| scholarly article | Q13442814 |
| P2093 | author name string | Bernhard T Baune | |
| Gaurav Singhal | |||
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| Stress in puberty unmasks latent neuropathological consequences of prenatal immune activation in mice | Q28286419 | ||
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| Alterations in 5-HT1B receptor function by p11 in depression-like states | Q28290425 | ||
| Immune cells contribute to the maintenance of neurogenesis and spatial learning abilities in adulthood | Q28292031 | ||
| Identification of a unique TGF-β-dependent molecular and functional signature in microglia | Q28303557 | ||
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| The inflammasome NLRs in immunity, inflammation, and associated diseases | Q29616025 | ||
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| Inflammation is detrimental for neurogenesis in adult brain | Q29619040 | ||
| Two types of mouse T helper cell. IV. Th2 clones secrete a factor that inhibits cytokine production by Th1 clones | Q29622840 | ||
| Activation of P2X7 receptor and NLRP3 inflammasome assembly in hippocampal glial cells mediates chronic stress-induced depressive-like behaviors | Q29994732 | ||
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| Neurotoxic kynurenine metabolism is increased in the dorsal hippocampus and drives distinct depressive behaviors during inflammation | Q30839124 | ||
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| Hippocampal volume and depression: a meta-analysis of MRI studies | Q30974294 | ||
| Microglia shape adult hippocampal neurogenesis through apoptosis-coupled phagocytosis | Q33560182 | ||
| Age differences in major depression: results from the National Comorbidity Survey Replication (NCS-R) | Q33619096 | ||
| Reduced density of calbindin immunoreactive GABAergic neurons in the occipital cortex in major depression: relevance to neuroimaging studies | Q33664090 | ||
| A two-way communication between microglial cells and angiogenic sprouts regulates angiogenesis in aortic ring cultures | Q33802916 | ||
| Cytokines and the brain: implications for clinical psychiatry | Q33900651 | ||
| Proinflammatory cytokines | Q33913139 | ||
| Genetic epidemiology of major depression: review and meta-analysis | Q33919509 | ||
| Inflammatory Cytokines in Nonpathological States | Q33949887 | ||
| Environmental enrichment enhances neurogenesis and improves functional outcome after cranial irradiation | Q34002090 | ||
| Social defeat induces depressive-like states and microglial activation without involvement of peripheral macrophages | Q37224361 | ||
| Differential effects of homotypic vs. heterotypic chronic stress regimens on microglial activation in the prefrontal cortex. | Q37232659 | ||
| Fluoxetine Inhibits NLRP3 Inflammasome Activation: Implication in Depression | Q37299370 | ||
| Evidence for a cytokine model of cognitive function | Q37321439 | ||
| Depression and cardiovascular disease | Q37344801 | ||
| GABAergic neurons immunoreactive for calcium binding proteins are reduced in the prefrontal cortex in major depression | Q37408446 | ||
| Neuroinflammation and comorbidity of pain and depression | Q37432089 | ||
| Inflammasome signaling at the heart of central nervous system pathology | Q37686413 | ||
| EAAT expression by macrophages and microglia: still more questions than answers | Q37849616 | ||
| Role of pro-inflammatory cytokines released from microglia in neurodegenerative diseases | Q37949182 | ||
| Inflammasomes in carcinogenesis and anticancer immune responses | Q37995072 | ||
| Post-ischemic inflammation in the brain | Q38029598 | ||
| Review: microglia of the aged brain: primed to be activated and resistant to regulation | Q38049597 | ||
| Microglia: actively surveying and shaping neuronal circuit structure and function. | Q38069248 | ||
| Microglia: new roles for the synaptic stripper. | Q38073391 | ||
| Microglia control neuronal network excitability via BDNF signalling | Q38148753 | ||
| Repression of inflammatory responses in the absence of DNA binding by the glucocorticoid receptor | Q38293939 | ||
| Etanercept and clinical outcomes, fatigue, and depression in psoriasis: double-blind placebo-controlled randomised phase III trial. | Q38410039 | ||
| Role of the Kynurenine Metabolism Pathway in Inflammation-Induced Depression: Preclinical Approaches | Q38844375 | ||
| Stress-Induced Microglia Activation and Monocyte Trafficking to the Brain Underlie the Development of Anxiety and Depression | Q38879652 | ||
| NLRP3 inflammasome-driven pathways in depression: Clinical and preclinical findings | Q38926968 | ||
| Immune activation promotes depression 1 month after diffuse brain injury: a role for primed microglia | Q38976143 | ||
| Associations between serum levels of inflammatory markers and change in knee pain over 5 years in older adults: a prospective cohort study | Q39118341 | ||
| Learned helplessness activates hippocampal microglia in rats: A potential target for the antidepressant imipramine. | Q39260354 | ||
| Altered microglia morphology and higher resilience to stress-induced depression-like behavior in CX3CR1-deficient mice | Q39283986 | ||
| Involvement of inflammasome activation in lipopolysaccharide-induced mice depressive-like behaviors | Q39307144 | ||
| NSAIDs are associated with lower depression scores in patients with osteoarthritis | Q39357958 | ||
| Minocycline selectively inhibits M1 polarization of microglia | Q39496127 | ||
| Effect of treatment on serum glial cell line-derived neurotrophic factor in depressed patients | Q40014805 | ||
| Serum markers support disease-specific glial pathology in major depression | Q40100041 | ||
| Neuronal regulation by which microglia enhance the production of neurotrophic factors for GABAergic, catecholaminergic, and cholinergic neurons | Q40141093 | ||
| Prevalence and risk factors of depression among community dwelling elderly | Q40186922 | ||
| Microglia-derived tumor necrosis factor-alpha exaggerates death of newborn hippocampal progenitor cells in vitro | Q40424649 | ||
| Cytokines and their receptors in the central nervous system: physiology, pharmacology, and pathology | Q40674047 | ||
| Astrocytes, brain aging, and neurodegeneration | Q41048970 | ||
| Cytokines and adhesion molecules in stroke and related diseases | Q41091098 | ||
| Role of spinal microglia in visceral hyperalgesia and NK1R up-regulation in a rat model of chronic stress | Q41873671 | ||
| Aging exacerbates depressive-like behavior in mice in response to activation of the peripheral innate immune system. | Q41993255 | ||
| Glucocorticoids mediate stress-induced priming of microglial pro-inflammatory responses | Q42381161 | ||
| Aging and glial responses to lipopolysaccharide in vitro: greater induction of IL-1 and IL-6, but smaller induction of neurotoxicity | Q42443522 | ||
| Neurotrophins regulate dendritic growth in developing visual cortex | Q42479052 | ||
| A molecular and cellular theory of depression | Q34064955 | ||
| Inflammation-associated depression: from serotonin to kynurenine | Q34147377 | ||
| Gut feelings: the emerging biology of gut-brain communication | Q34199959 | ||
| Inflammasomes in neuroinflammation and changes in brain function: a focused review | Q34299338 | ||
| The role of the Schwann cell in trophic support and regeneration | Q34307306 | ||
| Microglia, the first line of defence in brain pathologies. | Q34311723 | ||
| Review: the role of inflammation in depression | Q34367973 | ||
| Glia and their cytokines in progression of neurodegeneration | Q34382722 | ||
| Microglia: a sensor to threats in the nervous system? | Q34405840 | ||
| Defining glial cells during CNS development | Q34443660 | ||
| Host microbiota constantly control maturation and function of microglia in the CNS. | Q34478756 | ||
| The Gut-Brain Axis: The Missing Link in Depression | Q34502723 | ||
| Minocycline, a tetracycline derivative, is neuroprotective against excitotoxicity by inhibiting activation and proliferation of microglia. | Q34514721 | ||
| MAP kinases in the immune response | Q34542231 | ||
| Minocycline treatment ameliorates interferon-alpha- induced neurogenic defects and depression-like behaviors in mice. | Q34667917 | ||
| Stress, depression, and neuroplasticity: a convergence of mechanisms | Q34686632 | ||
| Immune system to brain signaling: neuropsychopharmacological implications. | Q34769827 | ||
| The inflammatory & neurodegenerative (I&ND) hypothesis of depression: leads for future research and new drug developments in depression | Q34904703 | ||
| Associations of depression with C-reactive protein, IL-1, and IL-6: a meta-analysis | Q34935593 | ||
| TNF-Α may mediate inflammasome activation in the absence of bacterial infection in more than one way. | Q34937708 | ||
| Microglia as a source and target of cytokines | Q34963658 | ||
| Cytokine-induced changes in mood and behaviour: implications for 'depression due to a general medical condition', immunotherapy and antidepressive treatment | Q35017009 | ||
| Role of microglia in inflammation-mediated neurodegenerative diseases: mechanisms and strategies for therapeutic intervention. | Q35029780 | ||
| Stress proteins and glial functions: possible therapeutic targets for neurodegenerative disorders | Q35031242 | ||
| Inflammasome is a central player in the induction of obesity and insulin resistance | Q35216914 | ||
| The effect of antidepressant medication treatment on serum levels of inflammatory cytokines: a meta-analysis | Q35356649 | ||
| Intravenous immunoglobulins containing antibodies against beta-amyloid for the treatment of Alzheimer's disease | Q35477363 | ||
| The inflammasome: pathways linking psychological stress, depression, and systemic illnesses | Q35592049 | ||
| Effects of centrally administered etanercept on behavior, microglia, and astrocytes in mice following a peripheral immune challenge. | Q35647379 | ||
| Inflammasomes in cardiovascular diseases | Q35660178 | ||
| Tricyclic Antidepressant Amitriptyline-induced Glial Cell Line-derived Neurotrophic Factor Production Involves Pertussis Toxin-sensitive Gαi/o Activation in Astroglial Cells | Q35662230 | ||
| Contribution of glial cells to the development of amyloid plaques in Alzheimer's disease | Q35789671 | ||
| Local effects of BDNF on dendritic growth | Q35808549 | ||
| Brain-derived neurotrophic factor (BDNF) infusion restored astrocytic plasticity in the hippocampus of a rat model of depression | Q42613055 | ||
| The role of microglia in mediating the effect of the environment in brain plasticity and behavior. | Q43010674 | ||
| Long-term treatment with peony glycosides reverses chronic unpredictable mild stress-induced depressive-like behavior via increasing expression of neurotrophins in rat brain | Q43153875 | ||
| Chronic stress alters the density and morphology of microglia in a subset of stress-responsive brain regions | Q43163166 | ||
| Age-related activation of microglia and astrocytes: in vitro studies show persistent phenotypes of aging, increased proliferation, and resistance to down-regulation | Q43478741 | ||
| Cardiovascular disease, interleukin-6, and risk of mortality in older women: the women's health and aging study | Q43831921 | ||
| Brain volume abnormalities in major depressive disorder: a meta-analysis of magnetic resonance imaging studies | Q44066592 | ||
| Effects of norepinephrine on rat cultured microglial cells that express alpha1, alpha2, beta1 and beta2 adrenergic receptors | Q44210702 | ||
| Gastrodin ameliorates depressive-like behaviors and up-regulates the expression of BDNF in the hippocampus and hippocampal-derived astrocyte of rats | Q44285325 | ||
| Diabetes, hyperglycemia, and inflammation in older individuals: the health, aging and body composition study | Q44676231 | ||
| Neuroscience. Microglia: the enemy within? | Q44681258 | ||
| Toward a comprehensive developmental model for major depression in men. | Q44916290 | ||
| Pro- and anti-inflammatory cytokines expression in rat's brain and spleen exposed to chronic mild stress: involvement in depression | Q45192635 | ||
| Major depressive disorder and hypothalamic-pituitary-adrenal axis activity: results from a large cohort study. | Q45987152 | ||
| Impairments in endocannabinoid signaling and depressive illness | Q46085075 | ||
| Noradrenaline reuptake inhibitors limit neuroinflammation in rat cortex following a systemic inflammatory challenge: implications for depression and neurodegeneration | Q46220981 | ||
| Eighteen months of drug treatment for depression: predicting relapse and recovery | Q46355684 | ||
| Drugs with antidepressant properties affect tryptophan metabolites differently in rodent models with depression-like behavior. | Q46383849 | ||
| Probiotic treatment reduces depressive-like behaviour in rats independently of diet | Q46402201 | ||
| Early life stress alters behavior, immunity, and microbiota in rats: implications for irritable bowel syndrome and psychiatric illnesses. | Q46414083 | ||
| Dopamine and noradrenaline control distinct functions in rodent microglial cells. | Q46467964 | ||
| Social stress and the regulation of tumor necrosis factor-alpha secretion | Q46535205 | ||
| Stress-induced elevation of glucocorticoids increases microglia proliferation through NMDA receptor activation | Q46796904 | ||
| The involvement of norepinephrine and microglia in hypothalamic and splenic IL-1beta responses to stress. | Q46874243 | ||
| Reduced neuronal size and glial cell density in area 9 of the dorsolateral prefrontal cortex in subjects with major depressive disorder. | Q47191236 | ||
| Reduced glial cell density and neuronal size in the anterior cingulate cortex in major depressive disorder. | Q47207451 | ||
| P2X7 as a new target for chrysophanol to treat lipopolysaccharide-induced depression in mice | Q47584088 | ||
| Microglia Loss Contributes to the Development of Major Depression Induced by Different Types of Chronic Stresses | Q47901145 | ||
| Toll-like receptor 2 and nucleotide-binding oligomerization domain-2 play divergent roles in the recognition of gut-derived lactobacilli and bifidobacteria in dendritic cells | Q47961731 | ||
| Glial reduction in amygdala in major depressive disorder is due to oligodendrocytes. | Q47969861 | ||
| Decreased levels of kynurenic acid in prefrontal cortex in a genetic animal model of depression | Q48049046 | ||
| Microglia activation is associated with IFN-α induced depressive-like behavior | Q48073957 | ||
| Interferon-alpha treatment induces depression-like behaviour accompanied by elevated hippocampal quinolinic acid levels in rats | Q48077606 | ||
| Association of depression duration with reduction of global cerebral gray matter volume in female patients with recurrent major depressive disorder | Q48156362 | ||
| Differential production of MCP-1 and cytokine-induced neutrophil chemoattractant in the ischemic brain after transient focal ischemia in rats | Q48179025 | ||
| Orbitofrontal cortex volume in late life depression: influence of hyperintense lesions and genetic polymorphisms | Q48254650 | ||
| Imipramine induces brain-derived neurotrophic factor mRNA expression in cultured astrocytes | Q48332044 | ||
| NLRP3 inflammasome is activated in mononuclear blood cells from patients with major depressive disorder | Q48354329 | ||
| Dynamic microglial alterations underlie stress-induced depressive-like behavior and suppressed neurogenesis. | Q48385750 | ||
| Brain-derived neurotrophic factor (BDNF) is required for the enhancement of hippocampal neurogenesis following environmental enrichment | Q48397095 | ||
| BDNF release from single cells elicits local dendritic growth in nearby neurons | Q48473998 | ||
| Stress increases vulnerability to inflammation in the rat prefrontal cortex. | Q48523197 | ||
| Learning, memory, and glial cell changes following recovery from chronic unpredictable stress | Q48547013 | ||
| Is unpredictable chronic mild stress (UCMS) a reliable model to study depression-induced neuroinflammation? | Q48589388 | ||
| Central and systemic endotoxin challenges exacerbate the local inflammatory response and increase neuronal death during chronic neurodegeneration. | Q48741510 | ||
| Association between cytokines and cerebral MRI changes in the aging brain. | Q48765609 | ||
| Social deprivation stress is a triggering factor for the emergence of anxiety- and depression-like behaviours and leads to reduced brain BDNF levels in C57BL/6J mice. | Q48860107 | ||
| Evidence that microglia mediate the neurobiological effects of chronic psychological stress on the medial prefrontal cortex. | Q48925604 | ||
| Circulating levels of inflammatory markers and cancer risk in the health aging and body composition cohort. | Q51509450 | ||
| Patient-reported outcomes improve with etanercept plus methotrexate in active early rheumatoid arthritis and the improvement is strongly associated with remission: the COMET trial. | Q51764647 | ||
| Molecules that mediate mood. | Q51970578 | ||
| Cytokines in neuroinflammation and Alzheimer's disease | Q35843383 | ||
| Alterations of neuroplasticity in depression: the hippocampus and beyond. | Q35953971 | ||
| Microglia in Alzheimer brain: a neuropathological perspective | Q35986371 | ||
| Peripheral innate immune challenge exaggerated microglia activation, increased the number of inflammatory CNS macrophages, and prolonged social withdrawal in socially defeated mice. | Q36013009 | ||
| Role of glial cells in cerebral ischemia | Q36104660 | ||
| Hypercortisolemia and depression. | Q36161754 | ||
| Imaging cerebral tryptophan metabolism in brain tumor-associated depression | Q36171525 | ||
| Effects of cytokines and infections on brain neurochemistry | Q36262535 | ||
| Microglial phenotype: is the commitment reversible? | Q36365630 | ||
| Molecular mechanisms involved in T cell migration across the blood-brain barrier. | Q36426872 | ||
| Microglia in the aging brain | Q36465314 | ||
| Upregulated NLRP3 inflammasome activation in patients with type 2 diabetes. | Q36477239 | ||
| Mechanisms of disease: inflammasome activation and the development of type 2 diabetes | Q36668052 | ||
| Reducing the societal burden of depression: a review of economic costs, quality of care and effects of treatment | Q36693787 | ||
| Neuroprotective role of the innate immune system by microglia | Q36801872 | ||
| BDNF overexpression in mouse hippocampal astrocytes promotes local neurogenesis and elicits anxiolytic-like activities. | Q36809785 | ||
| Gliogenesis and glial pathology in depression | Q36825936 | ||
| Aging, microglial cell priming, and the discordant central inflammatory response to signals from the peripheral immune system | Q36882295 | ||
| Evidence for IL-1 receptor blockade as a therapeutic strategy for the treatment of depression | Q36904522 | ||
| Microglia biology in health and disease. | Q37015357 | ||
| NMDA receptor blockade by ketamine abrogates lipopolysaccharide-induced depressive-like behavior in C57BL/6J mice | Q37030206 | ||
| Neurobiological mechanisms in major depressive disorder | Q37071342 | ||
| Neuroplasticity in depressed individuals compared with healthy controls | Q37172753 | ||
| IL-1, IL-18, and IL-33 families of cytokines | Q37211243 | ||
| P921 | main subject | neuroplasticity | Q849491 |
| microglia | Q1622829 | ||
| P304 | page(s) | 270 | |
| P577 | publication date | 2017-09-08 | |
| P1433 | published in | Frontiers in Cellular Neuroscience | Q2131509 |
| P1476 | title | Microglia: An Interface between the Loss of Neuroplasticity and Depression | |
| P478 | volume | 11 |
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