Contactins: Emerging key roles in the development and function of the nervous system

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

Alarcón, M., Abrahams, B. S., Stone, J. L., Duvall, J. A., Perederiy, J. V., Bomar, J. M., Sebat, J., Wigler, M., Martin, C. L., Ledbetter, D. H., et al. (2008) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2007.09.005 · Cited by 818 · see citing works

Spatial regulation of axonal glycoprotein expression on subsets of embryonic spinal neurons

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The local differentiation of myelinated axons at nodes of Ranvier

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Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

Strauss, K. A., Puffenberger, E. G., Huentelman, M. J., Gottlieb, S., Dobrin, S. E., Parod, J. M., Stephan, D. A., & Morton, D. H. (2006) · New England Journal of Medicine · doi:10.1056/nejmoa052773 · Cited by 630 · see citing works

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

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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

The axonal glycoprotein TAG-1 is an immunoglobulin superfamily member with neurite outgrowth-promoting activity

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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

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

Bakkaloglu, B., O'Roak, B. J., Louvi, A., Gupta, A. R., Abelson, J. F., Morgan, T. M., Chawarska, K., Klin, A., Ercan-Sencicek, A. G., Stillman, A. A., et al. (2008) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2007.09.017 · Cited by 537 · 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

Structure and function of the β2 subunit of brain sodium channels, a transmembrane glycoprotein with a CAM motif

Isom, L. L., Ragsdale, D. S., Jongh, K. S. D., Westenbroek, R. E., Reber, B. F. X., Scheuer, T., & Catterall, W. A. (1995) · Cell · doi:10.1016/0092-8674(95)90121-3 · Cited by 461 · 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 · 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

Maps of Odorant Molecular Features in the Mammalian Olfactory Bulb

Mori, K., Takahashi, Y. K., Igarashi, K. M., & Yamaguchi, M. (2006) · Physiological Reviews · doi:10.1152/physrev.00021.2005 · Cited by 397 · see citing works

Calcium and reactive oxygen species mediate staurosporine-induced mitochondrial dysfunction and apoptosis in PC12 cells

Kruman, I. I., Guo, Q., & Mattson, M. P. (1998) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19980201)51:3 · Cited by 377 · 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

F3/Contactin Acts as a Functional Ligand for Notch during Oligodendrocyte Maturation

Hu, Q., Ang, B.-T., Karsak, M., Hu, W.-P., Cui, X., Duka, T., Takeda, Y., Chia, W., Sankar, N., Ng, Y., et al. (2003) · Cell · doi:10.1016/s0092-8674(03)00810-9 · Cited by 367 · 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

On the molecular architecture of myelinated fibers

Arroyo, E. J., & Scherer, S. S. (2000) · Histochemistry and Cell Biology · doi:10.1007/s004180050001 · Cited by 316 · see citing works

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

Friedman, J. I., Vrijenhoek, T., Markx, S., Janssen, I. M., van der Vliet, W. A., Faas, B. H. W., Knoers, N. V. A. M., Cahn, W., Kahn, R. S., Edelmann, L. J., et al. (2007) · Molecular Psychiatry · doi:10.1038/sj.mp.4002049 · Cited by 297 · see citing works

Neurofascin Is a Glial Receptor for the Paranodin/Caspr-Contactin Axonal Complex at the Axoglial Junction

Charles, P., Tait, S., Faivre‐Sarrailh, C., Barbin, G., Gunn‐Moore, F. J., Denisenko, N., Guennoc, A., Girault, J., Brophy, P., & Lubetzki, C. (2002) · Current Biology · doi:10.1016/s0960-9822(01)00680-7 · Cited by 297 · see citing works

Contactin-Associated Protein (Caspr) and Contactin Form a Complex That Is Targeted to the Paranodal Junctions during Myelination

Rios, J. C., Melendez-Vasquez, C., Einheber, S., Lustig, M., Grumet, M., Hemperly, J., Peles, E., & Salzer, J. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-08354.2000 · Cited by 287 · see citing works

Neurite outgrowth on immobilized axonin-1 is mediated by a heterophilic interaction with L1(G4).

Kuhn, T. B., Stoeckli, E. T., Condrau, M. A., Rathjen, F. G., & Sonderegger, P. (1991) · The Journal of Cell Biology · doi:10.1083/jcb.115.4.1113 · Cited by 279 · see citing works

Sequence of contactin, a 130-kD glycoprotein concentrated in areas of interneuronal contact, defines a new member of the immunoglobulin supergene family in the nervous system

Ranscht, B. (1988) · The Journal of Cell Biology · doi:10.1083/jcb.107.4.1561 · Cited by 262 · see citing works

Paranodin, a glycoprotein of neuronal paranodal membranes.

Menegoz, M., Gaspar, P., Bert, M. L., Galvez, T., Burgaya, F., Palfrey, C., Ezan, P., Arnos, F., & Girault, J. (1997) · Neuron · doi:10.1016/s0896-6273(00)80942-3 · Cited by 262 · see citing works

The mouse neuronal cell surface protein F3: a phosphatidylinositol-anchored member of the immunoglobulin superfamily related to chicken contactin.

Gennarini, G., Cibelli, G., Rougon, G. N., Mattéi, M., & Goridis, C. (1989) · The Journal of Cell Biology · doi:10.1083/jcb.109.2.775 · Cited by 261 · see citing works

One neuron–one receptor rule in the mouse olfactory system

Serizawa, S., Miyamichi, K., & Sakano, H. (2004) · Trends in Genetics · doi:10.1016/j.tig.2004.09.006 · Cited by 260 · see citing works

Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers

Traka, M., Goutebroze, L., Denisenko, N., Bessa, M. J., Nifli, A., Havaki, S., Iwakura, Y., Fukamauchi, F., Watanabe, K., Soliven, B. C., et al. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200305078 · Cited by 249 · see citing works

Molecular domains of myelinated axons.

Peles, E., & Salzer, J. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00122-7 · Cited by 242 · see citing works

The F3/11 cell adhesion molecule mediates the repulsion of neurons by the extracellular matrix glycoprotein J1-160/180

Pesheva, P., Gennarini, G., Goridis, C., & Schachner, M. (1993) · Neuron · doi:10.1016/0896-6273(93)90243-k · Cited by 241 · see citing works

Neural cell recognition molecule F11: Homology with fibronectin type III and immunoglobulin type C domains

Brümmendorf, T., Wolff, J. M., Frank, R. W., & Rathjen, F. G. (1989) · Neuron · doi:10.1016/0896-6273(89)90073-1 · Cited by 220 · see citing works

Ataxia and abnormal cerebellar microorganization in mice with ablated contactin gene expression.

Berglund, E., Murai, K., Fredette, B., Sekerkovâ, G., Marturano, B., Weber, L., Mugnaini, E., & Ranscht, B. (1999) · Neuron · doi:10.1016/s0896-6273(00)81126-5 · Cited by 216 · see citing works

TAG-1/Axonin-1 Is a High-affinity Ligand of Neurocan, Phosphacan/Protein-tyrosine Phosphatase-ζ/β, and N-CAM

Milev, P., Maurel, P., Häring, M., Margolis, R. K., & Margolis, R. U. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.26.15716 · Cited by 210 · see citing works

The adhesion molecule TAG-1 mediates the migration of cortical interneurons from the ganglionic eminence along the corticofugal fiber system

Denaxa, M., Chan, C., Schachner, M., Parnavelas, J. G., & Karagogeos, D. (2001) · Development · doi:10.1242/dev.128.22.4635 · Cited by 202 · see citing works

Contactin Associates with Na+ Channels and Increases Their Functional Expression

Kazarinova-Noyes, K., Malhotra, J., Mcewen, D. P., Mattei, L. N., Berglund, E., Ranscht, B., Levinson, S., Schachner, M., Shrager, P., Isom, L., et al. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-19-07517.2001 · Cited by 199 · see citing works

A TAG1-APP signalling pathway through Fe65 negatively modulates neurogenesis

Ma, Q., Futagawa, T., Yang, W.-L., Jiang, X., Zeng, L., Takeda, Y., Xu, R., Bagnard, D., Schachner, M., Furley, A. J., et al. (2008) · Nature Cell Biology · doi:10.1038/ncb1690 · Cited by 196 · see citing works

Disruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome

Fernandez, T. V., Morgan, T. M., Davis, N., Klin, A. J., Morris, A., Farhi, A., Lifton, R. P., & State, M. W. (2004) · The American Journal of Human Genetics · doi:10.1086/421474 · Cited by 191 · see citing works

The axonal recognition molecule F11 is a multifunctional protein: Specific domains mediate interactions with Ng-CAM and restrictin

Brm̈mendorf, T., Hubert, M. J., Treubert, U., Leuschner, R., Tárnok, A., & Rathjen, F. G. (1993) · Neuron · doi:10.1016/0896-6273(93)90172-n · Cited by 179 · see citing works

Induction of Neurite Outgrowth through Contactin and Nr-CAM by Extracellular Regions of Glial Receptor Tyrosine Phosphatase β

Sakurai, T., Lustig, M., Nativ, M., Hemperly, J., Schlessinger, J., Peles, E., & Grumet, M. (1997) · Journal of Cell Biology · doi:10.1083/jcb.136.4.907 · Cited by 176 · see citing works

Neuronal cell adhesion molecule contactin/F11 binds to tenascin via its immunoglobulin-like domains.

Zisch, A. H., D'Alessandri, L., Ranscht, B., Falchetto, R. A., Winterhalter, K. H., & Vaughan, L. (1992) · The Journal of Cell Biology · doi:10.1083/jcb.119.1.203 · Cited by 156 · 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

Overlapping and differential expression of BIG‐2, BIG‐1, TAG‐1, and F3: Four members of an axon‐associated cell adhesion molecule subgroup of the immunoglobulin superfamily

Yoshihara, Y., Kawasaki, M., Tamada, A., Nagata, S., Kagamiyama, H., & Mori, K. (1995) · Journal of Neurobiology · doi:10.1002/neu.480280106 · Cited by 154 · see citing works

Disruption of contactin 4 in three subjects with autism spectrum disorder

Roohi, J., Montagna, C., Tegay, D. H., Palmer, L. E., DeVincent, C. J., Pomeroy, J. C., Christian, S. L., Nowak, N., & Hatchwell, E. (2008) · Journal of Medical Genetics · doi:10.1136/jmg.2008.057505 · Cited by 151 · see citing works

Distribution of TAG‐1/Axonin‐1 in fibre tracts and migratory streams of the developing mouse nervous system

Wolfer, D. P., Henehan‐Beatty, A., Stoeckli, E. T., Sonderegger, P., & Lipp, H. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903450102 · Cited by 145 · see citing works

NB-3/Notch1 Pathway via Deltex1 Promotes Neural Progenitor Cell Differentiation into Oligodendrocytes

Cui, X., Hu, Q., Tekaya, M., Shimoda, Y., Ang, B.-T., Nie, D. A., Sun, L. J., Hu, W.-P., Karsak, M., Duka, T., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313505200 · Cited by 144 · see citing works

BIG-2 Mediates Olfactory Axon Convergence to Target Glomeruli

Kaneko-Goto, T., Yoshihara, S.-I., Miyazaki, H., & Yoshihara, Y. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.023 · Cited by 142 · see citing works

Distribution of stage-specific neurite-associated proteins in the developing murine nervous system recognized by a monoclonal antibody

Yamamoto, M., Boyer, A. M., Crandall, J., Edwards, M., & Tanaka, H. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-12-03576.1986 · Cited by 140 · see citing works

Restrictin: a chick neural extracellular matrix protein involved in cell attachment co-purifies with the cell recognition molecule F11

Rathjen, F. G., Wolff, M., & Chiquet‐Ehrismann, R. (1991) · Development · doi:10.1242/dev.113.1.151 · Cited by 140 · see citing works

F3/contactin, a neuronal cell adhesion molecule implicated in axogenesis and myelination

Falk, J., Bonnon, C., Girault, J., & Faivre-Sarrailh, C. (2002) · Biology of the Cell · doi:10.1016/s0248-4900(02)00006-0 · Cited by 139 · see citing works

The role of sodium channels in cell adhesion.

Isom, L. (2002) · Frontiers in Bioscience · doi:10.2741/isom · Cited by 133 · see citing works

Cell adhesion molecules NgCAM and axonin-1 form heterodimers in the neuronal membrane and cooperate in neurite outgrowth promotion.

Buchstaller, A., Kunz, S., Berger, P., Kunz, B., Ziegler, U., Rader, C. M., & Sonderegger, P. (1996) · The Journal of Cell Biology · doi:10.1083/jcb.135.6.1593 · Cited by 127 · see citing works

The Neuronal Adhesion Protein TAG-1 Is Expressed by Schwann Cells and Oligodendrocytes and Is Localized to the Juxtaparanodal Region of Myelinated Fibers

Traka, M., Dupree, J. L., Popko, B., & Karagogeos, D. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-08-03016.2002 · Cited by 124 · see citing works

The Glycosylphosphatidyl Inositol-Anchored Adhesion Molecule F3/Contactin Is Required for Surface Transport of Paranodin/Contactin-Associated Protein (Caspr)

Faivre-Sarrailh, C., Gauthier, F., Denisenko‐Nehrbass, N., Bivic, A. L., Rougon, G., & Girault, J. (2000) · Journal of Cell Biology · doi:10.1083/jcb.149.2.491 · Cited by 124 · see citing works

The axonally secreted cell adhesion molecule, axonin‐1

Zuellig, R. A., Rader, C. M., SCHROEDER, A., Kalousek, M. B., Halbach, F. V. B. U., Osterwalder, T., Canan, I. N. A. N., Stoeckli, E. T., Affolter, H., FRITZ, A., et al. (1992) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1992.tb16655.x · Cited by 120 · see citing works

Tenascin-C Promotes Neurite Outgrowth of Embryonic Hippocampal Neurons through the Alternatively Spliced Fibronectin Type III BD Domains via Activation of the Cell Adhesion Molecule F3/Contactin

Rigato, F., Garwood, J., Calco, V., Heck, N., Faivre‐Sarrailh, C., & Faissner, A. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06596.2002 · Cited by 118 · see citing works

Induction of axonal growth by heterophilic interactions between the cell surface recognition proteins Fll and Nr-CAM/Bravo

Morales, G., Hubert, M. J., Brümmendorf, T., Treubert, U., Tárnok, A., Schwarz, U., & Rathjen, F. G. (1993) · Neuron · doi:10.1016/0896-6273(93)90224-f · Cited by 116 · see citing works

Protein Tyrosine Phosphatase α (Ptpα) and Contactin Form a Novel Neuronal Receptor Complex Linked to the Intracellular Tyrosine Kinase Fyn

Zeng, L., D'Alessandri, L., Kalousek, M., Vaughan, L., & Pallen, C. (1999) · Journal of Cell Biology · doi:10.1083/jcb.147.4.707 · Cited by 112 · see citing works

Development of nodes of Ranvier.

Girault, J., & Peles, E. (2002) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(02)00370-7 · Cited by 110 · see citing works

Neurite Fasciculation Mediated by Complexes of Axonin-1 and Ng Cell Adhesion Molecule

Kunz, S., Spirig, M., Ginsburg, C., Buchstaller, A., Berger, P., Lanz, R. B., Rader, C. M., Vogt, L., Kunz, B., & Sonderegger, P. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.143.6.1673 · Cited by 104 · see citing works

F3/F11 cell surface molecule expression in the developing mouse cerebellum is polarized at synaptic sites and within granule cells

Faivre‐Sarrailh, C., Gennarini, G., Goridis, C., & Rougon, G. N. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-01-00257.1992 · Cited by 103 · 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

Contactin supports synaptic plasticity associated with hippocampal long-term depression but not potentiation.

Murai, K., Misner, D., & Ranscht, B. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00680-2 · Cited by 98 · see citing works

BIG-1: A new TAG-1/F3-related member of the immunoglobulin superfamily with neurite outgrowth-promoting activity

Yoshihara, Y., Kawasaki, M., Tani, A., Tamada, A., Nagata, S., Kagamiyama, H., & Mori, K. (1994) · Neuron · doi:10.1016/0896-6273(94)90357-3 · Cited by 97 · see citing works

Binding between the neural cell adhesion molecules axonin-1 and Nr-CAM/Bravo is involved in neuron-glia interaction.

Suter, D. M., Pollerberg, G. E., Buchstaller, A., Giger, R. J., Dreyer, W. J., & Sonderegger, P. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.131.4.1067 · Cited by 97 · see citing works

A Direct Interaction of Axonin-1 with Ngcam-Related Cell Adhesion Molecule (Nrcam) Results in Guidance, but Not Growth of Commissural Axons

Fitzli, D., Stoeckli, E. T., Kunz, S., Siribour, K., Rader, C. M., Kunz, B., Kozlov, S. V., Buchstaller, A., Lane, R. P., Suter, D. M., et al. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.149.4.951 · Cited by 89 · see citing works

Neural recognition molecules CHL1 and NB‐3 regulate apical dendrite orientation in the neocortex via PTPα

Ye, H., Tan, Y. L. J., Ponniah, S., Takeda, Y., Wang, S., Schachner, M., Watanabe, K., Pallen, C. J., & Xiao, Z. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601939 · Cited by 86 · see citing works

Direct Interaction with Contactin Targets Voltage-gated Sodium Channel Nav1.9/NaN to the Cell Membrane*

Liu, C.-J., Dib-Hajj, S., Black, J., Greenwood, J., Lian, Z., & Waxman, S. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m108699200 · Cited by 85 · see citing works

Interaction of amyloid precursor protein with contactins and NgCAM in the retinotectal system

Osterfield, M., Egelund, R., Young, L. M., & Flanagan, J. G. (2008) · Development · doi:10.1242/dev.007401 · Cited by 84 · see citing works

Transgenic mice expressing F3/contactin from the TAG-1 promoter exhibit developmentally regulated changes in the differentiation of cerebellar neurons

Bizzoca, A., Virgintino, D., Lorusso, L., Buttiglione, M., Yoshida, L., Polizzi, A. M., Tattoli, M., Cagiano, R., Rossi, F., Козлов, С. В., et al. (2002) · Development · doi:10.1242/dev.00183 · Cited by 83 · see citing works

Nr‐CAM expression in the developing mouse nervous system: Ventral midline structures, specific fiber tracts, and neuropilar regions

Lustig, M., Erskine, L., Mason, C. A., Grumet, M., & Sakurai, T. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1161 · Cited by 83 · see citing works

Cis-activation of L1-mediated Ankyrin Recruitment by TAG-1 Homophilic Cell Adhesion

Malhotra, J. D., Tsiotra, P. C., Karagogeos, D., & Hortsch, M. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.50.33354 · Cited by 78 · see citing works

Neural GPI anchored cell adhesion molecules

Karagogeos, D. (2003) · Frontiers in bioscience · doi:10.2741/1214 · Cited by 77 · see citing works

The Glypiated Neuronal Cell Adhesion Molecule Contactin/F11 Complexes with src-Family Protein Tyrosine Kinase Fyn

Zisch, A. H., D'Alessandri, L., Amrein, K. E., Ranscht, B., Winterhalter, K. H., & Vaughan, L. (1995) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1995.1021 · Cited by 76 · see citing works

The Paranodal Complex of F3/Contactin and Caspr/Paranodin Traffics to the Cell Surface via a Non-conventional Pathway*

Bonnon, C., Goutebroze, L., Denisenko-Nehrbass, N., Girault, J., & Faivre-Sarrailh, C. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m309120200 · Cited by 72 · see citing works

Impairment of learning and memory in TAG-1 deficient mice associated with shorter CNS internodes and disrupted juxtaparanodes

Savvaki, M., Panagiotaropoulos, T. I., Stamatakis, A., Sargiannidou, I., Karatzioula, P., Watanabe, K., Stylianopoulou, F., Karagogeos, D., & Kleopa, K. A. (2008) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2008.07.025 · Cited by 72 · see citing works

A combination of chain and neurophilic migration involving the adhesion molecule TAG-1 in the caudal medulla

Kyriakopoulou, K., de Diego, I., Wassef, M., & Karagogeos, D. (2002) · Development · doi:10.1242/dev.129.2.287 · Cited by 72 · see citing works

Impaired motor coordination in mice lacking neural recognition molecule NB‐3 of the contactin/F3 subgroup

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TAG-1-Deficient Mice Have Marked Elevation of Adenosine A1 Receptors in the Hippocampus

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Untitled work

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Contactin 1: An Important and Emerging Oncogenic Protein Promoting Cancer Progression and Metastasis

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Generation of megabase-scale deletions, inversions and duplications involving the Contactin-6 gene in mice by CRISPR/Cas9 technology

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Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells

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DNA Methylation Profiling Reveals the Change of Inflammation-Associated ZC3H12D in Leukoaraiosis

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LewisX: A neural stem cell specific glycan?

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Developmental role of the cell adhesion molecule Contactin-6 in the cerebral cortex and hippocampus

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Immunoglobulin-Like Receptors and Their Impact on Wiring of Brain Synapses

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Contactin-1 and contactin-2 in cerebrospinal fluid as potential biomarkers for axonal domain dysfunction in multiple sclerosis

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Cell Adhesion Molecules Involved in Neurodevelopmental Pathways Implicated in 3p-Deletion Syndrome and Autism Spectrum Disorder

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Loss of neural recognition molecule NB‐3 delays the normal projection and terminal branching of developing corticospinal tract axons in the mouse

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Allele-Specific Biased Expression of the CNTN6 Gene in iPS Cell-Derived Neurons from a Patient with Intellectual Disability and 3p26.3 Microduplication Involving the CNTN6 Gene

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Loss-of-function of PTPR γ and ζ, observed in sporadic schizophrenia, causes brain region-specific deregulation of monoamine levels and altered behavior in mice

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Pathophysiology of Trans-Synaptic Adhesion Molecules: Implications for Epilepsy

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A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism

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Paeonol Attenuates H2O2 -Induced NF-κB-Associated Amyloid Precursor Protein Expression

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Structural insights into the contactin 1 – neurofascin 155 adhesion complex

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A cis-complex of NB-2/contactin-5 with amyloid precursor-like protein 1 is localized on the presynaptic membrane

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Contactin 1: A potential therapeutic target and biomarker in gastric cancer

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Molecular logic for cellular specializations that initiate the auditory parallel processing pathways

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Missing and overexpressing proteins in domestic cat oocytes following vitrification and in vitro maturation as revealed by proteomic analysis

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Serum contactin-1 as a biomarker of long-term disease progression in natalizumab-treated multiple sclerosis

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Contactin 1 modulates pegylated arginase resistance in small cell lung cancer through induction of epithelial–mesenchymal transition

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SLC1A1, SLC16A9, and CNTN3 Are Potential Biomarkers for the Occurrence of Colorectal Cancer

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The contactin RIG-6 mediates neuronal and non-neuronal cell migration in Caenorhabditis elegans

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Incorporating Information of microRNAs into Pathway Analysis in a Genome-Wide Association Study of Bipolar Disorder

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Nanomechanics of multidomain neuronal cell adhesion protein contactin revealed by single molecule AFM and SMD

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Why nature evolved GPI-anchored proteins: unique structure characteristics enable versatile cell surface functions

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Combined Whole Methylome and Genomewide Association Study ImplicatesCNTN4in Alcohol Use

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Latrophilin’s Social Protein Network

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Intragenic CNTN4 copy number variants associated with a spectrum of neurobehavioral phenotypes

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Unexpected phenotypic effects of a transgene integration causing a knockout of the endogenous Contactin-5 gene in mice

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Host cell membrane proteins located near SARS-CoV-2 spike protein attachment sites are identified using proximity labeling and proteomic analysis

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Structural abnormalities in the primary somatosensory cortex and a normal behavioral profile in Contactin-5 deficient mice

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Sphingosine-1-phosphate can promote mast cell hyper-reactivity through regulation of contactin-4 expression

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Significant Down-Regulation of “Biological Adhesion” Genes in Porcine Oocytes after IVM

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Identification of tyrosine phosphatase ligands for contactin cell adhesion molecules

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Contactin 6, A Novel Causative Gene for Congenital Hypothyroidism, Mediates Thyroid Hormone Biosynthesis Through Notch Signaling

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CNTN4 modulates neural elongation through interplay with APP

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Genome-wide microarray analysis of Atlantic cod (Gadus morhua) oocyte and embryo

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Medaka and zebrafish contactin1 mutants as a model for understanding neural circuits for motor coordination

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Prognostic significance of contactin 3 expression and associated genes in glioblastoma multiforme

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Anatomy and Cell Biology of Autism Spectrum Disorder: Lessons from Human Genetics

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Cntn6 deficiency impairs allocentric navigation in mice

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Contactin-2/TAG-1, active on the front line for three decades

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Contactins in the central nervous system: role in health and disease

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