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 · see citing works

Wnt5a signaling directly affects cell motility and invasion of metastatic melanoma

Weeraratna, A. T., Jiang, Y., Hostetter, G. H., Rosenblatt, K. P., Duray, P. H., Bittner, M. L., & Trent, J. M. (2002) · Cancer Cell · doi:10.1016/s1535-6108(02)00045-4 · Cited by 960 · see citing works

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

Habas, R., Kato, Y., & He, X. (2001) · Cell · doi:10.1016/s0092-8674(01)00614-6 · Cited by 842 · see citing works

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

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Shaping the Vertebrate Body Plan by Polarized Embryonic Cell Movements

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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

Hall, A. C., Lucas, F. R., & Salinas, P. C. (2000) · Cell · doi:10.1016/s0092-8674(00)80689-3 · Cited by 687 · see citing works

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

Lyuksyutova, A. I., Lu, C.-C., Milanesio, N., King, L. A., Guo, N., Wang, Y., Nathans, J., Tessier‐Lavigne, M., & Zou, Y. (2003) · Science · doi:10.1126/science.1089610 · Cited by 557 · see citing works

The Wnt signalling pathway

Huelsken, J., & Behrens, J. (2002) · Journal of Cell Science · doi:10.1242/jcs.00089 · Cited by 537 · see citing works

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 · see citing works

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 · see citing works

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

Graef, I. A., Wang, F., Charron, F., Chen, L., Neilson, J., Tessier-Lavigne, M., & Crabtree, G. R. (2003) · Cell · doi:10.1016/s0092-8674(03)00390-8 · Cited by 379 · see citing works

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

Sheldahl, L. C., Slusarski, D. C., Pandur, P., Miller, J. R., Kühl, M., & Moon, R. T. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200211094 · Cited by 350 · see citing works

Van Gogh: A New Drosophila Tissue Polarity Gene

Taylor, J., Abramova, N. A., Charlton, J., & Adler, P. N. (1998) · Genetics · doi:10.1093/genetics/150.1.199 · Cited by 328 · see citing works

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

Hindges, R., McLaughlin, T., Genoud, N., Henkemeyer, M. J., & O’Leary, D. D. M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00799-7 · Cited by 302 · see citing works

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 301 · see citing works

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 275 · see citing works

Wnt signalling: Antagonistic Dickkopfs

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

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 · see citing works

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 · see citing works

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 217 · see citing works

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 214 · see citing works

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 · see citing works

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 209 · see citing works

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

Mann, F., Ray, S., Harris, W. A., & Holt, C. E. (2002) · Neuron · doi:10.1016/s0896-6273(02)00786-9 · Cited by 205 · see citing works

Control of Dendritic Field Formation in Drosophila

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

Rauch, G.-J., Hammerschmidt, M., Blader, P., Schauerte, H. E., Strähle, U., Ingham, P. W., McMahon, A., & Haffter, P. (1997) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1997.062.01.028 · Cited by 180 · see citing works

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

Kinoshita, N., Iioka, H., Miyakoshi, A., & Ueno, N. (2003) · Genes & Development · doi:10.1101/gad.1101303 · Cited by 173 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 142 · see citing works

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

Kühl, M. (2004) · Frontiers in bioscience · doi:10.2741/1307 · Cited by 136 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 59 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

Wnt signal transduction pathways

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

Regulation of salivary gland function by autonomic nerves.

Proctor, G., & Carpenter, G. (2007) · Autonomic Neuroscience: Basic & Clinical · doi:10.1016/j.autneu.2006.10.006 · Cited by 723 · see citing works

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

Freese, J. L., Pino, D., & Pleasure, S. J. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.09.003 · Cited by 219 · see citing works

WNT signaling underlies the pathogenesis of neuropathic pain in rodents

Zhang, Y., Huang, Z., Liu, S., Liu, Y.-P., Song, A. A., & Song, X. (2013) · Journal of Clinical Investigation · doi:10.1172/jci65364 · Cited by 214 · see citing works

Vangl2 Promotes Wnt/Planar Cell Polarity-like Signaling by Antagonizing Dvl1-Mediated Feedback Inhibition in Growth Cone Guidance

Shafer, B., Onishi, K., Lo, C. G., Çolakoğlu, G., & Zou, Y. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.01.002 · Cited by 199 · see citing works

The Versatile Roles of “Axon Guidance” Cues in Tissue Morphogenesis

Hinck, L. (2004) · Developmental Cell · doi:10.1016/j.devcel.2004.11.002 · Cited by 187 · see citing works

Wnt5a Induces Simultaneous Cortical Axon Outgrowth and Repulsive Axon Guidance through Distinct Signaling Mechanisms

Li, L., Hutchins, B. I., & Kalil, K. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0183-09.2009 · Cited by 164 · see citing works

Pax6 is required for production and maintenance of progenitor cells in postnatal hippocampal neurogenesis

Maekawa, M., Takashima, N., Arai, Y., Nomura, T., Inokuchi, K., Yuasa, S., & Osumi, N. (2005) · Genes to Cells · doi:10.1111/j.1365-2443.2005.00893.x · Cited by 156 · see citing works

Synaptic Wnt signaling—a contributor to major psychiatric disorders?

Okerlund, N. D., & Cheyette, B. N. R. (2011) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-011-9083-6 · Cited by 143 · see citing works

Axon guidance genes identified in a large-scale RNAi screen using the RNAi-hypersensitive Caenorhabditis elegans strain nre-1(hd20) lin-15b(hd126 )

Schmitz, C., Kinge, P., & Hutter, H. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510527104 · Cited by 131 · see citing works

Directional guidance of nerve growth cones

Wen, Z., & Zheng, J. Q. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.12.005 · Cited by 123 · see citing works

NMDA receptor activation stimulates transcription-independent rapid wnt5a protein synthesis via the MAPK signaling pathway

Li, Y.-C., Li, B., Wan, X.-Z., Zhang, W., Zhong, L., & Tang, S.-J. (2012) · Molecular Brain · doi:10.1186/1756-6606-5-1 · Cited by 91 · see citing works

‘Suicide’ of crickets harbouring hairworms: a proteomics investigation

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Morphogens as conserved axon guidance cues

Zou, Y., & Lyuksyutova, A. I. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.01.006 · Cited by 101 · see citing works

Wnt5a Regulates Midbrain Dopaminergic Axon Growth and Guidance

Blakely, B. D., Bye, C. R., Fernando, C. V., Horne, M. K., Macheda, M. L., Stacker, S. A., Arenas, E., & Parish, C. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018373 · Cited by 100 · see citing works

Transfer of Vesicles From Schwann Cells to Axons: a Novel Mechanism of Communication in the Peripheral Nervous System

Lopez‐Verrilli, M. A., & Court, F. A. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00205 · Cited by 100 · see citing works

Src family kinases are required for WNT5 signaling through the Derailed/RYK receptor in theDrosophilaembryonic central nervous system

Wouda, R. R., Bansraj, M. R. K. S., de Jong, A. W. M., Noordermeer, J. N., & Fradkin, L. G. (2008) · Development · doi:10.1242/dev.017319 · Cited by 96 · see citing works

Non‐conventional Frizzled ligands and Wnt receptors

Hendrickx, M., & Leyns, L. (2008) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2008.01016.x · Cited by 95 · see citing works

Phosphatidylinositol-3-Kinase–Atypical Protein Kinase C Signaling Is Required for Wnt Attraction and Anterior–Posterior Axon Guidance

Wolf, A. M., Lyuksyutova, A. I., Fenstermaker, A. G., Shafer, B., Lo, C. G., & Zou, Y. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0029-08.2008 · Cited by 94 · see citing works

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 · see citing works

Tumor-immune profiling of CT-26 and Colon 26 syngeneic mouse models reveals mechanism of anti-PD-1 response

Sato, Y., Fu, Y., Liu, H., Lee, M. Y., & Shaw, M. H. (2021) · BMC Cancer · doi:10.1186/s12885-021-08974-3 · Cited by 94 · see citing works

Wnt-Ryk Signaling Mediates Axon Growth Inhibition and Limits Functional Recovery after Spinal Cord Injury

Miyashita, T., Koda, M., Kitajo, K., Yamazaki, M., Takahashi, K., Kikuchi, A., & Yamashita, T. (2009) · Journal of Neurotrauma · doi:10.1089/neu.2008.0776 · Cited by 89 · see citing works

Wnt/β-Catenin Signaling Suppresses Rapsyn Expression and Inhibits Acetylcholine Receptor Clustering at the Neuromuscular Junction

Wang, J., Ruan, N.-J., Qian, L., Lei, W., Chen, F., & Luo, Z. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m709939200 · Cited by 85 · see citing works

Wnt/Ryk signaling contributes to neuropathic pain by regulating sensory neuron excitability and spinal synaptic plasticity in rats

Liu, S., Liu, Y., Huang, Z., Zhang, Y., Song, A. A., Ma, P., & Song, X. (2015) · Pain · doi:10.1097/j.pain.0000000000000366 · Cited by 85 · see citing works

Wnt signaling promotes axonal regeneration following optic nerve injury in the mouse

Patel, A. K., Park, K. K., & Hackam, A. S. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.12.020 · Cited by 84 · see citing works

Wnt signaling drives WRM-1/β-catenin asymmetries in early C. elegans embryosPreprint

Nakamura, K., Kim, S. Y., Ishidate, T., Bei, Y., Pang, K. M., Shirayama, M., Trzepacz, C., Brownell, D. R., & Mello, C. C. (2005) · Genes & Development · doi:10.1101/gad.1323705 · Cited by 81 · see citing works

Expression of Frizzled5, Frizzled7, and Frizzled10 during early mouse development and interactions with canonical Wnt signaling

Kemp, C. R., Willems, E., Wawrzak, D., Hendrickx, M., Agbor, T. A., & Leyns, L. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21198 · Cited by 78 · see citing works

Mutations of the Sonic Hedgehog Pathway Underlie Hypothalamic Hamartoma with Gelastic Epilepsy

Hildebrand, M. S., Griffin, N. G., Damiano, J. A., Cops, E. J., Burgess, R., Öztürk, E., Jones, N. C., Leventer, R. J., Freeman, J. L., Harvey, A. S., et al. (2016) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2016.05.031 · Cited by 74 · see citing works

A Wnt-Frz/Ror-Dsh Pathway Regulates Neurite Outgrowth in Caenorhabditis elegans

Song, S., Zhang, B., Sun, H. J., Li, X., Xiang, Y., Liu, Z., Huang, X., & Ding, M. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001056 · Cited by 73 · see citing works

JNK Signaling Pathway Involvement in Spinal Cord Neuron Development and Death

Schellino, R., Boido, M., & Vercelli, A. (2019) · Cells · doi:10.3390/cells8121576 · Cited by 70 · see citing works

The Plane Facts of PCP in the CNS

Goodrich, L. V. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.003 · Cited by 68 · see citing works

Casein kinase 2-dependent serine phosphorylation of MuSK regulates acetylcholine receptor aggregation at the neuromuscular junctionPreprint

Cheusova, T., Khan, M. A., Schubert, S. W., Gavin, A., Buchou, T., Jacob, G., Sticht, H., Allende, J. E., Boldyreff, B., Brenner, H. R., et al. (2006) · Genes & Development · doi:10.1101/gad.375206 · Cited by 64 · see citing works

An Overview of Neural Differentiation Potential of Human Adipose Derived Stem Cells

Salehi, H., Amirpour, N., Niapour, A., & Razavi, S. (2015) · Stem Cell Reviews and Reports · doi:10.1007/s12015-015-9631-7 · Cited by 63 · see citing works

Wnt and lithium: a common destiny in the therapy of nervous system pathologies?

Meffre, D., Grenier, J., Bernard, S., Courtin, F., Dudev, T., Shackleford, G., Jafarian-Tehrani, M., & Massaad, C. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1378-1 · Cited by 61 · see citing works

Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectives

Faravelli, I., Bucchia, M., Rinchetti, P., Nizzardo, M., Simone, C., Frattini, E., & Corti, S. P. (2014) · Stem Cell Research & Therapy · doi:10.1186/scrt476 · Cited by 61 · see citing works

Axon Guidance Molecules Guiding Neuroinflammation

Lee, W. S., Lee, W., Bae, Y. C., & Suk, K. (2019) · Experimental Neurobiology · doi:10.5607/en.2019.28.3.311 · Cited by 61 · see citing works

Prostaglandin E2 alters Wnt-dependent migration and proliferation in neuroectodermal stem cells: implications for autism spectrum disorders

Wong, C. T., Ahmad, E., Li, H., & Crawford, D. A. (2014) · Cell Communication and Signaling · doi:10.1186/1478-811x-12-19 · Cited by 60 · see citing works

Wnt5aIs a Transcriptional Target ofDlxHomeogenes and Promotes Differentiation of Interneuron ProgenitorsIn VitroandIn Vivo

Paina, S., Garzotto, D., Marchis, S. D., Marino, M., Moiana, A., Conti, L., Cattaneo, E. F., Perera, M., Corte, G., Calautti, E., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3110-10.2011 · Cited by 55 · see citing works

Characterization of loss-of-function and gain-of-function Eph receptor tyrosine kinase signaling in C. elegans axon targeting and cell migration

Mohamed, A. M., & Chin-Sang, I. D. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2005.11.019 · Cited by 50 · see citing works

A β-Catenin-Dependent Wnt Pathway Mediates Anteroposterior Axon Guidance in C. elegans Motor Neurons

Maro, G. S., Klassen, M. P., & Shen, K. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004690 · Cited by 45 · see citing works

DkkL1 (Soggy), a Dickkopf family member, localizes to the acrosome during mammalian spermatogenesis

Kohn, M. J., Kaneko, K. J., & Depamphilis, M. (2005) · Molecular Reproduction and Development · doi:10.1002/mrd.20314 · Cited by 41 · see citing works

Derailed regulates development of the Drosophila neuromuscular junction

Liebl, F. L. W., Wu, Y., Featherstone, D. E., Noordermeer, J. N., Fradkin, L. G., & Hing, H. K. (2007) · Developmental Neurobiology · doi:10.1002/dneu.20562 · Cited by 40 · see citing works

Activation of theWnt–βCatenin Pathway in a Cell Population on the Surface of the Forebrain Is Essential for the Establishment of Olfactory Axon Connections

Zaghetto, A. A., Paina, S., Mantero, S., Platonova, N., Peretto, P., Bovetti, S., Puché, A. C., Piccolo, S., & Merlo, G. R. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0763-07.2007 · Cited by 40 · see citing works

Does Planar Cell Polarity Signaling Steer Growth Cones?

Zou, Y. (2012) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-394592-1.00009-0 · Cited by 38 · see citing works

Molecular Gradients of Bioinertness Reveal a Mechanistic Difference between Mammalian Cell Adhesion and Bacterial Biofilm Formation

Burton, E. A., Simon, K. A., Hou, S., Ren, D., & Luk, Y. (2009) · Langmuir · doi:10.1021/la803261b · Cited by 38 · see citing works

Celsr3 and Fzd3 in axon guidance

Chai, G., Goffinet, A. M., & Tissir, F. (2015) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2015.03.013 · Cited by 36 · see citing works

Prickle1 regulates neurite outgrowth of apical spiral ganglion neurons but not hair cell polarity in the murine cochlea

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Neuronal Target Identification Requires AHA-1-Mediated Fine-Tuning of Wnt Signaling in C. elegans

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Transient activation of Wnt/β-catenin signaling reporter in fibrotic scar formation after compression spinal cord injury in adult mice

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Optimal Ratio of Wnt3a Expression in Human Mesenchymal Stem Cells Promotes Axonal Regeneration in Spinal Cord Injured Rat Model

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Ryk regulates Wnt5a repulsion of mouse corticospinal tract through modulating planar cell polarity signaling

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Delivery of Wnt inhibitor WIF1 via engineered polymeric microspheres promotes nerve regeneration after sciatic nerve crush

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Revealing phosphorylation regulatory networks during embryogenesis of honey bee worker and drone (Apis mellifera)

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Ablation of Protein Kinase CK2β in Skeletal Muscle Fibers Interferes with Their Oxidative Capacity

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The Nab2 RNA-binding protein patterns dendritic and axonal projections through a planar cell polarity-sensitive mechanism

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The Fragile X Messenger Ribonucleoprotein 1 Participates in Axon Guidance Mediated by the Wnt/Planar Cell Polarity Pathway

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β-Catenin Controls the Electrophysiologic Properties of Skeletal Muscle Cells by Regulating the α2 Isoform of Na+/K+-ATPase

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The effect of vestibular nerve section on the expression of the hyaluronan in the frog, Rana esculenta

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Gene Expression Meta-Analysis of Seven Candidate Gene Sets for Diabetes Traits Following a GWAS Pathway Study

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Lithium Therapy Effects on the Reproductive System

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Molecular Control of Circuit Plasticity and the Permanence of Imprinted Odor MemoryPreprint

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High-quality genome assemblies provide clues on the evolutionary advantage of blue peafowl over green peafowl

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D E V E

(2016)