Regulation of innate immune responses in the brain

Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo

Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827

Microglia: Active sensor and versatile effector cells in the normal and pathologic brain

Hanisch, U.-K., & Kettenmann, H. (2007) · Nature Neuroscience · doi:10.1038/nn1997 · Cited by 3,676

The NALP3 inflammasome is involved in the innate immune response to amyloid-β

Halle, A., Hornung, V., Petzold, G. C., Stewart, C. R., Monks, B. G., Reinheckel, T., Fitzgerald, K. A., Latz, E., Moore, K. J., & Golenbock, D. T. (2008) · Nature Immunology · doi:10.1038/ni.1636 · Cited by 2,441

Untitled work

Wyss-Coray (2006) · doi:10.1038/nm1484 · Cited by 1,284

Bone Marrow-Derived Microglia Play a Critical Role in Restricting Senile Plaque Formation in Alzheimer's Disease

Simard, A. R., Soulet, D., Gowing, G., Julien, J.-P., & Rivest, S. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.022 · Cited by 1,265

Inflammation in Neurodegenerative Disease—A Double-Edged Sword

Wyss-Coray, T., & Mucke, L. (2002) · Neuron · doi:10.1016/s0896-6273(02)00794-8 · Cited by 1,235

The inflammatory response in stroke

Wang, Q., Tang, X. N., & Yenari, M. A. (2007) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.11.014 · Cited by 1,196

Cytokines and acute neurodegeneration

Allan, S. M., & Rothwell, N. J. (2001) · Nature reviews. Neuroscience · doi:10.1038/35094583 · Cited by 1,145

Toll-like receptor 3 mediates West Nile virus entry into the brain causing lethal encephalitis

Wang, T., Town, T., Alexopoulou, L., Anderson, J. F., Fikrig, E., & Flavell, R. A. (2004) · Nature Medicine · doi:10.1038/nm1140 · Cited by 1,142

Modulating effects of environmental enrichment on stress-induced changes in the gut microbiome

Smith, K. B., Murack, M., Butcher, J., Hinterberger, A., Stintzi, A. P., Liang, J., Tata, D. Α., & Ismail, N. (2025) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2025.101023 · Cited by 1

Multi-tier signaling and chromatin remodeling coordinate microglia inflammatory states and activities associated with demyelination

Distéfano‐Gagné, F., Belhamiti, N., Saxon, W., Bitarafan, S., Xavier, A. M., Fiola, S., Rivest, S., & Gosselin, D. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117569 · Cited by 1

How do energy metabolism disorders and neuroinflammation collectively contribute to the pathogenesis of Alzheimer’s disease?

Lei, Y., Liu, L., & Tang, Y. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103287 · Cited by 1

The CNS Innate Immune System and the Emerging Roles of the Neuroimmune Regulators (NIRegs) in Response to Infection, Neoplasia and Neurodegeneration

W., J., Denizot, M., J., J., & Gasque, P. (2012) · InTech eBooks · doi:10.5772/37824 · Cited by 1

Glial and Axonal Pathology in Multiple Sclerosis

Robinson‐Agramonte, M. D. L. Á., González‐Quevedo, A., & Alberto, C. (2012) · InTech eBooks · doi:10.5772/38317 · Cited by 1

Biochemical Aspects of Neuroinflammation

Farooqui, A. A. (2014) · Springer eBooks · doi:10.1007/978-3-319-04111-7_2 · Cited by 1

Multiple Sclerosis, Alzheimer’s Disease, and Inflammation: A Hypothetical View

Bynoe, M. S., & Viret, C. (2012) · Molecular and integrative toxicology · doi:10.1007/978-1-61779-812-2_9 · Cited by 1

Bacterial UDP-Glucose Hydrolases and P2 Receptor-Mediated Responses to Infection: A Commentary

Beacham, I. R., & Headrick, J. P. (2013) · Advances in Infectious Diseases · doi:10.4236/aid.2013.32016 · Cited by 1

Psychoneuroimmune Phenomena: Neuroimmune Interactions

Dantzer, R., & Kelley, K. W. (2012) · Springer eBooks · doi:10.1007/978-1-4614-1997-6_21 · Cited by 1

The Blood-Brain Barrier and the Immune Privilege of the Central Nervous System

Clarkson, B. D. S., Harris, M. G., Rayasam, A., & Fábry, Z. (2015) · CRC Press eBooks · doi:10.1201/b18606-9 · Cited by 1

Physalis alkekengi L. var. francheti alleviates neuronal cell death caused by activated microglia in vitro

Park, B. H., Kwon, O. W., Kim, I. S., Lee, H. M., Roh, Y. J., Kim, M., Jo, Y., Cho, H., Park, J. K., Zhi, Z., et al. (2021) · Applied Biological Chemistry · doi:10.1186/s13765-021-00594-6 · Cited by 1

The Role of Adaptive and Innate Immunity in Alzheimer’s Disease

Holmes, C. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108539623.012 · Cited by 1

Microglia Properties☆

Hanisch, U. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.04665-1 · Cited by 1

Recurrent oxidant treatment induces dysregulation in the brain transcriptome of Atlantic salmon (Salmo salar) smolts

Carletto, D., Breiland, M. W., Hytterød, S., Timmerhaus, G., & Lazado, C. C. (2022) · Toxicology Reports · doi:10.1016/j.toxrep.2022.06.009 · Cited by 1

Oxytocine et neuroprotection en période néonatale : évidences conceptuelles et précliniques

Baud, O., & Knoop, M. S. (2023) · Gynécologie Obstétrique Fertilité & Sénologie · doi:10.1016/j.gofs.2023.12.005 · Cited by 1

Síntomas neuropsiquiátricos en encefalitis por anticuerpos contra el receptor N-metil-D-aspartato: a propósito de dos casos

Custodio, N., & Montalvo, J. E. (2016) · Anales de la Facultad de Medicina · doi:10.15381/anales.v77i3.12419 · Cited by 1

Essential contributions of enhancer genomic regulatory elements to microglial cell identity and functions

Xavier, A. M., Belhocine, S., & Gosselin, D. (2019) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1449 · Cited by 1

Steroid hormones differentially regulate expression of complement receptors immunoglobulin in human macrophages, involving the glucocorticoid receptor

Kooltheat, N., Potup, P., Thongsri, Y., Ferrante, A., & Usuwanthim, K. (2019) · Trends in Biomedical Research · doi:10.15761/jtbr.1000109 · Cited by 1

Solid Organ Injury

Land, W. G. (2020) · Springer eBooks · doi:10.1007/978-3-030-53868-2_9 · Cited by 1

Malaria

Tavares, J. C. (2013) · Colloquium Series on Integrated Systems Physiology From Molecule to Function · doi:10.4199/c00091ed1v01y201309isp045 · Cited by 1

Análise temporal de mediadores inflamatórios no tecido neuronal e na periferia em camundongos 3xTg-AD, um modelo animal para a Doença de Alzheimer

Kinoshita, D. (2012) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.10.2012.tde-26092012-140403 · Cited by 1

Heparan Sulfate in the Amyloidosis and Inflammation of Alzheimer’s Disease

O′Callaghan, P. W. (2011) · KTH Publication Database DiVA (KTH Royal Institute of Technology) · Cited by 1

WNT SIGNALING IN MICROGLIA

Halleskog, C. (2013) · Cited by 1

Traumatic Brain Injury and Neurodegenerative Disease

McGuire, D. (2018) · Wiley eBooks · doi:10.1002/9781118772034.ch26 · Cited by 2

Molecular Regulation of Inflammation and Angiogenesis in the Tumor Microenvironment

Dieterich, L. C. (2011) · KTH Publication Database DiVA (KTH Royal Institute of Technology) · Cited by 1

Intravital microscopy

Fonseca, I. M. G., Michael Schnoor, A., & Vadillo, E. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90195-6.00009-7 · Cited by 1

TLR2 genetic diversity associated with the risk of Schizophrenia development in a Tunisian populationPreprint

Ayari, F., Chaaben, A. B., Abbaza, H., Mihoub, O., Ouni, N., Mankaï, A., Boukouaci, W., kharat, M., Leboyer, M., & Tamouza, R. (2022) · Research Square · doi:10.21203/rs.3.rs-1678095/v1 · Cited by 1

Microglia Depletion Selectively Eliminates a Singular Form of Hippocampal Long-Term PotentiationPreprint

Chavez, J., Le, A. A., Quintanilla, J., Tagne, A. M., Piomelli, D., LYNCH, G. S., & Gall, C. M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.29.501926 · Cited by 1

Inflammatory Signatures of Microglia in the Mouse Model of Corticosterone-Induced DepressionPreprint

Zhao, Y., Huang, Y., Cao, Y., & Yang, J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.21.608928 · Cited by 1

Acute inflammation-mediated attenuation of behavioural sensitization in methamphetamine-sensitized mice via distinct COX-2 and TNF-α pathwaysPreprint

Shinohara, R. C., Ishikawa, S., Matsumoto, R., Ito, K., Tonosaki, M., Matsuyama, S., Ohgidani, M., Koga, M., Hashimoto, N., Kusumi, I., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.08.723429 · Cited by 1

Immune System, Innate; Overview

Gandhi, R., & Weiner, H. L. (2014) · Encyclopedia of the Neurological Sciences · doi:10.1016/b978-0-12-385157-4.00180-9 · Cited by 1

Toll-7 and Toll-6: central nervous system functions as Drosophila neurotrophin receptors

McIlroy, G. (2012) · University of Birmingham Institutional Research Archive (University of Birmingham) · Cited by 1

The cuprizone model and multiple sclerosis : disparities and similarities

Kipp, M., & Baumgärtner, W. (2011) · RWTH Publications (RWTH Aachen)

Tyrphostin AG126 modulates Toll-like receptor (TLR) activation-induced functions in microglia by protein tyrosine kinase (PTK) -dependent and -independent mechanisms

Menzfeld, C. (2010) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-395

Studies on poly-ICLC treatment as a potent neuroprotective therapy against ischemic brain injury

Packard, A. E. B. (2015) · doi:10.6083/m4qv3jjw

Cytokine genetics and expression : implications of an immunogenetic pathogenesis in autism spectrum disorders.

Mott, M. C. (2011) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/1016

Studies on the neurotrophic factor Manf and the pleiotropic factor Lin-28 during Drosophila development

Stratoulias, V. (2014) · Työväentutkimus Vuosikirja

Interactions between Neuronal Innate Immune Pattern Recognition Receptor Pathways and Neurotropic Arboviruses: Host Measures, Viral Countermeasures, and Potential Therapeutics.

Peltier, D. (2010) · Deep Blue (University of Michigan)

WNT SIGNALING IN MICROGLIA

Halleskog, C. (2013) · Figshare

The Role of Acid Sphingomyelinase in Experimental Autoimmune Encephalomyelitis

Davies, L. (2013) · Publications of the UdS (Saarland University) · doi:10.22028/d291-21752

In VivoImaging of Glial and Immune Cell Responses in Central Nervous System Injury and Disease

Paré, A., & Lacroix, S. (2015) · Wiley eBooks · doi:10.1002/9781118732748.ch2

Estudio de la expresión y función de los receptores tipo Toll (TLRs) en células madre de la retina de mamífero adulto

Flores, A. I. (2015) · Tesis Doctorals en Xarxa (Consorci de Serveis Universitaris de Catalunya)

Efeito da sinvastatina na evolução clínica e na resposta imune celular Th17 na encefalite auto-imune experimental

de Oliveira, D. M. (2009) · doi:10.11606/d.42.2009.tde-09022010-121315

Suppression of Smad-1 mRNA expression level by Smad-2 likely control dichotomy of NF-κB and Smads mediated activation

Slade, N., Zorić, A., Horvat, B., Vukšić, M., Kostović, I., & Poljak, L. (2014) · Immunobiology · doi:10.1016/j.imbio.2014.09.003

New light on white matter damage of the premature brain: a neonatologist's point of view

Marcialis, M. A., Dessì, A., Irmesi, R., Marinelli, V., & Pintus, M. C. (2014) · Journal of pediatric and neonatal individualized medicine · doi:10.7363/030237

Modulation of Sensory Nerve Activity and Pharmaceutical Treatments

Sartori, M. (2014) · Journal of Anesthesia & Critical Care Open Access · doi:10.15406/jaccoa.2014.01.00009

Inflammation in the immature brain: The role of Toll like receptors

Stridh, L. (2011) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Genetic Regulation of Neuroinflammation after Infection and Injury

Abdelmagid, N. (2012) · Figshare

An Examination of the Long-lasting Effects of Lipopolysaccharide-induced Sepsis on Cognitive and Affective Behaviour in Mice

Anderson, S. T. (2014) · Maynooth University ePrints and eTheses Archive (Maynooth University)

A fractalkina (CX3CL1) está envolvida nas etapas iniciais de ativação da inflamação no hipotálamo de roedores obesos

Morari, J. (2013) · doi:10.47749/t/unicamp.2013.917221

[Albumin and IGG in the CSF as demonstration of blood-brain barrier damage and of immune response within the CNS (author's transl)].

Cognazzo, A., Promis, P. C. G., & Grasso, E. A. (1981) · PubMed

A Study of Brain Biomechanics Using Hamilton’s Principle: Application to Hydrocephalus

Drapaca, C. S., & Kauffman, J. A. (2015) · Springer proceedings in mathematics & statistics · doi:10.1007/978-3-319-12307-3_27

Microglia and Pain

Beggs, S., Trang, T., & Salter, M. W. (2012) · doi:10.1093/med/9780199794591.003.0068

Organization and consequences of functional responses in microglia upon activation of the TLR4 complex

Jáňová, H. (2014) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-4704

Neuroinflammation in Huntington’s & Related Neurodegenerative Disorders

Tripathi, V. K., & Jana, N. R. (2016) · Springer eBooks · doi:10.1007/978-981-10-1711-7_6

Defining microglial phenotypic diversity and the impact of ageing

Grabert, K. (2015) · ERA

Advances in the Treatment of Primary Brain Tumors: The Realm of Immunotherapy

Strong, M. J., & Ware, M. L. (2017) · InTech eBooks · doi:10.5772/65791

Standarization of a Protocol of Immunohistochemistry for the Detection of Brain Microglia in Wistar Rats

Ramírez, K., & Trías, J. F. (2017) · Odovtos - International Journal of Dental Sciences · doi:10.15517/ijds.v19i3.29698

Self-Uptake by Microglia Contributes to Amyloid Beta-Induced Receptor-Mediated Pinocytosis 4 P2Y

Duan, S., Lou, H., Zhang, J., Li, X., Wang, H., Li, H.-Q., Chen, C., Dou, Y., Wu, H., & Liu, Y. (2014)

Inflammatory Changes in Cerebral Ischemic Injury: Cellular and Molecular Involvement

Ooboshi, H. (2017) · Royal Society of Chemistry eBooks · doi:10.1039/9781788012539-00015

Axonal Transport, Parkin, And Α-Synuclein; Novel Therapeutic Targets To Treat Methamphetamine Neurotoxicity

Killinger, B. A. (2017) · Human Biology

The Effect of Docosahexaenoic Acid in a Mouse Model of Neuroinflammation

Orr, S. K. (2012) · TSpace (University of Toronto)

The Role of Age and Model Severity on Cortical Vascular Response Following Traumatic Brain Injury

Brickler, T. (2017) · VTechWorks (Virginia Tech)

L’immunopsychiatrie existe-t-elle ?

Fond, G. B. (2018) · Phytothérapie · doi:10.3166/phyto-2018-0092

Assessment of the visual thalamic circuitry in hallucinations in dementia with Lewy bodies

Erskine, D. (2017)

Signalisation par les récepteurs toll-like dans un contexte d'excitotoxicité

Larochelle, A. (2014) · Corpus Université Laval (Université Laval)

Oligodendroglial anillin facilitates septin assembly to prevent myelin outfoldings

Erwig, M. S. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7308

Early-life stress and inflammatory cytokines in psychoses: from bench to community-based research

Zuelli, F. M. D. G. C. (2020) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.17.2020.tde-26072019-154034

Efeitos dos glicocorticoides nas interações celulares de astrócitos, microglia e neurônios durante inflamação induzida por LPS em modelo in vitro.

Duque, É. D. A. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2019.tde-15102019-100704

Roles of the Choroid Plexus in CNS Infections

Schwerk, C., Tenenbaum, T., & Schroten, H. (2020) · Physiology in health and disease · doi:10.1007/978-1-0716-0536-3_11

Microglia

Cardona, A. E., Ransohoff, R. M., & Akassoglou, K. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00085-x · Cited by 2

Brain-Immune Interactions as the Basis of Gulf War Illness: Gulf War Illness Consortium (GWIC)

Sullivan, K. A. (2014) · doi:10.21236/ada613555

Roles in Immune Responses

Hanamsagar, R., Cardona, S. M., Kielian, T., & Cardona, A. E. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1429-6_5

Histopathological Evaluation of LAG-3, TIM-3 AND CD38 Levels in Meningiomas

Erdoğan, U., Haşimoğlu, O., Oflezer, C., Tanrıverdi, O., Tanık, C. T., & Günaldı, Ö. (2021) · Cam and Sakura Medical Journal · doi:10.4274/csmedj.galenos.2021.2021-11-5

Psychoneuroimmune Phenomena: Neuroimmune Interactions

Dantzer, R. (2021) · Springer eBooks · doi:10.1007/978-1-4614-6434-1_21-3

Faculty Opinions recommendation of Toll-6 and Toll-7 function as neurotrophin receptors in the Drosophila melanogaster CNS.

Imler, J. (2013) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718049779.793482844

Faculty Opinions recommendation of Brain infiltration of leukocytes contributes to the pathophysiology of temporal lobe epilepsy.

Avoli, M., & Biagini, G. (2011) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.10796957.11701055

Stressor re-exposure effects on behaviour and expression of pro-inflammatory cytokines in male and female mice

Hudson, S. E. (2014) · doi:10.22215/etd/2014-10260

Faculty Opinions recommendation of Neuroinflammation in Alzheimer's disease.

Perani, D. (2017) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.725413893.793537457

Faculty Opinions recommendation of The link between chronic pain and Alzheimer's disease.

Bergese, S. D., & Echeverria-Villalobos, M. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736867128.793567607

References

(2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811351-6.00026-7

Stressor and cytokine interactions : implications in depressive-like pathology

Gibb, J. (2011) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2011-09658

Neuroinflammatory mechanisms of Parkinson's Disease

Mangano, E. N. (2011) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2011-09648

Neuroprotective action of α-Klotho against LPS- activated glia conditioned medium in primary neuronal culturePreprint

Nakao, V. W., Mazucanti, C. H., Lima, L. S., Mello, P. S. D., Port’s, N. M. D. S., Kinoshita, P. F., Leite, J. A., Kawamoto, E. M., & Scavone, C. (2022) · Research Square · doi:10.21203/rs.3.rs-1632930/v1

TLR2 genetic diversity and the risk of SchizophreniaPreprint

Ayari, F., Chaaben, A. B., Abbaza, H., Mihoub, O., Ouni, N., Mankaï, A., Boukouaci, W., kharat, M., Leboyer, M., & Tamouza, R. (2022) · Research Square · doi:10.21203/rs.3.rs-1678095/v2

Neuroprotective action of α-Klotho against LPS- activated glia conditioned medium in primary neuronal culturePreprint

Nakao, V. W., Mazucanti, C. H., Lima, L. S., Mello, P. S. D., Port’s, N. M. D. S., Kinoshita, P. F., Leite, J. A., Kawamoto, E. M., & Scavone, C. (2022) · Research Square · doi:10.21203/rs.3.rs-1632930/v2

Infection-Induced Systemic Inflammation and Dementia

Osafo, N., Dei, S. O., Akwei, N. A., & Yeboah, K. O. (2022) · Springer eBooks · doi:10.1007/978-981-16-7606-2_2

Application of 9.4 Tesla resting-state functional MRI to Assess Neuronal function and Detect Microglial Density in AKI Rat ModelPreprint

Yu, Z., Pang, H., Yang, Y., Xu, C., Zheng, H., Huang, Z., Wu, Z., Hu, J., & Ren, K. (2022) · Research Square · doi:10.21203/rs.3.rs-1584210/v1

Psychoneuroimmune Phenomena: Neuroimmune Interactions

Dantzer, R. (2022) · Springer eBooks · doi:10.1007/978-3-030-88832-9_21

Binding of electrophilic chemicals to SH(thiol)-group of proteins and /or to seleno-proteins involved in protection against oxidative stress during brain development leading to impairment of learning and memory

Monnet‐Tschudi, F., Zurich, M., Nunes, C., Sandström, J., FitzGerald, R., Aschner, M., & da Rocha, J. B. T. (2022) · OECD series on adverse outcome pathways · doi:10.1787/4df0e9e4-en · Cited by 2

Ocytocine : une nouvelle cible de neuroprotection ?

Baud, O., Knoop, M. S., Jacquens, A., & Possovre, M.-L. (2022) · Biologie Aujourd hui · doi:10.1051/jbio/2022012

Protection against Microglia Senescence by the Dietary Supplement Dekosilhue® in BV2 Cells: A New Perspective for Obesity and Related Complications

Borgonetti, V., Sasia, C., Morozzi, M., Cenci, L., & Galeotti, N. (2023) · Nutraceuticals · doi:10.3390/nutraceuticals3020020

Detection of Toxoplasma Gondii DNA in Uterine and Malignant Prostate Tissues of Cancer Patients

Saeed, R. E., & Majali, A. A. A.-H. (2023) · International Journal of Research in Medical Sciences & Technology · doi:10.37648/ijrmst.v16i01.004

Alzheimer’s disease beyond the amyloid accumulation

Urkon, M., & Nagy, E. E. (2022) · Orvostudományi Értesítö · doi:10.2478/orvtudert-2022-0002

Merkezi Sinir Sisteminde MSS Mikroglia Mast Hücrelerinin Rolü ve Nörodejeneratif Hastalıklar Açısından Önemi

KUŞAT, T., & Emrah, S. U. R. (2023) · doi:10.59287/sbyc.582

Hyperoside Alleviates Macrophage-mediated Neuroinflammation And Oxidative Stress Through Activating PI3K/AKT And Nrf2/HO-1 Signaling Pathway Post Spinal Cord InjuryPreprint

Zhang, Q., Liu, X., Zhu, Q., Xia, M., & Li, H. (2023) · Research Square · doi:10.21203/rs.3.rs-3627565/v1

Microbiota intestinal y modulación central del síndrome dolor - depresión. ¿Mito o realidad?

Maresca, T. (2021) · NeuroTarget · doi:10.47924/neurotarget20215

Neurobiology of Neuroimmune Encephalitic Disorders

Laje, G. (2023) · Springer eBooks · doi:10.1007/978-3-030-42825-9_167-1

Associaçao entre microbiota intestinal e transtorno depressivo maior: uma revisão da literatura

Bochi, G. V., & Quincozes, J. A. V. (2021) · Revista Ciência & Humanização do Hospital de Clínicas de Passo Fundo · doi:10.29327/2185320.1.2-10

Neurobiology of Neuroimmune Encephalitic Disorders

Laje, G. (2024) · Springer eBooks · doi:10.1007/978-3-030-51366-5_167

Molecular and cellular immune mediators of neuroprotection

Turrin, N. P., & Rivest, S. (2006) · Molecular Neurobiology · doi:10.1385/mn:34:3:221 · Cited by 85

Microglia and their roles in response to injury of the central nervous system

Jia, Y. (2012) · Yixue yanjiusheng xuebao · Cited by 2

The role of the microglia in acute CNS injury

Kawabori, M., & Yenari, M. A. (2014) · Metabolic Brain Disease · doi:10.1007/s11011-014-9531-6 · Cited by 145

The Brain innate immune response in neuroprotection and repair

Serge, R. (2009) · Frontiers in Neuroscience · doi:10.3389/conf.neuro.01.2009.11.001

Microglia and neuroinflammation: a pathological perspective

Streit (2004) · Journal of Neuroinflammation · doi:10.1186/1742-2094-1-14 · Cited by 1,039