Brain Development in Normal and reeler Mice: the Phenotype

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

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

Reelin and brain development

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

Lipoprotein receptors in the nervous system

Herz, J., & Bock, H. H. (2002) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.71.110601.135342 · Cited by 457 · see citing works

The origin and migration of cortical neurones: new vistas

Parnavelas, J. G. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01553-8 · Cited by 393 · 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

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

Comparative aspects of cerebral cortical development

Molnár, Z., Métin, C., Stoykova, A., Tarabykin, V. S., Price, D. J., Francis, F., Meyer, G., Dehay, C., & Kennedy, H. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04611.x · Cited by 266 · 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

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

Neurodevelopment, GABA System Dysfunction, and Schizophrenia

Schmidt, M. J., & Mirnics, K. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.95 · Cited by 239 · see citing works

The LDL Receptor Gene Family

Herz, J. (2001) · Neuron · doi:10.1016/s0896-6273(01)00234-3 · Cited by 233 · see citing works

Reelin Regulates Neuronal Progenitor Migration in Intact and Epileptic Hippocampus

Gong, C., Wang, T., Huang, H. S., & Parent, J. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3111-06.2007 · Cited by 233 · see citing works

Homozygous Deletion of the Very Low Density Lipoprotein Receptor Gene Causes Autosomal Recessive Cerebellar Hypoplasia with Cerebral Gyral Simplification

Boycott, K. M., Flavelle, S. C., Bureau, A., Glass, H. C., Fujiwara, T., Wirrell, E. C., Davey, K., Chudley, A. E., Scott, J. N., McLeod, D. R., et al. (2005) · The American Journal of Human Genetics · doi:10.1086/444400 · Cited by 221 · see citing works

Embryonic and Early Fetal Development of the Human Neocortex

Meyer, G., Schaaps, J. P., Moreau, L., & Goffinet, A. M. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-05-01858.2000 · Cited by 215 · 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

Interstitial white matter neurons express less reelin and are abnormally distributed in schizophrenia: towards an integration of molecular and morphologic aspects of the neurodevelopmental hypothesis

Eastwood, S. L., & Harrison, P. J. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001399 · Cited by 208 · see citing works

Expression of p73 and Reelin in the Developing Human Cortex

Meyer, G., Pérez‐García, C. G., Ábrahám, H., & Caput, D. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-12-04973.2002 · Cited by 204 · see citing works

The Central Fragment of Reelin, Generated by Proteolytic ProcessingIn Vivo, Is Critical to Its Function during Cortical Plate Development

Jossin, Y., Ignatova, N. G., Hiesberger, T., Herz, J., de Rouvroit, C. L., & Goffinet, A. M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3408-03.2004 · Cited by 198 · see citing works

Dendritic Spine Hypoplasticity and Downregulation of Reelin and GABAergic Tone in Schizophrenia Vulnerability

Costa, E., Davis, J. M., Grayson, D. R., Guidotti, A., Pappas, G. D., & Pesold, C. (2001) · Neurobiology of Disease · doi:10.1006/nbdi.2001.0436 · Cited by 197 · see citing works

Regulation of N-cadherin-mediated adhesion by the p35–Cdk5 kinase

Kwon, Y. T., Gupta, A., Zhou, Y., Nikolić, M., & Tsai, L. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00411-5 · Cited by 178 · see citing works

Colocalization of integrin receptors and reelin in dendritic spine postsynaptic densities of adult nonhuman primate cortex

Rodríguez, M. Á., Pesold, C., Liu, W. S., Kriho, V., Guidotti, A., Pappas, G. D., & Costa, E. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.050589797 · Cited by 178 · see citing works

Neuronal migration

de Rouvroit, C. L., & Goffinet, A. M. (2001) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00396-3 · Cited by 176 · 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

Expression of reelin in adult mammalian blood, liver, pituitary pars intermedia, and adrenal chromaffin cells

Smalheiser, N. R., Costa, E., Guidotti, A., Impagnatiello, F., Auta, J., Lacor, P., Kriho, V., & Pappas, G. D. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.3.1281 · Cited by 158 · see citing works

Interstitial white matter neurons express less reelin and are abnormally distributed in schizophrenia: towards an integration of molecular and morphologic aspects of the neurodevelopmental hypothesis

Eastwood, S. L., & Harrison, P. J. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001371 · Cited by 158 · see citing works

Role for Reelin in stabilizing cortical architecture

Frotscher, M. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.06.001 · Cited by 157 · see citing works

Reelin, the Extracellular Matrix Protein Deficient in Reeler Mutant Mice, Is Processed by a Metalloproteinase

de Rouvroit, C. L., Bergeyck, V. D., Cortvrindt, C., Bar, I., Eeckhout, Y., & Goffinet, A. M. (1999) · Experimental Neurology · doi:10.1006/exnr.1998.7007 · Cited by 157 · see citing works

Human disorders of cortical development: from past to present

Francis, F., Meyer, G., Fallet‐Bianco, C., Moreno, S., Kappeler, C., Socorro, A. C., Tuy, F. P. D., Beldjord, C., & Chelly, J. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04649.x · Cited by 152 · see citing works

DeltaNp73 regulates neuronal survival in vivo

Tissir, F., Ravni, A., Achouri, Y., Riethmacher, D., Meyer, G., & Goffinet, A. M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903191106 · Cited by 153 · see citing works

New insights into Reelin-mediated signaling pathways

Lee, G. H., & D’Arcangelo, G. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00122 · Cited by 144 · see citing works

Reelin molecules assemble together to form a large protein complex, which is inhibited by the function-blocking CR-50 antibody

Utsunomiya-Tate, N., Kubo, K.-I., Tate, S.-I., Kainosho, M., Katayama, E., Nakajima, K., & Mikoshiba, K. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.160272497 · Cited by 131 · see citing works

Emerging topics in Reelin function

Förster, E., Bock, H. H., Herz, J., Chai, X., Frotscher, M., & Zhao, S. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07222.x · Cited by 130 · see citing works

Crystal Structures of the Dab Homology Domains of Mouse Disabled 1 and 2

Yun, M., Keshvara, L. M., Park, C., Zhang, Y.-M., Dickerson, J. B., Zheng, J., Rock, C. O., Curran, T., & Park, H.-W. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m304384200 · Cited by 129 · see citing works

Heterozygous Reelin Mutations Cause Autosomal-Dominant Lateral Temporal Epilepsy

Dazzo, E., Fanciulli, M., Serioli, E., Minervini, G., Pulitano, P., Binelli, S., Bonaventura, C. D., Luisi, C., Pasini, E., Striano, S., et al. (2015) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2015.04.020 · Cited by 128 · see citing works

Genetics and mechanisms leading to human cortical malformations

Romero, D. M., Bahi‐Buisson, N., & Francis, F. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.09.031 · Cited by 126 · see citing works

Developmental Roles of p73 in Cajal-Retzius Cells and Cortical Patterning

Meyer, G., Socorro, A. C., Pérez‐García, C. G., Millán, L. M., Walker, N., & Caput, D. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3060-04.2004 · Cited by 124 · see citing works

Reelin in the years: controlling neuronal migration and maturation in the mammalian brain

D'Arcangelo, G. (2014) · Advances in Neuroscience · doi:10.1155/2014/597395 · Cited by 120 · see citing works

Collapsin Response Mediator Proteins Regulate Neuronal Development and Plasticity by Switching Their Phosphorylation Status

Yamashita, N., & Goshima, Y. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8242-4 · Cited by 115 · 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

Expression of the chemokine receptor Cxcr4 mRNA during mouse brain development

Tissir, F., Wang, C.-E., & Goffinet, A. M. (2004) · Developmental Brain Research · doi:10.1016/j.devbrainres.2004.01.002 · Cited by 114 · see citing works

Reelin mouse mutants as models of cortical development disorders

D’Arcangelo, G. (2005) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2005.09.005 · Cited by 110 · see citing works

Reelin controls position of autonomic neurons in the spinal cord

Yip, J. W., Yip, Y. P., Nakajima, K., & Capriotti, C. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.150040497 · Cited by 112 · see citing works

Reelin secretion from glutamatergic neurons in culture is independent from neurotransmitter regulation

Lacor, P. N., Grayson, D. R., Auta, J., Sugaya, I., Costa, E., & Guidotti, A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.050589597 · Cited by 110 · see citing works

Canonical and non-canonical Reelin signaling

Bock, H. H., & May, P. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00166 · Cited by 107 · see citing works

Hippocampal development – Old and new findings

Khalaf‐Nazzal, R., & Francis, F. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.05.061 · Cited by 103 · see citing works

Role of heat-shock factor 2 in cerebral cortex formation and as a regulatorof p35 expressionPreprint

Chang, Y., Östling, P., Åkerfelt, M., Trouillet, D., Rallu, M., Gitton, Y., El Fatimy, R., Fardeau, V., Crom, S. L., Morange, M., et al. (2006) · Genes & Development · doi:10.1101/gad.366906 · Cited by 101 · 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

Building a human cortex: the evolutionary differentiation of Cajal‐Retzius cells and the cortical hem

Meyer, G. (2010) · Journal of Anatomy · doi:10.1111/j.1469-7580.2010.01266.x · Cited by 96 · see citing works

Role of BRCA1 in brain development

Pao, G. M., Zhu, Q., Pérez‐García, C. G., Chou, S., Suh, H., Gage, F. H., O’Leary, D. D. M., & Verma, I. M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1400783111 · Cited by 95 · see citing works

Reelin deficiency causes specific defects in the molecular composition of the synapses in the adult brain

Ventruti, A., Kazdoba, T. M., Niu, S., & D’Arcangelo, G. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.05.050 · Cited by 94 · see citing works

A Role of Netrin-1 in the Formation of the Subcortical Structure Striatum: Repulsive Action on the Migration of Late-Born Striatal Neurons

Hamasaki, T., Goto, S., Nishikawa, S., & Ushio, Y. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-12-04272.2001 · Cited by 94 · see citing works

Reduction of Crk and CrkL expression blocks reelin-induced dendritogenesis

Matsuki, T., Pramatarova, A., & Howell, B. W. (2008) · Journal of Cell Science · doi:10.1242/jcs.027334 · Cited by 92 · see citing works

Fyn Tyrosine Kinase as Harmonizing Factor in Neuronal Functions and Dysfunctions

Matrone, C., Petrillo, F., Nasso, R., & Ferretti, G. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124444 · Cited by 86 · see citing works

Collapsin Response Mediator Protein 1 Mediates Reelin Signaling in Cortical Neuronal Migration

Yamashita, N., Uchida, Y., Ohshima, T., Hirai, S.-I., Nakamura, F., Taniguchi, M., Mikoshiba, K., Honnorat, J., Kolattukudy, P. E., Thomasset, N., et al. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4276-06.2006 · Cited by 88 · see citing works

Reelin supplementation recovers sensorimotor gating, synaptic plasticity and associative learning deficits in the heterozygous reeler mouse

Rogers, J. T., Zhao, L., Trotter, J. H., Rusiana, I., Peters, M. M., Li, Q., Donaldson, E., Banko, J. L., Keenoy, K. E., Rebeck, G. W., et al. (2012) · Journal of Psychopharmacology · doi:10.1177/0269881112463468 · Cited by 87 · see citing works

Lipoprotein Receptors

Cooper, J. A., & Howell, B. W. (1999) · Cell · doi:10.1016/s0092-8674(00)80778-3 · Cited by 84 · see citing works

Conserved and divergent patterns of Reelin expression in the zebrafish central nervous system

Costagli, A., Kapsimali, M., Wilson, S. W., & Mione, M. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10292 · Cited by 82 · see citing works

The paleocortical ventricle is the origin of reelin‐expressing neurons in the marginal zone of the foetal human neocortex

Meyer, G., & Wahle, P. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00818.x · Cited by 80 · see citing works

The LDL receptor gene family: signaling functions during development

Howell, B. W., & Herz, J. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00176-8 · Cited by 79 · see citing works

The Reeler Mouse: Anatomy of a Mutant

D’Arcangelo, G. (2005) · International review of neurobiology · doi:10.1016/s0074-7742(05)71016-3 · Cited by 77 · see citing works

Role for Reelin in neurotransmitter release

Hellwig, S., Hack, I., Kowalski, J., Brunne, B., Jarowyj, J., Unger, A., Bock, H. H., Junghans, D., & Frotscher, M. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3984-10.2011 · Cited by 74 · see citing works

The role of RELN in lissencephaly and neuropsychiatric disease

Chang, B. S., Düzcan, F., Kim, S., Cinbiş, M., Aggarwal, A., Apse, K. A., Özdel, O. İ., Atmaca, M., Zencir, S., Bağcı, H., et al. (2006) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30392 · Cited by 74 · see citing works

Inhibition of Src Family Kinases and Non-Classical Protein Kinases C Induce a Reeler-Like Malformation of Cortical Plate Development

Jossin, Y., Ogawa, M., Métin, C., Tissir, F., & Goffinet, A. M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-30-09953.2003 · Cited by 74 · see citing works

Reelin provides an inhibitory signal in the migration of gonadotropin-releasing hormone neurons

Cariboni, A. M., Rakić, S., Liapi, A., Maggi, R., Goffinet, A. M., & Parnavelas, J. G. (2005) · Development · doi:10.1242/dev.02033 · Cited by 72 · see citing works

Developmental anatomy of reeler mutant mouse

Katsuyama, Y., & Terashima, T. (2009) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2009.01102.x · Cited by 75 · 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

Comparative aspects of p73 and Reelin expression in Cajal-Retzius cells and the cortical hem in lizard, mouse and human

Cabrera‐Socorro, A., Hernandez-Acosta, N. C., González‐Gómez, M., & Meyer, G. (2007) · Brain Research · doi:10.1016/j.brainres.2006.11.015 · Cited by 68 · see citing works

Abnormal laminar position and dendrite development of interneurons in the reeler forebrain

Yabut, O., Renfro, A., Niu, S., Swann, J. W., Marín, Ó., & D’Arcangelo, G. (2006) · Brain Research · doi:10.1016/j.brainres.2005.09.070 · Cited by 68 · see citing works

Reelin-immunoreactive neurons in the adult vertebrate pallium

Pérez‐García, C. G., Delgado, F. J. G., Suárez-Solá, M. L., Castro-Fuentes, R., Martin-Trujillo, J. M., Ferres-Torres, R., & Meyer, G. (2001) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(00)00104-6 · Cited by 66 · see citing works

Axonal secretion of reelin by cajal‐retzius cells: Evidence from comparison of normal and RelnOrl mutant mice

Derer, P., Derer, M., & Goffinet, A. M. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1375 · Cited by 66 · see citing works

Reelin receptors in developing laminated brain structures of mouse and human

Pérez‐García, C. G., Tissir, F., Goffinet, A. M., & Meyer, G. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03733.x · Cited by 61 · see citing works

Differential cellular and subcellular localization of protein phosphatase 1 isoforms in brain

Strack, S., Kini, S., Ebner, F. F., Wadzinski, B. E., & Colbran, R. J. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19991025)413:3 · Cited by 87 · see citing works

Methodological factors influencing measurement and processing of plasma reelin in humans

Lugli, G., Krueger, J. M., Davis, J. M., Persico, A. M., Keller, F., & Smalheiser, N. R. (2003) · BMC Biochemistry · doi:10.1186/1471-2091-4-9 · Cited by 60 · see citing works

Reelin expression during embryonic brain development in lacertilian lizards

Goffinet, A. M., Bar, I., Bernier, B., Trujillo, C. M., Raynaud, A., & Meyer, G. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19991129)414:4 · Cited by 61 · see citing works

Reelin expression during embryonic brain development in Crocodylus niloticus

Tissir, F., de Rouvroit, C. L., Sire, J., Meyer, G., & Goffinet, A. M. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10573 · Cited by 60 · see citing works

Altered cortico‐striatal synaptic plasticity and related behavioural impairments in reeler mice

Marrone, M. C., Marinelli, S., Biamonte, F., Keller, F., Sgobio, C., Ammassari‐Teule, M., Bernardi, G., & Mercuri, N. B. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05083.x · Cited by 58 · see citing works

The disabled 1 gene is disrupted by a replacement with L1 fragment in yotari mice

Kojima, T., Nakajima, K., & Mikoshiba, K. (2000) · Molecular Brain Research · doi:10.1016/s0169-328x(99)00313-7 · Cited by 54 · see citing works

Neuronal cell migration for the developmental formation of the mammalian striatum

Hamasaki, T., Goto, S., Nishikawa, S., & Ushio, Y. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(02)00216-3 · Cited by 52 · see citing works

N-cadherin-regulated FGFR ubiquitination and degradation control mammalian neocortical projection neuron migration

Kon, E., Calvo-Jiménez, E., Cossard, A., Na, Y., Cooper, J. A., & Jossin, Y. (2019) · eLife · doi:10.7554/elife.47673 · Cited by 50 · see citing works

Characterization of the various forms of the Reelin protein in the cerebrospinal fluid of normal subjects and in neurological diseases

Ignatova, N. G., Sindic, C., & Goffinet, A. M. (2004) · Neurobiology of Disease · doi:10.1016/j.nbd.2003.11.008 · Cited by 50 · see citing works

Mutations in MICAL‐1cause autosomal‐dominant lateral temporal epilepsy

Dazzo, E., Rehberg, K., Michelucci, R., Passarelli, D., Boniver, C., Dri, V. V., Striano, P., Striano, S., Pasterkamp, R. J., & Nobile, C. (2018) · Annals of Neurology · doi:10.1002/ana.25167 · Cited by 49 · see citing works

Absence of Reelin results in altered nociception and aberrant neuronal positioning in the dorsal spinal cord

Villeda, S., Akopians, A. L., Babayan, A. H., Basbaum, A. I., & Phelps, P. E. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.01.042 · Cited by 48 · see citing works

Polarity Regulation in Migrating Neurons in the Cortex

Reiner, O., & Sapir, T. (2009) · Molecular Neurobiology · doi:10.1007/s12035-009-8065-0 · Cited by 46 · see citing works

The Gene Encoding Disabled-1 (DAB1), the Intracellular Adaptor of the Reelin Pathway, Reveals Unusual Complexity in Human and Mouse

Bar, I., Tissir, F., de Rouvroit, C. L., Backer, O. D., & Goffinet, A. M. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m207178200 · Cited by 46 · see citing works

A new view of early cortical development

de Rouvroit, C. L., & Goffinet, A. M. (1998) · Biochemical Pharmacology · doi:10.1016/s0006-2952(98)00209-3 · Cited by 46 · see citing works

RareRELNvariants affect Reelin-DAB1 signal transduction in autism spectrum disorder

Sánchez-Sánchez, S. M., Magdalon, J., Griesi‐Oliveira, K., Yamamoto, G. L., Santacruz-Pérez, C., Fogo, M. S., Passos‐Bueno, M. R., & Sertie, A. L. (2018) · Human Mutation · doi:10.1002/humu.23584 · Cited by 45 · see citing works

Reelin-Related Disturbances in Depression: Implications for Translational Studies

Caruncho, H. J., Brymer, K. J., Romay-Tallón, R., Mitchell, M. A., Baltanás, T. R., Botterill, J. J., Olivares, J. M., & Kalynchuk, L. E. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00048 · Cited by 42 · see citing works

The heterogeneity of human Cajal-Retzius neurons

Meyer, G., & González‐Gómez, M. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.08.059 · Cited by 37 · see citing works

Making Ramón y Cajal proud: Development of cell identity and diversity in the cerebral cortex

Bella, D. J. D., Domıńguez-Iturza, N., Brown, J. R., & Arlotta, P. (2024) · Neuron · doi:10.1016/j.neuron.2024.04.021 · Cited by 37 · see citing works

Dispersion of the neurons expressing layer specific markers in the reeler brain

Dekimoto, H., Terashima, T., & Katsuyama, Y. (2010) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2009.01153.x · Cited by 36 · see citing works

Structural Insights into Reelin Function: Present and Future

Ranaivoson, F. M., von Daake, S., & Comoletti, D. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00137 · Cited by 34 · see citing works

Temporal proteomics of human cerebrospinal fluid after severe traumatic brain injury

Shultz, S. R., Shah, A. D., Huang, C., Dill, L. K., Schittenhelm, R. B., Morganti-Kossmann, M. C., & Semple, B. D. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02654-0 · Cited by 36 · see citing works

Evolutionarily Conserved, Alternative Splicing of Reelin during Brain Development

de Rouvroit, C. L., Bernier, B., Royaux, I. E., Bergeyck, V. D., & Goffinet, A. M. (1999) · Experimental Neurology · doi:10.1006/exnr.1999.7019 · Cited by 36 · see citing works

Reelin haploinsufficiency reduces the density of PV+ neurons in circumscribed regions of the striatum and selectively alters striatal-based behaviors

Ammassari‐Teule, M., Sgobio, C., Biamonte, F., Marrone, C., Mercuri, N. B., & Keller, F. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1483-x · Cited by 35 · see citing works

Absence of Layer-Specific Cadherin Expression Profiles in the Neocortex of the Reeler Mutant Mouse

Hertel, N., & Redies, C. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq183 · Cited by 35 · see citing works

Reelin signals survival through Src‐family kinases that inactivate BAD activity

Ohkubo, N., Vitek, M. P., Morishima, A., Suzuki, Y., Miki, T., Maeda, N., & Mitsuda, N. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04804.x · Cited by 35 · see citing works

Stereological estimates of total neuron numbers in the hippocampus of adult reeler mutant mice: Evidence for an increased survival of Cajal‐Retzius cells

Coulin, C., Drakew, A., Frotscher, M., & Deller, T. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1332 · Cited by 34 · see citing works

The molecular basis of central nervous system development

Hermanson, O., & Lendahl, U. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511711848.004

Embryology

Moini, J., Avgeropoulos, N. G., & Samsam, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821736-8.00024-8

Development of the Nervous System

Rubenstein, J. L. R., & Puelles, L. (2008) · doi:10.1093/oso/9780195306910.003.0007 · Cited by 6 · see citing works

Developmental Aspects of the Nervous System

Arslan, O. E. (2014) · CRC Press eBooks · doi:10.1201/b17094-6

Normal development of the nervous system

Monuki, E. S., Hevner, R. F., & Rose, M. F. (2024) · CRC Press eBooks · doi:10.1201/9781003389699-12 · Cited by 2 · see citing works