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Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death.

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Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality.

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Scrambler and yotari disrupt the disabled gene and produce a reeler -like phenotype in mice

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

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

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A role for Cajal–Retzius cells and reelin in the development of hippocampal connections

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Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor

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Constructing the cerebral cortex: Neurogenesis and fate determination

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Reelin is preferentially expressed in neurons synthesizing γ-aminobutyric acid in cortex and hippocampus of adult rats

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<i>Disabled-1</i> acts downstream of <i>Reelin</i> in a signaling pathway that controls laminar organization in the mammalian brain

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The VAB-1 Eph Receptor Tyrosine Kinase Functions in Neural and Epithelial Morphogenesis in C. elegans

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Aberrant Splicing of a Mouse disabled Homolog, mdab1, in the scrambler Mouse

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Involvement of Receptor-like Protein Tyrosine Phosphatase ζ/RPTPβ and Its Ligand Pleiotrophin/Heparin-binding Growth-associated Molecule (HB-GAM) in Neuronal Migration

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The Reeler Mouse as a Model of Brain Development

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Disruption of hippocampal development <i>in vivo</i> by CR-50 mAb against Reelin

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Cerebellar Disorganization Characteristic of Reeler in Scrambler Mutant Mice Despite Presence of Reelin

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The role of migration in central nervous system neuronal development

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A novel neurological mutant mouse, yotari, which exhibits reeler-like phenotype but expresses CR-50 antigen/Reelin

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Abnormal reorganization of preplate neurons and their associated extracellular matrix: An early manifestation of altered neocortical development in the reeler mutant mouse

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New directions for neuronal migration

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Birthdate and Cell Marker Analysis of Scrambler: A Novel Mutation Affecting Cortical Development with a Reeler-Like Phenotype

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Distribution of a reeler gene-related antigen in the developing cerebellum: An immunohistochemical study with an allogeneic antibody CR-50 on normal and reeler mice

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Detection of the reelin breakpoint in reeler mice

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The Eph family in the patterning of neural development

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Cerebellar abnormalities in the disabled (mdab1-1) mouse

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The mouse mutation reeler causes increased adhesion within a subpopulation of early postmitotic cortical neurons

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Tyrosine phosphorylation and axon guidance: of mice and flies

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Roles of Eph receptors and ephrins in neural crest pathfinding

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Molecular mechanisms of axon guidance and target recognition

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Cell-contact-dependent signalling in axon growth and guidance: Eph receptor tyrosine kinases and receptor protein tyrosine phosphatase β

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Neocortical Neurons: Where Do They Come From?

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Roles of Eph receptors and ephrins in neural crest pathfinding

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

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

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Reelin Is a Ligand for Lipoprotein Receptors

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Role of the Reelin Signaling Pathway in Central Nervous System Development

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

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Reelin Binds α3β1 Integrin and Inhibits Neuronal Migration

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Reelin, lipoprotein receptors and synaptic plasticity

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Extracellular Matrix: Functions in the Nervous System

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

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Guiding Neuronal Cell Migrations

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

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The Reelin signaling pathway promotes dendritic spine development in hippocampal neurons

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Proteins of the CNR Family Are Multiple Receptors for Reelin

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

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The reelin receptor ApoER2 recruits JNK-interacting proteins-1 and -2

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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 regulates postnatal neurogenesis and enhances spine hypertrophy and long-term potentiation

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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

Receptor Clustering Is Involved in Reelin Signaling

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Reelin and neuropsychiatric disorders

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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

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

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

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

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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

Layer acquisition by cortical GABAergic interneurons is independent of Reelin signaling

Pla, R., Borrell, V., Flames, N., & Marín, O. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.0245-06.2006 · Cited by 151 · see citing works

New insights into Reelin-mediated signaling pathways

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Reelin delays amyloid-beta fibril formation and rescues cognitive deficits in a model of Alzheimer’s disease

Pujadas, L., Rossi, D., Andrés, R., Teixeira, C. M., Serra-Vidal, B., Parcerisas, A., Maldonado, R., Giralt, E., Carulla, N., & Soriano, E. (2014) · Nature Communications · doi:10.1038/ncomms4443 · Cited by 129 · see citing works

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

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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

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

Canonical and non-canonical Reelin signaling

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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

Reelin deficiency causes granule cell dispersion in epilepsy

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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

Reelin-mediated signaling in neuropsychiatric and neurodegenerative diseases

Knuesel, I. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.04.002 · Cited by 89 · see citing works

A secreted soluble form of ApoE receptor 2 acts as a dominant-negative receptor and inhibits Reelin signaling

Koch, S., Strasser, V., Hauser, C., Fasching, D., Brandes, C., Bajari, T. M., Schneider, W. J., & Nimpf, J. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf599 · Cited by 80 · see citing works

BDNF-modulated Spatial Organization of Cajal–Retzius and GABAergic Neurons in the Marginal Zone Plays a Role in the Development of Cortical Organization

Alcántara, S., Pozas, E., Ibañez, C. F., & Soriano, E. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhi128 · Cited by 71 · see citing works

Reelin regulates the maturation of dendritic spines, synaptogenesis and glial ensheathment of newborn granule cells

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Cullin 5 Regulates Cortical Layering by Modulating the Speed and Duration of Dab1-Dependent Neuronal Migration

Simó, S., Jossin, Y., & Cooper, J. A. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.0035-10.2010 · Cited by 72 · see citing works

The Reelin Receptors Apoer2 and Vldlr Coordinate the Patterning of Purkinje Cell Topography in the Developing Mouse Cerebellum

Larouche, M., Beffert, U., Herz, J., & Hawkes, R. (2008) · PLoS ONE · doi:10.1371/journal.pone.0001653 · Cited by 49 · see citing works

Whole genome analysis in APOE4 homozygotes identifies the DAB1-RELN pathway in Alzheimer's disease pathogenesis

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Trajectory analysis unveils reelin’s role in the directed migration of granule cells in the dentate gyrus

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Neurotrophins regulate ApoER2 proteolysis through activation of the Trk signaling pathway

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Postnatal injection of Reelin protein into the cerebellum ameliorates the motor functions in reeler mouse

Ishii, K., Kohno, T., & Hattori, M. (2023) · Neuroscience Research · doi:10.1016/j.neures.2023.03.004 · Cited by 4 · see citing works

Localization of ApoER2, VLDLR and Dab1 in radial glia: groundwork for a new model of reelin action during cortical development

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

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Regulation of Cortical Neuron Migration by the Reelin Signaling Pathway

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PO4-101 EFFECT OF ENDOTHELIN RECEPTOR ANTAGONISTS ON SYMPATHETIC INNERVATION IN HYPERLIPIDEMIC RABBITS

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