Reelin Is a Serine Protease of the Extracellular Matrix

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

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

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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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Decrease in Reelin and Glutamic Acid Decarboxylase67 (GAD67) Expression in Schizophrenia and Bipolar Disorder

Guidotti, A., Auta, J., Davis, J. M., Gerevini, V. D. G., Dwivedi, Y., Grayson, D. R., Impagnatiello, F., Pandey, G. N., Pesold, C., Sharma, R. P., et al. (2000) · Archives of General Psychiatry · doi:10.1001/archpsyc.57.11.1061 · Cited by 1,222

Activity-based protein profiling: The serine hydrolases

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

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Reelin Is a Ligand for Lipoprotein Receptors

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Reelin Binds α3β1 Integrin and Inhibits Neuronal Migration

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Schizophrenia as a Disorder of Neurodevelopment

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Consensus Paper: Pathological Role of the Cerebellum in Autism

Fatemi, S. H., Aldinger, K. A., Ashwood, P., Bauman, M. L., Blaha, C. D., Blatt, G. J., Chauhan, A., Chauhan, V., Dager, S. R., Dickson, P. E., et al. (2012) · The Cerebellum · doi:10.1007/s12311-012-0355-9 · Cited by 723

Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

Persico, A. M., & Bourgeron, T. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.05.010 · Cited by 575

Environmental toxicants and autism spectrum disorders: a systematic review

Rossignol, D. A., Genuis, S. J., & Frye, R. E. (2014) · Translational Psychiatry · doi:10.1038/tp.2014.4 · Cited by 458

Genome-Wide Association Identifies a Common Variant in the Reelin Gene That Increases the Risk of Schizophrenia Only in Women

Shifman, S., Johannesson, M., Bronstein, M., Chen, S. X., Collier, D. A., Craddock, N. J., Kendler, K. S., Li, T., O’Donovan, M. C., O’Neill, F. A., et al. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.0040028 · Cited by 348

Integrins in regulation of tissue development and function

Danen, E. H. J., & Sonnenberg, A. (2003) · The Journal of Pathology · doi:10.1002/path.1416 · Cited by 318

Reelin is a detachment signal in tangential chain-migration during postnatal neurogenesis

Hack, I., Bancila, M., Loulier, K., Carroll, P., & Cremer, H. (2002) · Nature Neuroscience · doi:10.1038/nn923 · Cited by 327

GABAergic dysfunction in schizophrenia and mood disorders as reflected by decreased levels of glutamic acid decarboxylase 65 and 67 kDa and Reelin proteins in cerebellum

Fatemi, S. H., Stary, J. M., Earle, J. A., Araghi‐Niknam, M., & Eagan, E. (2004) · Schizophrenia Research · doi:10.1016/j.schres.2004.02.017 · Cited by 304

Reelin signaling is impaired in autism

Fatemi, S. H., Snow, A. V., Stary, J. M., Araghi-Niknam, M., Reutiman, T. J., Lee, S., Brooks, A. I., & Pearce, D. A. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.12.018 · Cited by 280

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

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 209

A proteomic study of serum from children with autism showing differential expression of apolipoproteins and complement proteins

Corbett, B. A., Kantor, A. B., Schulman, H., Walker, W. L., Lit, L., Ashwood, P., Rocke, D. M., & Sharp, F. R. (2007) · Molecular Psychiatry · doi:10.1038/sj.mp.4001943 · Cited by 197

Erratum: Integrins in regulation of tissue development and function. J Pathol ; 200: 471–480

Danen, E. H. J., & Sonnenberg, A. (2003) · The Journal of Pathology · doi:10.1002/path.1472 · Cited by 193

Behavioral and regulatory abnormalities in mice deficient in the NPAS1 and NPAS3 transcription factors

Erbel-Sieler, C., Dudley, C., Zhou, Y., Wu, X., Estill, S. J., Han, T., Diaz-Arrastia, R., Brunskill, E. W., Potter, S. S., & McKnight, S. L. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0405310101 · Cited by 178

Chemokines Promote Quiescence and Survival of Human Neural Progenitor Cells

Krathwohl, M. D., & Kaiser, J. L. (2004) · Stem Cells · doi:10.1634/stemcells.22-1-109 · Cited by 166

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

Viral infection, inflammation and schizophrenia

Kneeland, R. E., & Fatemi, S. H. (2013) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2012.02.001 · Cited by 152

The axonal chemorepellant semaphorin 3A is increased in the cerebellum in schizophrenia and may contribute to its synaptic pathology

Eastwood, S. L., Law, A. J., Everall, I., & Harrison, P. J. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001233 · Cited by 145

Converting juvenile into adult plasticity: a role for the brain's extracellular matrix

Gundelfinger, E. D., Frischknecht, R., Choquet, D., & Heine, M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07253.x · Cited by 136

A heterogeneity-based genome search meta-analysis for autism-spectrum disorders

Trikalinos, T. A., Karvouni, A., Zintzaras, E., Ylisaukko‐oja, T., Peltonen, L., Järvelä, I. E., & Ioannidis, J. P. A. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001750 · Cited by 141

Lymphatic Endothelial Cells, Lymphangiogenesis, and Extracellular Matrix

Ji, R. (2006) · Lymphatic Research and Biology · doi:10.1089/lrb.2006.4.83 · Cited by 134

Smooth, rough and upside-down neocortical development

Olson, E. C., & Walsh, C. A. (2002) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(02)00305-2 · Cited by 137

Role of Integrins in the Development of the Cerebral Cortex

Schmid, R. S. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.3.219 · Cited by 132

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 133

Analysis of reelin as a candidate gene for autism

Bonora, E., Beyer, K. S., Lamb, J. A., Parr, J. R., Klauck, S. M., Benner, A., Paolucci, M., Abbott, A., Ragoussis, J., Poustka, A., et al. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001310 · Cited by 132

Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene–environment interactions

D'Amelio, M., Ricci, I., Sacco, R., Liu, X., D'Agruma, L., Muscarella, L. A., Guarnieri, V, Militerni, R., Bravaccio, C., Elia, M., et al. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001714 · Cited by 125

Neuronal connectivity as a convergent target of gene × environment interactions that confer risk for Autism Spectrum Disorders

Stamou, M., Streifel, K. M., Goines, P. E., & Lein, P. J. (2013) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2012.12.001 · Cited by 128

Reduced Blood Levels of Reelin as a Vulnerability Factor in Pathophysiology of Autistic Disorder

Fatemi, S. H., Stary, J. M., & Egan, E. A. (2002) · Cellular and Molecular Neurobiology · doi:10.1023/a:1019857620251 · Cited by 122

Agent-based modeling of morphogenetic systems: advantages and challenges.

Glen, C. M., Kemp, M. L., & Voit, E. O. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006577 · Cited by 116

Integrins in the development function and dysfunction of the nervous system

Clegg, D. (2003) · Frontiers in bioscience · doi:10.2741/1020 · Cited by 119

The Neurobiological Context of Autism

Keller, F., & Persico, A. M. (2003) · Molecular Neurobiology · doi:10.1385/mn:28:1:1 · Cited by 115

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 109

A reelin–integrin receptor interaction regulates Arc mRNA translation in synaptoneurosomes

Dong, E., Caruncho, H. J., Liu, W., Smalheiser, N. R., Grayson, D. R., Costa, E., & Guidotti, A. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1031602100 · Cited by 107

Age-related accumulation of Reelin in amyloid-like deposits

Knuesel, I., Nyffeler, M., Mormède, C., Muhia, M., Meyer, U., Pietropaolo, S., Yee, B. K., Pryce, C. R., LaFerla, F. M., Marighetto, A., et al. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.08.011 · Cited by 94

Reelin‐expressing neurons in the postnatal and adult human hippocampal formation

Ábrahám, H., & Meyer, G. (2003) · Hippocampus · doi:10.1002/hipo.10125 · Cited by 93

The role of reelin in adult synaptic function and the genetic and epigenetic regulation of the reelin gene

Levenson, J. M., Qiu, S., & Weeber, E. J. (2008) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2008.01.001 · Cited by 93

Syndromic autism: causes and pathogenetic pathways

Benvenuto, A., Moavero, R., Alessandrelli, R., Manzi, B., & Curatolo, P. (2009) · World Journal of Pediatrics · doi:10.1007/s12519-009-0033-2 · Cited by 93

Transcriptomic and proteomic analyses of seasonal photoperiodism in the pea aphid

Trionnaire, G. L., Francis, F., Jaubert‐Possamai, S., Bonhomme, J., Pauw, E. D., Gauthier, J.-P., Haubruge, É., Legeai, F., Prunier‐Leterme, N., Simon, J., et al. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-456 · Cited by 93

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

Luque, J. M., Morante, J., & Fairén, A. (2003) · Developmental Brain Research · doi:10.1016/s0165-3806(02)00604-1 · Cited by 86

The Structure of Human Prokallikrein 6 Reveals a Novel Activation Mechanism for the Kallikrein Family

Gomis‐Rüth, F. X., Bayés, À., Sotiropoulou, G., Pampalakis, G., Tsetsenis, T., Villegas, S., Avilés, F. X., & Coll, M. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m201534200 · Cited by 83

Reelin function in neural stem cell biology

Kim, H. M., Qu, T., Kriho, V., Lacor, P., Smalheiser, N. R., Pappas, G. D., Guidotti, A., Costa, E., & Sugaya, K. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.062698299 · Cited by 84

C2GnT-M is downregulated in colorectal cancer and its re-expression causes growth inhibition of colon cancer cells

Huang, M.-C., Chen, H., Huang, H.-C., Huang, J. C., Liang, J.-T., Shen, T.-L., Lin, N.-Y., Ho, C., Cho, I.-M., & Hsu, S.-M. (2006) · Oncogene · doi:10.1038/sj.onc.1209350 · Cited by 79

The role of Reelin in pathology of autism

Fatemi, S. H. (2002) · Molecular Psychiatry · doi:10.1038/sj.mp.4001248 · Cited by 79

Teneurin 2 is expressed by the neurons of the thalamofugal visual system in situ and promotes homophilic cell-cell adhesion in vitro

Rubin, B. P., Tucker, R. P., Brown-Luedi, M., Martin, D., & Chiquet‐Ehrismann, R. (2002) · Development · doi:10.1242/dev.129.20.4697 · Cited by 73

A Genome-wide Analysis Identifies Genetic Variants in the RELN Gene Associated with Otosclerosis

Schrauwen, I., Ealy, M., Huentelman, M. J., Thys, M., Homer, N., Vanderstraeten, K., Fransén, E., Corneveaux, J. J., Craig, D. W., Claustres, M., et al. (2009) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2009.01.023 · Cited by 71

iTRAQ‐Based Proteomic Analysis Reveals Protein Profile in Plasma from Children with Autism

Shen, L., Zhang, K., Feng, C., Chen, Y., Li, S., Iqbal, J., Liao, L., Zhao, Y., & Zhai, J. (2017) · PROTEOMICS - CLINICAL APPLICATIONS · doi:10.1002/prca.201700085 · Cited by 70

Extracellular factors that regulate neuronal migration in the central nervous system

Sobeih, M. M., & Corfas, G. (2002) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(02)00040-0 · Cited by 68

Casting a net on dendritic spines: The extracellular matrix and its receptors

Dansie, L. E., & Ethell, I. M. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20963 · Cited by 68

Physiological and Pathological Roles of α3β1 Integrin

Tsuji, T. (2004) · The Journal of Membrane Biology · doi:10.1007/s00232-004-0696-5 · Cited by 65

Neuroimmunologic and Neurotrophic Interactions in Autism Spectrum Disorders: Relationship to Neuroinflammation

Ohja, K., Gozal, E., Fahnestock, M. L., Cai, L., Cai, J., Freedman, J. H., Switala, A., El-Baz, A. S., & Barnes, G. N. (2018) · NeuroMolecular Medicine · doi:10.1007/s12017-018-8488-8 · Cited by 66

Reelin Immunoreactivity in the Adult Primate Brain: Intracellular Localization in Projecting and Local Circuit Neurons of the Cerebral Cortex, Hippocampus and Subcortical Regions

Martínez‐Cerdeño, V. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.12.1298 · Cited by 64

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

Reelin Glycoprotein in Autism and Schizophrenia

Fatemi, S. H. (2005) · International review of neurobiology · doi:10.1016/s0074-7742(05)71008-4 · Cited by 60

The Genetics of otosclerosis

Ealy, M., & Smith, R. J. (2009) · Hearing Research · doi:10.1016/j.heares.2009.07.002 · Cited by 57

Cellular Form of Prion Protein Inhibits Reelin-Mediated Shedding of Caspr from the Neuronal Cell Surface to Potentiate Caspr-Mediated Inhibition of Neurite Outgrowth

Devanathan, V., Jakovcevski, I., Santuccione, A., Li, S., Lee, H. J., Peles, E., Leshchyns’ka, I., Sytnyk, V., & Schachner, M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5657-09.2010 · Cited by 52

Polymorphic GGC repeat differentially regulates human reelin gene expression levels

Persico, A. M., Levitt, P., & Pimenta, A. F. (2006) · Journal of Neural Transmission · doi:10.1007/s00702-006-0441-6 · Cited by 52

Go or Stop? Divergent Roles of Reelin in Radial Neuronal Migration

Zhao, S., & Frotscher, M. (2010) · The Neuroscientist · doi:10.1177/1073858410367521 · Cited by 53

Expression and localization of reelin in human odontoblasts

Maurin, J.-C., Couble, M., Didier‐Bazès, M., Brisson, C., Magloire, H., & Bleicher, F. (2004) · Matrix Biology · doi:10.1016/j.matbio.2004.06.005 · Cited by 51

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

Lintas, C., Sacco, R., & Persico, A. M. (2016) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-016-9151-z · Cited by 50

An immune-induced Reeler protein is involved in the Bombyx mori melanization cascade

Bao, Y., Xue, J., Wu, W., Wang, Y., Lv, Z.-Y., & Zhang, C. (2011) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2011.05.001 · Cited by 51

Reelin and apoE actions on signal transduction, synaptic function and memory formation

Rogers, J. T., & Weeber, E. J. (2008) · Neuron Glia Biology · doi:10.1017/s1740925x09990184 · Cited by 48

Seasonal photoperiodism regulates the expression of cuticular and signalling protein genes in the pea aphid

Trionnaire, G. L., Jaubert‐Possamai, S., Sabater‐Muñoz, B., Benedetto, A., Bonhomme, J., Prunier‐Leterme, N., Martinez-Torres, D., Simon, J., & Tagu, D. (2007) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2007.06.008 · Cited by 49

Action control processes in autism spectrum disorder – Insights from a neurobiological and neuroanatomical perspective

Chmielewski, W. X., & Beste, C. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2014.11.002 · Cited by 51

Structural and mechanistic insight into how antibodies inhibit serine proteases

Ganesan, R., Eigenbrot, C. W., & Kirchhofer, D. (2010) · Biochemical Journal · doi:10.1042/bj20100634 · Cited by 49

Extracellular proteases in epilepsy

Łukasiuk, K., Wilczynski, G. M., & Kaczmarek, L. (2011) · Epilepsy Research · doi:10.1016/j.eplepsyres.2011.08.002 · Cited by 47

Reelin Signaling and Cdk5 in the Control of Neuronal Positioning

Ohshima, T., & Mikoshiba, K. (2002) · Molecular Neurobiology · doi:10.1385/mn:26:2-3:153 · Cited by 46

Reelin immunoreactivity in lymphatics and liver during development and adult life

Samama, B., & Boehm, N. (2005) · The Anatomical Record Part A Discoveries in Molecular Cellular and Evolutionary Biology · doi:10.1002/ar.a.20202 · Cited by 43

Neocortical RELN promoter methylation increases significantly after puberty

Lintas, C., & Persico, A. M. (2010) · Neuroreport · doi:10.1097/wnr.0b013e328334b343 · Cited by 43

In Patas monkey, glutamic acid decarboxylase‐67 and reelin mRNA coexpression varies in a manner dependent on layers and cortical areas

Rodriguez, M. A., Caruncho, H. J., Costa, E., Pesold, C., Liu, W., & Guidotti, A. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10341 · Cited by 42

Reelin Signaling in Neurodevelopmental Disorders and Neurodegenerative Diseases

Joly‐Amado, A., Kulkarni, N., & Nash, K. R. (2023) · Brain Sciences · doi:10.3390/brainsci13101479 · Cited by 47

Longistatin is an unconventional serine protease and induces protective immunity against tick infestation

Anisuzzaman, A., Islam, M. K., Alim, M. A., Miyoshi, T., Hatta, T., Yamaji, K., Matsumoto, Y., Fujisaki, K., & Tsuji, N. (2011) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2011.12.002 · Cited by 41

Reelin‐immunoreactive neurons, axons, and neuropil in the adult ferret brain: Evidence for axonal secretion of reelin in long axonal pathways

Martínez‐Cerdeño, V., Galazo, M. J., & Clascá, F. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10748 · Cited by 43

Retardation of neurobehavioral development and reelin down-regulation regulated by further DNA methylation in the hippocampus of the rat pups are associated with maternal deprivation

Qin, L., Tu, W.-Q., Sun, X.-M., Zhang, J., Chen, Y., & Zhao, H. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.10.018 · Cited by 42

Treadmill exercise ameliorates motor disturbance through inhibition of apoptosis in the cerebellum of valproic acid-induced autistic rat pups

Kim, J., Shin, M., Seo, T.-B., Ji, E., BAEK, S.-S., Lee, S., Park, J.-K., & Kim, C. (2013) · Molecular Medicine Reports · doi:10.3892/mmr.2013.1518 · Cited by 38

Abnormal Cell Properties and Down-Regulated FAK-Src Complex Signaling in B Lymphoblasts of Autistic Subjects

Wei, H., Malik, M. N., Sheikh, A. M., Merz, G., Brown, W. T., & Li, X. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2011.03.034 · Cited by 40

Extracellular proteases and their inhibitors ingenetic diseases of the central nervous system

Molinari, F., Meskanaite, V., Münnich, A., Sonderegger, P., & Colleaux, L. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddg276 · Cited by 36

Analysis of common genetic variants identifiesRELNas a risk gene for schizophrenia in Chinese population

Li, M., Luo, X., Xiao, X., Shi, L., Liu, X., Yin, L.-D., Ma, X., Yang, S.-Y., Pu, X., Yu, J. S., et al. (2011) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2011.587891 · Cited by 35

Enhanced APOE2 transmission rates in families with autistic probands

Persico, A. M., D’Agruma, L., Zelante, L., Militerni, R., Bravaccio, C., Schneider, C., Melmed, R. D., Trillo, S., Montecchi, F., Elia, M., et al. (2004) · Psychiatric Genetics · doi:10.1097/01.ypg.0000128768.37838.17 · Cited by 34

Reelin is a platelet protein and functions as a positive regulator of platelet spreading on fibrinogen

Tseng, W.-L., Huang, C., Chong, K., Liao, C.-H., Stern, A., Cheng, J.-C., & Tseng, C. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-0201-5 · Cited by 31

Serine proteases regulating synaptic plasticity

Shiosaka, S. (2004) · Anatomical Science International · doi:10.1111/j.1447-073x.2004.00080.x · Cited by 29

Targeting Glycoproteins as a therapeutic strategy for diabetes mellitus and its complications

Naseri, R., Navabi, S. J., Samimi, Z., Mishra, A. P., Nigam, M., Chandra, H., Olatunde, A., Tijjani, H., Morais‐Urano, R. P., & Farzaei, M. H. (2020) · DARU Journal of Pharmaceutical Sciences · doi:10.1007/s40199-020-00327-y · Cited by 31

Integrin α3β1 Represses Reelin Expression in Breast Cancer Cells to Promote Invasion

Ndoye, A., Miskin, R. P., & DiPersio, C. M. (2021) · Cancers · doi:10.3390/cancers13020344 · Cited by 27

Reelin signalling in neuroblastoma: Migratory switch in metastatic stages

Becker, J., Fröhlich, J., Perske, C., Pavlaković, H., & Wilting, J. (2012) · International Journal of Oncology · doi:10.3892/ijo.2012.1488 · Cited by 29

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

Environmental Factors in the Onset of Autism Spectrum Disorder

Persico, A. M., & Merelli, S. (2014) · Current Developmental Disorders Reports · doi:10.1007/s40474-013-0002-2 · Cited by 26

cDNA cloning and expression of bacteria-induced Hdd11 gene from eri-silkworm, Samia cynthia ricini

Bao, Y., Mega, K., Yamano, Y., & Morishima, I. (2003) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cca.2003.10.007 · Cited by 26

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