Brain Development in Normal and reeler Mice: the Phenotype

Liver X receptor β and thyroid hormone receptor α in brain cortical layering

Tan, X.-J., Fan, X., Kim, H., Butler, R., Webb, P., Warner, M. N., & Gustafsson, J.-Α. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006162107 · Cited by 32

Ectopic corticospinal tract and corticothalamic tract neurons in the cerebral cortex of yotari and reeler mice

Yamamoto, T., Sakakibara, S., Mikoshiba, K., & Terashima, T. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10678 · Cited by 33

Developmental distribution of reelin‐positive cells and their secreted product in the rodent spinal cord

Kubasak, M. D., Brooks, R., Chen, S., Villeda, S., & Phelps, P. E. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10946 · Cited by 33

Unusual Patch-Matrix Organization in the Retrosplenial Cortex of the reeler Mouse and Shaking Rat Kawasaki

Ichinohe, N., Knight, A., Ogawa, M., Ohshima, T., Mikoshiba, K., Yoshihara, Y., Terashima, T., & Rockland, K. S. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm148 · Cited by 30

Disabled‐1 mRNA and protein expression in developing human cortex

Meyer, G., de Rouvroit, C. L., Goffinet, A. M., & Wahle, P. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02480.x · Cited by 28

Molecular specializations of deep cortical layer analogs in songbirds

Nevue, A. A., Lovell, P. V., Wirthlin, M. E., & Mello, C. V. (2020) · Scientific Reports · doi:10.1038/s41598-020-75773-4 · Cited by 28

The superficial layers of the superior colliculus are cytoarchitectually and myeloarchitectually disorganized in the reelin-deficient mouse, reeler

Baba, K., Sakakibara, S., Setsu, T., & Terashima, T. (2006) · Brain Research · doi:10.1016/j.brainres.2006.09.113 · Cited by 27

Reelin immunoreactivity in the larval sea lamprey brain

Pérez‐Costas, E., Meléndez‐Ferro, M., Santos, Y., Anadón, R., Rodicio, M. C., & Caruncho, H. J. (2002) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(01)00156-9 · Cited by 26

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

Wang, S., Brunne, B., Zhao, S., Chai, X., Li, J., Lau, J., Failla, A. V., Zobiak, B., Sibbe, M., Westbrook, G. L., et al. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.0988-17.2017 · Cited by 26

Transient and compartmental expression of the reeler gene product Reelin in the developing rat striatum

Nishikawa, S., Goto, S., Hamasaki, T., Ogawa, M., & Ushio, Y. (1999) · Brain Research · doi:10.1016/s0006-8993(99)02136-8 · Cited by 25

Book Review: Human Neocortical Development: The Importance of Embryonic and Early Fetal Events

Meyer, G. (2001) · The Neuroscientist · doi:10.1177/107385840100700407 · Cited by 24

Crosstalk of thyroid hormone receptor and liver X receptor in lipid metabolism and beyond [Review]

Hashimoto, K., & Mori, M. (2011) · Endocrine Journal · doi:10.1507/endocrj.ej11-0114 · Cited by 23

Spatiotemporal distribution of tenascin‐R in the developing human cerebral cortex parallels neuronal migration

Ayachi, I. E., Fernandez, C., Baeza, N., de Paula, A. M., Pesheva, P., & Figarella‐Branger, D. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22632 · Cited by 25

Reelin signaling modulates GABAB receptor function in the neocortex

Hamad, M. I. K., Jbara, A., Rabaya, O., Petrova, P., Daoud, S., Melliti, N., Meseke, M., Lutz, D., Petrasch‐Parwez, E., Schwitalla, J. C., et al. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.14990 · Cited by 22

Changes in reelin expression in the mouse olfactory bulb after chemical lesion to the olfactory epithelium

Okuyama‐Yamamoto, A., Yamamoto, T., Miki, A., & Terashima, T. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04082.x · Cited by 21

Two Novel CNRs from the CNR Gene Cluster Have Molecular Features Distinct from Those of CNR1 to 8

Takei, Y., Hamada, S., Senzaki, K., Mutoh, T., Sugino, H., & Yagi, T. (2001) · Genomics · doi:10.1006/geno.2000.6468 · Cited by 21

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

Krüger, M. T., Zhao, S., Chai, X., Brunne, B., Bouché, E., Bock, H. H., & Frotscher, M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07433.x · Cited by 20

Cajal‐Retzius neurons are required for the development of the human hippocampal fissure

Meyer, G., González‐Arnay, E., Moll, U. M., Nemajerová, A., Tissir, F., & González‐Gómez, M. (2019) · Journal of Anatomy · doi:10.1111/joa.12947 · Cited by 19

Epilepsy-causing Reelin mutations result in impaired secretion and intracellular degradation of mutant proteins

Dazzo, E., & Nobile, C. (2021) · Human Molecular Genetics · doi:10.1093/hmg/ddab271 · Cited by 18

Laminar distribution of neurotransmitter receptors in different reeler mouse brain regions

Cremer, C. M., Lübke, J. H. R., Palomero-Gallagher, N., & Zilles, K. (2011) · Brain Structure and Function · doi:10.1007/s00429-011-0303-3 · Cited by 17

Neuronal migration and its disorders affecting the CA3 region

Belvindrah, R., Nosten-Bertrand, M., & Francis, F. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00063 · Cited by 18

Cell death and neurodegeneration in the postnatal development of cerebellar vermis in normal and Reeler mice

Castagna, C., Merighi, A., & Lossi, L. (2016) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2016.01.010 · Cited by 18

Animal Models of Epilepsy

(2009) · Neuromethods · doi:10.1007/978-1-60327-263-6 · Cited by 18

Reelin-expressing neurons in the anterior commissure and corpus callosum of the rat

Misaki, K., Kikkawa, S., & Terashima, T. (2004) · Developmental Brain Research · doi:10.1016/j.devbrainres.2003.10.009 · Cited by 18

Reduced Reelin Expression in the Hippocampus after Traumatic Brain Injury

Pozzo, V. D., Crowell, B., Briski, N., Crockett, D. P., & D’Arcangelo, G. (2020) · Biomolecules · doi:10.3390/biom10070975 · Cited by 16

RBX2 maintains final retinal cell position in a DAB1-dependent and -independent fashion

Fairchild, C. L. A., Hino, K., Han, J. S., Miltner, A. M., Peinado, G., Brown, C. E., Burns, M. E., Torre, A. L., & Simó, S. (2018) · Development · doi:10.1242/dev.155283 · Cited by 17

Reelin is expressed in the accessory olfactory system, but is not a guidance cue for vomeronasal axons

Teillon, S., Yiu, G. C., & Walsh, C. A. (2003) · Developmental Brain Research · doi:10.1016/s0165-3806(02)00616-8 · Cited by 17

Laminar distribution of synaptopodin in normal and reeler mouse brain depends on the position of spine‐bearing neurons

Deller, T., Haas, C. A., LaFaver, K., Turco, D. D., Coulin, C., Gebhardt, C., Drakew, A., Schwarz, K., Mundel, P. H., & Frotscher, M. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10362 · Cited by 17

Histological study in the brain of the reelin/Dab1-compound mutant mouse

Yamamoto, T., Setsu, T., Okuyama‐Yamamoto, A., & Terashima, T. (2009) · Anatomical Science International · doi:10.1007/s12565-008-0009-7 · Cited by 16

Post-natal development of the Reeler mouse cerebellum: An ultrastructural study

Castagna, C., Aimar, P., Alasia, S., & Lossi, L. (2013) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2013.11.004 · Cited by 15

Distribution and orientation of nerve fibers and myelin assembly in a brain section retrieved by small-angle neutron scattering

Maiti, S., Frielinghaus, H., Gräßel, D., Dulle, M., Axer, M., & Förster, S. (2021) · Scientific Reports · doi:10.1038/s41598-021-92995-2 · Cited by 13

Expression of reelin in the dorsal cochlear nucleus of the mouse

Takaoka, Y., Setsu, T., Misaki, K., Yamauchi, T., & Terashima, T. (2005) · Developmental Brain Research · doi:10.1016/j.devbrainres.2005.07.014 · Cited by 13

The Control of Cortical Folding: Multiple Mechanisms, Multiple Models

Moffat, A., & Schuurmans, C. J. (2023) · The Neuroscientist · doi:10.1177/10738584231190839 · Cited by 12

Migrating neurons cross a reelin‐rich territory to form an organized tissue out of embryonic cortical slices

Hedin‐Pereira, C., DeMoraes, E. C. P., Santiago, M. F., Méndez‐Otero, R., & Lent, R. (2000) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2000.01332.x · Cited by 12

The Subpial Granular Layer in the Developing Cerebral Cortex of Rodents

Meyer, G., Castro, R., Soria, J. M., & Fairén, A. (2000) · Results and problems in cell differentiation · doi:10.1007/978-3-540-48002-0_12 · Cited by 11

The Reelin-Signaling Pathway and Mouse Cortical Development

Bar, I., de Rouvroit, C. L., & Goffinet, A. M. (2000) · Results and problems in cell differentiation · doi:10.1007/978-3-540-48002-0_11 · Cited by 10

Development and Developmental Disorders of the Cerebral Cortex

ten Donkelaar, H. J., Lammens, M. M. Y., Aronica, E., van Bokhoven, H., Ulzen, K. K.-V., & Hori, A. (2014) · Springer eBooks · doi:10.1007/978-3-642-54687-7_10 · Cited by 9

The structure-function relationship of a signaling-competent, dimeric Reelin fragment

Turk, L. S., Kuang, X., Pozzo, V. D., Patel, K., Chen, M., Huynh, K. W., Currie, M. J., Mitchell, D., Dobson, R. C. J., D’Arcangelo, G., et al. (2021) · Structure · doi:10.1016/j.str.2021.05.012 · Cited by 9

Reelin immunoreactivity in the adult sea lamprey brain

Pérez‐Costas, E., Meléndez‐Ferro, M., Pérez‐García, C. G., Caruncho, H. J., & Rodicio, M. C. (2003) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2003.08.005 · Cited by 9

Cloning of HumanDAB1and Mapping to Chromosome 1p31–p32

de Rouvroit, C. L., & Goffinet, A. M. (1998) · Genomics · doi:10.1006/geno.1998.5523 · Cited by 10

Reelin Alleviates Mesenchymal Stem Cell Senescence and Reduces Pathological α-Synuclein Expression in an In Vitro Model of Parkinson’s Disease

Cho, E., Park, J., Kim, K., Kim, M., & Cho, S. (2021) · Genes · doi:10.3390/genes12071066 · Cited by 8

Defective Reelin/Dab1 signaling pathways associated with disturbed hippocampus development of homozygous yotari mice

Arimitsu, N. N., Mizukami, Y., Shimizu, J., Takai, K., Tomoko, S., & Suzuki, N. (2021) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2021.103614 · Cited by 7

Increased Callosal Connectivity in Reeler Mice Revealed by Brain-Wide Input Mapping of VIP Neurons in Barrel Cortex

Hafner, G., Guy, J., Witte, M., Truschow, P., Rüppel, A., Sirmpilatze, N., Dadarwal, R., Boretius, S., & Staiger, J. F. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa280 · Cited by 10

The Reelin Gene and Its Functions in Brain Development

Huang, C.-C., & D’Arcangelo, G. (2008) · Springer eBooks · doi:10.1007/978-0-387-76761-1_1 · Cited by 8

Neuronal Migration in the Developing Brain

Polleux, F., & Anton, E. S. (2006) · Kluwer Academic Publishers-Plenum Publishers eBooks · doi:10.1007/0-387-28117-7_8 · Cited by 7

Multifaceted roles of MeCP2 in cellular regulation and phase separation: implications for neurodevelopmental disorders, depression, and oxidative stress

Good, K., Kalani, L., Vincent, J. B., & Ausió, J. (2025) · Biochemistry and Cell Biology · doi:10.1139/bcb-2024-0237 · Cited by 6

A modification of Representational Difference Analysis, with application to the cloning of a candidate in the Reelin signalling pathway

Kuvbachieva, A. A., & Goffinet, A. M. (2002) · BMC Molecular Biology · doi:10.1186/1471-2199-3-6 · Cited by 6

Radial Migration of Neurons in the Cerebral Cortex

Stanco, A., & Anton, E. S. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00028-4 · Cited by 5

Functional Analysis of RELN S2486G Mutation and its Contribution to Pathogenesis of Ankylosing Spondylitis

Esmaeilzadeh‐Gharehdaghi, E., Razmara, E., Bitaraf, A., Jamshidi, A., Mahmoudi, M., & Garshasbi, M. (2020) · Archives of Iranian Medicine · doi:10.34172/aim.2020.87 · Cited by 6

From Spontaneous to Induced Neurological Mutations: A Personal Witness of the Ascent of the Mouse Model

RAKIC, P. T. (2000) · Results and problems in cell differentiation · doi:10.1007/978-3-540-48002-0_1 · Cited by 5

Normal connectivity of thalamorecipient networks in barrel equivalents of the reeler cortex

Meeuwissen, A., Möck, M., Staiger, J. F., & Guy, J. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad072 · Cited by 4

Development and Developmental Disorders of the Cerebral Cortex

ten Donkelaar, H. J., Vasung, L., Molnár, Z., Aronica, E., Lammens, M. M. Y., van Bokhoven, H., Ulzen, K. K.-V., & Hori, A. (2023) · Springer eBooks · doi:10.1007/978-3-031-26098-8_10 · Cited by 3

Animal Models of Epilepsy

Calcagnotto, M. E., & Baraban, S. C. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-5316-3.00051-4 · Cited by 2

Structure of Reelin repeat 8 and the adjacent C-terminal region

Turk, L. S., Currie, M. J., Dobson, R. C. J., & Comoletti, D. (2022) · Biophysical Journal · doi:10.1016/j.bpj.2022.06.002 · Cited by 2

Neuropathology of schizophrenia: is there evidence for a neurodevelopmental disorder?

Falkai, P., Vogeley, K. T., Tepest, R., & Schneider-Axmann, T. (2002) · Steinkopff eBooks · doi:10.1007/978-3-642-57516-7_5 · Cited by 1

Ultrastructural Localization of Reelin

Roberts, R. C., & Pérez‐Costas, E. (2008) · Springer eBooks · doi:10.1007/978-0-387-76761-1_8

Reelin and Lissencephaly

Parrini, E., & Guerrini, R. (2008) · Springer eBooks · doi:10.1007/978-0-387-76761-1_21

Ethanol, Vitamins, and Brain Dysfunction

González‐Reimers, E., Fernández-Rodríguez, C. M., González‐Arnay, E., & Santolaria-Fernández, F. J. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800213-1.00044-4

Clinical Aspects of the Inherited Cerebellar Malformations

Marzban, A., Vafaee‐Shahi, M., & Azarkhish, K. (2017) · Contemporary clinical neuroscience · doi:10.1007/978-3-319-59749-2_19

Clinical Aspects of the Inherited Cerebellar Malformations

Marzban, A., Ghiyamihoor, F., Vafaee‐Shahi, M., & Azarkhish, K. (2023) · Contemporary clinical neuroscience · doi:10.1007/978-3-031-23104-9_22

Early postnatal reelin treatment suppresses epileptic spasms in a rat model of cortical malformation

Lee, M., Kim, E.-J., & Yum, M.-S. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110637

KIAA 0510, Ténascine R, et astrocytomes pilocytiques

Ayachi, I. E. (2010) · theses.fr (ABES) · doi:10.70675/0e9b78fcz07aaz49baz9438z0925e5029be4

Dysfonctionnements préfrontaux et pharmacothérapies dans des modèles murins de maladies spychiatriques

Bouamrane, L. (2015) · theses.fr (ABES) · doi:10.70675/00597159za953z4221z95b8z57a6c1d48c8e

Reelin promotes cerebral angiogenesis via mTOR/HIF-1α-mediated transcriptional upregulation of Netrin-4

Feng, Z., Pan, M., Liu, H., Liu, M., Yang, J., Wang, C., Yao, R., Liu, H., & Fu, Y. (2026) · Tissue and Cell · doi:10.1016/j.tice.2026.103727

Broca's region revisited: Cytoarchitecture and intersubject variability

Amunts, K., Schleicher, A., B�rgel, U., Mohlberg, H., Uylings, H. B. M., & Zilles, K. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990920)412:2

Untitled work

Herman (2000) · doi:10.1002/1096-9861(20000703)422:3

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

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