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Evidence for morphological alterations in prefrontal white matter glia in schizophrenia and bipolar disorder

https://doi.org/10.1503/jpn.130277
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What this work says

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

inferredcites →https://doi.org/10.1001/archpsyc.65.9.1017openalex-snapshot
Meta-analysis, Database, and Meta-regression of 98 Structural Imaging Studies in Bipolar Disorder
inferredcites →https://doi.org/10.1002/(sici)1097-0185(199803)250:3<373::aid-ar12>3.0.co;2-lopenalex-snapshot
What was wrong with the Abercrombie and empirical cell counting methods? A review
inferredcites →https://doi.org/10.1002/ar.1090940210openalex-snapshot
Estimation of nuclear population from microtome sections
inferredcites →https://doi.org/10.1002/jnr.10858openalex-snapshot
ADAM (a disintegrin and metalloprotease) 12 is expressed in rat and human brain and localized to oligodendrocytes
inferredcites →https://doi.org/10.1007/s00401-006-0090-8openalex-snapshot
Distribution of HLA-DR-positive microglia in schizophrenia reflects impaired cerebral lateralization
inferredcites →https://doi.org/10.1007/s00401-008-0379-xopenalex-snapshot
Spatial distribution and density of oligodendrocytes in the cingulum bundle are unaltered in schizophrenia
inferredcites →https://doi.org/10.1007/s00406-011-0197-3openalex-snapshot
Protective effects of haloperidol and clozapine on energy-deprived OLN-93 oligodendrocytes
inferredcites →https://doi.org/10.1007/s00406-012-0328-5openalex-snapshot
Astrocyte decrease in the subgenual cingulate and callosal genu in schizophrenia
inferredcites →https://doi.org/10.1007/s004290050191openalex-snapshot
Variation of fractionator estimates and its prediction
inferredcites →https://doi.org/10.1007/s12017-012-8185-yopenalex-snapshot
Increased Density of Prohibitin-Immunoreactive Oligodendrocytes in the Dorsolateral Prefrontal White Matter of Subjects with Schizophrenia Suggests Extraneuronal Roles for the Protein in the Disease
inferredcites →https://doi.org/10.1016/0165-0270(94)90025-6openalex-snapshot
Evaluation of neuronal numerical density by Dirichlet tessellation
inferredcites →https://doi.org/10.1016/b978-012373960-5.00335-xopenalex-snapshot
Global Burden of Disease
inferredcites →https://doi.org/10.1016/j.biopsych.2007.08.018openalex-snapshot
Effect of Chronic Antipsychotic Exposure on Astrocyte and Oligodendrocyte Numbers in Macaque Monkeys
inferredcites →https://doi.org/10.1016/j.eurpsy.2010.01.009openalex-snapshot
Stress, genetics and epigenetic effects on the neurobiology of suicidal behavior and depression
inferredcites →https://doi.org/10.1016/j.jad.2013.05.034openalex-snapshot
Systematic review and voxel-based meta-analysis of diffusion tensor imaging studies in bipolar disorder
inferredcites →https://doi.org/10.1016/j.jpsychires.2013.03.018openalex-snapshot
Increased nuclear Olig1-expression in the pregenual anterior cingulate white matter of patients with major depression: A regenerative attempt to compensate oligodendrocyte loss?
inferredcites →https://doi.org/10.1016/j.neubiorev.2006.02.001openalex-snapshot
Neuropathological, neurogenetic and neuroimaging evidence for white matter pathology in schizophrenia
inferredcites →https://doi.org/10.1016/j.pnpbp.2009.01.015openalex-snapshot
Chronic lithium treatment decreases NG2 cell proliferation in rat dentate hilus, amygdala and corpus callosum
inferredcites →https://doi.org/10.1016/j.schres.2006.11.017openalex-snapshot
Expression of transcripts for myelination-related genes in the anterior cingulate cortex in schizophrenia☆
inferredcites →https://doi.org/10.1016/j.schres.2007.09.032openalex-snapshot
Expression of oligodendrocyte-associated genes in dorsolateral prefrontal cortex of patients with schizophrenia
inferredcites →https://doi.org/10.1016/j.schres.2007.09.034openalex-snapshot
Schizophrenia and sex associated differences in the expression of neuronal and oligodendrocyte-specific genes in individual thalamic nuclei
inferredcites →https://doi.org/10.1016/j.schres.2008.01.005openalex-snapshot
Meta-analysis of magnetic resonance imaging studies of the corpus callosum in schizophrenia
inferredcites →https://doi.org/10.1016/j.schres.2008.11.021openalex-snapshot
Meta-analysis of diffusion tensor imaging studies in schizophrenia
inferredcites →https://doi.org/10.1016/j.schres.2009.01.017openalex-snapshot
Metabolic abnormalities in fronto-striatal-thalamic white matter tracts in schizophrenia
inferredcites →https://doi.org/10.1016/j.schres.2009.04.019openalex-snapshot
Subcortical oligodendrocyte- and astrocyte-associated gene expression in subjects with schizophrenia, major depression and bipolar disorder
inferredcites →https://doi.org/10.1016/j.schres.2009.09.028openalex-snapshot
Two-dimensional assessment of cytoarchitecture in the superior temporal white matter in schizophrenia, major depressive disorder and bipolar disorder
inferredcites →https://doi.org/10.1016/j.schres.2010.02.1068openalex-snapshot
Haloperidol activates quiescent oligodendroglia precursor cells in the adult mouse brain
inferredcites →https://doi.org/10.1016/j.tins.2011.11.008openalex-snapshot
The neurodevelopmental origins of suicidal behavior
inferredcites →https://doi.org/10.1016/s0006-3223(03)00114-8openalex-snapshot
Two-dimensional assessment of cytoarchitecture in the anterior cingulate cortex in major depressive disorder, bipolar disorder, and schizophrenia: evidence for decreased neuronal somal size and increased neuronal density
inferredcites →https://doi.org/10.1016/s0006-3223(03)00237-3openalex-snapshot
Loss and altered spatial distribution of oligodendrocytes in the superior frontal gyrus in schizophrenia
inferredcites →https://doi.org/10.1016/s0006-3223(99)00113-4openalex-snapshot
Increased volume and glial density in primate prefrontal cortex associated with chronic antipsychotic drug exposure
inferredcites →https://doi.org/10.1016/s0166-2236(00)01660-xopenalex-snapshot
Two-dimensional versus three-dimensional cell counting: a practical perspective
inferredcites →https://doi.org/10.1016/s0891-0618(00)00064-8openalex-snapshot
Voronoi tessellation to study the numerical density and the spatial distribution of neurones
inferredcites →https://doi.org/10.1016/s0920-9964(02)00339-0openalex-snapshot
Layer-specific reductions in GFAP-reactive astroglia in the dorsolateral prefrontal cortex in schizophrenia
inferredcites →https://doi.org/10.1016/s0920-9964(03)00181-6openalex-snapshot
Oligodendroglial density in the prefrontal cortex in schizophrenia and mood disorders: a study from the Stanley Neuropathology Consortium
inferredcites →https://doi.org/10.1016/s0920-9964(99)00192-9openalex-snapshot
The Stanley Foundation brain collection and Neuropathology Consortium
inferredcites →https://doi.org/10.1038/mp.2012.110openalex-snapshot
Increased inflammatory markers identified in the dorsolateral prefrontal cortex of individuals with schizophrenia
inferredcites →https://doi.org/10.1038/npp.2012.172openalex-snapshot
Lithium and GSK3-β Promoter Gene Variants Influence White Matter Microstructure in Bipolar Disorder
inferredcites →https://doi.org/10.1038/nrn2480openalex-snapshot
Remyelination in the CNS: from biology to therapy
inferredcites →https://doi.org/10.1046/j.1365-2990.1999.00162.xopenalex-snapshot
No evidence for astrogliosis in brains of schizophrenic patients. A post‐mortem study
inferredcites →https://doi.org/10.1046/j.1471-4159.2003.02247.xopenalex-snapshot
Gene expression profile of the nucleus accumbens of human cocaine abusers: evidence for dysregulation of myelin
inferredcites →https://doi.org/10.1093/brain/123.1.105openalex-snapshot
Oligodendrocyte survival, loss and birth in lesions of chronic-stage multiple sclerosis
inferredcites →https://doi.org/10.1097/00005072-199802000-00001openalex-snapshot
The Neuropathology of Alcohol-specific Brain Damage, or Does Alcohol Damage the Brain?
inferredcites →https://doi.org/10.1097/fpc.0b013e328011b5b2openalex-snapshot
A microarray gene expression study of the molecular pharmacology of lithium carbonate on mouse brain mRNA to understand the neurobiology of mood stabilization and treatment of bipolar affective disorder
inferredcites →https://doi.org/10.1101/gad.188326.112openalex-snapshot
Astrocytes and disease: a neurodevelopmental perspective
inferredcites →https://doi.org/10.1111/j.1399-5618.2010.00804.xopenalex-snapshot
Sex dependence of brain size and shape in bipolar disorder: an exploratory study
inferredcites →https://doi.org/10.1111/j.1460-9568.2006.05219.xopenalex-snapshot
Calprotectin in microglia from frontal cortex is up‐regulated in schizophrenia: evidence for an inflammatory process?
inferredcites →https://doi.org/10.1111/j.1471-4159.2008.05570.xopenalex-snapshot
The life, death, and replacement of oligodendrocytes in the adult CNS
inferredcites →https://doi.org/10.1111/jnc.12316openalex-snapshot
Specific subcellular changes in oxidative stress in prefrontal cortex from patients with bipolar disorder
inferredcites →https://doi.org/10.1523/jneurosci.4707-08.2009openalex-snapshot
Uniquely Hominid Features of Adult Human Astrocytes
inferredcites →https://doi.org/10.3109/15622970903497936openalex-snapshot
Reduced density of ADAM 12-immunoreactive oligodendrocytes in the anterior cingulate white matter of patients with schizophrenia
inferredcites →https://doi.org/10.4049/jimmunol.181.1.338openalex-snapshot
Lithium Prevents and Ameliorates Experimental Autoimmune Encephalomyelitis

What points at this work

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

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Corollary Discharge Dysfunction Related to Anomalous Self-Experiences in Schizophrenia and Bipolar Disorder. A Specificity Analysis
inferred← citeshttps://doi.org/10.1002/ctd2.70128openalex-snapshot
Astrocytes as central integrators of neural circuit function: Mechanisms and dysregulation in neuropsychiatric disorders
inferred← citeshttps://doi.org/10.1002/glia.23166openalex-snapshot
Drug discovery for remyelination and treatment of MS
inferred← citeshttps://doi.org/10.1002/glia.23962openalex-snapshot
A loss of mature microglial markers without immune activation in schizophrenia
inferred← citeshttps://doi.org/10.1002/glia.23994openalex-snapshot
Implication of cerebral astrocytes in major depression: A review of fine neuroanatomical evidence in humans
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Microscopic anisotropy misestimation in spherical‐mean single diffusion encoding MRI
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Microglial Activation and Psychotic Disorders: Evidence from Pre-clinical and Clinical Studies
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A Drug-Inducible Transgenic Zebrafish Model for Myelinating Glial Cell Ablation
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inferred← citeshttps://doi.org/10.1007/978-3-030-61721-9_16openalex-snapshot
Glial Cells in the Schizophrenia Puzzle: Angiotensin II Role
inferred← citeshttps://doi.org/10.1007/978-3-030-68308-5_11openalex-snapshot
The Neuropathology of White Matter in Schizophrenia
inferred← citeshttps://doi.org/10.1007/978-3-030-68308-5_12openalex-snapshot
Glial Cells
inferred← citeshttps://doi.org/10.1007/978-3-030-68308-5_4openalex-snapshot
Frontal Cortex
inferred← citeshttps://doi.org/10.1007/978-3-030-68308-5_7openalex-snapshot
The Cingulate Cortex
inferred← citeshttps://doi.org/10.1007/978-3-030-77375-5_4openalex-snapshot
Morphological Features of Astrocytes in Health and Neuropsychiatric Disorders
inferred← citeshttps://doi.org/10.1007/978-3-030-77375-5_5openalex-snapshot
Astrocytes in Bipolar Disorder
inferred← citeshttps://doi.org/10.1007/978-3-030-77375-5_8openalex-snapshot
Astrocytes in Neuropsychiatric Disorders: A Review of Postmortem Evidence
inferred← citeshttps://doi.org/10.1007/978-3-319-31689-5_8openalex-snapshot
Neuroimaging Studies of Bipolar Depression: Therapeutic Implications
inferred← citeshttps://doi.org/10.1007/s00406-020-01107-0openalex-snapshot
Lateralization of increased density of Iba1-immunopositive microglial cells in the anterior midcingulate cortex of schizophrenia and bipolar disorder
inferred← citeshttps://doi.org/10.1007/s00406-023-01621-xopenalex-snapshot
Microglia-neuron interactions in prefrontal gray matter in schizophrenia: a postmortem ultrastructural morphometric study
inferred← citeshttps://doi.org/10.1007/s11055-023-01491-9openalex-snapshot
Characteristics of the Interaction of Microglia and Oligodendrocytes in the White Matter in Continuous Schizophrenia
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Role of Astrocytes in Major Neuropsychiatric Disorders
inferred← citeshttps://doi.org/10.1007/s12035-021-02672-8openalex-snapshot
Glial Cell Abnormalities in Major Psychiatric Diseases: A Systematic Review of Postmortem Brain Studies
inferred← citeshttps://doi.org/10.1007/s12035-024-03987-yopenalex-snapshot
GABAergic and inflammatory changes in the frontal cortex following neonatal PCP plus isolation rearing, as a dual-hit neurodevelopmental model for schizophrenia
inferred← citeshttps://doi.org/10.1016/b978-0-12-819182-8.00004-1openalex-snapshot
Immune mechanisms in bipolar disorder: Evidence and implications
inferred← citeshttps://doi.org/10.1016/b978-0-12-819182-8.00015-6openalex-snapshot
Bipolar disorder as a gliopathy
inferred← citeshttps://doi.org/10.1016/b978-0-12-821565-4.00001-8openalex-snapshot
Neuropsychiatric disorders
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The fetal origins of mental illness
inferred← citeshttps://doi.org/10.1016/j.ajp.2026.104959openalex-snapshot
Cell type-specific transcriptional features associated with gray matter volume alterations in schizophrenia with predominantly negative symptoms
inferred← citeshttps://doi.org/10.1016/j.bbi.2023.02.021openalex-snapshot
Suicide in bipolar disorder patients is associated with hippocampal microglia activation and reduction of lymphocytes-activation gene 3 (LAG3) microglial checkpoint expression
inferred← citeshttps://doi.org/10.1016/j.bbi.2026.106276openalex-snapshot
Midbrain microglial and macrophage mRNAs distinguish neuroinflammatory schizophrenia from bipolar disorder
inferred← citeshttps://doi.org/10.1016/j.bbi.2026.106598openalex-snapshot
Choroid plexus inflammation in bipolar disorder
inferred← citeshttps://doi.org/10.1016/j.bbih.2020.100038openalex-snapshot
Overlapping evidence of innate immune dysfunction in psychotic and affective disorders
inferred← citeshttps://doi.org/10.1016/j.bnd.2026.04.003openalex-snapshot
Astrocyte subtype dynamics in mood disorders: Current insights and future directions
inferred← citeshttps://doi.org/10.1016/j.brainres.2017.05.027openalex-snapshot
QKI6B mRNA levels are upregulated in schizophrenia and predict GFAP expression
inferred← citeshttps://doi.org/10.1016/j.cels.2019.01.002openalex-snapshot
Genome-Scale Transcriptional Regulatory Network Models of Psychiatric and Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.1016/j.clinph.2024.07.014openalex-snapshot
Corollary discharge and anomalous self-experiences in schizophrenia and bipolar disorder: A specificity analysis
inferred← citeshttps://doi.org/10.1016/j.comppsych.2016.12.008openalex-snapshot
Decreased S100B serum levels after treatment in bipolar patients in a manic phase
inferred← citeshttps://doi.org/10.1016/j.euroneuro.2016.07.009openalex-snapshot
Increased mRNA expression of peripheral glial cell markers in bipolar disorder: The effect of long-term lithium treatment
inferred← citeshttps://doi.org/10.1016/j.jad.2019.02.015openalex-snapshot
Effects of illness duration on cognitive performances in bipolar depression are mediated by white matter microstructure
inferred← citeshttps://doi.org/10.1016/j.jad.2024.06.032openalex-snapshot
The blood-brain barrier in bipolar disorders: A systematic review
inferred← citeshttps://doi.org/10.1016/j.jaut.2022.102962openalex-snapshot
Infectious diseases, autoantibodies, and autoimmunity
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2017.08.009openalex-snapshot
Evidence for altered cell membrane lipid composition in postmortem prefrontal white matter in bipolar disorder and schizophrenia
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2019.11.002openalex-snapshot
Prefrontal cortex alterations in glia gene expression in schizophrenia with and without suicide
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2023.01.008openalex-snapshot
A fatal alliance: Glial connexins, myelin pathology and mental disorders
inferred← citeshttps://doi.org/10.1016/j.mcn.2015.11.006openalex-snapshot
Neurodevelopmental origins of bipolar disorder: iPSC models
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Neuroadaptations to antipsychotic drugs: Insights from pre-clinical and human post-mortem studies
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2019.01.005openalex-snapshot
From the microscope to the magnet: Disconnection in schizophrenia and bipolar disorder
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2019.05.027openalex-snapshot
Neurons and glial cells in bipolar disorder: A systematic review of postmortem brain studies of cell number and size
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2021.09.023openalex-snapshot
The emerging tale of microglia in psychiatric disorders
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2015.05.018openalex-snapshot
The role of inflammation and microglial activation in the pathophysiology of psychiatric disorders
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2026.04.003openalex-snapshot
Schizophrenia and frontotemporal dementia: distinct diseases with converging circuit dysfunctions
inferred← citeshttps://doi.org/10.1016/j.nicl.2018.09.033openalex-snapshot
Physical activity is associated with left corticospinal tract microstructure in bipolar depression
inferred← citeshttps://doi.org/10.1016/j.pbb.2018.12.006openalex-snapshot
Revisiting inflammation in bipolar disorder
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2017.06.013openalex-snapshot
Stem cells, pluripotency and glial cell markers in peripheral blood of bipolar patients on long-term lithium treatment
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2017.10.002openalex-snapshot
Astroglial correlates of neuropsychiatric disease: From astrocytopathy to astrogliosis
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2019.02.006openalex-snapshot
Structural connectivity in schizophrenia and bipolar disorder: Effects of chronicity and antipsychotic treatment
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2023.110773openalex-snapshot
A consideration of the increased risk of schizophrenia due to prenatal maternal stress, and the possible role of microglia
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2024.111229openalex-snapshot
Alterations in white matter microstructure in bipolar disorder patients with and without psychosis
inferred← citeshttps://doi.org/10.1016/j.pscychresns.2016.10.001openalex-snapshot
SREBF-2 polymorphism influences white matter microstructure in bipolar disorder
inferred← citeshttps://doi.org/10.1016/j.psychres.2016.09.029openalex-snapshot
Cognitive dysfunction correlates with elevated serum S100B concentration in drug-free acutely relapsed patients with schizophrenia
inferred← citeshttps://doi.org/10.1016/j.schres.2015.05.017openalex-snapshot
Dysfunctional glycosynapses in schizophrenia: Disease and regional specificity
inferred← citeshttps://doi.org/10.1016/j.schres.2015.07.018openalex-snapshot
Clinical studies of neuroinflammatory mechanisms in schizophrenia
inferred← citeshttps://doi.org/10.1016/j.schres.2015.10.042openalex-snapshot
Differentiation of oligodendrocyte precursors is impaired in the prefrontal cortex in schizophrenia
inferred← citeshttps://doi.org/10.1016/j.schres.2016.04.023openalex-snapshot
Ultrastructural alterations of oligodendrocytes in prefrontal white matter in schizophrenia: A post-mortem morphometric study
inferred← citeshttps://doi.org/10.1016/j.schres.2018.08.021openalex-snapshot
Widespread white-matter microstructure integrity reduction in first-episode schizophrenia patients after acute antipsychotic treatment
inferred← citeshttps://doi.org/10.1016/j.schres.2020.11.053openalex-snapshot
Markers of copper transport in the cingulum bundle in schizophrenia
inferred← citeshttps://doi.org/10.1038/mp.2016.90openalex-snapshot
Postmortem evidence of cerebral inflammation in schizophrenia: a systematic review
inferred← citeshttps://doi.org/10.1038/s41380-018-0213-3openalex-snapshot
The neuropathology of bipolar disorder: systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1038/s41380-018-0235-xopenalex-snapshot
Increased macrophages and changed brain endothelial cell gene expression in the frontal cortex of people with schizophrenia displaying inflammation
inferred← citeshttps://doi.org/10.1038/s41380-019-0448-7openalex-snapshot
Postmortem evidence of brain inflammatory markers in bipolar disorder: a systematic review
inferred← citeshttps://doi.org/10.1038/s41380-023-02162-4openalex-snapshot
Cytomegalovirus antibodies are associated with mood disorders, suicide, markers of neuroinflammation, and microglia activation in postmortem brain samples
inferred← citeshttps://doi.org/10.1038/s41380-024-02861-6openalex-snapshot
Glial cell deficits are a key feature of schizophrenia: implications for neuronal circuit maintenance and histological differentiation from classical neurodegeneration
inferred← citeshttps://doi.org/10.1038/s41386-022-01338-wopenalex-snapshot
Astrocyte regulation of synaptic signaling in psychiatric disorders
inferred← citeshttps://doi.org/10.1038/s41392-023-01628-9openalex-snapshot
Astrocytes in human central nervous system diseases: a frontier for new therapies
inferred← citeshttps://doi.org/10.1038/s41398-019-0490-xopenalex-snapshot
Microglia in post-mortem brain tissue of patients with bipolar disorder are not immune activated
inferred← citeshttps://doi.org/10.1038/s41398-019-0542-2openalex-snapshot
Astrocytes are direct cellular targets of lithium treatment: novel roles for lysyl oxidase and peroxisome-proliferator activated receptor-γ as astroglial targets of lithium
inferred← citeshttps://doi.org/10.1038/s41398-021-01607-0openalex-snapshot
Neuroinflammation in schizophrenia: the role of nuclear factor kappa B
inferred← citeshttps://doi.org/10.1038/s41398-021-01681-4openalex-snapshot
A human iPSC-astroglia neurodevelopmental model reveals divergent transcriptomic patterns in schizophrenia
inferred← citeshttps://doi.org/10.1038/s41398-022-02197-1openalex-snapshot
Microglia sequelae: brain signature of innate immunity in schizophrenia
inferred← citeshttps://doi.org/10.1038/s41398-024-03166-6openalex-snapshot
Long-term effects of a double hit murine model for schizophrenia on parvalbumin expressing cells and plasticity-related molecules in the thalamic reticular nucleus and the habenula
inferred← citeshttps://doi.org/10.1038/s41398-026-04072-9openalex-snapshot
Myo-inositol concentration in the medial prefrontal cortex is associated with changes in brain white matter microstructure in early psychosis
inferred← citeshttps://doi.org/10.1038/s41537-018-0068-2openalex-snapshot
Ultrastructural pathology of oligodendrocytes adjacent to microglia in prefrontal white matter in schizophrenia
inferred← citeshttps://doi.org/10.1038/s41537-019-0078-8openalex-snapshot
White matter neuron biology and neuropathology in schizophrenia
inferred← citeshttps://doi.org/10.1038/tp.2016.278openalex-snapshot
Inflammation and the neural diathesis-stress hypothesis of schizophrenia: a reconceptualization
inferred← citeshttps://doi.org/10.1080/15622975.2020.1789217openalex-snapshot
An overview of the human brain myelin proteome and differences associated with schizophrenia
inferred← citeshttps://doi.org/10.1080/15622975.2021.2013042openalex-snapshot
Correlation between S100B and severity of depression in MDD: A meta-analysis
inferred← citeshttps://doi.org/10.1084/jem.20180794openalex-snapshot
Microbiome–microglia connections via the gut–brain axis
inferred← citeshttps://doi.org/10.1093/cercor/bhy061openalex-snapshot
Microglial Pruning of Synapses in the Prefrontal Cortex During Adolescence
inferred← citeshttps://doi.org/10.1093/ijnp/pyw035openalex-snapshot
Valproic Acid and Other HDAC Inhibitors Upregulate FGF21 Gene Expression and Promote Process Elongation in Glia by Inhibiting HDAC2 and 3
inferred← citeshttps://doi.org/10.1093/jnen/nlz113openalex-snapshot
Fasciculation and Elongation Protein Zeta-1 Expression in Reactive Astrocytes in a Rat Model of Frontal Lobe Injury
inferred← citeshttps://doi.org/10.1093/med/9780197574522.003.0002openalex-snapshot
Structural brain abnormalities in bipolar disorder
inferred← citeshttps://doi.org/10.1093/med/9780197574522.003.0012openalex-snapshot
MiRNAs as predictors of bipolar disorder diagnosis and treatment response
inferred← citeshttps://doi.org/10.1093/schbul/sby088openalex-snapshot
(Micro)Glia as Effectors of Cortical Volume Loss in Schizophrenia
inferred← citeshttps://doi.org/10.1101/2021.09.22.461367openalex-snapshot
Assessing the relationships between neurological and psychiatric diseases with astrocyte subtypes and psychotropic medications
inferred← citeshttps://doi.org/10.1111/bdi.12395openalex-snapshot
Deficits in axon‐associated proteins in prefrontal white matter in bipolar disorder but not schizophrenia
inferred← citeshttps://doi.org/10.1111/bdi.12447openalex-snapshot
Chronic LiCl pretreatment suppresses thrombin‐stimulated intracellular calcium mobilization through TRPC 3 in astroglioma cells
inferred← citeshttps://doi.org/10.1111/bpa.13003openalex-snapshot
Microglia activation in postmortem brains with schizophrenia demonstrates distinct morphological changes between brain regions
inferred← citeshttps://doi.org/10.1111/bph.13364openalex-snapshot
Microglial activation and progressive brain changes in schizophrenia
inferred← citeshttps://doi.org/10.1111/bph.14612openalex-snapshot
Pathology of white matter integrity in three major white matter fasciculi: A post‐mortem study of schizophrenia and treatment status
inferred← citeshttps://doi.org/10.1111/jnc.16098openalex-snapshot
The emerging neuroimmune hypothesis of bipolar disorder: An updated overview of neuroimmune and microglial findings
inferred← citeshttps://doi.org/10.1111/jnc.70559openalex-snapshot
Adolescent Exposure to a THC ‐Rich Cannabis Extract Produces Genotype‐Dependent Effects on Cognition and Glial Morphology in Serine Racemase Mutant Mice
inferred← citeshttps://doi.org/10.1111/jog.14149openalex-snapshot
Oxytocin induced labor causes region and sex‐specific transient oligodendrocyte cell death in neonatal mouse brain
inferred← citeshttps://doi.org/10.1126/sciadv.ads6841openalex-snapshot
Supervised and unsupervised learning reveal heroin-induced impairments in astrocyte structural plasticity
inferred← citeshttps://doi.org/10.1126/science.abm5224openalex-snapshot
Fate mapping of neural stem cell niches reveals distinct origins of human cortical astrocytes
inferred← citeshttps://doi.org/10.1152/ajpendo.00331.2024openalex-snapshot
Neuroimmunometabolism: how metabolism orchestrates immune response in healthy and diseased brain
inferred← citeshttps://doi.org/10.1159/000511887openalex-snapshot
Transcriptomic Deconvolution of Dorsal Striata Reveals Increased Monocyte Fractions in Bipolar Disorder
inferred← citeshttps://doi.org/10.1186/s12987-018-0097-2openalex-snapshot
Brain vascular heterogeneity: implications for disease pathogenesis and design of in vitro blood–brain barrier models
inferred← citeshttps://doi.org/10.1186/s13024-015-0061-4openalex-snapshot
Loss of Munc18-1 long splice variant in GABAergic terminals is associated with cognitive decline and increased risk of dementia in a community sample
inferred← citeshttps://doi.org/10.14288/1.0384590openalex-snapshot
Fractalkine signaling in psychiatric disorder : observations in the postmortem brain
inferred← citeshttps://doi.org/10.1515/nipt-2024-0017openalex-snapshot
The challenges to detect, quantify, and characterize viral reservoirs in the current antiretroviral era
inferred← citeshttps://doi.org/10.1590/0004-282x20160101openalex-snapshot
Are astrocytes executive cells within the central nervous system?
inferred← citeshttps://doi.org/10.1590/2237-6089-2015-0088openalex-snapshot
Frontal lobe alterations in schizophrenia: a review
inferred← citeshttps://doi.org/10.17116/jnevro20171179176-81openalex-snapshot
Ultrastructural pathology of oligodendrocytes in the white matter in continuous paranoid schizophrenia: a role for microglia
inferred← citeshttps://doi.org/10.17116/jnevro2022122121128openalex-snapshot
Specific interactions between microglia and oligodendrocytes in white matter in continuous schizophrenia
inferred← citeshttps://doi.org/10.29328/journal.jnnd.1001011openalex-snapshot
Discrepancy in Microglia and Peripheral Monocytic Cells - A scope in the Pathophysiology of Psychiatric maladies
inferred← citeshttps://doi.org/10.30629/2618-6667-2022-20-4-84-95openalex-snapshot
Microglia-Oligodendrocyte Interactions in White Matter of the Prefrontal Cortex in Attack-Like Schizophrenia
inferred← citeshttps://doi.org/10.31083/jin27636openalex-snapshot
Neuroinflammation in Schizophrenia: An Overview of Evidence and Implications for Pathophysiology
inferred← citeshttps://doi.org/10.3233/nib-160110openalex-snapshot
Microglial Gene Expression Alterations in the Brains of Patients with Psychiatric Disorders
inferred← citeshttps://doi.org/10.3325/cmj.2020.61.354openalex-snapshot
Axon morphology of rapid Golgi-stained pyramidal neurons in the prefrontal cortex in schizophrenia
inferred← citeshttps://doi.org/10.3389/fimmu.2020.01818openalex-snapshot
Affective Immunology: The Crosstalk Between Microglia and Astrocytes Plays Key Role?
inferred← citeshttps://doi.org/10.3389/fnagi.2022.873697openalex-snapshot
Glymphatic System Dysfunction in Central Nervous System Diseases and Mood Disorders
inferred← citeshttps://doi.org/10.3389/fncel.2015.00451openalex-snapshot
Advancements in the Underlying Pathogenesis of Schizophrenia: Implications of DNA Methylation in Glial Cells
inferred← citeshttps://doi.org/10.3389/fncel.2015.00468openalex-snapshot
A New Outlook on Mental Illnesses: Glial Involvement Beyond the Glue
inferred← citeshttps://doi.org/10.3389/fncel.2016.00033openalex-snapshot
Serum S100B Protein is Specifically Related to White Matter Changes in Schizophrenia
inferred← citeshttps://doi.org/10.3389/fncel.2016.00119openalex-snapshot
Astrocytes in Oligodendrocyte Lineage Development and White Matter Pathology
inferred← citeshttps://doi.org/10.3389/fncel.2016.00144openalex-snapshot
Linking Activation of Microglia and Peripheral Monocytic Cells to the Pathophysiology of Psychiatric Disorders
inferred← citeshttps://doi.org/10.3389/fncel.2018.00323openalex-snapshot
Bidirectional Microglia–Neuron Communication in Health and Disease
inferred← citeshttps://doi.org/10.3389/fncel.2019.00405openalex-snapshot
The Evolving Concept of the Blood Brain Barrier (BBB): From a Single Static Barrier to a Heterogeneous and Dynamic Relay Center
inferred← citeshttps://doi.org/10.3389/fncel.2020.00274openalex-snapshot
The Inflamed Brain in Schizophrenia: The Convergence of Genetic and Environmental Risk Factors That Lead to Uncontrolled Neuroinflammation
inferred← citeshttps://doi.org/10.3389/fncel.2024.1345349openalex-snapshot
Microglia-neuron interactions in schizophrenia
inferred← citeshttps://doi.org/10.3389/fncel.2026.1784522openalex-snapshot
Altered lipid peroxidation, perineuronal net and oligodendrocyte markers in the frontal cortex of a dual-hit neurodevelopmental model support its relevance to schizophrenia
inferred← citeshttps://doi.org/10.3389/fnins.2019.00351openalex-snapshot
Robust Generation of Person-Specific, Synchronously Active Neuronal Networks Using Purely Isogenic Human iPSC-3D Neural Aggregate Cultures
inferred← citeshttps://doi.org/10.3389/fnins.2025.1551764openalex-snapshot
Cognitive and anti-inflammatory effects of Palmaria palmata in a schizophrenia mouse model: insights into CREB signaling, Iba-1 expression, and CD4+ cell modulation
inferred← citeshttps://doi.org/10.3389/fnmol.2018.00056openalex-snapshot
Clinical Findings Documenting Cellular and Molecular Abnormalities of Glia in Depressive Disorders
inferred← citeshttps://doi.org/10.3389/fpsyt.2015.00116openalex-snapshot
Kynurenine 3-Monooxygenase: An Influential Mediator of Neuropathology
inferred← citeshttps://doi.org/10.3389/fpsyt.2016.00021openalex-snapshot
DTI and Myelin Plasticity in Bipolar Disorder: Integrating Neuroimaging and Neuropathological Findings
inferred← citeshttps://doi.org/10.3389/fpsyt.2018.00675openalex-snapshot
Low Field Magnetic Stimulation Ameliorates Schizophrenia-Like Behavior and Up-Regulates Neuregulin-1 Expression in a Mouse Model of Cuprizone-Induced Demyelination
inferred← citeshttps://doi.org/10.3389/fpsyt.2021.658340openalex-snapshot
Glymphatic Dysfunction: A Bridge Between Sleep Disturbance and Mood Disorders
inferred← citeshttps://doi.org/10.3389/fpsyt.2022.863734openalex-snapshot
Inflammatory Markers in Substance Use and Mood Disorders: A Neuroimaging Perspective
inferred← citeshttps://doi.org/10.3390/brainsci12111513openalex-snapshot
Astrocytes in the Neuropathology of Bipolar Disorder: Review of Current Evidence
inferred← citeshttps://doi.org/10.3390/brainsci13081221openalex-snapshot
Can Brain-Derived Neurotrophic Factor Be Considered a Biomarker for Bipolar Disorder? An Analysis of the Current Evidence
inferred← citeshttps://doi.org/10.3390/cells11203315openalex-snapshot
Gene Enrichment Analysis of Astrocyte Subtypes in Psychiatric Disorders and Psychotropic Medication Datasets
inferred← citeshttps://doi.org/10.3390/ijms22147671openalex-snapshot
Hidden Role of Gut Microbiome Dysbiosis in Schizophrenia: Antipsychotics or Psychobiotics as Therapeutics?
inferred← citeshttps://doi.org/10.35376/10324/51849openalex-snapshot
Conectividad de la red cerebral en el trastorno bipolar y la esquizofrenia
inferred← citeshttps://doi.org/10.35376/10324/72377openalex-snapshot
Exploration of self-integrity in psychotic disorders through electroencephalographic activity analysis during a speech production and perception task
inferred← citeshttps://doi.org/10.36253/ijae-15787openalex-snapshot
A narrative review of astrocytes and suicide in psychiatric disorders
inferred← citeshttps://doi.org/10.4103/2347-8659.167309openalex-snapshot
Neuroinflammation in bipolar disorders
inferred← citeshttps://doi.org/10.4103/indianjpsychiatry.indianjpsychiatry_104_21openalex-snapshot
Glial changes in schizophrenia
inferred← citeshttps://doi.org/10.4103/nrr.nrr-d-24-01375openalex-snapshot
Schizophrenia: Genetics, neurological mechanisms, and therapeutic approaches
inferred← citeshttps://doi.org/10.4172/2329-6488.1000e123openalex-snapshot
Astrocyte Function in Alcohol Reward and Addiction
inferred← citeshttps://doi.org/10.47626/2237-6089openalex-snapshot
Trends in Psychiatry and Psychotherapy
inferred← citeshttps://doi.org/10.53846/goediss-7396openalex-snapshot
Molecular Interactions between Neurons and Oligodendrocytes during Myelin Formation
inferred← citeshttps://doi.org/10.5498/wjp.v12.i2.264openalex-snapshot
Insights into myelin dysfunction in schizophrenia and bipolar disorder
inferred← citeshttps://doi.org/10.5498/wjp.v12.i2.268openalex-snapshot
Insights into myelin dysfunction in schizophrenia and bipolar disorder
inferred← citeshttps://doi.org/10.64898/2026.05.09.722417openalex-snapshot
Cell Type-informed Characterization of Spatial Niches from Spatial Multimodal and Multi-omics Data
inferred← citeshttps://doi.org/10.7554/elife.35136openalex-snapshot
An automated high-resolution in vivo screen in zebrafish to identify chemical regulators of myelination
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