The DOI matches its Crossref record; 109 of the 109 references it cites were found in a registry or an index.
Emerging topics in Reelin function
Open accessAbstract
Reelin signalling in the early developing cortex regulates radial migration of cortical neurons. Later in development, Reelin promotes maturation of dendrites and dendritic spines. Finally, in the mature brain, it is involved in modulating synaptic function. In recent years, efforts to identify downstream signalling events induced by binding of Reelin to lipoprotein receptors led to the characterization of novel components of the Reelin signalling cascade. In the present review, we first address distinct functions of the Reelin receptors Apoer2 and Vldlr in cortical layer formation, followed by a discussion on the recently identified downstream effector molecule n‐cofilin, involved in regulating actin cytoskeletal dynamics required for coordinated neuronal migration. Next, we discuss possible functions of the recently identified Reelin–Notch signalling crosstalk, and new aspects of the role of Reelin in the formation of the dentate radial glial scaffold. Finally, progress in characterizing the function of Reelin in modulating synaptic function in the adult brain is summarized. The present review has been inspired by a session entitled ‘Functions of Reelin in the developing and adult hippocampus’, held at the Spring Hippocampal Research Conference in Verona/Italy, June 2009.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“The defective migration of Nova2−/− upper-layer neurons was attributed to the mis-splicing of disabled 1 (Dab1), a component of the Reelin signalling pathway that controls cortical neuronal migration and lamination40–42.”
From The neurogenetics of alternative splicing (2016) · cites this paper as [42]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
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
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
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×
“Incubation of hippocampal neurons with Aβ-oligomers impaired endocytosis and trafficking of AMPA- and NMDA-receptors and thus decreased LTP (Hsieh et al., 2006; Kamenetz et al., 2003; Snyder et al., 2005).”
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
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
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
Self-citationIsolation 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
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
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
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
Self-citationNotch signalling in vertebrate neural development
Louvi, A., & Artavanis‐Tsakonas, S. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1847 · Cited by 909
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 896
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
Tissir, F., & Goffinet, A. M. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1113 · Cited by 767
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
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
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 716
Modes of neuronal migration in the developing cerebral cortex
Nadarajah, B., & Parnavelas, J. G. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn845 · Cited by 712
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
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
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
Self-citationNotch 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
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
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
Reelin, lipoprotein receptors and synaptic plasticity
Herz, J., & Chen, Y. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn2009 · Cited by 524
Self-citationEstablishment 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
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
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
Self-citationTrommsdorff, M., Borg, J.-P., Margolis, B., & Herz, J. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.50.33556 · Cited by 453
Self-citationLKB1 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 418
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
Reelin-induced tryosine phosphorylation of Disabled 1 during neuronal positioning
Howell, B. W., Herrick, T. M., & Cooper, J. A. (1999) · Genes & Development · doi:10.1101/gad.13.6.643 · Cited by 411
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
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
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 358
Self-citationMammalian 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 345
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 323
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
Self-citationReelin 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
Self-citationCortical 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
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 287
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 285
Self-citationFyn 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 284
Self-citationThe 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
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
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
Self-citationA 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 251
Förster, E., Zhao, S., & Frotscher, M. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1882 · Cited by 247
Self-citationCurran, T., & D'Arcangelo, G. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00035-0 · Cited by 246
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 243
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
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
Self-citationJossin, Y., & Goffinet, A. M. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.00928-07 · Cited by 235
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
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
Apolipoprotein E receptors: linking brain development and alzheimer's disease
Herz, J., & Beffert, U. (2000) · Nature reviews. Neuroscience · doi:10.1038/35036221 · Cited by 224
Self-citationInteraction 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 223
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
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
Self-citationAbsence 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 205
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
Self-citationADF/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
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
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
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
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
Kiuchi, T., Ohashi, K., Kurita, S., & Mizuno, K. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200610005 · Cited by 172
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
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 166
Self-citationLord, M., & Caviness, V. S. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901870104 · Cited by 164
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
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
A Role for Abl in Notch Signaling
Giniger, E. (1998) · Neuron · doi:10.1016/s0896-6273(00)81007-7 · Cited by 161
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
Self-citationCullin 5 regulates Dab1 protein levels and neuron positioning during cortical development
Feng, L., Allen, N. S., Simo, S., & Cooper, J. A. (2007) · Genes & Development · doi:10.1101/gad.1604207 · Cited by 148
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
Self-citationRamos‐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 133
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 129
Self-citationBeffert, 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
Self-citationLi, G., Kataoka, H., Coughlin, S. R., & Pleasure, S. J. (2008) · Development · doi:10.1242/dev.025742 · Cited by 120
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 116
Self-citationBinding 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 109
Asada, N., Sanada, K., & Fukada, Y. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1938-07.2007 · Cited by 108
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 106
Self-citationRadial ‘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
Bock, H. H., Jossin, Y., May, P., Bergner, O., & Herz, J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m401770200 · Cited by 102
Self-citationModulation 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
Self-citationMolecular 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
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
Self-citationGenetic 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 84
Self-citationDrakew, A., Frotscher, M., Deller, T., Ogawa, M., & Heimrich, B. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00326-6 · Cited by 77
Self-citationDuit, 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
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 65
Reelin Promotes Neuronal Orientation and Dendritogenesis during Preplate Splitting
Nichols, A. J., & Olson, E. C. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhp303 · Cited by 65
Reelin induces a radial glial phenotype in human neural progenitor cells by activation of Notch-1
Keilani, S., & Sugaya, K. (2008) · BMC Developmental Biology · doi:10.1186/1471-213x-8-69 · Cited by 58
Terashima, T., Inoue, K., Inoue, Y., Mikoshiba, K., & Tsukada, Y. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902320108 · Cited by 52
Miyata, T., & Ogawa, M. (2007) · Current Biology · doi:10.1016/j.cub.2006.11.023 · Cited by 46
Functional interactions of APP with the apoE receptor family
Hoe, H., & Rebeck, G. W. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05517.x · Cited by 44
Doehner, J., Madhusudan, A., Konietzko, U., Fritschy, J., & Knuesel, I. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-1333 · Cited by 43
Inverted pyramidal neurons and their axons in the neocortex of reeler mutant mice
Landrieu, P., & Goffinet, A. M. (1981) · Cell and Tissue Research · doi:10.1007/bf00210345 · Cited by 43
Mouse Disabled1 (DAB1) Is a Nucleocytoplasmic Shuttling Protein
Honda, T., & Nakajima, K. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m609061200 · Cited by 42
Zhao, S., Chai, X., Bock, H. H., Brunne, B., Förster, E., & Frotscher, M. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20846 · Cited by 39
Self-citationThe fyn art of N -methyl- d -aspartate receptor phosphorylation
Sala, C., & Sheng, M. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.2.335 · Cited by 38
Hartfuss, E., Förster, E., Bock, H. H., Hack, M. A., Leprince, P., Luque, I. M., Herz, J., Frotscher, M., & Götz, M. (2003) · Cited by 31
Self-citationGaiano, N. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.009 · Cited by 29
Proper Layering Is Important for Precisely Timed Activation of Hippocampal Mossy Cells
Kowalski, J., Geuting, M., Paúl, S., Dieni, S., Laurens, J., Zhao, S., Drakew, A., Haas, C. A., Frotscher, M., & Vida, I. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhp267 · Cited by 21
Self-citationFatemi, S. H. (2008) · Springer eBooks · doi:10.1007/978-0-387-76761-1 · Cited by 6
Apolipoprotein E Receptor 2 and Very-Low-Density Lipoprotein Receptor: An Overview
Bock, H. H., & Herz, J. (2008) · Springer eBooks · doi:10.1007/978-0-387-76761-1_2 · Cited by 3
Self-citation
Cited by
Sorted by citations
Alternative splicing as a regulator of development and tissue identity
Baralle, F. E., & Giudice, J. (2017) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.27 · Cited by 1,333
Apolipoprotein E and Apolipoprotein E Receptors: Normal Biology and Roles in Alzheimer Disease
Holtzman, D. M., Herz, J., & Bu, G. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a006312 · Cited by 782
Self-citationExtracellular Matrix: Functions in the Nervous System
Barros, C. S., Franco, S. J., & Muller, U. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005108 · Cited by 506
The neurogenetics of alternative splicing
Vuong, C. K., Black, D. L., & Zheng, S. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.27 · Cited by 340
The involvement of Reelin in neurodevelopmental disorders
Folsom, T. D., & Fatemi, S. H. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.08.015 · Cited by 275
Metadata
- Authors
- Förster, E., Bock, H. H., Herz, J., Chai, X., Frotscher, M., & Zhao, S.
- Affiliations
- Universität Hamburg (DE)
- University of Freiburg (DE)
- Corresponding author
- Förster, Eckart
- Venue
- European Journal of Neuroscience
- Publisher
- Wiley
- Published
- 2010-04-30
- Volume
- 31
- Issue
- 9
- Pages
- 1511-1518
- ISSN
- 0953-816X (ISSN-L)
- 1460-9568
- PMC
- PMC2942760
- OpenAlex
- W1795146795
- Cited by
- 130
- References
- 109
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 4 · 2023: 4 · 2022: 5 · 2021: 6 · 2020: 5 · 2019: 5 · 2018: 5 · 2017: 8 · 2016: 14 · 2015: 12 · 2014: 8 · 2013: 20 · 2012: 12
- FWCI
- 1.28
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- European Journal of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- National Heart, Lung, and Blood Institute (R01HL063762, R37HL063762, P01HL020948)
- National Institute of Neurological Disorders and Stroke (RC1NS068697, R01NS043408)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- cortical development, radial neuronal migration, cortical lamination, dendritic spine maturation, synaptic function, ApoER2, VLDLR, actin cytoskeleton, dentate gyrus, hippocampus, lipoprotein receptors
- MeSH terms
- Reelin Protein, Animals, Cytoskeleton, Humans, Models, Neurological, Nerve Tissue Proteins, Neuroglia, Neurons, Receptors, Cell Surface, Serine Endopeptidases, Cell Adhesion Molecules, Neuronal, Extracellular Matrix Proteins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review