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Exploring the full spectrum of macrophage activation

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Copper-Zinc Superoxide Dismutase (SOD1) Is Released by Microglial Cells and Confers Neuroprotection against 6-OHDA Neurotoxicity

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Neuroinflammation in Alzheimer's disease

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Consensus Nomenclature for in vivo Imaging of Reversibly Binding Radioligands

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Immune modulation of learning, memory, neural plasticity and neurogenesis

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Translocator protein (18kDa): new nomenclature for the peripheral-type benzodiazepine receptor based on its structure and molecular function

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Neuroinflammatory and Immunological Aspects of Fibromyalgia

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The Role of Brain Structure and Function in the Association Between Inflammation and Depressive Symptoms

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Low-dose lipopolysaccharide as an immune regulator for homeostasis maintenance in the central nervous system through transformation to neuroprotective microglia

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Gut Dysbiosis and Western Diet in the Pathogenesis of Essential Arterial Hypertension: A Narrative Review

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Neuro-Inflammation Modulation and Post-Traumatic Brain Injury Lesions: From Bench to Bed-Side

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Microglial depletion and activation: A [11C]PBR28 PET study in nonhuman primates

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Microglial activation and responses to vasculature that result from an acute LPS exposure

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Meta-analysis of the Glial Marker TSPO in Psychosis Revisited: Reconciling Inconclusive Findings of Patient–Control Differences

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PET imaging shows no changes in TSPO brain density after IFN-α immune challenge in healthy human volunteers

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Mechanisms of long-term cognitive dysfunction of sepsis: from blood-borne leukocytes to glial cells

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Influenza infection triggers disease in a genetic model of experimental autoimmune encephalomyelitis

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Shared microglial mechanisms underpinning depression and chronic fatigue syndrome and their comorbidities

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Kinetic modeling and parameter estimation of TSPO PET imaging in the human brain

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Inflammatory neuronal loss in the substantia nigra induced by systemic lipopolysaccharide is prevented by knockout of the P2Y6 receptor in mice

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Systemic inflammation induced the delayed reduction of excitatory synapses in the CA3 during ageing

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Orthopedic Surgery Causes Gut Microbiome Dysbiosis and Intestinal Barrier Dysfunction in Prodromal Alzheimer Disease Patients

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Characterization and modulation of microglial phenotypes in an animal model of severe sepsis

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Lifetime modulation of the pain system via neuroimmune and neuroendocrine interactions

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Downregulation of synapse-associated protein expression and loss of homeostatic microglial control in cerebrospinal fluid of infectious patients with delirium and patients with Alzheimer’s disease

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Intestinal Permeability and Its Significance in Psychiatric Disorders—A Narrative Review and Future Perspectives

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A binge high sucrose diet provokes systemic and cerebral inflammation in rats without inducing obesity

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Maresin 2 is an analgesic specialized pro-resolution lipid mediator in mice by inhibiting neutrophil and monocyte recruitment, nociceptor neuron TRPV1 and TRPA1 activation, and CGRP release

Fattori, V., Zaninelli, T. H., Ferraz, C. R., Brasil-Silva, L., Borghi, S. M., da Cunha, J. M., Chichorro, J. G., Casagrande, R., & Verri, W. A., Jr. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109189 · Cited by 44

Exploring the Significance of Gut Microbiota in Diabetes Pathogenesis and Management—A Narrative Review

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Recent Developments in Diagnosis of Epilepsy: Scope of MicroRNA and Technological Advancements

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Diffusion-weighted MR spectroscopy (DW-MRS) is sensitive to LPS-induced changes in human glial morphometry: A preliminary study

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Effects of Antipsychotic Drugs: Cross Talk Between the Nervous and Innate Immune System

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Systemic inflammation as a central player in the initiation and development of Alzheimer’s disease

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What Makes You Feel Sick After Inflammation? Predictors of Acute and Persisting Physical Sickness Symptoms Induced by Experimental Endotoxemia

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Histidine Decarboxylase Knockout Mice as a Model of the Pathophysiology of Tourette Syndrome and Related Conditions

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Peripheral inflammation in behavioural variant frontotemporal dementia: associations with central degeneration and clinical measures

Chu, M., Wen, L., Jiang, D., Liu, L., Nan, H., Yue, A., Wang, Y., Wang, Y., Qu, M., Wang, N., et al. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02746-5 · Cited by 33

Biomarker Predictors of Delirium in Acutely Ill Patients: A Systematic Review

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Gut Microbiota and Gut–Brain Axis in Hypertension: Implications for Kidney and Cardiovascular Health—A Narrative Review

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LPS and palmitic acid Co-upregulate microglia activation and neuroinflammatory response

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Systemic Inflammation and Anhedonic Responses to an Inflammatory Challenge in Adults With Major Depressive Disorder: A Randomized Controlled Trial

Savitz, J. B., Figueroa‐Hall, L. K., Teague, T. K., Yeh, H., Zheng, H., Kuplicki, R., Burrows, K., El-Sabbagh, N. S., Thomas, M., Ewers, I., et al. (2025) · American Journal of Psychiatry · doi:10.1176/appi.ajp.20240142 · Cited by 34

In vivo PET imaging of the neuroinflammatory response in rat spinal cord injury using the TSPO tracer [18F]GE-180 and effect of docosahexaenoic acid

Tremoleda, J. L., Thau‐Zuchman, O., Davies, M., Foster, J., Khan, I., Vadivelu, K. C., Yip, P. K., Sosabowski, J. K., Trigg, W., & Michael-Titus, A. T. (2016) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-016-3391-8 · Cited by 34

Why Are Some People with Lower Urinary Tract Symptoms (LUTS) Depressed? New Evidence That Peripheral Inflammation in the Bladder Causes Central Inflammation and Mood Disorders

Hughes, F. M., Odom, M. R., Cervantes, A., Livingston, A. J., & Purves, J. T. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032821 · Cited by 33

In VivoMRI of Functionalized Iron Oxide Nanoparticles for Brain Inflammation

Tang, T., Valenzuela, A. E., Petit, F., Chow, S. S. L., Leung, K. H., Gorin, F. A., Louie, A. Y., & Dhénain, M. (2018) · Contrast Media & Molecular Imaging · doi:10.1155/2018/3476476 · Cited by 35

The mind–skin connection: A narrative review exploring the link between inflammatory skin diseases and psychological stress

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Metabolic Endotoxemia: From the Gut to Neurodegeneration

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Neuroinflammation trajectories precede cognitive impairment after experimental meningitis—evidence from an in vivo PET study

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What can neuroimmunology teach us about the symptoms of long-COVID?

Mondelli, V., & Pariante, C. M. (2021) · Oxford Open Immunology · doi:10.1093/oxfimm/iqab004 · Cited by 32

A Modest Increase in 11C-PK11195-Positron Emission Tomography TSPO Binding in Depression Is Not Associated With Serum C-Reactive Protein or Body Mass Index

Schubert, J. J., Veronese, M., Fryer, T. D., Manavaki, R., Kitzbichler, M. G., Nettis, M. A., Mondelli, V., Pariante, C. M., Bullmore, E. T., Wlazly, D., et al. (2021) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2020.12.017 · Cited by 33

Evidence of fatigue, disordered sleep and peripheral inflammation, but not increased brain TSPO expression, in seasonal allergy: A [11C]PBR28 PET study

Tamm, S., Červenka, S., Forsberg, A., Estelius, J., Grünewald, J., Gyllfors, P., Karshikoff, B., Kosek, E., Lampa, J., Lensmar, C., et al. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.10.013 · Cited by 32

Potential efficacy and mechanism of eight mild-natured and bitter-flavored TCMs based on gut microbiota: A review

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Evaluation of Brain Nuclear Medicine Imaging Tracers in a Murine Model of Sepsis-Associated Encephalopathy

Szöllősi, D., Hegedűs, N., Veres, D. S., Futó, I., Horváth, I., Kovács, N., Martinecz, B., Dénes, Á., Seifert, D., Bergmann, R., et al. (2018) · Molecular Imaging and Biology · doi:10.1007/s11307-018-1201-3 · Cited by 31

Correlation between interleukin-6 levels and methadone maintenance therapy outcomes

Lu, R., Wang, T., Lee, S.-Y., Chen, S., Chang, Y.-H., Chen, P. S., Lin, S., Chu, C., Huang, S., Tzeng, N., et al. (2019) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2019.06.018 · Cited by 29

Heterogeneity of Microglia Phenotypes: Developmental, Functional and Some Therapeutic Considerations

Yuan, Y., Wu, C., & Ling, E. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666190722114248 · Cited by 31

In vivo monitoring of remnant undifferentiated neural cells following human induced pluripotent stem cell-derived neural stem/progenitor cells transplantation

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Advances of Molecular Imaging in Epilepsy

Galovic, M., & Koepp, M. J. (2016) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-016-0660-7 · Cited by 30

Translocator protein in late stage Alzheimer’s disease and Dementia with Lewy bodies brains

Xu, J., Sun, J., Perrin, R. J., Mach, R. H., Bales, K. R., Morris, J. C., Benzinger, T. L. S., & Holtzman, D. M. (2019) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.50837 · Cited by 31

Development of a 18F-Labeled Radiotracer with Improved Brain Kinetics for Positron Emission Tomography Imaging of Translocator Protein (18 kDa) in Ischemic Brain and Glioma

Fujinaga, M., Luo, R., Kumata, K., Zhang, Y., Hatori, A., Yamasaki, T., Xie, L., Mori, W., Kurihara, Y., Ogawa, M., et al. (2017) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.7b00374 · Cited by 30

Neuroimmune Mechanisms and Sex/Gender-Dependent Effects in the Pathophysiology of Mental Disorders

Kokkosis, A. G., & Tsirka, S. E. (2020) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.120.266163 · Cited by 29

From “Leaky Gut” to Impaired Glia-Neuron Communication in Depression

Rudzki, L., & Maes, M. H. J. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-981-33-6044-0_9 · Cited by 31

Nicotinic Acetylcholine Receptors and Microglia as Therapeutic and Imaging Targets in Alzheimer’s Disease

Takata, K., Kimura, H., Yanagisawa, D., Harada, K., Nishimura, K., Kitamura, Y., Shimohama, S., & Tooyama, I. (2022) · Molecules · doi:10.3390/molecules27092780 · Cited by 29

Imaging the inflammatory phenotype in migraine

Christensen, R. H., Gollion, C., Amin, F. M., Moskowitz, M. A., Hadjikhani, N. K., & Ashina, M. (2022) · The Journal of Headache and Pain · doi:10.1186/s10194-022-01430-y · Cited by 29

The translocator protein (18 kDa) and its role in neuropsychiatric disorders

Barichello, T., Simões, L. R., Collodel, A., Giridharan, V. V., Dal‐Pizzol, F., Macêdo, D. S., & Quevedo, J. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.10.010 · Cited by 30

Resolving the cellular specificity of TSPO imaging in a rat model of peripherally-induced neuroinflammation

Vicente-Rodríguez, M., Singh, N., Turkheimer, F., Peris-Yague, A., Randall, K., Veronese, M., Simmons, C., Karim Haji-Dheere, A., Bordoloi, J., Sander, K., et al. (2021) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2021.05.025 · Cited by 28

Postmortem Evidence of Brain Inflammatory Markers and Injury in Septic Patients: A Systematic Review

Barichello, T., Generoso, J. S., Dominguini, D., Córneo, E. D. S., Giridharan, V. V., Sahrapour, T. A., Simões, L. R., da Rosa, M. I., Petronilho, F. C., Ritter, C., et al. (2021) · Critical Care Medicine · doi:10.1097/ccm.0000000000005307 · Cited by 30

The Effects of Peripheral Inflammation on the Brain—A Neuroimaging Perspective

Millett, C. E., Burdick, K. E., & Kubicki, M. R. (2022) · Harvard Review of Psychiatry · doi:10.1097/hrp.0000000000000323 · Cited by 27

Microglial activation and neuroinflammation in acute and chronic cognitive deficits in sepsis

Denver, P., & Cunningham, C. M. (2024) · Neuropharmacology · doi:10.1016/j.neuropharm.2024.110285 · Cited by 33

Replicating predictive serum correlates of greater translocator protein distribution volume in brain

Attwells, S., Setiawan, E., Wilson, A. A., Rusjan, P., Miler, L., Xu, C., Hutton, C., Husain, M. I., Kish, S. J., Vasdev, N., et al. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0561-y · Cited by 27

Imaging the Neuroimmune Dynamics Across Space and Time

Carrier, M., Robert, M.-È., Ibáñez, F. G., Desjardins, M., & Tremblay, M. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00903 · Cited by 28

A potential mechanistic role for neuroinflammation in reward processing impairments in autism spectrum disorder

Greene, R. K., Walsh, E. C., Mosner, M. G., & Dichter, G. S. (2018) · Biological Psychology · doi:10.1016/j.biopsycho.2018.12.008 · Cited by 29

Extra-axial inflammatory signal and its relationship to peripheral and central immunity in depression

Eiff, B., Bullmore, E. T., Clatworthy, M. R., Fryer, T. D., Pariante, C. M., Mondelli, V., Maccioni, L., Hadjikhani, N. K., Loggia, M. L., Moskowitz, M. A., et al. (2024) · Brain · doi:10.1093/brain/awae343 · Cited by 27

Systemic immunization with altered myelin basic protein peptide produces sustained antidepressant-like effects

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Minocycline as adjunctive treatment for treatment-resistant depression: study protocol for a double blind, placebo-controlled, randomized trial (MINDEP2)

Husain, M. I., Cullen, C., Umer, M., Carvalho, A. F., Kloiber, S. M., Meyer, J. H., Ortiz, A., Knyahnytska, Y., Husain, M. O., Giddens, J. L., et al. (2020) · BMC Psychiatry · doi:10.1186/s12888-020-02553-9 · Cited by 26

The Bidirectional Signal Communication of Microbiota‐Gut‐Brain Axis in Hypertension

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Neuroinflammation in the Brain and Role of Intestinal Microbiota: An Overview of the Players

Cavaliere, G., & Traina, G. (2023) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2206148 · Cited by 29

Neuroinflammatory mechanisms of hypertension

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Imaging Biomarkers of the Neuroimmune System among Substance Use Disorders: A Systematic Review

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Emerging Developments in Human Induced Pluripotent Stem Cell-Derived Microglia: Implications for Modelling Psychiatric Disorders With a Neurodevelopmental Origin

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Investigating whether depressed youth exhibiting elevated C reactive protein perform worse on measures of executive functioning, verbal fluency and episodic memory in a large, population based sample of Dutch adolescents

Giollabhui, N. M., Alloy, L. B., & Hartman, C. A. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.08.030 · Cited by 24

Preclinical Neuropathic Pain Assessment; the Importance of Translatability and Bidirectional Research

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Inflammation, Obsessive-Compulsive Disorder, and Related Disorders

Meyer, J. H. (2021) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_210 · Cited by 26

Risk of Dementia and Structural Brain Changes Following Nonneurological Infections During 9-Year Follow-Up*

van Ton, A. M. P., Leijsen, E. M. C. M.-V., Bergkamp, M. I., Bronkhorst, E. M., Pickkers, P., de Leeuw, F., Tuladhar, A. M., & Abdo, W. F. (2021) · Critical Care Medicine · doi:10.1097/ccm.0000000000005313 · Cited by 26

The isozyme selective phosphodiesterase-4 inhibitor, ABI-4, attenuates the effects of lipopolysaccharide in human cells and rodent models of peripheral and CNS inflammation

Hedde, J. R., Hanks, A. N., Schmidt, C. J., & Hughes, Z. A. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.04.015 · Cited by 24

Microglial Hyperreactivity Evolved to Immunosuppression in the Hippocampus of a Mouse Model of Accelerated Aging and Alzheimer’s Disease Traits

Molina‐Martínez, P., Corpas, R., García-Lara, E., Cosín‐Tomás, M., Cristòfol, R. M., Kaliman, P., Solà, C., Molinuevo, J. L., Sánchez‐Valle, R., Antonell, A., et al. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.622360 · Cited by 24

Traumatic Brain Injury and Gut Brain Axis: The Disruption of an Alliance

Ferrara, M., Bertozzi, G., Zanza, C., Longhitano, Y., Piccolella, F., Lauritano, E. C., Volonnino, G., Manetti, A. C., Maiese, A., & Russa, R. L. (2022) · Reviews on Recent Clinical Trials · doi:10.2174/1574887117666220622143423 · Cited by 23

HDL and LDL have distinct, opposing effects on LPS-induced brain inflammation

Radford‐Smith, D. E., Yates, A. G., Rizvi, L., Anthony, D. C., & Probert, F. (2023) · Lipids in Health and Disease · doi:10.1186/s12944-023-01817-z · Cited by 24

Single Inflammatory Trigger Leads to Neuroinflammation in LRRK2 Rodent Model without Degeneration of Dopaminergic Neurons

Schildt, A., Walker, M. D., Dinelle, K., Miao, Q., Schulzer, M., OʼKusky, J. R., Farrer, M. J., Doudet, D. J., & Sossi, V. (2018) · Journal of Parkinson s Disease · doi:10.3233/jpd-181446 · Cited by 25

Disease activity in rheumatoid arthritis is inversely related to cerebral TSPO binding assessed by [11C]PBR28 positron emission tomography

Forsberg, A., Lampa, J., Estelius, J., Červenka, S., Farde, L., Halldin, C., Lekander, M., Höglund, C. O., & Kosek, E. (2019) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2019.577000 · Cited by 25

Acute Morphine Exposure Increases the Brain Distribution of [18F]DPA-714, a PET Biomarker of Glial Activation in Nonhuman Primates

Auvity, S., Saba, W., Goutal, S., Leroy, C., Buvat, I., Cayla, J., Caillé, F., Bottlaender, M., Cisternino, S., & Tournier, N. (2016) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyw077 · Cited by 22

Microglia-mediated neuroimmune suppression in PTSD is associated with anhedonia

Bonomi, R. E., Hillmer, A. T., Woodcock, E. A., Bhatt, S., Rusowicz, A., Angarita, G. A., Carson, R. E., Davis, M. T., Esterlis, I., Nabulsi, N., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2406005121 · Cited by 22

Insights into electrochemical decomposition mechanism of lipopolysaccharide using TiO2 nanotubes arrays electrode

Wang, K., Li, Y., Huang, J., Xu, L., Yin, L., Ji, Y., Wang, C., Xu, Z., & Niu, J. (2020) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2020.122259 · Cited by 21

Perspective: Solving the Heterogeneity Conundrum of TSPO PET Imaging in Psychosis

Picker, L. D., & Morrens, M. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00362 · Cited by 21

Depression Phenotype, Inflammation, and the Brain

Krishnadas, R., & Harrison, N. A. (2016) · Psychosomatic Medicine · doi:10.1097/psy.0000000000000339 · Cited by 21

[18F]DAA1106: Automated radiosynthesis using spirocyclic iodonium ylide and preclinical evaluation for positron emission tomography imaging of translocator protein (18 kDa)

Kumata, K., Zhang, Y., Fujinaga, M., Ohkubo, T., Mori, W., Yamasaki, T., Hanyu, M., Xie, L., Hatori, A., & Zhang, M. (2018) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2018.08.017 · Cited by 21

Evidence of microglial activation following exposure to serum from first-onset drug-naïve schizophrenia patients

van Rees, G. F., Lago, S. G., Cox, D., Tomasik, J., Rustogi, N., Weigelt, K., Özcan, S., Cooper, J. D., Drexhage, H. A., Leweke, F. M., et al. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.10.003 · Cited by 22

Indications of success: Strategies for utilizing neuroimaging biomarkers in CNS drug discovery and development

Suhara, T., Chaki, S., Kimura, H., Furusawa, M., Matsumoto, M., Ogura, H., Negishi, T., Saijo, T., Higuchi, M., Omura, T., et al. (2016) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyw111 · Cited by 19

Perioperative neurocognitive disorders: Advances in molecular mechanisms and bioactive molecules

Mao, L., Wang, L., Huang, Z., Switzer, J. A., Hess, D. C., & Zhang, Q. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102885 · Cited by 24

Mediterranean diet and prudent diet are both associated with low circulating esterified 3-hydroxy fatty acids, a proxy of LPS burden, among older adults

André, P., de Barros, J.-P. P., Merle, B. M. J., Samieri, C., Helmer, C., Delcourt, C., & Féart, C. (2021) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/nqab126 · Cited by 20

Dietary fiber ameliorates lead‐induced gut microbiota disturbance and alleviates neuroinflammation

Yao, M., Shao, X., Wei, Y., Zhang, X., Wang, H., & Xu, F. (2022) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.12074 · Cited by 20

Current status of PET tracers for the early diagnosis of Alzheimer's disease

Li, Y., Liu, T., Zeng, Q., & Cui, M. (2024) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2024.117546 · Cited by 20

Quinic Acid Alleviates Behavior Impairment by Reducing Neuroinflammation and MAPK Activation in LPS-Treated Mice

Park, Y., Paing, Y. M. M., Cho, N., Kim, C., Yoo, J., Choi, J. W., & Lee, S. H. (2024) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2023.184 · Cited by 19

Associations of Microbiota and Nutrition with Cognitive Impairment in Diseases

Młynarska, E., Jakubowska, P., Frąk, W., Gajewska, A., Sornowska, J., Skwira, S., Wasiak, J., Rysz, J., & Franczyk, B. (2024) · Nutrients · doi:10.3390/nu16203570 · Cited by 19

Anxiogenic-like effect of chronic lipopolysaccharide is associated with increased expression of matrix metalloproteinase 9 in the rat amygdala

Shishkina, G. T., Bannova, A. V., Komysheva, N. P., & Дыгало, Н. Н. (2020) · Stress · doi:10.1080/10253890.2020.1793943 · Cited by 19

The brain-gut axis: A prime therapeutic target in traumatic brain injury

Weaver, J. L. (2020) · Brain Research · doi:10.1016/j.brainres.2020.147225 · Cited by 18

Pharmacological and Genetic Inhibition of Translocator Protein 18 kDa Ameliorated Neuroinflammation in Murine Endotoxemia Model

Giga, H., Ji, B., Kikutani, K., Fukuda, S., Kitajima, T., Katsumata, S., Matsumata, M., Suhara, T., Yamawaki, S., Shime, N., et al. (2020) · Shock · doi:10.1097/shk.0000000000001703 · Cited by 18

Leaky Gut Biomarkers as Predictors of Depression and Suicidal Risk: A Systematic Review and Meta-Analysis

Morena, D., Lippi, M., Scopetti, M., Turillazzi, E., & Fineschi, V. (2025) · Diagnostics · doi:10.3390/diagnostics15131683 · Cited by 24

Lipopolysaccharide-induced inflammation leads to acute elevations in pro-inflammatory cytokine expression in a mouse model of Fragile X syndrome

Hodges, S. L., Nolan, S. O., Tomac, L. A., Muhammad, I. D. A., Binder, M. S., Taube, J. H., & Lugo, J. N. (2019) · Physiology & Behavior · doi:10.1016/j.physbeh.2019.112776 · Cited by 20

Endotoxin-induced systemic inflammation activates microglia: [11C]PBR28 positron emission tomography in nonhuman primates

Hannestad, J. O., Gallezot, J., Schafbauer, T., Lim, K., Kloczynski, T., Morris, E. D., Carson, R. E., Ding, Y., & Cosgrove, K. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.06.055 · Cited by 218

Systemic endotoxin induces a robust increase in microglial activation measured with [11C]PBR28 and PET in humans

Sandiego, C. M., Gallezot, J., Lim, K., Lin, S.-F., Devine, L., O’Connor, K. C., Huang, Y. H., Hannestad, J. O., Carson, R. E., & Cosgrove, K. (2015) · Journal of Nuclear Medicine · Cited by 1

Peripheral benzodiazepine receptor/18 kDa translocator protein positron emission tomography imaging in a rat model of acute brain injury

Nomura, M., Toyama, H., Suzuki, H., Yamada, T., Hatano, K., Wilson, A. A., Ito, K., & Sawada, M. (2020) · Annals of Nuclear Medicine · doi:10.1007/s12149-020-01530-2 · Cited by 5

Two activated stages of microglia and PET imaging of peripheral benzodiazepine receptors with [11C]PK11195 in rats

Ito, F., Toyama, H., Kudo, G., Suzuki, H., Hatano, K., Ichise, M., Katada, K., Ito, K., & Sawada, M. (2010) · Annals of Nuclear Medicine · doi:10.1007/s12149-009-0339-0 · Cited by 23

Perivascular microglia defined

Graeber, M. B., & Streit, W. J. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90020-b · Cited by 91