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Reelin-Related Disturbances in Depression: Implications for Translational Studies

https://doi.org/10.3389/fncel.2016.00048

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/archpsyc.57.11.1061openalex-snapshot

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

inferredcites →https://doi.org/10.1002/(sici)1097-0177(199710)210:2<157::aid-aja8>3.0.co;2-fopenalex-snapshot

Expression ofreelin, the gene responsible for the reeler mutation, in embryonic development and adulthood in the mouse

inferredcites →https://doi.org/10.1002/ar.a.20202openalex-snapshot

Reelin immunoreactivity in lymphatics and liver during development and adult life

inferredcites →https://doi.org/10.1002/cne.10341openalex-snapshot

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

inferredcites →https://doi.org/10.1002/cne.20408openalex-snapshot

Ultrastructural localization of reelin in the cortex in post-mortem human brain

inferredcites →https://doi.org/10.1006/brbi.1995.1005openalex-snapshot

Suppressed T Cell and Macrophage Function in the "Reeler" (rl/rl) Mutant, a Murine Strain with Elevated Cerebellar Norepinephrine Concentration

inferredcites →https://doi.org/10.1007/978-3-642-72257-8openalex-snapshot

The Reeler Mouse as a Model of Brain Development

inferredcites →https://doi.org/10.1007/978-3-642-72257-8_1openalex-snapshot

Brain Development in Normal and reeler Mice: the Phenotype

inferredcites →https://doi.org/10.1007/s00018-009-0201-5openalex-snapshot

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

inferredcites →https://doi.org/10.1007/s00418-012-0912-9openalex-snapshot

Congruence of vascular network remodeling and neuronal dispersion in the hippocampus of reelin-deficient mice

inferredcites →https://doi.org/10.1007/s11011-008-9118-1openalex-snapshot

The inflammatory & neurodegenerative (I&ND) hypothesis of depression: leads for future research and new drug developments in depression

inferredcites →https://doi.org/10.1007/s11920-011-0210-6openalex-snapshot

Inflammatory Biomarkers in Depression: An Opportunity for Novel Therapeutic Interventions

inferredcites →https://doi.org/10.1016/0896-6273(95)90258-9openalex-snapshot

Cortical development: View from neurological mutants two decades later

inferredcites →https://doi.org/10.1016/j.bbi.2010.10.008openalex-snapshot

Immune suppression and immune activation in depression

inferredcites →https://doi.org/10.1016/j.bbr.2004.05.013openalex-snapshot

Effect of repeated corticosterone injections and restraint stress on anxiety and depression-like behavior in male rats

inferredcites →https://doi.org/10.1016/j.bbr.2005.11.019openalex-snapshot

Effect of different doses of corticosterone on depression-like behavior and HPA axis responses to a novel stressor

inferredcites →https://doi.org/10.1016/j.biopsych.2004.10.019openalex-snapshot

Neurochemical markers for schizophrenia, bipolar disorder, and major depression in postmortem brains

inferredcites →https://doi.org/10.1016/j.biopsych.2004.12.018openalex-snapshot

Reelin signaling is impaired in autism

inferredcites →https://doi.org/10.1016/j.biopsych.2008.02.022openalex-snapshot

Drug-Dependent Requirement of Hippocampal Neurogenesis in a Model of Depression and of Antidepressant Reversal

inferredcites →https://doi.org/10.1016/j.biopsych.2008.11.029openalex-snapshot

Inflammation and Its Discontents: The Role of Cytokines in the Pathophysiology of Major Depression

inferredcites →https://doi.org/10.1016/j.brainres.2005.12.049openalex-snapshot

NMDA-receptor proteins are upregulated in the hippocampus of postnatal heterozygous reeler mice

inferredcites →https://doi.org/10.1016/j.brainres.2014.10.050openalex-snapshot

Differential effects of corticosterone on the colocalization of reelin and neuronal nitric oxide synthase in the adult hippocampus in wild type and heterozygous reeler mice

inferredcites →https://doi.org/10.1016/j.cell.2014.07.035openalex-snapshot

Reelin Signaling Specifies the Molecular Identity of the Pyramidal Neuron Distal Dendritic Compartment

inferredcites →https://doi.org/10.1016/j.ejphar.2011.05.008openalex-snapshot

Repeated citalopram administration counteracts kainic acid-induced spreading of PSA-NCAM-immunoreactive cells and loss of reelin in the adult mouse hippocampus

inferredcites →https://doi.org/10.1016/j.expneurol.2008.12.029openalex-snapshot

Exogenous reelin prevents granule cell dispersion in experimental epilepsy

inferredcites →https://doi.org/10.1016/j.febslet.2013.11.002openalex-snapshot

Erythroid differentiation is augmented in Reelin‐deficient K562 cells and homozygous reeler mice

inferredcites →https://doi.org/10.1016/j.it.2005.11.006openalex-snapshot

Cytokines sing the blues: inflammation and the pathogenesis of depression

inferredcites →https://doi.org/10.1016/j.jad.2011.12.041openalex-snapshot

Serotonin transporter clustering in blood lymphocytes as a putative biomarker of therapeutic efficacy in major depressive disorder

inferredcites →https://doi.org/10.1016/j.jad.2013.06.004openalex-snapshot

CRP, IL-6 and depression: A systematic review and meta-analysis of longitudinal studies

inferredcites →https://doi.org/10.1016/j.jad.2014.03.011openalex-snapshot

Serotonin 2A receptor clustering in peripheral lymphocytes is altered in major depression and may be a biomarker of therapeutic efficacy

inferredcites →https://doi.org/10.1016/j.jad.2014.07.032openalex-snapshot

A review of the relationship between proinflammatory cytokines and major depressive disorder

inferredcites →https://doi.org/10.1016/j.jchemneu.2003.08.005openalex-snapshot

Reelin immunoreactivity in the adult sea lamprey brain

inferredcites →https://doi.org/10.1016/j.mcn.2014.05.001openalex-snapshot

Expression and regulation of reelin and its receptors in the enteric nervous system

inferredcites →https://doi.org/10.1016/j.neubiorev.2006.04.001openalex-snapshot

Reelin down-regulation in mice and psychosis endophenotypes

inferredcites →https://doi.org/10.1016/j.neulet.2009.05.050openalex-snapshot

Repeated exposure to corticosterone, but not restraint, decreases the number of reelin-positive cells in the adult rat hippocampus

inferredcites →https://doi.org/10.1016/j.neures.2014.12.013openalex-snapshot

Reelin has a preventive effect on phencyclidine-induced cognitive and sensory-motor gating deficits

inferredcites →https://doi.org/10.1016/j.neuron.2005.07.007openalex-snapshot

Modulation of Synaptic Plasticity and Memory by Reelin Involves Differential Splicing of the Lipoprotein Receptor Apoer2

inferredcites →https://doi.org/10.1016/j.neuron.2009.04.017openalex-snapshot

Neurogenesis-Dependent and -Independent Effects of Fluoxetine in an Animal Model of Anxiety/Depression

inferredcites →https://doi.org/10.1016/j.neuron.2013.08.024openalex-snapshot

Reelin Mobilizes a VAMP7-Dependent Synaptic Vesicle Pool and Selectively Augments Spontaneous Neurotransmission

inferredcites →https://doi.org/10.1016/j.neuropharm.2010.09.007openalex-snapshot

Reelin as a putative vulnerability factor for depression: Examining the depressogenic effects of repeated corticosterone in heterozygous reeler mice

inferredcites →https://doi.org/10.1016/j.neuropharm.2011.09.003openalex-snapshot

The neurogenesis hypothesis of affective and anxiety disorders: Are we mistaking the scaffolding for the building?

inferredcites →https://doi.org/10.1016/j.neuropharm.2012.08.015openalex-snapshot

The involvement of Reelin in neurodevelopmental disorders

inferredcites →https://doi.org/10.1016/j.neuropharm.2013.04.012openalex-snapshot

The progressive development of depression-like behavior in corticosterone-treated rats is paralleled by slowed granule cell maturation and decreased reelin expression in the adult dentate gyrus

inferredcites →https://doi.org/10.1016/j.neuroscience.2010.04.023openalex-snapshot

Chronic high corticosterone reduces neurogenesis in the dentate gyrus of adult male and female rats

inferredcites →https://doi.org/10.1016/j.neuroscience.2011.05.050openalex-snapshot

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

inferredcites →https://doi.org/10.1016/j.neuroscience.2012.11.037openalex-snapshot

Altered GABAergic and glutamatergic activity within the rat hippocampus and amygdala in rats subjected to repeated corticosterone administration but not restraint stress

inferredcites →https://doi.org/10.1016/j.neuroscience.2015.01.031openalex-snapshot

Reelin influences the expression and function of dopamine D2 and serotonin 5-HT2A receptors: A comparative study

inferredcites →https://doi.org/10.1016/j.neuroscience.2015.11.006openalex-snapshot

Effectiveness of different corticosterone administration methods to elevate corticosterone serum levels, induce depressive-like behavior, and affect neurogenesis levels in female rats

inferredcites →https://doi.org/10.1016/j.physbeh.2009.04.014openalex-snapshot

Repeated exposure to corticosterone increases depression-like behavior in two different versions of the forced swim test without altering nonspecific locomotor activity or muscle strength

inferredcites →https://doi.org/10.1016/j.pnpbp.2010.03.005openalex-snapshot

Behavioral and neurobiological consequences of prolonged glucocorticoid exposure in rats: Relevance to depression

inferredcites →https://doi.org/10.1016/j.pnpbp.2012.02.005openalex-snapshot

Altered N-methyl-d-aspartate receptor function in reelin heterozygous mice: Male–female differences and comparison with dopaminergic activity

inferredcites →https://doi.org/10.1016/j.pnpbp.2012.10.006openalex-snapshot

Immune changes and neurotransmitters: Possible interactions in depression?

inferredcites →https://doi.org/10.1016/j.pnpbp.2015.02.001openalex-snapshot

Imipramine protects against the deleterious effects of chronic corticosterone on depression-like behavior, hippocampal reelin expression, and neuronal maturation

inferredcites →https://doi.org/10.1016/j.schres.2007.09.029openalex-snapshot

Decreased expression of reelin receptor VLDLR in peripheral lymphocytes of drug-naive schizophrenic patients

inferredcites →https://doi.org/10.1016/j.schres.2010.01.018openalex-snapshot

Co-occurrence of neurodevelopmental genes in etiopathogenesis of autism and schizophrenia

inferredcites →https://doi.org/10.1016/s0001-4079(19)32062-xopenalex-snapshot

Inflammation et VIH

inferredcites →https://doi.org/10.1016/s0002-9440(10)63988-0openalex-snapshot

Hippocampal Apoptosis in Major Depression Is a Minor Event and Absent from Subareas at Risk for Glucocorticoid Overexposure

inferredcites →https://doi.org/10.1016/s0074-7742(05)71008-4openalex-snapshot

Reelin Glycoprotein in Autism and Schizophrenia

inferredcites →https://doi.org/10.1016/s0889-1591(02)00011-9openalex-snapshot

Further evidence for the depressive effects of cytokines: Anhedonia and neurochemical changes

inferredcites →https://doi.org/10.1016/s0891-0618(01)00156-9openalex-snapshot

Reelin immunoreactivity in the larval sea lamprey brain

inferredcites →https://doi.org/10.1017/s1461145714000121openalex-snapshot

Corticosterone treatment during adolescence induces down-regulation of reelin and NMDA receptor subunit GLUN2C expression only in male mice: implications for schizophrenia

inferredcites →https://doi.org/10.1023/a:1013234708757openalex-snapshot

Dysregulation of Reelin and Bcl-2 Proteins in Autistic Cerebellum

inferredcites →https://doi.org/10.1023/a:1015017710332openalex-snapshot

Reelin in the extracellular matrix and dendritic spines of the cortex and hippocampus: a comparison between wild type and heterozygous reeler mice by immunoelectron microscopy

inferredcites →https://doi.org/10.1023/a:1019857620251openalex-snapshot

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

inferredcites →https://doi.org/10.1034/j.1600-0447.2001.103002122.xopenalex-snapshot

Determinants of poor 1‐year outcome of DSM‐III‐R major depression in the general population: results of the Netherlands Mental Health Survey and Incidence Study (NEMESIS)

inferredcites →https://doi.org/10.1037/0735-7044.118.6.1365openalex-snapshot

Corticosterone Increases Depression-Like Behavior, With Some Effects on Predator Odor-Induced Defensive Behavior, in Male and Female Rats.

inferredcites →https://doi.org/10.1038/374719a0openalex-snapshot

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

inferredcites →https://doi.org/10.1038/mp.2008.119openalex-snapshot

The mood-improving actions of antidepressants do not depend on neurogenesis but are associated with neuronal remodeling

inferredcites →https://doi.org/10.1038/mp.2013.20openalex-snapshot

The vascular depression hypothesis: mechanisms linking vascular disease with depression

inferredcites →https://doi.org/10.1038/mp.2013.66openalex-snapshot

Reelin, an extracellular matrix protein linked to early onset psychiatric diseases, drives postnatal development of the prefrontal cortex via GluN2B-NMDARs and the mTOR pathway

inferredcites →https://doi.org/10.1038/ncomms4443openalex-snapshot

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

inferredcites →https://doi.org/10.1038/npp.2011.153openalex-snapshot

Overexpression of Reelin Prevents the Manifestation of Behavioral Phenotypes Related to Schizophrenia and Bipolar Disorder

inferredcites →https://doi.org/10.1038/npp.2012.125openalex-snapshot

The Dynamics of DNA Methylation in Schizophrenia and Related Psychiatric Disorders

inferredcites →https://doi.org/10.1038/npp.2014.230openalex-snapshot

Adult Neurogenesis and Mental Illness

inferredcites →https://doi.org/10.1038/npp.2014.256openalex-snapshot

Lateral Diffusion of Gαs in the Plasma Membrane Is Decreased after Chronic but not Acute Antidepressant Treatment: Role of Lipid Raft and Non-Raft Membrane Microdomains

inferredcites →https://doi.org/10.1038/nrn1113openalex-snapshot

Reelin and brain development

inferredcites →https://doi.org/10.1038/nrn1115openalex-snapshot

Extracellular matrix molecules and synaptic plasticity

inferredcites →https://doi.org/10.1038/sj.mp.4000712openalex-snapshot

Adult brain neurogenesis and psychiatry: a novel theory of depression

inferredcites →https://doi.org/10.1038/sj.mp.4000783openalex-snapshot

Reduction in Reelin immunoreactivity in hippocampus of subjects with schizophrenia, bipolar disorder and major depression

inferredcites →https://doi.org/10.1038/sj.mp.4001248openalex-snapshot

The role of Reelin in pathology of autism

inferredcites →https://doi.org/10.1038/sj.mp.4001371openalex-snapshot

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

inferredcites →https://doi.org/10.1038/sj.mp.4001399openalex-snapshot

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

inferredcites →https://doi.org/10.1038/sj.mp.4001471openalex-snapshot

Molecular abnormalities of the hippocampus in severe psychiatric illness: postmortem findings from the Stanley Neuropathology Consortium

inferredcites →https://doi.org/10.1038/sj.mp.4001613openalex-snapshot

Reelin glycoprotein: structure, biology and roles in health and disease

inferredcites →https://doi.org/10.1038/sj.mp.4001791openalex-snapshot

Neural stem cell proliferation is decreased in schizophrenia, but not in depression

inferredcites →https://doi.org/10.1038/tp.2012.141openalex-snapshot

Sustained remission from depressive-like behavior depends on hippocampal neurogenesis

inferredcites →https://doi.org/10.1046/j.1460-9568.2002.01952.xopenalex-snapshot

Preferential alterations in the mesolimbic dopamine pathway of heterozygous reeler mice: an emerging animal‐based model of schizophrenia

inferredcites →https://doi.org/10.1073/pnas.0337481100openalex-snapshot

Course of illness, hippocampal function, and hippocampal volume in major depression

inferredcites →https://doi.org/10.1073/pnas.050589797openalex-snapshot

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

inferredcites →https://doi.org/10.1073/pnas.051614698openalex-snapshot

Down-regulation of dendritic spine and glutamic acid decarboxylase 67 expressions in the reelin haploinsufficient heterozygous reeler mouse

inferredcites →https://doi.org/10.1073/pnas.0810764106openalex-snapshot

The N-terminal region of reelin regulates postnatal dendritic maturation of cortical pyramidal neurons

inferredcites →https://doi.org/10.1073/pnas.1031602100openalex-snapshot

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

inferredcites →https://doi.org/10.1073/pnas.2637013100openalex-snapshot

DNA-methyltransferase 1 mRNA is selectively overexpressed in telencephalic GABAergic interneurons of schizophrenia brains

inferredcites →https://doi.org/10.1073/pnas.95.26.15718openalex-snapshot

A decrease of reelin expression as a putative vulnerability factor in schizophrenia

inferredcites →https://doi.org/10.1073/pnas.95.6.3221openalex-snapshot

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

inferredcites →https://doi.org/10.1073/pnas.96.6.3217openalex-snapshot

Cortical bitufted, horizontal, and Martinotti cells preferentially express and secrete reelin into perineuronal nets, nonsynaptically modulating gene expression

inferredcites →https://doi.org/10.1073/pnas.97.3.1281openalex-snapshot

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

inferredcites →https://doi.org/10.1074/jbc.m205147200openalex-snapshot

Reelin and ApoE Receptors Cooperate to Enhance Hippocampal Synaptic Plasticity and Learning

inferredcites →https://doi.org/10.1074/jbc.m400831200openalex-snapshot

Partitioning of the Serotonin Transporter into Lipid Microdomains Modulates Transport of Serotonin

inferredcites →https://doi.org/10.1080/15622970701263303openalex-snapshot

Consensus paper of the WFSBP Task Force on Biological Markers: Biological Markers in Depression

inferredcites →https://doi.org/10.1083/jcb.201110132openalex-snapshot

Smooth muscle–endothelial cell communication activates Reelin signaling and regulates lymphatic vessel formation

inferredcites →https://doi.org/10.1093/cercor/12.12.1298openalex-snapshot

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

inferredcites →https://doi.org/10.1097/00001756-199904260-00032openalex-snapshot

The phenotypic characteristics of heterozygous reeler mouse

inferredcites →https://doi.org/10.1097/00001756-200110290-00014openalex-snapshot

Altered levels of Reelin and its isoforms in schizophrenia and mood disorders

inferredcites →https://doi.org/10.1097/psy.0b013e3181907c1bopenalex-snapshot

Associations of Depression With C-Reactive Protein, IL-1, and IL-6: A Meta-Analysis

inferredcites →https://doi.org/10.1101/lm.2153511openalex-snapshot

Reelin supplementation enhances cognitive ability, synaptic plasticity, and dendritic spine density

inferredcites →https://doi.org/10.1111/ejn.12893openalex-snapshot

Reelin supplementation recovers synaptic plasticity and cognitive deficits in a mouse model for Angelman syndrome

inferredcites →https://doi.org/10.1111/j.1365-2826.2012.02380.xopenalex-snapshot

Postpartum Corticosterone Administration Reduces Dendritic Complexity and Increases the Density of Mushroom Spines of Hippocampal CA 3 Arbours in Dams

inferredcites →https://doi.org/10.1111/j.1460-9568.2005.04567.xopenalex-snapshot

Extracellular matrix molecules and synaptic plasticity: immunomapping of intracellular and secreted Reelin in the adult rat brain

inferredcites →https://doi.org/10.1111/j.1460-9568.2010.07563.xopenalex-snapshot

Region-specific alteration of GABAergic markers in the brain of heterozygous reeler mice

inferredcites →https://doi.org/10.1111/jth.12736openalex-snapshot

Impaired thrombin generation in Reelin‐deficient mice: a potential role of plasma Reelin in hemostasis

inferredcites →https://doi.org/10.1124/jpet.109.162644openalex-snapshot

Chronic Treatment with Escitalopram but Not R-Citalopram Translocates Gαs from Lipid Raft Domains and Potentiates Adenylyl Cyclase: A 5-Hydroxytryptamine Transporter-Independent Action of This Antidepressant Compound

inferredcites →https://doi.org/10.1126/science.1083328openalex-snapshot

Requirement of Hippocampal Neurogenesis for the Behavioral Effects of Antidepressants

inferredcites →https://doi.org/10.1128/mcb.24.3.1378-1386.2004openalex-snapshot

Receptor Clustering Is Involved in Reelin Signaling

inferredcites →https://doi.org/10.1146/annurev-clinpsy-050212-185606openalex-snapshot

Depression, Stress, and Anhedonia: Toward a Synthesis and Integrated Model

inferredcites →https://doi.org/10.1155/2010/130429openalex-snapshot

The Coexpression of Reelin and Neuronal Nitric Oxide Synthase in a Subpopulation of Dentate Gyrus Neurons Is Downregulated in Heterozygous Reeler Mice

inferredcites →https://doi.org/10.1155/2010/396282openalex-snapshot

Serotonin Transporter Clustering in Blood Lymphocytes of Reeler Mice

inferredcites →https://doi.org/10.1159/000337129openalex-snapshot

Decreased Reelin Expression in the Left Prefrontal Cortex (BA9) in Chronic Schizophrenia Patients

inferredcites →https://doi.org/10.1159/000444713openalex-snapshot

Epigenetic Regulations of GABAergic Neurotransmission: Relevance for Neurological Disorders and Epigenetic Therapy

inferredcites →https://doi.org/10.1176/appi.ajp.161.4.598openalex-snapshot

Lower Hippocampal Volume in Patients Suffering From Depression: A Meta-Analysis

inferredcites →https://doi.org/10.1176/appi.ajp.2007.06091564openalex-snapshot

Association of Different Adverse Life Events With Distinct Patterns of Depressive Symptoms

inferredcites →https://doi.org/10.1177/0269881112463468openalex-snapshot

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

inferredcites →https://doi.org/10.1186/1742-2094-10-142openalex-snapshot

Neurovascular unit dysfunction with blood-brain barrier hyperpermeability contributes to major depressive disorder: a review of clinical and experimental evidence

inferredcites →https://doi.org/10.1186/s12868-015-0156-4openalex-snapshot

Reelin expression in brain endothelial cells: an electron microscopy study

inferredcites →https://doi.org/10.1186/s12991-015-0085-8openalex-snapshot

Serotonin transporter clustering in blood lymphocytes predicts the outcome on anhedonia scores in naïve depressive patients treated with antidepressant medication

inferredcites →https://doi.org/10.1371/journal.pone.0005505openalex-snapshot

Reelin Secreted by GABAergic Neurons Regulates Glutamate Receptor Homeostasis

inferredcites →https://doi.org/10.1371/journal.pone.0119643openalex-snapshot

Stem- and Progenitor Cell Proliferation in the Dentate Gyrus of the Reeler Mouse

inferredcites →https://doi.org/10.1523/jneurosci.1757-05.2005openalex-snapshot

Reelin, Very-Low-Density Lipoprotein Receptor, and Apolipoprotein E Receptor 2 Control Somatic NMDA Receptor Composition during Hippocampal MaturationIn Vitro

inferredcites →https://doi.org/10.1523/jneurosci.1772-07.2007openalex-snapshot

NMDA Receptor Surface Trafficking and Synaptic Subunit Composition Are Developmentally Regulated by the Extracellular Matrix Protein Reelin

inferredcites →https://doi.org/10.1523/jneurosci.18-19-07779.1998openalex-snapshot

Regional and Cellular Patterns ofreelinmRNA Expression in the Forebrain of the Developing and Adult Mouse

inferredcites →https://doi.org/10.1523/jneurosci.1857-12.2012openalex-snapshot

Cell-Autonomous Inactivation of the Reelin Pathway Impairs Adult Neurogenesis in the Hippocampus

inferredcites →https://doi.org/10.1523/jneurosci.1917-08.2008openalex-snapshot

The Reelin Signaling Pathway Promotes Dendritic Spine Development in Hippocampal Neurons

inferredcites →https://doi.org/10.1523/jneurosci.1951-05.2005openalex-snapshot

Reelin Modulates NMDA Receptor Activity in Cortical Neurons

inferredcites →https://doi.org/10.1523/jneurosci.2278-14.2015openalex-snapshot

Lymphocytes from Chronically Stressed Mice Confer Antidepressant-Like Effects to Naive Mice

inferredcites →https://doi.org/10.1523/jneurosci.2561-06.2006openalex-snapshot

Differential Reelin-Induced Enhancement of NMDA and AMPA Receptor Activity in the Adult Hippocampus

inferredcites →https://doi.org/10.1523/jneurosci.3984-10.2011openalex-snapshot

Role for Reelin in Neurotransmitter Release

inferredcites →https://doi.org/10.1523/jneurosci.4566-05.2006openalex-snapshot

Functional Dissection of Reelin Signaling by Site-Directed Disruption of Disabled-1 Adaptor Binding to Apolipoprotein E Receptor 2: Distinct Roles in Development and Synaptic Plasticity

inferredcites →https://doi.org/10.1523/jneurosci.5284-09.2010openalex-snapshot

Reelin Regulates Postnatal Neurogenesis and Enhances Spine Hypertrophy and Long-Term Potentiation

inferredcites →https://doi.org/10.1615/critrevneurobiol.v16.i12.02openalex-snapshot

Prolog to Special Issue

inferredcites →https://doi.org/10.2174/157339510791823835openalex-snapshot

The Concept of Depression as a Dysfunction of the Immune System

inferredcites →https://doi.org/10.3109/09540261.2013.813442openalex-snapshot

Cytokines as biomarkers in depressive disorder: Current standing and prospects

inferredcites →https://doi.org/10.31887/dcns.2014.16.3/aguidottiopenalex-snapshot

DNA methylation and demethylation as targets for antipsychotic therapy

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/hipo.22991openalex-snapshot

Global epigenetic analysis of BDNF Val66Met mice hippocampus reveals changes in dendrite and spine remodeling genes

inferred← citeshttps://doi.org/10.1007/s11011-026-01855-3openalex-snapshot

Neurobiology of co-morbid stress and a western diet in mice: mitochondrial, proteomic and behavioral outcomes

inferred← citeshttps://doi.org/10.1016/b978-0-323-85666-9.00017-6openalex-snapshot

Mitochondrial dysfunction and affective disorders: Focus on diet, exercise, and aging

inferred← citeshttps://doi.org/10.1016/j.bbi.2017.09.012openalex-snapshot

Chronic stress induced disturbances in Laminin: A significant contributor to modulating microglial pro-inflammatory tone?

inferred← citeshttps://doi.org/10.1016/j.bbr.2021.113291openalex-snapshot

Altered acoustic startle, prepulse facilitation, and object recognition memory produced by corticosterone withdrawal in male rats

inferred← citeshttps://doi.org/10.1016/j.comppsych.2022.152363openalex-snapshot

The diagnostic utility of miRNA and elucidation of pathological mechanisms in major depressive disorder

inferred← citeshttps://doi.org/10.1016/j.drudis.2021.07.027openalex-snapshot

Positive AMPA receptor modulation in the treatment of neuropsychiatric disorders: A long and winding road

inferred← citeshttps://doi.org/10.1016/j.ijdevneu.2019.04.004openalex-snapshot

Fetal exposure to high levels of maternal glucocorticoids alters reelin signaling in the prefrontal cortex of rat pups

inferred← citeshttps://doi.org/10.1016/j.jneuroim.2026.579050openalex-snapshot

Neuroimmune mechanisms of the gut–brain axis in treatment-resistant depression: Implications for microbiome-based therapeutic strategies

inferred← citeshttps://doi.org/10.1016/j.jpsychires.2018.04.012openalex-snapshot

The impact of body mass index in gene expression of reelin pathway mediators in individuals with schizophrenia and mood disorders: A post-mortem study

inferred← citeshttps://doi.org/10.1016/j.jpsychires.2019.04.007openalex-snapshot

Unravelling the genetic basis of schizophrenia and bipolar disorder with GWAS: A systematic review

inferred← citeshttps://doi.org/10.1016/j.mito.2020.11.010openalex-snapshot

Severe life stress, mitochondrial dysfunction, and depressive behavior: A pathophysiological and therapeutic perspective

inferred← citeshttps://doi.org/10.1016/j.molmet.2019.06.001openalex-snapshot

Reelin is modulated by diet-induced obesity and has direct actions on arcuate proopiomelanocortin neurons

inferred← citeshttps://doi.org/10.1016/j.neulet.2024.137770openalex-snapshot

Chronic corticosterone exposure in rats induces sex-specific alterations in hypothalamic reelin fragments, MeCP2, and DNMT3a protein levels

inferred← citeshttps://doi.org/10.1016/j.neuropharm.2022.109043openalex-snapshot

Reelin has antidepressant-like effects after repeated or singular peripheral injections

inferred← citeshttps://doi.org/10.1016/j.physbeh.2020.113070openalex-snapshot

Cyclical administration of corticosterone results in aggravation of depression-like behaviors and accompanying downregulations in reelin in an animal model of chronic stress relevant to human recurrent depression

inferred← citeshttps://doi.org/10.1016/j.pnpbp.2025.111563openalex-snapshot

Sirtuin 3, a mitochondrial metabolic enzyme, links the mitochondrial function to neurophysiology in depression

inferred← citeshttps://doi.org/10.1016/j.schres.2019.09.007openalex-snapshot

Psychiatric drugs impact mitochondrial function in brain and other tissues

inferred← citeshttps://doi.org/10.1016/j.yebeh.2019.04.052openalex-snapshot

Reelin, tau phosphorylation and psychiatric complications in patients with hippocampal sclerosis and structural abnormalities in temporal lobe epilepsy

inferred← citeshttps://doi.org/10.1038/s41386-020-0609-zopenalex-snapshot

Fast-acting antidepressant-like effects of Reelin evaluated in the repeated-corticosterone chronic stress paradigm

inferred← citeshttps://doi.org/10.1038/s41398-025-03370-yopenalex-snapshot

Music therapy as a preventive intervention for postpartum depression: modulation of synaptic plasticity, oxidative stress, and inflammation in a mouse model

inferred← citeshttps://doi.org/10.1038/s41598-017-04300-9openalex-snapshot

Altered miRNA expression network in locus coeruleus of depressed suicide subjects

inferred← citeshttps://doi.org/10.1038/s41598-025-85276-9openalex-snapshot

Sugemule-7 alleviates oxidative stress, neuroinflammation, and cell death, promoting synaptic plasticity recovery in mice with postpartum depression

inferred← citeshttps://doi.org/10.1093/cercor/bhy024openalex-snapshot

PDK1 Deficit Impairs the Development of the Dentate Gyrus in Mice

inferred← citeshttps://doi.org/10.1093/ijnp/pyaa093openalex-snapshot

Neuroinflammation Induction and Alteration of Hippocampal Neurogenesis in Mice Following Developmental Exposure to Gossypol

inferred← citeshttps://doi.org/10.1111/ahe.12496openalex-snapshot

Adult neurogenesis in the mammalian dentate gyrus

inferred← citeshttps://doi.org/10.1139/bcb-2024-0237openalex-snapshot

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

inferred← citeshttps://doi.org/10.1155/2022/3714857openalex-snapshot

A Famous Chinese Medicine Formula: Yinhuo Decoction Antagonizes the Damage of Corticosterone to PC12 Cells and Improves Depression by Regulating the SIRT1/PGC‐1α Pathway

inferred← citeshttps://doi.org/10.1177/1179069519870182openalex-snapshot

A Further Analysis and Commentary on: Profiling Changes in Cortical Astroglial Cells Following Chronic Stress

inferred← citeshttps://doi.org/10.1186/s40364-017-0107-6openalex-snapshot

Comparative study of two protocols for quantitative image-analysis of serotonin transporter clustering in lymphocytes, a putative biomarker of therapeutic efficacy in major depression

inferred← citeshttps://doi.org/10.1194/jlr.r075507openalex-snapshot

The ApoE receptors Vldlr and Apoer2 in central nervous system function and disease

inferred← citeshttps://doi.org/10.1371/journal.pone.0200268openalex-snapshot

Reelin controls the positioning of brainstem serotonergic raphe neurons

inferred← citeshttps://doi.org/10.1523/jneurosci.0125-20.2020openalex-snapshot

The Secreted Glycoprotein Reelin Suppresses the Proliferation and Regulates the Distribution of Oligodendrocyte Progenitor Cells in the Embryonic Neocortex

inferred← citeshttps://doi.org/10.15547/tjs.2019.01.013openalex-snapshot

THE ROLE OF OXIDATIVE STRESS IN THE ETIOPATHOGENESIS OF DEPRESSION

inferred← citeshttps://doi.org/10.3389/fcell.2021.664535openalex-snapshot

A Selective Review of the Excitatory-Inhibitory Imbalance in Schizophrenia: Underlying Biology, Genetics, Microcircuits, and Symptoms

inferred← citeshttps://doi.org/10.3389/fnins.2018.00386openalex-snapshot

Mitochondria and Mood: Mitochondrial Dysfunction as a Key Player in the Manifestation of Depression

inferred← citeshttps://doi.org/10.3389/fnins.2019.00098openalex-snapshot

Exploring the Potential Antidepressant Mechanisms of TNFα Antagonists

inferred← citeshttps://doi.org/10.3389/fphar.2018.00121openalex-snapshot

Peripheral Etanercept Administration Normalizes Behavior, Hippocampal Neurogenesis, and Hippocampal Reelin and GABAA Receptor Expression in a Preclinical Model of Depression

inferred← citeshttps://doi.org/10.3389/fphar.2018.01149openalex-snapshot

Changes in Membrane Protein Clustering in Peripheral Lymphocytes in an Animal Model of Depression Parallel Those Observed in Naïve Depression Patients: Implications for the Development of Novel Biomarkers of Depression

inferred← citeshttps://doi.org/10.3389/fphar.2019.00190openalex-snapshot

Patterns of Membrane Protein Clustering in Peripheral Lymphocytes as Predictors of Therapeutic Outcomes in Major Depressive Disorder

inferred← citeshttps://doi.org/10.3390/cimb47050382openalex-snapshot

The Role of Mitochondrial Energy Metabolism in the Mechanism of Exercise Improving Depression

inferred← citeshttps://doi.org/10.3390/ijms25020814openalex-snapshot

Molecular Mechanisms of Reelin in the Enteric Nervous System and the Microbiota–Gut–Brain Axis: Implications for Depression and Antidepressant Therapy

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