Wnt Signaling in Neural Circuit Assembly

Wnt/β-Catenin Signaling in Development and Disease

Clevers, H. (2006) · Cell · doi:10.1016/j.cell.2006.10.018 · Cited by 5,568

The Wnt Signaling Pathway in Development and Disease

Logan, C. Y., & Nusse, R. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.113126 · Cited by 5,325

The Molecular Biology of Axon Guidance

Tessier‐Lavigne, M., & Goodman, C. S. (1996) · Science · doi:10.1126/science.274.5290.1123 · Cited by 3,311

Wnt Signaling: Multiple Pathways, Multiple Receptors, and Multiple Transcription Factors

Gordon, M. D., & Nusse, R. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.r600015200 · Cited by 1,333

Morphological Changes in Dendritic Spines Associated with Long-Term Synaptic Plasticity

Yuste, R., & Bonhoeffer, T. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1071 · Cited by 1,269

Purified Wnt5a Protein Activates or Inhibits β-Catenin–TCF Signaling Depending on Receptor Context

Mikels, A. J., & Nusse, R. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040115 · Cited by 1,244

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

Zebrafish Prickle, a Modulator of Noncanonical Wnt/Fz Signaling, Regulates Gastrulation Movements

Veeman, M. T., Slusarski, D. C., Kaykas, A., Louie, S. H., & Moon, R. T. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00240-9 · Cited by 945

Cytoskeletal Dynamics and Transport in Growth Cone Motility and Axon Guidance

Dent, E. W., & Gertler, F. B. (2003) · Neuron · doi:10.1016/s0896-6273(03)00633-0 · Cited by 922

Wnt and calcium signaling: β-Catenin-independent pathways

Kohn, A. D., & Moon, R. T. (2005) · Cell Calcium · doi:10.1016/j.ceca.2005.06.022 · Cited by 730

Neuroligins and neurexins link synaptic function to cognitive disease

Südhof, T. C. (2008) · Nature · doi:10.1038/nature07456 · Cited by 1,849

Microtubule assembly, organization and dynamics in axons and dendrites

Conde, C., & Cáceres, A. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2631 · Cited by 1,086

Can we safely target the WNT pathway?

Kahn, M. (2014) · Nature Reviews Drug Discovery · doi:10.1038/nrd4233 · Cited by 1,063

Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses

Gilman, S. R., Iossifov, I., Levy, D., Ronemus, M., Wigler, M., & Vitkup, D. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.021 · Cited by 701

Mechanisms underlying development of visual maps and receptive fields

Huberman, A. D., Feller, M. B., & Chapman, B. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125533 · Cited by 628

Mechanisms and Molecules of Neuronal Wiring: A PrimerPreprint

Kolodkin, A. L., & Tessier‐Lavigne, M. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a001727 · Cited by 641

Emerging roles of Wnts in the adult nervous system

Inestrosa, N. C., & Arenas, E. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2755 · Cited by 622

Trans-Synaptic Transmission of Vesicular Wnt Signals through Evi/Wntless

Korkut, C., Ataman, B., Ramachandran, P., Ashley, J., Barria, R., Gherbesi, N., & Budnik, V. (2009) · Cell · doi:10.1016/j.cell.2009.07.051 · Cited by 443

A de novo convergence of autism genetics and molecular neuroscience

Krumm, N., O’Roak, B. J., Shendure, J., & Eichler, E. E. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2013.11.005 · Cited by 423

Many paths to synaptic specificity.

Sanes, J., & Yamagata, M. (2009) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.24.110707.175402 · Cited by 315

Mitotic and mitogenic Wnt signalling

Niehrs, C., & Acebron, S. P. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.124 · Cited by 305

Synaptic organizing complexes

Siddiqui, T. J., & Craig, A. M. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.08.016 · Cited by 276

Signalling pathways in autism spectrum disorder: mechanisms and therapeutic implications

Jiang, C.-C., Lin, L., Long, S., Ke, X., Fukunaga, K., Lu, Y., & Han, F. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01081-0 · Cited by 295

Long noncoding RNA genes: conservation of sequence and brain expression among diverse amniotes

Chodroff, R. A., Goodstadt, L., Sirey, T., Oliver, P. L., Davies, K. E., Green, E. D., Molnár, Z., & Ponting, C. P. (2010) · Genome biology · doi:10.1186/gb-2010-11-7-r72 · Cited by 257

Ror‐family receptor tyrosine kinases in noncanonical Wnt signaling: Their implications in developmental morphogenesis and human diseases

Minami, Y., Oishi, I., Endo, M., & Nishita, M. (2009) · Developmental Dynamics · doi:10.1002/dvdy.21991 · Cited by 240

Wnt7a signaling promotes dendritic spine growth and synaptic strength through Ca 2+ /Calmodulin-dependent protein kinase II

Ciani, L., Boyle, K. A., Dickins, E. M., Sahores, M., Anane, D., Lopes, D. M., Gibb, A. J., & Salinas, P. C. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018132108 · Cited by 214

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

Use of human neuroblastoma SH-SY5Y cells to evaluate glyphosate-induced effects on oxidative stress, neuronal development and cell death signaling pathways

Martínez, M., Rodríguez, J.-L., López-Torres, B., Martínez, M., Martínez‐Larrañaga, M., Maximiliano, J.-E., Anadón, A., & Arés, I. (2019) · Environment International · doi:10.1016/j.envint.2019.105414 · Cited by 215

Wnt-5a/JNK Signaling Promotes the Clustering of PSD-95 in Hippocampal Neurons

Farı́as, G. G., Alfaro, I. E., Cerpa, W. F., Grabowski, C. P., Godoy, J. A., Bonansco, C., & Inestrosa, N. C. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m808986200 · Cited by 205

Wingless-type family member 5A (Wnt-5a) stimulates synaptic differentiation and function of glutamatergic synapses

Varela-Nallar, L., Alfaro, I. E., Serrano, F. G., Parodi, J., & Inestrosa, N. C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010011107 · Cited by 197

Wnt/β-Catenin Signaling Is an Essential and Direct Driver of Myelin Gene Expression and Myelinogenesis

Tawk, M., Makoukji, J., Belle, M., Fonte, C., Trousson, A., Hawkins, T. A., Li, H., Ghandour, S., Schumacher, M., & Massaad, C. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4270-10.2011 · Cited by 196

Wnt Signaling in the Vertebrate Central Nervous System: From Axon Guidance to Synaptic FunctionPreprint

Salinas, P. C. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a008003 · Cited by 195

Wnt Signaling: Role in Alzheimer Disease and Schizophrenia

Inestrosa, N. C., Montecinos-Oliva, C., & Fuenzalida, M. (2012) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-012-9417-5 · Cited by 192

Initiating and Growing an AxonPreprint

Polleux, F., & Snider, W. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a001925 · Cited by 200

Connecting Vascular and Nervous System Development: Angiogenesis and the Blood-Brain Barrier

Tam, S. J., & Watts, R. J. (2010) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-152829 · Cited by 197

Wnt Signaling Mediates Experience-Related Regulation of Synapse Numbers and Mossy Fiber Connectivities in the Adult Hippocampus

Gogolla, N., Galimberti, I., Deguchi, Y., & Caroni, P. (2009) · Neuron · doi:10.1016/j.neuron.2009.04.022 · Cited by 181

Wnt signaling networks in autism spectrum disorder and intellectual disability

Kwan, V., Unda, B. K., & Singh, K. K. (2016) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-016-9176-3 · Cited by 176

Unifying Views of Autism Spectrum Disorders: A Consideration of Autoregulatory Feedback Loops

Mullins, C., Fishell, G., & Tsien, R. W. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.017 · Cited by 167

Wnt/Planar Cell Polarity Signaling Controls the Anterior–Posterior Organization of Monoaminergic Axons in the Brainstem

Fenstermaker, A. G., Prasad, A. A., Bechara, A., Adolfs, Y., Tissir, F., Goffinet, A. M., Zou, Y., & Pasterkamp, R. J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4508-10.2010 · Cited by 162

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 172

Autism spectrum disorder: insights into convergent mechanisms from transcriptomics

Quesnel-Vallières, M., Weatheritt, R. J., Cordes, S. P., & Blencowe, B. J. (2018) · Nature Reviews Genetics · doi:10.1038/s41576-018-0066-2 · Cited by 167

Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autism

Urresti, J., Zhang, P., Losada, P. M., Yu, N., Negraes, P. D., Trujillo, C. A., Antaki, D., Amar, M., Chau, K. K., Pramod, A. B., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01243-6 · Cited by 135

WNT signaling increases proliferation and impairs differentiation of stem cells in the developing cerebellum

Pei, Y., Brun, S. N., Markant, S. L., Lento, W. E., Gibson, P., Taketo, M. M., Giovannini, M., Gilbertson, R. J., & Wechsler‐Reya, R. J. (2012) · Development · doi:10.1242/dev.050104 · Cited by 138

Chapter 2 Synapse Formation in Developing Neural Circuits

Colón‐Ramos, D. A. (2009) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(09)01202-2 · Cited by 141

Wnt signaling promotes AChR aggregation at the neuromuscular synapse in collaboration with agrin

Henríquez, J. P., Webb, A., Bence, M., Bildsoe, H., Sahores, M., Hughes, S. M., & Salinas, P. C. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806300105 · Cited by 136

Frizzled-5, a receptor for the synaptic organizer Wnt7a, regulates activity-mediated synaptogenesis

Sahores, M., Gibb, A. J., & Salinas, P. C. (2010) · Development · doi:10.1242/dev.046722 · Cited by 128

Wnts in action: from synapse formation to synaptic maintenance

Dickins, E. M., & Salinas, P. C. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00162 · Cited by 122

Wnt-5a Modulates Recycling of Functional GABAA Receptors on Hippocampal Neurons

Cuitiño, L., Godoy, J. A., Farı́as, G. G., Couve, A., Bonansco, C., Fuenzalida, M., & Inestrosa, N. C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5736-09.2010 · Cited by 125

Wnt5a cooperates with canonical Wnts to generate midbrain dopaminergic neurons in vivo and in stem cells

Andersson, E. R., Saltó, C., Villaescusa, C., Čajánek, L., Yang, S., Bryjová, L., Nagy, I. I., Vainio, S. J., Ramírez, C., Bryja, V., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1208524110 · Cited by 125

Role of glial cells in the formation and maintenance of synapses

Pfrieger, F. W. (2010) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.11.002 · Cited by 124

Neuronal connectivity as a convergent target of gene × environment interactions that confer risk for Autism Spectrum Disorders

Stamou, M., Streifel, K. M., Goines, P. E., & Lein, P. J. (2013) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2012.12.001 · Cited by 128

Wnt signaling in midbrain dopaminergic neuron development and regenerative medicine for Parkinson's disease

Arenas, E. (2014) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mju001 · Cited by 128

Wnt-5aoccludes Aβ oligomer-induced depression of glutamatergic transmission in hippocampal neurons

Cerpa, W. F., Farı́as, G. G., Godoy, J. A., Fuenzalida, M., Bonansco, C., & Inestrosa, N. C. (2010) · Molecular Neurodegeneration · doi:10.1186/1750-1326-5-3 · Cited by 119

Role of Wnt Signaling in Central Nervous System Injury

Lambert, C., Cisternas, P., & Inestrosa, N. C. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9138-x · Cited by 121

Targeting Wnt Pathways in DiseasePreprint

Zimmerman, Z. F., Moon, R. T., & Chien, A. J. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a008086 · Cited by 111

En1 and Wnt signaling in midbrain dopaminergic neuronal development

dos Santos, M. T. A., & Smidt, M. P. (2011) · Neural Development · doi:10.1186/1749-8104-6-23 · Cited by 116

WNTs in synapse formation and neuronal circuitry

Park, M., & Shen, K. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.145 · Cited by 107

Ryks: new partners for Wnts in the developing and regenerating nervous system

Fradkin, L. G., Dura, J., & Noordermeer, J. N. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.11.005 · Cited by 110

Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity

Darbandi, S. F., Schwartz, S. E. R., Qi, Q., Catta-Preta, R., Pai, E. L.-L., Mandell, J. D., Everitt, A., Rubin, A. N., Krasnoff, R., Katzman, S. J., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.027 · Cited by 100

Canonical Wnt Signaling is Necessary for Object Recognition Memory Consolidation

Fortress, A. M., Schram, S., Tuscher, J. J., & Frick, K. M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0659-13.2013 · Cited by 105

Collagen XIX is expressed by interneurons and contributes to the formation of hippocampal synapses

Su, J., Gorse, K. M., Ramirez, F., & Fox, M. A. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22228 · Cited by 101

Molecular mechanisms of dendrite morphogenesis

Arikkath, J. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00061 · Cited by 113

Cell Adhesion, the Backbone of the Synapse: "Vertebrate" and "Invertebrate" Perspectives

Giagtzoglou, N., Ly, C. V., & Bellen, H. J. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a003079 · Cited by 97

Wnt/calcium signaling mediates axon growth and guidance in the developing corpus callosum

Hutchins, B. I., Li, L., & Kalil, K. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20846 · Cited by 95

Wnt Signaling in the Pathogenesis of Multiple Sclerosis-Associated Chronic Pain

Yuan, S., Shi, Y., & Tang, S. (2012) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-012-9370-3 · Cited by 95

Structural Perspectives on Axon Guidance

Seiradake, E., Jones, E. Y., & Klein, R. (2016) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-111315-125008 · Cited by 96

Perturbed Wnt signaling leads to neuronal migration delay, altered interhemispheric connections and impaired social behavior

Bocchi, R., Égervári, K., Carol-Perdiguer, L., Viale, B., Quairiaux, C., Roo, M. D., Boitard, M., Oskouie, S. K., Salmon, P., & Kiss, J. Z. (2017) · Nature Communications · doi:10.1038/s41467-017-01046-w · Cited by 95

Emerging mechanisms in morphogen‐mediated axon guidance

Sánchez‐Camacho, C., & Bovolenta, P. (2009) · BioEssays · doi:10.1002/bies.200900063 · Cited by 93

The nuclear import of Frizzled2-C by Importins-β11 and α2 promotes postsynaptic development

Mosca, T. J., & Schwarz, T. L. (2010) · Nature Neuroscience · doi:10.1038/nn.2593 · Cited by 84

Molecular Remodeling of the Presynaptic Active Zone of Drosophila Photoreceptors via Activity-Dependent Feedback

Sugie, A., Hakeda‐Suzuki, S., Suzuki, E., Silies, M., Shimozono, M., Möhl, C., Suzuki, T., & Tavosanis, G. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.046 · Cited by 91

The Role of Wnt Signaling in the Development of Alzheimer’s Disease: A Potential Therapeutic Target?

Wan, W., Xia, S., Kalionis, B., Liu, L., & Li, Y. (2014) · BioMed Research International · doi:10.1155/2014/301575 · Cited by 86

Loss of neuronal GSK3β reduces dendritic spine stability and attenuates excitatory synaptic transmission via β-catenin

Ochs, S. M., Dorostkar, M. M., Aramuni, G., Schön, C., Filser, S., Pöschl, J., Kremer, A., Leuven, F. V., Ovsepian, S. V., & Herms, J. W. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.55 · Cited by 86

Transcriptome of embryonic and neonatal mouse cortex by high-throughput RNA sequencing

Han, X., Wu, X., Chung, W.-Y., Li, T., Nekrutenko, A., Altman, N. S., Chen, G., & Ma, H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902417106 · Cited by 83

How the Wnt signaling pathway protects from neurodegeneration: the mitochondrial scenario

Arrázola, M. S., Silva-Álvarez, C., & Inestrosa, N. C. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00166 · Cited by 80

The Tangled Web of Non-Canonical Wnt Signalling in Neural Migration

Clark, C., Nourse, C. C., & Cooper, H. M. (2012) · Neurosignals · doi:10.1159/000332153 · Cited by 85

Synaptogenesis in the developing mouse visual cortex

Ming-shan, L., Cui, Z., Niu, Y., Liu, B., Fan, W., Yu, D., & Deng, J. (2009) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2009.08.028 · Cited by 77

Perlecan regulates bidirectional Wnt signaling at the Drosophila neuromuscular junction

Kamimura, K., Ueno, K., Nakagawa, J., Hamada, R., Saitoe, M., & Maeda, N. (2013) · The Journal of Cell Biology · doi:10.1083/jcb.201207036 · Cited by 78

Extracellular matrix and its receptors indrosophilaneural development

Broadie, K. S., Baumgartner, S., & Prokop, A. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20935 · Cited by 77

Chronic hypoxia induces the activation of the Wnt/β-catenin signaling pathway and stimulates hippocampal neurogenesis in wild-type and APPswe-PS1ΔE9 transgenic mice in vivo

Varela‐Nallar, L., Rojas-Abalos, M., Abbott, A. C., Moya, E. A., Iturriaga, R., & Inestrosa, N. C. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00017 · Cited by 74

WNTs tune up the neuromuscular junction

Korkut, C., & Budnik, V. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2681 · Cited by 73

WNT5A Signaling Contributes to Aβ-Induced Neuroinflammation and Neurotoxicity

Li, B., Zhong, L., Yang, X., Andersson, T., Huang, M., & Tang, S.-J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022920 · Cited by 81

Evidence for opposing roles of Celsr3 and Vangl2 in glutamatergic synapse formation

Thakar, S., Wang, L., Yu, T., Ye, M., Onishi, K., Scott, J. C., Qi, J., Fernandes, C., Han, X., Yates, J. R., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1612062114 · Cited by 75

The Plane Facts of PCP in the CNS

Goodrich, L. V. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.003 · Cited by 73

Bcl11a is required for neuronal morphogenesis and sensory circuit formation in dorsal spinal cord development

John, A., Brylka, H., Wiegreffe, C., Simon, R., Liu, P., Jüttner, R., Crenshaw, E. B., Luyten, F. P., Jenkins, N. A., Copeland, N. G., et al. (2012) · Development · doi:10.1242/dev.072850 · Cited by 72

Crosstalk between Agrin and Wnt signaling pathways in development of vertebrate neuromuscular junction

Barik, A., Zhang, B., Sohal, G. S., Xiong, W., & Mei, L. (2014) · Developmental Neurobiology · doi:10.1002/dneu.22190 · Cited by 74

Interaction of estrogen receptors with insulin-like growth factor-I and Wnt signaling in the nervous system

Varea, O., Arévalo, M., Garrido, J. J., García‐Segura, L. M., Wandosell, F. G., & Méndez, P. (2009) · Steroids · doi:10.1016/j.steroids.2009.09.006 · Cited by 70

Neurotrophin and Wnt signaling cooperatively regulate dendritic spine formation

Hiester, B. G., Galati, D. F., Salinas, P. C., & Jones, K. R. (2013) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2013.04.006 · Cited by 70

Neuronal development and axon growth are altered by glyphosate through a WNT non-canonical signaling pathway

Coullery, R. P., Ferrari, M. E., & Rosso, S. B. (2015) · NeuroToxicology · doi:10.1016/j.neuro.2015.12.004 · Cited by 70

Signalling mechanisms regulating axonal branching in vivo

Schmidt, H., & Rathjen, F. G. (2010) · BioEssays · doi:10.1002/bies.201000054 · Cited by 69

Regulation of Wnt Signaling by Nociceptive Input in Animal Models

Shi, Y., Yuan, S., Li, B., Wang, J., Carlton, S. M., Chung, K., Chung, J. M., & Tang, S. (2012) · Molecular Pain · doi:10.1186/1744-8069-8-47 · Cited by 67

Netrin instructs synaptic vesicle clustering through Rac GTPase, MIG-10, and the actin cytoskeleton

Stavoe, A. K., & Colón‐Ramos, D. A. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201110127 · Cited by 64

Glycogen Synthase Kinase-3 as a Therapeutic Target for Cognitive Dysfunction in Neuropsychiatric Disorders

O’Leary, O. F., & Nolan, Y. M. (2014) · CNS Drugs · doi:10.1007/s40263-014-0213-z · Cited by 64

Reinduced Wnt signaling limits regenerative potential of sensory axons in the spinal cord following conditioning lesion

Hollis, E. R., II, & Zou, Y. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1206218109 · Cited by 63

An autocrine Wnt5a-Ror signaling loop mediates sympathetic target innervation

Ryu, Y. K., Collins, S. E., Ho, H. H., Zhao, H., & Kuruvilla, R. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.02.013 · Cited by 61

Wnt transmembrane signaling and long‐term spatial memory

Tabatadze, N., Tomas, C., McGonigal, R., Lin, B., Schook, A. C., & Routtenberg, A. (2011) · Hippocampus · doi:10.1002/hipo.20991 · Cited by 61

Andrographolide Stimulates Neurogenesis in the Adult Hippocampus

Varela‐Nallar, L., Arredondo, S. B., Tapia‐Rojas, C., Hancke, J. L., & Inestrosa, N. C. (2015) · Neural Plasticity · doi:10.1155/2015/935403 · Cited by 61

A Fox stops the Wnt: implications for forebrain development and diseases

Danesin, C., & Houart, C. (2012) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2012.05.001 · Cited by 60

Interaction of the mu-opioid receptor with GPR177 (Wntless) inhibits Wnt secretion: potential implications for opioid dependence

Jin, J., Kittanakom, S., Wong, V., Reyes, B. A. S., Bockstaele, E. J. V., Štagljar, I., Berrettini, W. H., & Levenson, R. G. (2010) · BMC Neuroscience · doi:10.1186/1471-2202-11-33 · Cited by 60

Neuron activity–induced Wnt signaling up-regulates expression of brain-derived neurotrophic factor in the pain neural circuit

Zhang, W., Shi, Y., Peng, Y., Zhong, L., Zhu, S., Zhang, W., & Tang, S.-J. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.002840 · Cited by 59

Biosignatures for Parkinson’s Disease and Atypical Parkinsonian Disorders Patients

Potashkin, J. A., Santiago, J. A., Ravina, B. M., Watts, A., & Leontovich, A. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043595 · Cited by 61

Genome‐wide analysis of POU3F2/BRN2 promoter occupancy in human melanoma cells reveals Kitl as a novel regulated target gene

Kobi, D., Steunou, A., Dembélé, D., Gras, S. L., Larue, L., Nieto, L., & Davidson, I. (2010) · Pigment Cell & Melanoma Research · doi:10.1111/j.1755-148x.2010.00697.x · Cited by 69

SFRP1 and SFRP2 Dose‐Dependently Regulate Midbrain Dopamine Neuron Development In Vivo and in Embryonic Stem Cells

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