Wnt signaling in axon guidance

MECHANISMS OF WNT SIGNALING IN DEVELOPMENT

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Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation

Heisenberg, C.-P., Tada, M., Rauch, G.-J., Saúde, L., Concha, M. L., Geisler, R., Stemple, D. L., Smith, J. C., & Wilson, S. W. (2000) · Nature · doi:10.1038/35011068 · Cited by 1,013

Wnt5a signaling directly affects cell motility and invasion of metastatic melanoma

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Wnt/Frizzled Activation of Rho Regulates Vertebrate Gastrulation and Requires a Novel Formin Homology Protein Daam1

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Shaping the Vertebrate Body Plan by Polarized Embryonic Cell Movements

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Flamingo, a Seven-Pass Transmembrane Cadherin, Regulates Planar Cell Polarity under the Control of Frizzled

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Identification of Vangl2 and Scrb1 as planar polarity genes in mammals

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Axonal Remodeling and Synaptic Differentiation in the Cerebellum Is Regulated by WNT-7a Signaling

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Anterior-Posterior Guidance of Commissural Axons by Wnt-Frizzled Signaling

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The Wnt signalling pathway

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Wnt-mediated axon guidance via the Drosophila Derailed receptor

Yoshikawa, S., McKinnon, R. D., Kokel, M., & Thomas, J. B. (2003) · Nature · doi:10.1038/nature01522 · Cited by 416

Calcium signalling in the guidance of nerve growth by netrin-1

Hong, K., Nishiyama, M., Henley, J. R., Tessier‐Lavigne, M., & Poo, M. (2000) · Nature · doi:10.1038/47507 · Cited by 390

Neurotrophins and Netrins Require Calcineurin/NFAT Signaling to Stimulate Outgrowth of Embryonic Axons

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Dishevelled activates Ca2+ flux, PKC, and CamKII in vertebrate embryos

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Van Gogh: A New Drosophila Tissue Polarity Gene

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Inhibition of GSK-3β leading to the loss of phosphorylated MAP-1B is an early event in axonal remodelling induced by WNT-7a or lithium

Lucas, F. R., Goold, R., Gordon‐Weeks, P. R., & Salinas, P. C. (1998) · Journal of Cell Science · doi:10.1242/jcs.111.10.1351 · Cited by 307

EphB Forward Signaling Controls Directional Branch Extension and Arborization Required for Dorsal-Ventral Retinotopic Mapping

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WNT-7a Induces Axonal Remodeling and Increases Synapsin I Levels in Cerebellar Neurons

Lucas, F. R., & Salinas, P. C. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8734 · Cited by 280

Wnt signalling: Antagonistic Dickkopfs

Zorn, A. M. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00360-8 · Cited by 238

Nerve growth cone guidance mediated by G protein–coupled receptors

Xiang, Y., Yan, L., Zhang, Z., Cui, K., Wang, S., Yuan, X., Wu, C.-P., Poo, M., & Duan, S. (2002) · Nature Neuroscience · doi:10.1038/nn899 · Cited by 231

A divergent canonical WNT-signaling pathway regulates microtubule dynamics

Ciani, L., Krylova, O. Y., Smalley, M. J., Dale, T. C., & Salinas, P. C. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200309096 · Cited by 226

Antagonistic regulation of convergent extension movements in Xenopus by Wnt/β-catenin and Wnt/Ca2+ signaling

Kühl, M., Geis, K., Sheldahl, L. C., Pukrop, T., Moon, R. T., & Wedlich, D. (2001) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00416-6 · Cited by 219

Eph receptors and ephrins: Regulators of guidance and assembly

Wilkinson, D. G. (2000) · International review of cytology · doi:10.1016/s0074-7696(00)96005-4 · Cited by 218

Wnt signaling mediates reorientation of outer hair cell stereociliary bundles in the mammalian cochlea

Dabdoub, A., Donohue, M. J., Brennan, A., Wolf, V., Montcouquiol, M., Sassoon, D. A., Hseih, J.-C., Rubin, J. S., Salinas, P. C., & Kelley, M. W. (2003) · Development · doi:10.1242/dev.00448 · Cited by 211

Non-canonical Wnt signalling and regulation of gastrulation movements

Tada, M., Concha, M. L., & Heisenberg, C. (2002) · Seminars in Cell and Developmental Biology · doi:10.1016/s1084-9521(02)00052-6 · Cited by 211

Topographic Mapping in Dorsoventral Axis of the Xenopus Retinotectal System Depends on Signaling through Ephrin-B Ligands

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Control of Dendritic Field Formation in Drosophila

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Wnt5 is required for tail formation in the zebrafish embryo.Preprint

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Control of neuronal pathway selection by a Drosophila receptor protein-tyrosine kinase family member

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PKCδ is essential for Dishevelled function in a noncanonical Wnt pathway that regulates Xenopus convergent extension movementsPreprint

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Ryk-deficient mice exhibit craniofacial defects associated with perturbed Eph receptor crosstalk

Halford, M. M., Armes, J. E., Büchert, M., Meskenaïte, V., Grail, D., Hibbs, M. L., Wilks, A. F., Farlie, P. G., Newgreen, D. F., Hovens, C. M., et al. (2000) · Nature Genetics · doi:10.1038/78099 · Cited by 172

The protocadherin Flamingo is required for axon target selection in the Drosophila visual system

Lee, R. C., Clandinin, T. R., Lee, C., Chen, P.-L., Meinertzhagen, I. A., & Zipursky, S. L. (2003) · Nature Neuroscience · doi:10.1038/nn1063 · Cited by 170

Axon routing across the midline controlled by the Drosophila Derailed receptor

Bonkowsky, J. L., Yoshikawa, S., O’Keefe, D. D., Scully, A. L., & Thomas, J. B. (1999) · Nature · doi:10.1038/990122 · Cited by 146

DWnt4 Regulates Cell Movement and Focal Adhesion Kinase during Drosophila Ovarian Morphogenesis

Cohen, E. D., Mariol, M., Wallace, R. M. H., Weyers, J., Kamberov, Y. G., Pradel, J., & Wilder, E. L. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00142-9 · Cited by 140

The WNT/Calcium pathway: biochemical mediators, tools and future requirements

Kühl, M. (2004) · Frontiers in bioscience · doi:10.2741/1307 · Cited by 140

Flamingo Regulates R8 Axon-Axon and Axon-Target Interactions in the Drosophila Visual System

Senti, K.-A., Usui, T., Boucke, K., Greber, U. F., Uemura, T., & Dickson, B. J. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00291-4 · Cited by 126

Frizzled signaling and cell–cell interactions in planar polarity

Adler, P. N., & Lee, H. (2001) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(00)00263-5 · Cited by 119

The Drosophila Wnt Protein DWnt-3 Is a Secreted Glycoprotein Localized on the Axon Tracts of the Embryonic CNS

Fradkin, L. G., Noordermeer, J. N., & Nusse, R. (1995) · Developmental Biology · doi:10.1006/dbio.1995.1072 · Cited by 69

Dephrin, a transmembrane ephrin with a unique structure, prevents interneuronal axons from exiting theDrosophilaembryonic CNS

Bossing, T., & Brand, A. H. (2002) · Development · doi:10.1242/dev.129.18.4205 · Cited by 63

Isolation and Characterization of Dek, a Drosophila Eph Receptor Protein Tyrosine Kinase

Scully, A. L., McKeown, M., & Thomas, J. B. (1999) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1999.0752 · Cited by 60

The Derailed Guidance Receptor Does Not Require Kinase ActivityIn Vivo

Yoshikawa, S., Bonkowsky, J. L., Kokel, M., Shyn, S. I., & Thomas, J. B. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-01-j0002.2001 · Cited by 48

RYK, a Catalytically Inactive Receptor Tyrosine Kinase, Associates with EphB2 and EphB3 but Does Not Interact with AF-6

Trivier, E., & Ganesan, T. S. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m202486200 · Cited by 48

Xwnt11 and the regulation of gastrulation in Xenopus

Smith, J. C., Conlon, F. L., Saka, Y., & Tada, M. (2000) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2000.0627 · Cited by 47

Synaptogenesis: Wnt and TGF-β Take Centre Stage

Salinas, P. C. (2003) · Current Biology · doi:10.1016/s0960-9822(02)01429-x · Cited by 47

Wnts as Retrograde Signals for Axon and Growth Cone Differentiation

Burden, S. J. (2000) · Cell · doi:10.1016/s0092-8674(00)80685-6 · Cited by 37

Wnt signal transduction pathways

Komiya, Y., & Habas, R. (2008) · Organogenesis · doi:10.4161/org.4.2.5851 · Cited by 1,528

Regulation of salivary gland function by autonomic nerves.

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Wnt/Ca2+ signaling pathway: a brief overview

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Dishevelled promotes axon differentiation by regulating atypical protein kinase C

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Wnt signaling in development and disease

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Axon guidance and injury — lessons from Wnts and Wnt signaling

Onishi, K., Hollis, E. R., II, & Zou, Y. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.05.005 · Cited by 92

Wnt signaling and neurite outgrowth: Insights and questions

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Expression of the Wnt signaling system in central nervous system axon guidance and regeneration

eHollis, E., & eZou, Y. (2012) · Frontiers in Molecular Neuroscience

Signaling from Axon Guidance ReceptorsPreprint

Bashaw, G. J., & Klein, R. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a001941 · Cited by 260

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