Emerging topics in Reelin function

Neurons derived from radial glial cells establish radial units in neocortex

Noctor, S. C., Flint, A. C., Weissman, T. A., Dammerman, R. S., & Kriegstein, A. R. (2001) · Nature · doi:10.1038/35055553 · Cited by 2,016 · see citing works

A protein related to extracellular matrix proteins deleted in the mouse mutant reeler

D'Arcangelo, G., G. Miao, G., Chen, S.-C., Scares, H. D., Morgan, J. I., & Curran, T. (1995) · Nature · doi:10.1038/374719a0 · Cited by 1,748 · see citing works

APP Processing and Synaptic Function

Kamenetz, F., Tomita, T., Hsieh, H., Seabrook, G., Borchelt, D., Iwatsubo, T., Sisodia, S., & Malinow, R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00124-7 · Cited by 1,644 · see citing works

Regulation of NMDA receptor trafficking by amyloid-β

Snyder, E. M., Nong, Y., Almeida, C. G., Paul, S., Moran, T., Choi, E. Y., Nairn, A. C., Salter, M. W., Lombroso, P. J., Gouras, G. K., et al. (2005) · Nature Neuroscience · doi:10.1038/nn1503 · Cited by 1,561 · cited 2× · see citing works

Cellular prion protein mediates impairment of synaptic plasticity by amyloid-β oligomers

Laurén, J., Gimbel, D. A., Nygaard, H. B., Gilbert, J. W., & Strittmatter, S. M. (2009) · Nature · doi:10.1038/nature07761 · Cited by 1,560 · see citing works

Regulation of actin dynamics through phosphorylation of cofilin by LIM-kinase

Arber, S., Barbayannis, F. A., Hanser, H., Schneider, C., Stanyon, C. A., Bernard, O., & Caroni, P. (1998) · Nature · doi:10.1038/31729 · Cited by 1,426 · see citing works

Reeler/Disabled-like Disruption of Neuronal Migration in Knockout Mice Lacking the VLDL Receptor and ApoE Receptor 2

Trommsdorff, M., Gotthardt, M., Hiesberger, T., Shelton, J., Stockinger, W., Nimpf, J., Hammer, R. E., Richardson, J. A., & Herz, J. (1999) · Cell · doi:10.1016/s0092-8674(00)80782-5 · Cited by 1,261 · see citing works

Isolation of radial glial cells by fluorescent-activated cell sorting reveals a neuronal lineage

Malatesta, P., Hartfuss, E., & Götz, M. (2000) · Development · doi:10.1242/dev.127.24.5253 · Cited by 1,157 · see citing works

AMPAR Removal Underlies Aβ-Induced Synaptic Depression and Dendritic Spine Loss

Hsieh, H., Boehm, J., Sato, C., Iwatsubo, T., Tomita, T., Sisodia, S., & Malinow, R. (2006) · Neuron · doi:10.1016/j.neuron.2006.10.035 · Cited by 1,042 · see citing works

Proteins of the ADF/Cofilin Family: Essential Regulators of Actin Dynamics

Bamburg, J. R. (1999) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.15.1.185 · Cited by 1,015 · see citing works

Direct Binding of Reelin to VLDL Receptor and ApoE Receptor 2 Induces Tyrosine Phosphorylation of Disabled-1 and Modulates Tau Phosphorylation

Hiesberger, T., Trommsdorff, M., Howell, B. W., Goffinet, A., Mumby, M. C., Cooper, J. A., & Herz, J. (1999) · Neuron · doi:10.1016/s0896-6273(00)80861-2 · Cited by 916 · see citing works

Notch signalling in vertebrate neural development

Louvi, A., & Artavanis‐Tsakonas, S. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1847 · Cited by 887 · see citing works

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

Hong, S. E., Shugart, Y. Y., Huang, D. T.-C., Shahwan, S. A., Grant, P. E., Hourihane, J. O., Martin, N. D. T., & Walsh, C. A. (2000) · Nature Genetics · doi:10.1038/79246 · Cited by 878 · see citing works

Reelin Is a Ligand for Lipoprotein Receptors

D'Arcangelo, G., Homayouni, R., Keshvara, L., Rice, D. S., Sheldon, M., & Curran, T. (1999) · Neuron · doi:10.1016/s0896-6273(00)80860-0 · Cited by 808 · see citing works

Direct inhibition of the NOTCH transcription factor complex

Moellering, R. E., Cornejo, M., Davis, T. N., Bianco, C. D., Aster, J. C., Blacklow, S. C., Kung, A. L., Gilliland, D. G., Verdine, G. L., & Bradner, J. E. (2009) · Nature · doi:10.1038/nature08543 · Cited by 752 · see citing works

Reelin and brain development

Tissir, F., & Goffinet, A. M. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1113 · Cited by 748 · see citing works

Radial Glial Identity Is Promoted by Notch1 Signaling in the Murine Forebrain

Gaiano, N., Nye, J. S., & Fishell, G. (2000) · Neuron · doi:10.1016/s0896-6273(00)81172-1 · Cited by 727 · see citing works

Two modes of radial migration in early development of the cerebral cortex

Nadarajah, B., Brunstrom, J. E., Grutzendler, J., Wong, R., & Pearlman, A. L. (2001) · Nature Neuroscience · doi:10.1038/83967 · Cited by 689 · see citing works

Modes of neuronal migration in the developing cerebral cortex

Nadarajah, B., & Parnavelas, J. G. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn845 · Cited by 683 · see citing works

Role of the Reelin Signaling Pathway in Central Nervous System Development

Rice, D. S., & Curran, T. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1005 · Cited by 667 · see citing works

Cofilin Promotes Actin Polymerization and Defines the Direction of Cell Motility

Ghosh, M., Song, X., Mouneimne, G., Sidani, M., Lawrence, D. S., & Condeelis, J. S. (2004) · Science · doi:10.1126/science.1094561 · Cited by 657 · see citing works

Reelin and ApoE receptors cooperate to enhance hippocampal synaptic plasticity and learning

Weeber, E. J., Beffert, U., Jones, C., Christian, J. M., Förster, E., Sweatt, J. D., & Herz, J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m205147200 · Cited by 623 · see citing works

Notch signaling in the mammalian central nervous system: insights from mouse mutants

Yoon, K., & Gaiano, N. (2005) · Nature Neuroscience · doi:10.1038/nn1475 · Cited by 587 · see citing works

Regional and Cellular Patterns of<i>reelin</i>mRNA Expression in the Forebrain of the Developing and Adult Mouse

Alcántara, S., Ruiz, M., D’Arcangelo, G., Ezan, F., de Lecea, L., Curran, T., Sotelo, C., & Soriano, E. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-19-07779.1998 · Cited by 568 · see citing works

Interaction of Cytosolic Adaptor Proteins with Neuronal Apolipoprotein E Receptors and the Amyloid Precursor Protein

Trommsdorff, M., Borg, J., Margolis, B. L., & Herz, J. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.50.33556 · Cited by 540 · see citing works

The Role of Local Actin Instability in Axon Formation

Bradke, F., & Dotti, C. G. (1999) · Science · doi:10.1126/science.283.5409.1931 · Cited by 534 · see citing works

Reelin, lipoprotein receptors and synaptic plasticity

Herz, J., & Chen, Y. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn2009 · Cited by 524 · see citing works

Establishment of axon-dendrite polarity in developing neurons.

Barnes, A. P., & Polleux, F. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125536 · Cited by 523 · see citing works

Reelin Is a Secreted Glycoprotein Recognized by the CR-50 Monoclonal Antibody

D’Arcangelo, G., Nakajima, K., Miyata, T., Ogawa, M., Mikoshiba, K., & Curran, T. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-01-00023.1997 · Cited by 515 · see citing works

Modulation of synaptic plasticity and memory by Reelin involves differential splicing of the lipoprotein receptor Apoer2

Beffert, U., Weeber, E. J., Durudas, A., Qiu, S., Masiulis, I., Sweatt, J. D., Li, W.-P., Adelmann, G., Frotscher, M., Hammer, R. E., et al. (2005) · Neuron · doi:10.1016/j.neuron.2005.07.007 · Cited by 497 · see citing works

Phosphorylation of Ser‐3 of cofilin regulates its essential function on actin

Moriyama, K., Iida, K., & Yahara, I. (1996) · Genes to Cells · doi:10.1046/j.1365-2443.1996.05005.x · Cited by 415 · see citing works

Reelin-induced tryosine phosphorylation of Disabled 1 during neuronal positioning

Howell, B. W., Herrick, T. M., & Cooper, J. A. (1999) · Genes &amp; Development · doi:10.1101/gad.13.6.643 · Cited by 411 · see citing works

LKB1 and SAD Kinases Define a Pathway Required for the Polarization of Cortical Neurons

Barnes, A. P., Lilley, B. N., Pan, Y. A., Plummer, L. J., Powell, A. W., Raines, A. N., Sanes, J. R., & Polleux, F. (2007) · Cell · doi:10.1016/j.cell.2007.03.025 · Cited by 401 · see citing works

Reelin promotes hippocampal dendrite development through the VLDLR/ApoER2-Dab1 pathway

Niu, S., Renfro, A., Quattrocchi, C. C., Sheldon, M., & D'Arcangelo, G. (2004) · Neuron · doi:10.1016/s0896-6273(03)00819-5 · Cited by 375 · see citing works

A Critical Function for β-Amyloid Precursor Protein in Neuronal Migration Revealed by <i>In Utero</i> RNA Interference

Young-Pearse, T. L., Bai, J., Chang, R., Zheng, J. B., LoTurco, J. J., & Selkoe, D. J. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4701-07.2007 · Cited by 369 · see citing works

Reelin Activates Src Family Tyrosine Kinases in Neurons

Bock, H. H., & Herz, J. (2003) · Current Biology · doi:10.1016/s0960-9822(02)01403-3 · Cited by 355 · see citing works

Mammalian SAD Kinases Are Required for Neuronal Polarization

Kishi, M., Pan, Y. A., Crump, J. G., & Sanes, J. R. (2005) · Science · doi:10.1126/science.1107403 · Cited by 343 · see citing works

Mouse disabled (mDab1): a Src binding protein implicated in neuronal development

Howell, B. W., Gertler, F. B., & Cooper, J. A. (1997) · The EMBO Journal · doi:10.1093/emboj/16.1.121 · Cited by 339 · see citing works

The Actin Cytoskeleton in T Cell Activation

Burkhardt, J. K., Carrizosa, E., & Shaffer, M. H. (2008) · Annual Review of Immunology · doi:10.1146/annurev.immunol.26.021607.090347 · Cited by 314 · see citing works

Reelin-mediated Signaling Locally Regulates Protein Kinase B/Akt and Glycogen Synthase Kinase 3β

Beffert, U., Morfini, G., Bock, H. H., Reyna, H., Brady, S. T., & Herz, J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m209205200 · Cited by 306 · see citing works

Reelin modulates NMDA receptor activity in cortical neurons

Chen, Y., Beffert, U., Ertunc, M., Tang, T.-S., Kavalali, E. T., Bezprozvanny, I., & Herz, J. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1951-05.2005 · Cited by 299 · see citing works

Cortical development: View from neurological mutants two decades later

Rakic, P., & Caviness, V. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90258-9 · Cited by 287 · see citing works

Fyn Tyrosine Kinase Is a Critical Regulator of Disabled-1 during Brain Development

Arnaud, L., Ballif, B. A., Förster, E., & Cooper, J. A. (2003) · Current Biology · doi:10.1016/s0960-9822(02)01397-0 · Cited by 283 · see citing works

Cajal—Retzius cells, Reelin, and the formation of layers

Frotscher, M. (1998) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(98)80082-2 · Cited by 275 · see citing works

The Reelin signaling pathway promotes dendritic spine development in hippocampal neurons

Niu, S., Yabut, O., & D'Arcangelo, G. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1917-08.2008 · Cited by 266 · see citing works

Dab1 tyrosine phosphorylation sites relay positional signals during mouse brain development

Howell, B. W., Herrick, T. M., Hildebrand, J. D., Zhang, Y., & Cooper, J. A. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00608-4 · Cited by 258 · see citing works

Reelin, Disabled 1, and β ₁ integrins are required for the formation of the radial glial scaffold in the hippocampus

Förster, E., Tielsch, A., Saum, B., Weiss, K. H., Johanssen, C., Graus-Porta, D., Müller, U., & Frotscher, M. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.202035899 · Cited by 254 · see citing works

Role of reelin in the control of brain development1Published on the World Wide Web on 21 October 1997.1

Curran, T., & D'Arcangelo, G. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00035-0 · Cited by 246 · see citing works

Laminating the hippocampus

Förster, E., Zhao, S., & Frotscher, M. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1882 · Cited by 242 · see citing works

Reelin glycoprotein: structure, biology and roles in health and disease

Fatemi, S. H. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001613 · Cited by 241 · see citing works

Reelin signaling directly affects radial glia morphology and biochemical maturation

Hartfuss, E., Förster, E., Bock, H. H., Hack, M. A., Leprince, P., Luque, J. M., Herz, J., Frotscher, M., & Götz, M. (2003) · Development · doi:10.1242/dev.00654 · Cited by 237 · see citing works

The Cells of Cajal-Retzius: Still a Mystery One Century After

Soriano, E., & del Rı́o, J. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.019 · Cited by 237 · see citing works

A mechanism for inside-out lamination in the neocortex

Cooper, J. A. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2007.12.003 · Cited by 236 · see citing works

Reelin signals through phosphatidylinositol 3-kinase and Akt to control cortical development and through mTor to regulate dendritic growth

Jossin, Y., & Goffinet, A. M. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.00928-07 · Cited by 235 · see citing works

Myosin II Motors and F-Actin Dynamics Drive the Coordinated Movement of the Centrosome and Soma during CNS Glial-Guided Neuronal Migration

Solecki, D. J., Trivedi, N., Govek, E., Kerekes, R. A., Gleason, S. S., & Hatten, M. E. (2009) · Neuron · doi:10.1016/j.neuron.2009.05.028 · Cited by 233 · see citing works

The morphology of the hippocampus and dentate gyrus in normal and reeler mice

Stanfield, B. B., & Cowan, W. M. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901850302 · Cited by 228 · see citing works

Interaction of Reelin with Amyloid Precursor Protein Promotes Neurite Outgrowth

Hoe, H.-S., Lee, K. J., Carney, R. S. E., Lee, J., Markova, A., Lee, J.-Y., Howell, B. W., Hyman, B. T., Pak, D. T. S., Bu, G., et al. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4872-08.2009 · Cited by 219 · see citing works

Apolipoprotein E receptors: linking brain development and alzheimer's disease

Herz, J., & Beffert, U. (2000) · Nature reviews. Neuroscience · doi:10.1038/35036221 · Cited by 218 · see citing works

Interaction between Reelin and Notch Signaling Regulates Neuronal Migration in the Cerebral Cortex

Hashimoto‐Torii, K., Torii, M., Sarkisian, M. R., Bartley, C. M., Shen, J., Radtke, F., Gridley, T., Šestan, N., & RAKIC, P. T. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.026 · Cited by 216 · see citing works

Phosphatidylinositol 3-kinase interacts with the adaptor protein Dab1 in response to Reelin signaling and is required for normal cortical lamination

Bock, H. H., Jossin, Y., Liu, P., Förster, E., May, P., Goffinet, A. M., & Herz, J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m306416200 · Cited by 213 · see citing works

Reelin stabilizes the actin cytoskeleton of neuronal processes by inducing n-cofilin phosphorylation at serine3

Chai, X., Förster, E., Zhao, S., Bock, H. H., & Frotscher, M. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2934-08.2009 · Cited by 202 · see citing works

Absence of Fyn and Src Causes a Reeler-Like Phenotype

Kuo, G., Arnaud, L., Kronstad-O'Brien, P., & Cooper, J. A. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1656-05.2005 · Cited by 200 · see citing works

ADF/Cofilin Controls Cell Polarity during Fibroblast Migration

Dawe, H. R., Minamide, L. S., Bamburg, J. R., & Cramer, L. P. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00040-x · Cited by 189 · see citing works

N-cofilin is associated with neuronal migration disorders and cell cycle control in the cerebral cortexPreprint

Bellenchi, G. C., Gurniak, C. B., Perlas, E., Middei, S., Ammassari‐Teule, M., & Witke, W. (2007) · Genes & Development · doi:10.1101/gad.434307 · Cited by 187 · see citing works

Differential reelin-induced enhancement of NMDA and AMPA receptor activity in the adult hippocampus

Qiu, S., Zhao, L. F., Korwek, K. M., & Weeber, E. J. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2561-06.2006 · Cited by 186 · see citing works

The Reeler Mouse as a Model of Brain Development

de Rouvroit, C. L., & Goffinet, A. M. (1998) · Advances in anatomy, embryology and cell biology · doi:10.1007/978-3-642-72257-8 · Cited by 179 · see citing works

DAB1 and Reelin effects on amyloid precursor protein and ApoE receptor 2 trafficking and processing

Hoe, H.-S., Tran, T. S., Matsuoka, Y., Howell, B. W., & Rebeck, G. W. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m602162200 · Cited by 174 · see citing works

Cofilin promotes stimulus-induced lamellipodium formation by generating an abundant supply of actin monomers

Kiuchi, T., Ohashi, K., Kurita, S., & Mizuno, K. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200610005 · Cited by 172 · see citing works

Brain Development in Normal and reeler Mice: the Phenotype

Lambert de Rouvroit, C., & Goffinet, A. M. (1998) · Advances in Anatomy Embryology and Cell Biology · doi:10.1007/978-3-642-72257-8_1 · Cited by 166 · see citing works

Regulation of Protein Tyrosine Kinase Signaling by Substrate Degradation during Brain Development

Arnaud, L., Ballif, B. A., & Cooper, J. A. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.24.9293-9302.2003 · Cited by 164 · see citing works

Determinants of cell shape and orientation: A comparative Golgi analysis of cell‐axon interrelationships in the developing neocortex of normal and reeler mice

Lord, M., & Caviness, V. S. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901870104 · Cited by 163 · see citing works

Begacestat (GSI-953): A Novel, Selective Thiophene Sulfonamide Inhibitor of Amyloid Precursor Protein γ-Secretase for the Treatment of Alzheimer's Disease

Martone, R., Zhou, H., Atchison, K., Comery, T., Xu, J. Z., Huang, X.-Y., Gong, X., Jin, M., Kreft, A., Harrison, B., et al. (2009) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.109.152975 · Cited by 163 · see citing works

Divergent roles of ApoER2 and Vldlr in the migration of cortical neurons

Hack, I., Hellwig, S., Junghans, D., Brunne, B., Bock, H. H., Zhao, S., & Frotscher, M. (2007) · Development · doi:10.1242/dev.005447 · Cited by 162 · see citing works

A Role for Abl in Notch Signaling

Giniger, E. (1998) · Neuron · doi:10.1016/s0896-6273(00)81007-7 · Cited by 161 · see citing works

Reelin signaling antagonizes β-amyloid at the synapse

Durakoglugil, M. S., Chen, Y., White, C. L., Kavalali, E. T., & Herz, J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908176106 · Cited by 153 · see citing works

Cullin 5 regulates Dab1 protein levels and neuron positioning during cortical development

Feng, L., Allen, N. S., Simo, S., & Cooper, J. A. (2007) · Genes &amp; Development · doi:10.1101/gad.1604207 · Cited by 148 · see citing works

Differential glycosylation regulates processing of lipoprotein receptors by γ-secretase

May, P., Bock, H. H., Nimpf, J., & Herz, J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m305858200 · Cited by 142 · see citing works

Extracellular matrix molecules and synaptic plasticity: immunomapping of intracellular and secreted Reelin in the adult rat brain

Ramos‐Moreno, T., Galazo, M. J., Porrero, C., Martínez‐Cerdeño, V., & Clascá, F. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04567.x · Cited by 129 · see citing works

Reelin is a positional signal for the lamination of dentate granule cells

Zhao, S., Chai, X., Förster, E., & Frotscher, M. (2004) · Development · doi:10.1242/dev.01387 · Cited by 127 · see citing works

Functional Dissection of Reelin Signaling by Site-Directed Disruption of Disabled-1 Adaptor Binding to Apolipoprotein E Receptor 2: Distinct Roles in Development and Synaptic Plasticity

Beffert, U., Durudas, A., Weeber, E. J., Stolt, P. C., Giehl, K. M., Sweatt, J. D., Hammer, R. E., & Herz, J. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4566-05.2006 · Cited by 121 · see citing works

Identification of a transient subpial neurogenic zone in the developing dentate gyrus and its regulation by Cxcl12 and reelin signaling

Li, G., Kataoka, H., Coughlin, S. R., & Pleasure, S. J. (2008) · Development · doi:10.1242/dev.025742 · Cited by 120 · see citing works

Recent progress in understanding the role of Reelin in radial neuronal migration, with specific emphasis on the dentate gyrus

Förster, E., Jossin, Y., Zhao, S., Chai, X., Frotscher, M., & Goffinet, A. M. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04612.x · Cited by 114 · see citing works

Binding of purified Reelin to ApoER2 and VLDLR mediates tyrosine phosphorylation of Disabled-1

Benhayon, D., Magdaleno, S. M., & Curran, T. (2003) · Molecular Brain Research · doi:10.1016/s0169-328x(03)00032-9 · Cited by 110 · see citing works

Radial ‘glial’ progenitors: neurogenesis and signaling

Ever, L., & Gaiano, N. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.01.005 · Cited by 104 · see citing works

Malformation of the radial glial scaffold in the dentate gyrus of reeler mice, scrambler mice, and ApoER2/VLDLR‐deficient mice

Weiss, K. H., Johanssen, C., Tielsch, A., Herz, J., Deller, T., Frotscher, M., & Förster, E. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10644 · Cited by 103 · see citing works

Apolipoprotein E Receptors Are Required for Reelin-induced Proteasomal Degradation of the Neuronal Adaptor Protein Disabled-1

Bock, H. H., Jossin, Y., May, P., Bergner, O., & Herz, J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m401770200 · Cited by 102 · see citing works

LKB1 Regulates Neuronal Migration and Neuronal Differentiation in the Developing Neocortex through Centrosomal Positioning

Asada, N., Sanada, K., & Fukada, Y. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1938-07.2007 · Cited by 102 · see citing works

Modulation of lipoprotein receptor functions by intracellular adaptor proteins

Stolt-Bergner, P. C., & Bock, H. H. (2006) · Cellular Signalling · doi:10.1016/j.cellsig.2006.03.008 · Cited by 101 · see citing works

Molecular separation of two signaling pathways for the receptor, Notch

Gall, M. L., Mattei, C. D., & Giniger, E. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.10.030 · Cited by 86 · see citing works

Reelin and Notch1 Cooperate in the Development of the Dentate Gyrus

Sibbe, M., Forster, E., Başak, O., Taylor, V., & Frotscher, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0958-09.2009 · Cited by 86 · see citing works

Genetic Modulation of Tau Phosphorylation in the Mouse

Brich, J., Shie, F., Howell, B. W., Li, R., Tus, K., Wakeland, E. K., Jin, L., Mumby, M. C., Churchill, G. A., Herz, J., et al. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00187.2003 · Cited by 83 · see citing works

Developmental distribution of a reeler gene-related antigen in the rat hippocampal formation visualized by CR-50 immunocytochemistry

Drakew, A., Frotscher, M., Deller, T., Ogawa, M., & Heimrich, B. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00326-6 · Cited by 77 · see citing works

Differential functions of ApoER2 and very low density lipoprotein receptor in Reelin signaling depend on differential sorting of the receptors

Duit, S., Mayer, H., Blake, S. M., Schneider, W. J., & Nimpf, J. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.025973 · Cited by 71 · see citing works

β-amyloid controls altered Reelin expression and processing in Alzheimer's disease

Botella-López, A., Cuchillo‐Ibáñez, I., Cotrufo, T., Mok, S. S., Li, Q., Jiménez, M. S. B., Dierssen, M., Soriano, E., & Sáez‐Valero, J. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.12.006 · Cited by 64 · see citing works

Reelin Promotes Neuronal Orientation and Dendritogenesis during Preplate Splitting

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Mouse Disabled1 (DAB1) Is a Nucleocytoplasmic Shuttling Protein

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Proper Layering Is Important for Precisely Timed Activation of Hippocampal Mossy Cells

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Extracellular Matrix: Functions in the Nervous System

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CORTECON: A Temporal Transcriptome Analysis of In Vitro Human Cerebral Cortex Development from Human Embryonic Stem Cells

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Reelin and Stk25 Have Opposing Roles in Neuronal Polarization and Dendritic Golgi Deployment

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Development of Patient-Specific Neurons in Schizophrenia Using Induced Pluripotent Stem Cells

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Extracellular matrix functions during neuronal migration and lamination in the mammalian central nervous system

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In Sickness and in Health: Perineuronal Nets and Synaptic Plasticity in Psychiatric Disorders

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Networks of Cultured iPSC-Derived Neurons Reveal the Human Synaptic Activity-Regulated Adaptive Gene Program

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Role for Reelin in neurotransmitter release

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Convergent and Divergent Mechanisms of Epileptogenesis in mTORopathies

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Impaired Reelin-Dab1 Signaling Contributes to Neuronal Migration Deficits of Tuberous Sclerosis Complex

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Reelin Induces Branching of Neurons and Radial Glial Cells during Corticogenesis

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Development of Layer 1 Neurons in the Mouse Neocortex

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Genome-wide target analysis of NEUROD2 provides new insights into regulation of cortical projection neuron migration and differentiation

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Molecular mechanisms of developmental pathways in neurological disorders: a pharmacological and therapeutic review

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Dietary-induced obesity disrupts trace fear conditioning and decreases hippocampal reelin expression

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A disintegrin and metalloproteinase with thrombospondin motifs 4 (ADAMTS‐4) cleaves Reelin in an isoform‐dependent manner

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Molecular and Electrophysiological Characterization of GFP-Expressing CA1 Interneurons in GAD65-GFP Mice

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Early Effects of Lipopolysaccharide-Induced Inflammation on Foetal Brain Development in Rat

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Systematic Evaluation of Candidate Ligands Regulating Ectodomain Shedding of Amyloid Precursor Protein

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Differential methylation at the RELN gene promoter in temporal cortex from autistic and typically developing post-puberal subjects

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Characterization and Distribution of Reelin-Positive Interneuron Subtypes in the Rat Barrel Cortex

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RELN and VLDLR mutations underlie two distinguishable clinico‐radiological phenotypes

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The β-amyloid peptide compromises Reelin signaling in Alzheimer’s disease

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Lineage divergence of activity-driven transcription and evolution of cognitive ability

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Update on neuroimaging phenotypes of mid-hindbrain malformations

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Sex Differences in Alzheimer’s Disease: Where Do We Stand?

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Cell Polarity in Cerebral Cortex Development—Cellular Architecture Shaped by Biochemical Networks

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Plasticity of Blood- and Lymphatic Endothelial Cells and Marker Identification

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Impaired Structural and Functional Development of Cerebellum Following Gestational Exposure of Deltamethrin in Rats: Role of Reelin

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Reelin in the Years: decline in the number of reelin immunoreactive neurons in layer II of the entorhinal cortex in aged monkeys with memory impairment

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ApoER2 and Reelin are expressed in regenerating peripheral nerve and regulate Schwann cell migration by activating the Rac1 GEF protein, Tiam1

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Invasive cells in animals and plants: searching for LECA machineries in later eukaryotic life

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Inhibition of excessive kallikrein-8 improves neuroplasticity in Alzheimer's disease mouse model

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A Deletion in the VLDLR Gene in Eurasier Dogs with Cerebellar Hypoplasia Resembling a Dandy-Walker-Like Malformation (DWLM)

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Extracellular molecular signals shaping dendrite architecture during brain development

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An Intricate Connection between Alternative Splicing and Phenotypic Plasticity in Development and Cancer

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Reelin Depletion Protects Against Atherosclerosis by Decreasing Vascular Adhesion of Leukocytes

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Heat stress attenuates new cell generation in the hypothalamus: A role for miR-138

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Reelin Signaling Controls the Preference for Social Novelty in Zebrafish

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Reelin expression in brain endothelial cells: an electron microscopy study

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Effects of β4 integrin expression on microRNA patterns in breast cancer

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M1 muscarinic receptor for the development of auditory cortical function

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Reciprocal Regulation of Very Low Density Lipoprotein Receptors (VLDLRs) in Neurons by Brain-derived Neurotrophic Factor (BDNF) and Reelin

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Role for Reelin‐induced cofilin phosphorylation in the assembly of sympathetic preganglionic neurons in the murine intermediolateral column

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Intracortical Network Effects Preserve Thalamocortical Input Efficacy in a Cortex Without Layers

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MiR-138 promotes the migration of cultured chicken embryonic hypothalamic cells by targeting reelin

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Neurobehavioral performances and brain regional metabolism in Dab1scm (scrambler) mutant mice

Jacquelin, C., Lalonde, R., Jantzen-Ossola, C., & Strazielle, C. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.05.024 · Cited by 17 · see citing works

Regulation of Lymphatic Vasculature by Extracellular Matrix

Lutter, S., & Mäkinen, T. (2013) · Advances in anatomy, embryology and cell biology · doi:10.1007/978-3-7091-1646-3_5 · Cited by 18 · see citing works

Subarachnoid cerebrospinal fluid is essential for normal development of the cerebral cortex

Miyan, J. A., Cains, S., Larcombe, S. J., Naz, N., Jimenez, A. R., Bueno, D., & Gato, A. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.11.011 · Cited by 17 · see citing works

Loss of the Reelin-signaling pathway differentially disrupts heat, mechanical and chemical nociceptive processing

Wang, X., Babayan, A. H., Basbaum, A. I., & Phelps, P. E. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.09.027 · Cited by 17 · see citing works

NOT THAT RIGID MIDGETS AND NOT SO FLEXIBLE GIANTS: ON THE ABUNDANCE AND ROLES OF INTRINSIC DISORDER IN SHORT AND LONG PROTEINS

Howell, M., Green, R. J., Killeen, A., WEDDERBURN, L., Picascio, V., Rabionet, A., Peng, Z., Larina, M., Xue, B., Kurgan, L., et al. (2012) · Journal of Biological Systems · doi:10.1142/s0218339012400086 · Cited by 17 · see citing works

Reelin influences the expression and function of dopamine D2 and serotonin 5-HT2A receptors: A comparative study

Varela, M. J., Lage, S., Caruncho, H. J., Cadavid, M. I., Loza, M. I., & Brea, J. M. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.01.031 · Cited by 16 · see citing works

Reelin and aromatase cooperate in ovarian follicle development

Meseke, M., Pröls, F., Schmahl, C., Seebo, K., Kruse, C., Brandt, N., Fester, L., Zhou, L., Bender, R., & Rune, G. M. (2018) · Scientific Reports · doi:10.1038/s41598-018-26928-x · Cited by 15 · see citing works

Neuroinflammation Induction and Alteration of Hippocampal Neurogenesis in Mice Following Developmental Exposure to Gossypol

Zhu, X., Wu, Y., Pan, J., Li, C., Huang, J., Cui, E., Chen, Z., Zhou, W., Chai, X., & Zhao, S. (2020) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyaa093 · Cited by 14 · see citing works

Protection of Beta Boswellic Acid against Streptozotocin-induced Alzheimerʼs Model by Reduction of Tau Phosphorylation Level and Enhancement of Reelin Expression

Shasaltaneh, M. D., Naghdi, N., Ramezani, S., Alizadeh, L., & Riazi, G. H. (2021) · Planta Medica · doi:10.1055/a-1502-7083 · Cited by 14 · see citing works

Sexually Dimorphic Expression of Reelin in the Brain of a Mouse Model of Alzheimer Disease

Palladino, G., Nicolia, V., Kovács, G. G., Canterini, S., Ciraci, V., Fuso, A., Mangia, F., Scarpa, S., & Fiorenza, M. T. (2016) · Journal of Molecular Neuroscience · doi:10.1007/s12031-016-0865-x · Cited by 14 · see citing works

Microcompartments in the Drosophila heart and the mammalian brain: general features and common principles

Brandt, R., & Paululat, A. (2013) · Biological Chemistry · doi:10.1515/hsz-2012-0261 · Cited by 13 · see citing works

Neurotrophins regulate ApoER2 proteolysis through activation of the Trk signaling pathway

Larios, J. A., Jausoro, I., Benitez, M.-L., Bronfman, F. C., & Marzolo, M.-P. (2014) · BMC Neuroscience · doi:10.1186/1471-2202-15-108 · Cited by 12 · see citing works

Reelin differentially shapes dendrite morphology of medial entorhinal cortical ocean and island cells

Hamad, M. I. K., Daoud, S., Petrova, P., Rabaya, O., Jbara, A., Houqani, S. A., BaniYas, S., Alblooshi, M., Almheiri, A., Nakhal, M. M., et al. (2024) · Development · doi:10.1242/dev.202449 · Cited by 12 · see citing works

Early-Life Stress Caused by Maternal Deprivation Impacts Dendritic Morphology of Adult Male Mouse Neocortical Interneurons

Nakhal, M. M., Yassin, L. K., Houqani, S. A., Mydeen, A. B., Ibrahim, M. F., Shehab, S. A. S., Allouh, M. Z., & Hamad, M. I. K. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26051909 · Cited by 12 · see citing works

Characterization of NGF, trkA NGFR , and p75 NTR in Retina of Mice Lacking Reelin Glycoprotein

Balzamino, B. O., Biamonte, F., Esposito, G., Marino, R., Fanelli, F., Keller, F., & Micera, A. (2014) · International Journal of Cell Biology · doi:10.1155/2014/725928 · Cited by 12 · see citing works

NGF Expression in Reelin-Deprived Retinal Cells: A Potential Neuroprotective Effect

Balzamino, B. O., Esposito, G., Marino, R., Keller, F., & Micera, A. (2015) · NeuroMolecular Medicine · doi:10.1007/s12017-015-8360-z · Cited by 12 · see citing works

Regulation of the hippocampal translatome by Apoer2-ICD release

Wasser, C. R., Werthmann, G. C., Hall, E. M., Kuhbandner, K., Wong, C. H. Y., Durakoglugil, M. S., & Herz, J. (2023) · Molecular Neurodegeneration · doi:10.1186/s13024-023-00652-1 · Cited by 11 · see citing works

The Reelin receptors ApoER2 and VLDLR are direct target genes of HIC1 (Hypermethylated In Cancer 1)

Dubuissez, M., Faiderbe, P., Pinte, S., Dehennaut, V., Rood, B. R., & Leprince, D. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.09.091 · Cited by 11 · see citing works

Pinocembrin Ameliorates Cognitive Impairment Induced by Vascular Dementia: Contribution of Reelin-dab1 Signaling Pathway

Kang, Z.-C., Wang, H.-G., Yang, Y.-L., Zhao, X., Zhou, Q., Yang, Y., Yang, J., & Du, G. (2020) · Drug Design Development and Therapy · doi:10.2147/dddt.s249176 · Cited by 10 · see citing works

Neuroserpin Is Strongly Expressed in the Developing and Adult Mouse Neocortex but Its Absence Does Not Perturb Cortical Lamination and Synaptic Proteome

Kement, D., Reumann, R., Schostak, K., Voß, H., Douceau, S., Dottermusch, M., Schweizer, M., Schlüter, H., Vivien, D., Glatzel, M., et al. (2021) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.627896 · Cited by 10 · see citing works

Correction: Plasticity of Blood- and Lymphatic Endothelial Cells and Marker Identification

Keuschnigg, J., Karinen, S., Auvinen, K., Irjala, H., Mpindi, J.-P., Kallioniemi, O., Hautaniemi, S., Jalkanen, S., & Salmi, M. (2013) · PLoS ONE · doi:10.1371/annotation/cfda269a-cb46-4735-b87f-42afccb6aeb1 · Cited by 9 · see citing works

Integrity of Cajal–Retzius cells in thereeler‐mouse hippocampus

Anstötz, M., Karsak, M., & Rune, G. M. (2018) · Hippocampus · doi:10.1002/hipo.23049 · Cited by 8 · see citing works

Environmental Factors and Autism Spectrum Disorder

Persico, A. M., & Merelli, S. (2015) · Key issues in mental health (Online)/Key issues in mental health (Print) · doi:10.1159/000363611 · Cited by 8 · see citing works

Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review

Chen, C., Su, Y., Chen, C.-Y., Chern, S., Wu, P.-S., Su, J.-W., Lee, C., Chen, L., & Wang, W. (2013) · Genomics · doi:10.1016/j.ygeno.2013.08.003 · Cited by 8 · see citing works

Controversies in RELN/reelin expression in otosclerosis

Csomor, P., Sziklai, I., & Karosi, T. (2011) · European Archives of Oto-Rhino-Laryngology · doi:10.1007/s00405-011-1653-4 · Cited by 7 · see citing works

BASIC NEUROSCIENCES, GENETICS AND IMMUNOLOGY- REVIEW ARTICLE Role of Reelin in the development and maintenance of cortical lamination

(2015)

Reelin acts as a stop signal for radially migrating neurons by inducing phosphorylation of n-cofilin at the leading edge

Chai, X., Förster, E., Zhao, S., Bock, H. H., & Frotscher, M. (2009) · Communicative & Integrative Biology · doi:10.4161/cib.2.4.8614 · Cited by 34 · see citing works

Role of Reelin in the development and maintenance of cortical lamination

Frotscher, M., Chai, X., Bock, H. H., Haas, C. A., Förster, E., & Zhao, S. (2009) · Journal of Neural Transmission · doi:10.1007/s00702-009-0228-7 · Cited by 68 · see citing works

The Reelin signaling pathway promotes dendritic spine development in hippocampal neurons

Niu, S., Yabut, O., & D'Arcangelo, G. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1917-08.2008 · Cited by 266 · see citing works

The functions of Reelin in membrane trafficking and cytoskeletal dynamics: implications for neuronal migration, polarization and differentiation

Santana, J., & Marzolo, M. (2017) · Biochemical Journal · doi:10.1042/bcj20160628 · Cited by 74 · see citing works