y. C., Garcia-Fresco, G. P., Ching, W., Martin, M. S. S., Li, J., Einheber, S., Chesler, M., Rosenbluth, J., et al. (2001) · Neuron · doi:10.1016/s0896-6273(01)00294-x · Cited by 585 · see citing works

Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1

Poliak, S., Salomon, D., Elhanany, H., Sabanay, H., Kiernan, B. W., Pevny, L., Stewart, C., Xu, X.-R., Chiu, S., Shrager, P., et al. (2003) · Journal of Cell Biology · doi:10.1083/jcb.200305018 · Cited by 542 · see citing works

Contactin orchestrates assembly of the septate-like junctions at the paranode in myelinated peripheral nerve.

Boyle, M. E., Berglund, E., Murai, K., Weber, L., Peles, E., & Ranscht, B. (2001) · Neuron · doi:10.1016/s0896-6273(01)00296-3 · Cited by 539 · see citing works

Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels.

Poliak, S., Gollan, L., Martinez, R., Custer, A., Einheber, S., Salzer, J., Trimmer, J., Shrager, P., & Peles, E. (1999) · Neuron · doi:10.1016/s0896-6273(00)81049-1 · Cited by 530 · see citing works

Identification of a novel contactin‐associated transmembrane receptor with multiple domains implicated in protein–protein interactions

Peles, E., Nativ, M., Lustig, M., Grumet, M., Schilling, J., Martinez, R., Plowman, G. D., & Schlessinger, J. (1997) · The EMBO Journal · doi:10.1093/emboj/16.5.978 · Cited by 400 · cited 2× · see citing works

Polarized Domains of Myelinated Axons

Salzer, J. L. (2003) · Neuron · doi:10.1016/s0896-6273(03)00628-7 · Cited by 399 · see citing works

The carbonic anhydrase domain of receptor tyrosine phosphatase β is a functional ligand for the axonal cell recognition molecule contactin

Peles, E., Nativ, M., Campbell, P. L., Sakurai, T., Martinez, R., Lev, S., Clary, D. O., Schilling, J., Barnea, G., Plowman, G. D., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90312-7 · Cited by 397 · see citing works

The axonal membrane protein Caspr, a homologue of neurexin IV, is a component of the septate-like paranodal junctions that assemble during myelination

Einheber, S., Zanazzi, G., Ching, W., Scherer, S., Milner, T. A., Peles, E., & Salzer, J. L. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.139.6.1495 · Cited by 369 · see citing works

Molecular dissection of the myelinated axon

Waxman, S. G., & Ritchie, J. M. (1993) · Annals of Neurology · doi:10.1002/ana.410330202 · Cited by 356 · see citing works

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.

Davis, J. Q., Lambert, S., & Bennett, V. (1996) · The Journal of Cell Biology · doi:10.1083/jcb.135.5.1355 · Cited by 347 · see citing works

An Oligodendrocyte Cell Adhesion Molecule at the Site of Assembly of the Paranodal Axo-Glial Junction

Tait, S., Gunn-Moore, F., Collinson, J., Huang, J., Lubetzki, C., Pedraza, L., Sherman, D., Colman, D., & Brophy, P. (2000) · Journal of Cell Biology · doi:10.1083/jcb.150.3.657 · Cited by 339 · see citing works

Induction of sodium channel clustering by oligodendrocytes

Kaplan, M. R., Meyer‐Franke, A., Lambert, S., Bennett, V., Duncan, I. D., Levinson, S. R., & Barres, B. A. (1997) · Nature · doi:10.1038/386724a0 · Cited by 332 · see citing works

Differential Control of Clustering of the Sodium Channels Nav1.2 and Nav1.6 at Developing CNS Nodes of Ranvier

Kaplan, M. R., Cho, M.-H., Ullian, E. M., Isom, L. L., Levinson, S. R., & Barres, B. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00266-5 · Cited by 304 · see citing works

βIV-spectrin regulates sodium channel clustering through ankyrin-G at axon initial segments and nodes of Ranvier

Komada, M., & Soriano, P. M. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200110003 · Cited by 291 · see citing works

α-Latrotoxin Receptor, Latrophilin, Is a Novel Member of the Secretin Family of G Protein-coupled Receptors

Lelianova, V. G., Davletov, B. A., Sterling, A., Rahman, M. A., Grishin, E. V., Totty, N. F., & Ushkaryov, Y. A. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.34.21504 · Cited by 288 · see citing works

Axo-Glial Interactions Regulate the Localization of Axonal Paranodal Proteins

Dupree, J., Girault, J., & Popko, B. (1999) · Journal of Cell Biology · doi:10.1083/jcb.147.6.1145 · Cited by 278 · see citing works

βiv Spectrin, a New Spectrin Localized at Axon Initial Segments and Nodes of Ranvier in the Central and Peripheral Nervous System

Berghs, S., Aggujaro, D., Dirkx, R. A., Maksimova, E. M., Stabach, P. R., Hermel, J., Zhang, J.-P., Philbrick, W. M., Slepnev, V. I., Ort, T., et al. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.5.985 · Cited by 276 · see citing works

Sodium Channel β Subunits Mediate Homophilic Cell Adhesion and Recruit Ankyrin to Points of Cell-Cell Contact

Malhotra, J. D., Kazen-Gillespie, K. A., Hortsch, M., & Isom, L. L. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.15.11383 · Cited by 272 · see citing works

Unique Role of Dystroglycan in Peripheral Nerve Myelination, Nodal Structure, and Sodium Channel Stabilization

Saito, F., Moore, S. A., Barresi, R., Henry, M. D., Messing, A., Ross, S. E., Cohn, R. D., Williamson, R. A., Sluka, K. A., Sherman, D. L., et al. (2003) · Neuron · doi:10.1016/s0896-6273(03)00301-5 · Cited by 250 · see citing works

Identification of a Conserved Ankyrin-binding Motif in the Family of Sodium Channel α Subunits

Lemaillet, G., Walker, B. J., & Lambert, S. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m303327200 · Cited by 243 · see citing works

Tyrosine Phosphorylation at a Site Highly Conserved in the L1 Family of Cell Adhesion Molecules Abolishes Ankyrin Binding and Increases Lateral Mobility of Neurofascin

Garver, T. D., Ren, Q., Tuvia, S., & Bennett, V. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.137.3.703 · Cited by 242 · see citing works

Morphogenesis of the Node of Ranvier: Co-Clusters of Ankyrin and Ankyrin-Binding Integral Proteins Define Early Developmental Intermediates

Lambert, S. B., Davis, J. Q., & Bennett, V. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-18-07025.1997 · Cited by 216 · see citing works

Clustering of Na+ channels and node of Ranvier formation in remyelinating axons

Novaković, S. D., Koszowski, A. G., Levinson, S. R., & Shrager, P. G. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00492.1995 · Cited by 210 · see citing works

Restricted growth of Schwann cells lacking Cajal bands slows conduction in myelinated nerves

Court, F. A., Sherman, D. L., Pratt, T., Garry, E. M., Ribchester, R. R., Cottrell, D. F., Fleetwood-Walker, S. M., & Brophy, P. (2004) · Nature · doi:10.1038/nature02841 · Cited by 205 · see citing works

Abnormal sodium channel distribution in optic nerve axons in a model of inflammatory demyelination

Craner, M. J. (2003) · Brain · doi:10.1093/brain/awg153 · Cited by 187 · see citing works

Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cells

Poliak, S., Matlis, S., Ullmer, C., Scherer, S. S., & Peles, E. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200207050 · Cited by 182 · see citing works

Sodium channel β1 and β3 subunits associate with neurofascin through their extracellular immunoglobulin-like domain

Ratcliffe, C. F., Westenbroek, R. E., Curtis, R., & Catterall, W. A. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.200102086 · Cited by 173 · see citing works

An isoform of ankyrin is localized at nodes of Ranvier in myelinated axons of central and peripheral nerves.

Kordeli, E., Davis, J. Q., Trapp, B. D., & Bennett, V. (1990) · The Journal of Cell Biology · doi:10.1083/jcb.110.4.1341 · Cited by 160 · see citing works

The perinodal astrocyte

Black, J. A., & Waxman, S. G. (1988) · Glia · doi:10.1002/glia.440010302 · Cited by 155 · see citing works

Caspr regulates the processing of contactin and inhibits its binding to neurofascin

Gollan, L., Salomon, D., Salzer, J., & Peles, E. (2003) · Journal of Cell Biology · doi:10.1083/jcb.200309147 · Cited by 154 · see citing works

The Clustering of Axonal Sodium Channels during Development of the Peripheral Nervous System

Vabnick, I., Novaković, S. D., Levinson, S. R., Schachner, M., & Shrager, P. G. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-04914.1996 · Cited by 153 · see citing works

βIV Spectrins Are Essential for Membrane Stability and the Molecular Organization of Nodes of Ranvier

Yang, Y., Lacas-Gervais, S., Morest, D., Solimena, M., & Rasband, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2125-04.2004 · Cited by 153 · see citing works

Does Paranode Formation and Maintenance Require Partitioning of Neurofascin 155 into Lipid Rafts?

Schafer, D. P., Bansal, R., Hedstrom, K. L., Pfeiffer, S., & Rasband, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5427-03.2004 · Cited by 146 · see citing works

A Conserved Postsynaptic Transmembrane Protein Affecting Neuromuscular Signaling in Caenorhabditis elegans

Loria, P. M., Hodgkin, J., & Hobert, O. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5462-03.2004 · Cited by 137 · see citing works

βIVΣ1 spectrin stabilizes the nodes of Ranvier and axon initial segments

Lacas‐Gervais, S., Guo, J., Strenzke, N., Scarfone, E., Kolpe, M., Jähkel, M., Camilli, P. V. D., Moser, T., Rasband, M. N., & Solimena, M. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200408007 · Cited by 134 · see citing works

Noelin-1 is a secreted glycoprotein involved in generation of the neural crest

Barembaum, M., Moreno, T. A., LaBonne, C., Sechrist, J. W., & Bronner-Fraser, M. E. (2000) · Nature Cell Biology · doi:10.1038/35008643 · Cited by 132 · see citing works

Mutant β-spectrin 4 causes auditory and motor neuropathies in quivering mice

Parkinson, N., Olsson, C. L., Hallows, J. L., McKee-Johnson, J. W., Keogh, B. P., Noben‐Trauth, K., Kujawa, S. G., & Tempel, B. L. (2001) · Nature Genetics · doi:10.1038/ng710 · Cited by 127 · see citing works

Nodes of Ranvier form in association with ezrin-radixin-moesin (ERM)-positive Schwann cell processes

Melendez‐Vasquez, C. V., Rios, J. C., Zanazzi, G. J., Lambert, S., Bretscher, A. P., & Salzer, J. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.3.1235 · Cited by 127 · see citing works

Heterophilic Interactions of Sodium Channel β1 Subunits with Axonal and Glial Cell Adhesion Molecules*

Mcewen, D. P., & Isom, L. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m405990200 · Cited by 121 · see citing works

Rho Kinase Regulates Schwann Cell Myelination and Formation of Associated Axonal Domains

Melendez‐Vasquez, C. V., Einheber, S., & Salzer, J. L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4920-03.2004 · Cited by 115 · see citing works

Molecular cloning of olfactomedin, an extracellular matrix protein specific to olfactory neuroepithelium.

Yokoe, H., & Anholt, R. R. H. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.10.4655 · Cited by 112 · see citing works

Caspr3 and caspr4, two novel members of the caspr family are expressed in the nervous system and interact with PDZ domains.

Spiegel, I., Salomon, D., Erne, B., Schaeren-Wiemers, N., & Peles, E. (2002) · Molecular and cellular neurosciences · doi:10.1006/mcne.2002.1110 · Cited by 103 · see citing works

Endocytotic elimination and domain-selective tethering constitute a potential mechanism of protein segregation at the axonal initial segment

Fache, M., Moussif, A., Fernandes, F., Giraud, P., Garrido, J. J., & Dargent, B. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200312155 · Cited by 103 · see citing works

Astrocytes protect neurons from neurotoxic injury by serum glutamate

Ye, Z., & Sontheimer, H. W. (1998) · Glia · doi:10.1002/(sici)1098-1136(199803)22:3 · Cited by 94 · see citing works

Clustering of neuronal sodium channels requires contact with myelinating Schwann cells

Ching, W., Zanazzi, G. J., Levinson, S. R., & Salzer, J. L. (1999) · Journal of Neurocytology · doi:10.1023/a:1007053411667 · Cited by 92 · see citing works

Amassin, an olfactomedin protein, mediates the massive intercellular adhesion of sea urchin coelomocytes

Hillier, B. J., & Vacquier, V. D. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200210053 · Cited by 87 · see citing works

The Role of the Ankyrin-Binding Protein NrCAM in Node of Ranvier Formation

Custer, A., Kazarinova-Noyes, K., Sakurai, T., Xu, X.-R., Simon, W., Grumet, M., & Shrager, P. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-31-10032.2003 · Cited by 83 · see citing works

Ezrin, radixin, and moesin are components of Schwann cell microvilli

Scherer, S. S., Xu, T., Crino, P. B., Arroyo, E. J., & Gutmann, D. H. (2001) · Journal of Neuroscience Research · doi:10.1002/jnr.1138 · Cited by 78 · see citing works

On the association between perinodal astrocytic processes and the node of Ranvier in the C.N.S.

Raine, C. S. (1984) · Journal of Neurocytology · doi:10.1007/bf01148316 · Cited by 77 · see citing works

Local ERM activation and dynamic growth cones at Schwann cell tips implicated in efficient formation of nodes of Ranvier

Gatto, C. L., Walker, B. J., & Lambert, S. B. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200303039 · Cited by 75 · see citing works

Three-dimensional fine structure of cytoskeletal-membrane interactions at nodes of Ranvier

Ichimura, T., & Ellisman, M. H. (1991) · Journal of Neurocytology · doi:10.1007/bf01187068 · Cited by 73 · see citing works

Electron microscopic serial section analysis of nodes of Ranvier in lumbosacral spinal roots of the cat: ultrastructural organization of nodal compartments in fibres of different sizes

Berthold, C. ‐., & Rydmark, M. (1983) · Journal of Neurocytology · doi:10.1007/bf01159386 · Cited by 71 · see citing works

Essential role of oligodendrocytes in the formation and maintenance of central nervous system nodal regions

Mathis, C., Denisenko, N., Girault, J., & Borrelli, E. (2001) · Development · doi:10.1242/dev.128.23.4881 · Cited by 71 · see citing works

Ankyrins

Mohler, P. J., Gramolini, A. O., & Bennett, V. (2002) · Journal of Cell Science · doi:10.1242/jcs.115.8.1565 · Cited by 71 · see citing works

Differences between the nodes of Ranvier of large and small diameter fibres in the P.N.S.

Raine, C. S. (1982) · Journal of Neurocytology · doi:10.1007/bf01148309 · Cited by 70 · see citing works

Acute demyelination disrupts the molecular organization of peripheral nervous system nodes

Arroyo, E., Sirkowski, E. E., Chitale, R. V., & Scherer, S. (2004) · The Journal of comparative neurology · doi:10.1002/cne.20321 · Cited by 70 · see citing works

Nr-CAM and neurofascin interactions regulate ankyrin G and sodium channel clustering at the node of Ranvier

Lustig, M., Zanazzi, G. J., Sakurai, T., Blanco, C., Levinson, S. R., Lambert, S., Grumet, M., & Salzer, J. L. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00586-3 · Cited by 69 · see citing works

Axolemmal differentiation in myelinated fibers of rat peripheral nerves

Tao-Cheng, J.-H., & Rosenbluth, J. (1983) · Developmental Brain Research · doi:10.1016/0165-3806(83)90023-8 · Cited by 57 · see citing works

Syndecan-3 and syndecan-4 are enriched in Schwann cell perinodal processes

Goutebroze, L., Carnaud, M., Denisenko, N., Boutterin, M., & Girault, J. (2003) · BMC Neuroscience · doi:10.1186/1471-2202-4-29 · Cited by 51 · see citing works

Dorsalization of the Neural Tube by Xenopus Tiarin, a Novel Patterning Factor Secreted by the Flanking Nonneural Head Ectoderm

Tsuda, H., Sasai, N., Matsuo‐Takasaki, M., Sakuragi, M., Murakami, Y., & Sasai, Y. (2002) · Neuron · doi:10.1016/s0896-6273(02)00590-1 · Cited by 50 · see citing works

Identification of Genes That Are Downregulated in the Absence of the POU Domain Transcription Factor pou3f1 (Oct-6, Tst-1, SCIP) in Sciatic Nerve

Bermingham, J. R., Shumas, S. R., Whisenhunt, T., Sirkowski, E. E., O’Connell, S. M., Scherer, S. S., & Rosenfeld, M. G. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-23-10217.2002 · Cited by 45 · see citing works

Neurofascin interactions play a critical role in clustering sodium channels, ankyrinG and βIV spectrin at peripheral nodes of Ranvier

Koticha, D. K., Maurel, P., Zanazzi, G. J., Kane‐Goldsmith, N., Basak, S., Babiarz, J. P., Salzer, J. L., & Grumet, M. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2005.05.028 · Cited by 43 · see citing works

Secreted glycoprotein myocilin is a component of the myelin sheath in peripheral nerves

Ohlmann, A., Goldwich, A., Flügel‐Koch, C., Fuchs, A. V., Schwager, K. A., & Tamm, E. R. (2003) · Glia · doi:10.1002/glia.10233 · Cited by 37 · see citing works

Identification and characterization of CRG-L2, a new marker for liver tumor development

Graveel, C. R., Harkins-Perry, S. R., Acevedo, L. G., & Farnham, P. (2003) · Oncogene · doi:10.1038/sj.onc.1206309 · Cited by 19 · see citing works

Untitled work

(1997) · doi:10.1002/(sici)1097-4547(19971015)50:2

The Mystery and Magic of Glia: A Perspective on Their Roles in Health and Disease

Barres, B. A. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.013 · Cited by 1,352 · see citing works

The axon initial segment and the maintenance of neuronal polarity

Rasband, M. N. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2852 · Cited by 442 · see citing works

Anti-GM1 Antibodies Cause Complement-Mediated Disruption of Sodium Channel Clusters in Peripheral Motor Nerve Fibers

Susuki, K., Rasband, M., Tohyama, K., Koibuchi, K., Okamoto, S., Funakoshi, K., Hirata, K., Baba, H., & Yuki, N. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4401-06.2007 · Cited by 381 · see citing works

Neurofascins Are Required to Establish Axonal Domains for Saltatory Conduction

Sherman, D. L., Tait, S., Melrose, S., Johnson, R., Zonta, B., Court, F. A., Macklin, W. B., Meek, S. E., Smith, A., Cottrell, D. F., et al. (2005) · Neuron · doi:10.1016/j.neuron.2005.10.019 · Cited by 342 · see citing works

Neurofascin assembles a specialized extracellular matrix at the axon initial segment

Hedstrom, K. L., Xu, X., Ogawa, Y., Frischknecht, R., Seidenbecher, C. I., Shrager, P., & Rasband, M. N. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200705119 · Cited by 268 · see citing works

The bone morphogenetic protein 1/Tolloid-like metalloproteinases

Hopkins, D. R., Keleş, S., & Greenspan, D. S. (2007) · Matrix Biology · doi:10.1016/j.matbio.2007.05.004 · Cited by 259 · see citing works

Neurofascin as a target for autoantibodies in peripheral neuropathies

Ng, J., Malotka, J., Kawakami, N., Derfuss, T., Khademi, M., Olsson, T., Linington, C., Odaka, M., Tackenberg, B., Prüss, H., et al. (2012) · Neurology · doi:10.1212/wnl.0b013e31827689ad · Cited by 270 · see citing works

Schwann cell functions in peripheral nerve development and repair

Bosch-Queralt, M., Fledrich, R., & Stassart, R. M. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105952 · Cited by 244 · see citing works

Wrapping it up: the cell biology of myelination

Simons, M., & Trotter, J. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.08.003 · Cited by 227 · see citing works

A central role for Necl4 (SynCAM4) in Schwann cell–axon interaction and myelination

Spiegel, I., Adamsky, K., Eshed, Y., Milo, R., Sabanay, H., Sarig-Nadir, O., Horresh, I., Scherer, S. S., Rasband, M. N., & Peles, E. (2007) · Nature Neuroscience · doi:10.1038/nn1915 · Cited by 226 · see citing works

Neuron-glia communication in the control of oligodendrocyte function and myelin biogenesis

Simons, M., & Trajković, K. (2006) · Journal of Cell Science · doi:10.1242/jcs.03242 · Cited by 218 · see citing works

Molecular domains of myelinated axons in the peripheral nervous system

Salzer, J., Brophy, P., & Peles, E. (2008) · Glia · doi:10.1002/glia.20750 · Cited by 240 · see citing works

Nodal, paranodal and juxtaparanodal axonal proteins during demyelination and remyelination in multiple sclerosis

Coman, I., Aigrot, M., Seilhean, D., Reynolds, R., Girault, J., Zalc, B., & Lubetzki, C. (2006) · Brain · doi:10.1093/brain/awl144 · Cited by 210 · see citing works

Adhesion Molecules in the Nervous System: Structural Insights into Function and Diversity

Shapiro, L. S., Love, J. M., & Colman, D. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.113034 · Cited by 207 · see citing works

Nodes of Ranvier and axon initial segments are ankyrin G–dependent domains that assemble by distinct mechanisms

Dzhashiashvili, Y., Zhang, Y., Galinska, J., Lam, I., Grumet, M., & Salzer, J. L. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200612012 · Cited by 206 · see citing works

A glial signal consisting of Gliomedin and NrCAM clusters axonal Na+ channels during the formation of nodes of Ranvier

Feinberg, K., Eshed-Eisenbach, Y., Frechter, S., Amor, V., Salomon, D., Sabanay, H., Dupree, J., Grumet, M., Brophy, P., Shrager, P., et al. (2010) · Neuron · doi:10.1016/j.neuron.2010.02.004 · Cited by 203 · see citing works

βIV spectrin is recruited to axon initial segments and nodes of Ranvier by ankyrinG

Yang, Y., Ogawa, Y., Hedstrom, K. L., & Rasband, M. (2007) · Journal of Cell Biology · doi:10.1083/jcb.200610128 · Cited by 200 · see citing works

Regulation of Schwann cell function by the extracellular matrix

Chernousov, M. A., Yu, W., Chen, Z., Carey, D. J., & Strickland, S. (2008) · Glia · doi:10.1002/glia.20740 · Cited by 197 · see citing works

Three mechanisms assemble central nervous system nodes of Ranvier

Susuki, K., Chang, K.-J., Zollinger, D. R., Liu, Y., Ogawa, Y., Eshed-Eisenbach, Y., Dours-Zimmermann, M. T., Oses-Prieto, J. A., Burlingame, A. L., Seidenbecher, C. I., et al. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.005 · Cited by 186 · see citing works

Membrane Domains Based on Ankyrin and Spectrin Associated with Cell-Cell InteractionsPreprint

Bennett, V., & Healy, J. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a003012 · Cited by 191 · see citing works

Specific Inhibition of p300-HAT Alters Global Gene Expression and Represses HIV Replication

Mantelingu, K., Reddy, B. A., Swaminathan, V., Kishore, A. H., Siddappa, N. B., Kumar, G. V. P., Nagashankar, G., Natesh, N., Roy, S., Sadhale, P. P., et al. (2007) · Chemistry & Biology · doi:10.1016/j.chembiol.2007.04.011 · Cited by 193 · see citing works

Nodal proteins are target antigens in Guillain‐Barré syndrome

Devaux, J. J., Odaka, M., & Yuki, N. (2012) · Journal of the Peripheral Nervous System · doi:10.1111/j.1529-8027.2012.00372.x · Cited by 192 · see citing works

The Nodes of Ranvier: Molecular Assembly and Maintenance

Rasband, M. N., & Peles, E. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020495 · Cited by 190 · see citing works

Glial and neuronal isoforms of Neurofascin have distinct roles in the assembly of nodes of Ranvier in the central nervous system

Zonta, B., Tait, S., Melrose, S., Anderson, H., Harroch, S., Higginson, J., Sherman, D. L., & Brophy, P. J. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200712154 · Cited by 188 · see citing works

Protein kinase CK2 contributes to the organization of sodium channels in axonal membranes by regulating their interactions with ankyrin G

Bréchet, A., Fache, M., Brachet, A., Ferracci, G., Baude, A., Irondelle, M., Pereira, S., Leterrier, C., & Dargent, B. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200805169 · Cited by 172 · see citing works

Mechanisms of node of Ranvier assembly

Rasband, M. N., & Peles, E. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-00406-8 · Cited by 168 · see citing works

Contactin-1 IgG4 antibodies cause paranode dismantling and conduction defects.

Manso, C., Querol, L., Mekaouche, M., Illa, I., & Devaux, J. (2016) · Brain : a journal of neurology · doi:10.1093/brain/aww062 · Cited by 155 · see citing works

Spectrins and AnkyrinB Constitute a Specialized Paranodal Cytoskeleton

Ogawa, Y., Schafer, D. P., Horresh, I., Bar, V., Hales, K., Yang, Y., Susuki, K., Peles, E., Stankewich, M. C., & Rasband, M. N. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0425-06.2006 · Cited by 162 · see citing works

A Critical Role for Neurofascin in Regulating Action Potential Initiation through Maintenance of the Axon Initial Segment

Zonta, B., Desmazières, A., Rinaldi, A., Tait, S., Sherman, D. L., Nolan, M. F., & Brophy, P. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.021 · Cited by 158 · see citing works

Transient auditory nerve demyelination as a new mechanism for hidden hearing loss

Wan, G., & Corfas, G. (2017) · Nature Communications · doi:10.1038/ncomms14487 · Cited by 157 · see citing works

Olfactomedin Domain-Containing Proteins: Possible Mechanisms of Action and Functions in Normal Development and Pathology

Tomarev, S. I., & Nakaya, N. (2009) · Molecular Neurobiology · doi:10.1007/s12035-009-8076-x · Cited by 155 · see citing works

G protein-coupled receptor 37 is a negative regulator of oligodendrocyte differentiation and myelination

Yang, H., Vainshtein, A., Maik-Rachline, G., & Peles, E. (2016) · Nature Communications · doi:10.1038/ncomms10884 · Cited by 150 · see citing works

The intriguing nature of dorsal root ganglion neurons: Linking structure with polarity and function

Nascimento, A. I., Mar, F. M., & Sousa, M. M. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.05.002 · Cited by 147 · see citing works

The role of NrCAM in neural development and disorders—Beyond a simple glue in the brain

Sakurai, T. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.12.002 · Cited by 143 · see citing works

Postsynaptic Density-93 Clusters Kv1 Channels at Axon Initial Segments Independently of Caspr2

Ogawa, Y., Horresh, I., Trimmer, J. S., Bredt, D. S., Peles, E., & Rasband, M. N. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4431-07.2008 · Cited by 141 · see citing works

Mechanisms of sodium channel clustering and its influence on axonal impulse conduction

Freeman, S. A., Desmazières, A., Fricker, D., Lubetzki, C., & Sol‐Foulon, N. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-2081-1 · Cited by 133 · see citing works

Molecular mechanisms of node of Ranvier formation

Susuki, K., & Rasband, M. N. (2008) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2008.09.007 · Cited by 135 · see citing works

Ion Channel Clustering at the Axon Initial Segment and Node of Ranvier Evolved Sequentially in Early Chordates

Hill, A. S., Nishino, A., Nakajo, K., Zhang, G., Fineman, J. R., Selzer, M. E., Okamura, Y., & Cooper, E. C. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000317 · Cited by 132 · see citing works

The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity

Oohashi, T., Edamatsu, M., Bekku, Y., & Carulli, D. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.09.010 · Cited by 131 · see citing works

Disruption of neurofascin and gliomedin at nodes of Ranvier precedes demyelination in experimental allergic neuritis

Lonigro, A., & Devaux, J. J. (2008) · Brain · doi:10.1093/brain/awn281 · Cited by 126 · see citing works

Ankyrin protein networks in membrane formation and stabilization

Cunha, S. R., & Mohler, P. J. (2009) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2009.00943.x · Cited by 125 · see citing works

Specific Contactin N-Glycans Are Implicated in Neurofascin Binding and Autoimmune Targeting in Peripheral Neuropathies

Labasque, M., Hivert, B., Nogales‐Gadea, G., Querol, L., Illa, I., & Faivre‐Sarrailh, C. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.528489 · Cited by 124 · see citing works

Ultrastructural anatomy of nodes of Ranvier in the peripheral nervous system as revealed by STED microscopy

D’Este, E., Kamin, D., Balzarotti, F., & Hell, S. W. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1619553114 · Cited by 124 · see citing works

Versican V2 Assembles the Extracellular Matrix Surrounding the Nodes of Ranvier in the CNS

Dours-Zimmermann, M. T., Maurer, K., Rauch, U., Stoffel, W., Fassler, R., & Zimmermann, D. R. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4158-08.2009 · Cited by 123 · see citing works

Mechanisms of C aspr2 antibodies in autoimmune encephalitis and neuromyotonia

Patterson, K. R., Dalmau, J. O., & Lancaster, E. (2017) · Annals of Neurology · doi:10.1002/ana.25120 · Cited by 121 · see citing works

Axonal Membranes and Their Domains: Assembly and Function of the Axon Initial Segment and Node of Ranvier

Nelson, A. D., & Jenkins, P. M. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00136 · Cited by 120 · see citing works

Multiple molecular interactions determine the clustering of Caspr2 and Kv1 channels in myelinated axons

Horresh, I., Poliak, S., Grant, S., Bredt, D., Rasband, M., & Peles, E. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3398-08.2008 · Cited by 116 · see citing works

Both Laminin and Schwann Cell Dystroglycan Are Necessary for Proper Clustering of Sodium Channels at Nodes of Ranvier

Occhi, S., Zambroni, D., Carro, U. D., Amadio, S., Sirkowski, E. E., Scherer, S. S., Campbell, K. P., Moore, S. A., Chen, Z.-L., Strickland, S., et al. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2068-05.2005 · Cited by 116 · see citing works

Multiple functions of the paranodal junction of myelinated nerve fibers

D, J. R. M. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.22013 · Cited by 114 · see citing works

The functional organization and assembly of the axon initial segment

Ogawa, Y., & Rasband, M. N. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.08.008 · Cited by 114 · see citing works

Ankyrin-Dependent and -Independent Mechanisms Orchestrate Axonal Compartmentalization of L1 Family Members Neurofascin and L1/Neuron–Glia Cell Adhesion Molecule

Boiko, T., Vakulenko, M., Ewers, H., Yap, C. C., Norden, C., & Winckler, B. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4302-06.2007 · Cited by 112 · see citing works

Anti–neurofascin-155 IgG4 antibodies prevent paranodal complex formation in vivo

Manso, C., Querol, L., Lleixà, C., Poncelet, M., Mekaouche, M., Vallat, J., Illa, I., & Devaux, J. J. (2019) · Journal of Clinical Investigation · doi:10.1172/jci124694 · Cited by 110 · see citing works

Molecular Reconstruction of Nodes of Ranvier after Remyelination by Transplanted Olfactory Ensheathing Cells in the Demyelinated Spinal Cord

Sasaki, M., Black, J. A., Lankford, K. L., Tokuno, H. A., Waxman, S. G., & Kocsis, J. D. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3611-05.2006 · Cited by 106 · see citing works

Secreted gliomedin is a perinodal matrix component of peripheral nerves

Eshed, Y., Feinberg, K., Carey, D. J., & Peles, E. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200612139 · Cited by 103 · see citing works

Axon‐oligodendrocyte interactions during developmental myelination, demyelination and repair

Piaton, G., Gould, R. M., & Lubetzki, C. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06831.x · Cited by 101 · see citing works

Assembly and Maintenance of Nodes of Ranvier Rely on Distinct Sources of Proteins and Targeting Mechanisms

Zhang, Y., Bekku, Y., Dzhashiashvili, Y., Armenti, S. T., Meng, X., Sasaki, Y., Milbrandt, J., & Salzer, J. L. (2012) · Neuron · doi:10.1016/j.neuron.2011.10.016 · Cited by 100 · see citing works

SH3TC2, a protein mutant in Charcot–Marie–Tooth neuropathy, links peripheral nerve myelination to endosomal recycling

Stendel, C., Roos, A., Kleine, H. O., Arnaud, E., Özçelik, M., Sidiropoulos, P. N. M., Zenker, J., Schüpfer, F., Lehmann, U., Sobota, R. M., et al. (2010) · Brain · doi:10.1093/brain/awq168 · Cited by 100 · see citing works

Olfactomedin proteins: central players in development and disease

Anholt, R. R. H. (2014) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2014.00006 · Cited by 100 · see citing works

No Pasaran! Role of the axon initial segment in the regulation of protein transport and the maintenance of axonal identity

Leterrier, C., & Dargent, B. (2013) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2013.11.001 · Cited by 96 · see citing works

Glia unglued: How signals from the extracellular matrix regulate the development of myelinating glia

Colognato, H., & Tzvetanova, I. D. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20966 · Cited by 90 · see citing works

Basal lamina: Schwann cells wrap to the rhythm of space-time

Court, F. A., Wrabetz, L. G., & Feltri, M. L. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.08.005 · Cited by 94 · see citing works

Cleavage and Oligomerization of Gliomedin, a Transmembrane Collagen Required for Node of Ranvier Formation

Maertens, B., Hopkins, D. R., Franzke, C.-W., Keene, D. R., Bruckner‐Tuderman, L., Greenspan, D. S., & Koch, M. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611339200 · Cited by 93 · see citing works

Organization and maintenance of molecular domains in myelinated axons

Buttermore, E. D., Thaxton, C., & Bhat, M. A. (2013) · Journal of Neuroscience Research · doi:10.1002/jnr.23197 · Cited by 92 · see citing works

Nodes of Ranvier Act as Barriers to Restrict Invasion of Flanking Paranodal Domains in Myelinated Axons

Thaxton, C., Pillai, A. M., Pribisko, A. L., Dupree, J. L., & Bhat, M. A. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.016 · Cited by 88 · see citing works

Neuro-glial interactions at the nodes of Ranvier: implication in health and diseases

Faivre‐Sarrailh, C., & Devaux, J. J. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00196 · Cited by 85 · see citing works

Neurofascin: A switch between neuronal plasticity and stability

Kriebel, M., Wuchter, J., Trinks, S., & Volkmer, H. (2012) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2012.01.012 · Cited by 86 · see citing works

Early events in node of Ranvier formation during myelination and remyelination in the PNS

Schafer, D. P., Custer, A. W., Shrager, P. G., & Rasband, M. N. (2006) · Neuron Glia Biology · doi:10.1017/s1740925x06000093 · Cited by 83 · see citing works

Acceleration of conduction velocity linked to clustering of nodal components precedes myelination

Freeman, S. A., Desmazières, A., Simonnet, J., Gatta, M., Pfeiffer, F., Aigrot, M. S., Rappeneau, Q., Guerreiro, S., Michel, P. P., Yanagawa, Y., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1419099112 · Cited by 80 · see citing works

N-WASP is required for membrane wrapping and myelination by Schwann cells

Novak, N., Bar, V., Sabanay, H., Frechter, S., Jaegle, M., Snapper, S., Meijer, D., & Peles, E. (2011) · Journal of Cell Biology · doi:10.1083/jcb.201010013 · Cited by 81 · see citing works

The role of sodium channels in chronic pain

Levinson, S. R., Luo, S., & Henry, M. A. (2012) · Muscle & Nerve · doi:10.1002/mus.23314 · Cited by 77 · see citing works

Reduced hGC-1 Protein Expression Is Associated with Malignant Progression of Colon Carcinoma

Liu, W., Liu, Y., Zhu, J., Wright, E., Ding, I., & Rodgers, G. P. (2008) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-07-4125 · Cited by 77 · see citing works

Novel roles for collagens in wiring the vertebrate nervous system

Fox, M. A. (2008) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2008.05.003 · Cited by 77 · see citing works

Axo-glial antigens as targets in multiple sclerosis: implications for axonal and grey matter injury

Derfuss, T. J., Linington, C., Hohlfeld, R., & Meinl, E. (2010) · Journal of Molecular Medicine · doi:10.1007/s00109-010-0632-3 · Cited by 76 · see citing works

Voltage-gated sodium channel organization in neurons: Protein interactions and trafficking pathways

Leterrier, C., Brachet, A., Fache, M., & Dargent, B. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.08.079 · Cited by 75 · see citing works

Myocilin Is a Modulator of Wnt Signaling

Kwon, H.-S., Lee, H.-S., Ji, Y., Rubin, J. S., & Tomarev, S. I. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.01274-08 · Cited by 75 · see citing works

Axonal targeting of Caspr2 in hippocampal neurons via selective somatodendritic endocytosis

Bel, C., Oguievetskaia, K., Pitaval, C., Goutebroze, L., & Faivre‐Sarrailh, C. (2009) · Journal of Cell Science · doi:10.1242/jcs.050526 · Cited by 74 · see citing works

Genetic Deletion of Cadm4 Results in Myelin Abnormalities Resembling Charcot-Marie-Tooth Neuropathy

Golan, N., Kartvelishvily, E., Spiegel, I., Salomon, D., Sabanay, H., Rechav, K., Vainshtein, A., Frechter, S., Maik-Rachline, G., Eshed-Eisenbach, Y., et al. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0571-13.2013 · Cited by 68 · see citing works

Trafficking and Cellular Distribution of Voltage‐Gated Sodium Channels

Cusdin, F. S., Clare, J. J., & Jackson, A. P. (2007) · Traffic · doi:10.1111/j.1600-0854.2007.00673.x · Cited by 72 · see citing works

The paranodal cytoskeleton clusters Na+ channels at nodes of Ranvier

Amor, V., Zhang, C., Vainshtein, A., Zhang, A., Zollinger, D. R., Eshed‐Eisenbach, Y., Brophy, P., Rasband, M. N., & Peles, E. (2017) · eLife · doi:10.7554/elife.21392 · Cited by 70 · see citing works

Node of Ranvier Disruption as a Cause of Neurological Diseases

Susuki, K. (2013) · ASN NEURO · doi:10.1042/an20130025 · Cited by 68 · see citing works

Beyond Wrapping: Canonical and Noncanonical Functions of Schwann Cells

Taveggia, C., & Feltri, M. L. (2022) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-110920-030610 · Cited by 67 · see citing works

Mutations in GLDN, Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal Arthrogryposis.

Maluenda, J., Manso, C., Quevarec, L., Vivanti, A., Marguet, F., Gonzalès, M., Guimiot, F., Petit, F., Toutain, A., Whalen, S., et al. (2016) · American Journal of Human Genetics · doi:10.1016/j.ajhg.2016.07.021 · Cited by 56 · see citing works

Intrinsic and extrinsic determinants of ion channel localization in neurons

Hedstrom, K. L., & Rasband, M. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04001.x · Cited by 67 · see citing works

Neuronal proteins are novel components of podocyte major processes and their expression in glomerular crescents supports their role in crescent formation

Sistani, L., Rodriguez, P. Q., Hultenby, K. R., Uhlén, M., Betsholtz, C., Jalanko, H., Tryggvason, K., Wernerson, A. M., & Patrakka, J. (2012) · Kidney International · doi:10.1038/ki.2012.321 · Cited by 64 · see citing works

Remyelination of the injured spinal cord

Sasaki, M., Li, B., Lankford, K. L., Radtke, C., & Kocsis, J. D. (2007) · Progress in brain research · doi:10.1016/s0079-6123(06)61030-3 · Cited by 64 · see citing works

CIDP – the relevance of recent advances in Schwann cell/axonal neurobiology

Pollard, J. D., & Armati, P. J. (2011) · Journal of the Peripheral Nervous System · doi:10.1111/j.1529-8027.2011.00323.x · Cited by 63 · see citing works

Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder.

Lossos, A., Elazar, N., Lerer, I., Schueler-Furman, O., Fellig, Y., Glick, B., Zimmerman, B.-E., Azulay, H., Dotan, S., Goldberg, S., et al. (2015) · Brain : a journal of neurology · doi:10.1093/brain/awv204 · Cited by 55 · see citing works

Antibodies to Gliomedin Cause Peripheral Demyelinating Neuropathy and the Dismantling of the Nodes of Ranvier

Devaux, J. J. (2012) · American Journal Of Pathology · doi:10.1016/j.ajpath.2012.06.034 · Cited by 59 · see citing works

Long-Term Maintenance of Na+ Channels at Nodes of Ranvier Depends on Glial Contact Mediated by Gliomedin and NrCAM

Amor, V., Feinberg, K., Eshed-Eisenbach, Y., Vainshtein, A., Frechter, S., Grumet, M., Rosenbluth, J., & Peles, E. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4752-13.2014 · Cited by 85 · see citing works

Composition, assembly, and maintenance of excitable membrane domains in myelinated axons

Rasband, M. N. (2010) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2010.09.010 · Cited by 59 · see citing works

Glial regulation of the axonal membrane at nodes of Ranvier

Schafer, D. P., & Rasband, M. N. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.08.003 · Cited by 59 · see citing works

Direct Genesis of Functional Rodent and Human Schwann Cells from Skin Mesenchymal Precursors

Krause, M. P., Dworski, S., Feinberg, K., Jones, K. L., Johnston, A. P. W., Paul, S., Paris, M., Peles, E., Bägli, D., Forrest, C. R., et al. (2014) · Stem Cell Reports · doi:10.1016/j.stemcr.2014.05.011 · Cited by 58 · see citing works

Axonal Neurofilaments Control Multiple Fiber Properties But Do Not Influence Structure or Spacing of Nodes of Ranvier

Perrot, R., Lonchampt, P., Peterson, A. C., & Eyer, J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1224-07.2007 · Cited by 58 · see citing works

Moesin is a possible target molecule for cytomegalovirus-related Guillain-Barré syndrome

Sawai, S., Satoh, M., Mori, M., Misawa, S., Sogawa, K., Kazami, T., Ishibashi, M., Beppu, M., Shibuya, K., Ishige, T., et al. (2014) · Neurology · doi:10.1212/wnl.0000000000000566 · Cited by 58 · see citing works

The secretome signature of reactive glial cells and its pathological implications

Jha, M. K., Seo, M., Kim, J., Kim, B., Cho, J., & Suk, K. (2012) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2012.12.006 · Cited by 56 · see citing works

In VivoDeletion of Immunoglobulin Domains 5 and 6 inNeurofascin(Nfasc) Reveals Domain-Specific Requirements in Myelinated Axons

Thaxton, C., Pillai, A. M., Pribisko, A. L., Labasque, M., Dupree, J. L., Faivre‐Sarrailh, C., & Bhat, M. A. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5951-09.2010 · Cited by 57 · see citing works

Na+Channel-Dependent Recruitment of Navβ4 to Axon Initial Segments and Nodes of Ranvier

Buffington, S. A., & Rasband, M. N. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4051-12.2013 · Cited by 56 · see citing works

Zebrafish Olfactomedin 1 Regulates Retinal Axon ElongationIn Vivoand Is a Modulator of Wnt Signaling Pathway

Nakaya, N., Lee, H.-S., Takada, Y., Tzchori, I., & Tomarev, S. I. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0617-08.2008 · Cited by 55 · see citing works

Disrupted axo-glial junctions result in accumulation of abnormal mitochondria at nodes of ranvier.

Einheber, S., Bhat, M., & Salzer, J. (2006) · Neuron Glia Biology · doi:10.1017/s1740925x06000275 · Cited by 53 · see citing works

Differential Stability of PNS and CNS Nodal Complexes When Neuronal Neurofascin Is Lost

Desmazières, A., Zonta, B., Zhang, A., Wu, L.-M. N., Sherman, D. L., & Brophy, P. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4662-13.2014 · Cited by 54 · see citing works

A glial signal consisting of Gliomedin and NrCAM clusters axonal Na+ channels during the formation of nodes of Ranvier

Feinberg, K., Eshed-Eisenbach, Y., Frechter, S., Amor, V., Salomon, D., Sabanay, H., Dupree, J., Grumet, M., Brophy, P., Shrager, P., et al. (2010) · Neuron · doi:10.1016/j.neuron.2010.02.004 · Cited by 203 · see citing works

Long-Term Maintenance of Na+ Channels at Nodes of Ranvier Depends on Glial Contact Mediated by Gliomedin and NrCAM

Amor, V., Feinberg, K., Eshed-Eisenbach, Y., Vainshtein, A., Frechter, S., Grumet, M., Rosenbluth, J., & Peles, E. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4752-13.2014 · Cited by 85 · see citing works

Coordination of Schwann cell myelination and node formation at the transcriptional level

Wegner, M., & Fröb, F. (2021) · Neural Regeneration Research · doi:10.4103/1673-5374.327343 · Cited by 2 · see citing works

Gathering at the nodes

Jones, R. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1758

Precise Spatiotemporal Control of Nodal Na+ Channel Clustering by Bone Morphogenetic Protein-1/Tolloid-like Proteinases.

Eshed-Eisenbach, Y., Devaux, J., Vainshtein, A., Golani, O., Lee, S.-J., Feinberg, K., Sukhanov, N., Greenspan, D., Susuki, K., Rasband, M., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.03.001 · Cited by 10 · see citing works