Microglia and neuroinflammation: a pathological perspective

Amyloid oligomers exacerbate tau pathology in a mouse model of tauopathy

Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359

Inflammation and Alzheimer’s disease

Akiyama, H. (2000) · Neurobiology of Aging · doi:10.1016/s0197-4580(00)00124-x · Cited by 4,514

Innate Immunity

Medzhitov, R. M., & Janeway, C. A. (2000) · New England Journal of Medicine · doi:10.1056/nejm200008033430506 · Cited by 1,827

Brain interleukin 1 and S-100 immunoreactivity are elevated in Down syndrome and Alzheimer disease.

Griffin, W. S., Stanley, L. C., Ling, C., White, L., MacLeod, V, Perrot, L. J., White, C. L., & Araoz, C. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.19.7611 · Cited by 1,777

Reactive microglia in patients with senile dementia of the Alzheimer type are positive for the histocompatibility glycoprotein HLA-DR

McGeer, P. L., Itagaki, S., Tago, H., & McGeer, E. G. (1987) · Neuroscience Letters · doi:10.1016/0304-3940(87)90696-3 · Cited by 836

APPSW Transgenic Mice Develop Age-related Aβ Deposits and Neuropil Abnormalities, but no Neuronal Loss in CA1

IRIZARRY, M. C., MCNAMARA, M., FEDORCHAK, K., HSIAO, K., & HYMAN, B. T. (1997) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/00005072-199709000-00002 · Cited by 649

Microglial response to amyloid plaques in APPsw transgenic mice.

Frautschy, S. A., Yang, F., Irrizarry, M., Hyman, B. T., Saido, T. C., Hsiao, K., & Cole, G. M. (1998) · Europe PMC (PubMed Central) · Cited by 592

Neuroinflammation in Alzheimer's disease and prion disease

Eikelenboom, P., Bate, C., van Gool, W. A., Hoozemans, J. J. M., Rozemüller, A. J. M., Veerhuis, R., & Williams, A. (2002) · Glia · doi:10.1002/glia.10146 · Cited by 412

Rats and mice exhibit distinct inflammatory reactions after spinal cord injury

Sroga, J. M., Jones, T. B., Kigerl, K. A., McGaughy, V. M., & Popovich, P. G. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10736 · Cited by 369

Fibrillar β-Amyloid Induces Microglial Phagocytosis, Expression of Inducible Nitric Oxide Synthase, and Loss of a Select Population of Neurons in the Rat CNS In Vivo

Weldon, D. T., Rogers, S. D., Ghilardi, J. R., Finke, M. P., Cleary, J. P., O’Hare, E., Esler, W. P., Maggio, J. E., & Mantyh, P. W. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-06-02161.1998 · Cited by 348

Autism, Development and Neural Plasticity

Robinson‐Agramonte, M. D. L. Á., Fraguela, M. E. G., & Bergado, J. A. (2015) · Springer eBooks · doi:10.1007/978-3-319-16321-5_7 · Cited by 1

Targeting leukotriene-mediated neuroinflammation in traumatic brain injury

Corser-Jensen, C. E. (2015) · doi:10.25677/t3c4-nq55 · Cited by 1

Potential Roles for the Neurotrophic Molecules Agrin and Neuregulin in Regulating Aspects of the Inflammatory Response

Mencel, M. (2014) · UWSpace (University of Waterloo) · Cited by 2

WNT SIGNALING IN MICROGLIA

Halleskog, C. (2013) · Cited by 1

Japanese Encephalitis Virus Infected Microglial Cells Secrete Exosomes Containing let-7a/b that Facilitate Neuronal Damage via Caspase ActivationPreprint

Mukherjee, S., Akbar, I., Kumari, B., Vrati, S., Basu, A., & Banerjee, A. K. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/324715 · Cited by 1

In vivo Imaging of Cerebral Microglial Activation and Glutathione in Regular Cannabis Users

Silva, D., & Sofia, T. (2018) · TSpace (University of Toronto) · Cited by 1

Blood and Brain Gene Expression Trajectories Underlying Neuropathology and Cognitive Impairment in NeurodegenerationPreprint

Iturria‐Medina, Y., Khan, A. F., Adewale, Q., & Initiative, A. D. N. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/548974 · Cited by 1

Role of Interferon-Gamma and Leucine-Rich Repeat Kinase 2 in Stress-Related Pathology

Litteljohn, D. (2016) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2016-11660

HIV-1 and microglia: EcoHIV and HIV-1 transgenic ratsPreprint

Li, H., McLaurin, K. A., Illenberger, J. M., Mactutus, C. F., & Booze, R. M. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.03.365494 · Cited by 1

Therapeutic Strategies to Treat Alcohol-Related Disorders Targeting Central Immune Signaling

Wu, Y. H., & Hutchinson, M. R. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4729-0_17

WNT SIGNALING IN MICROGLIA

Halleskog, C. (2013) · Figshare

Effects of Adoptive Transfer of Beta-Amyloid Sensitive Immune Cells in a Mouse Model for Alzheimer’s Disease

Shippy, D. C. (2005) · Digital Commons - University of South Florida (University of South Florida)

Genomic clues to secondary injury mechanisms in brain trauma

von Gertten, C. (2006) · Figshare

Chronic Ill Effects of Air Pollution in Children: Neurological Derailment

Kumar, H., & Sharma, A. (2012) · Global Journal of Human-Social Science

ANALYSIS OF RAT MICROGLIAL CELLULAR SENESCENCE AS DETERMINED BY MEASUREMENTS OF TELOMERE LENGTH AND TELOMERASE ACTIVITY

Flanary, B. E. (2005)

Modulation of ASIC1a function by sigma-1 receptors: Physiological and pathophysiological implications

Herrera, Y. (2009) · Digital Commons - University of South Florida (University of South Florida)

A ativação imune materna e os efeitos sobre a imunidade, neuroinflamação e desenvolvimento da encefalomielite autoimune experimental na prole de camundongos

Zager, A. (2013) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.10.2013.tde-21112013-113642

Functional analysis of microglial signal regulatory protein β 1 (SIRPβ1)

Gaikwad, S. M. (2007) · bonndoc (University of Bonn)

Diagnosis and Management of Posttraumatic Pancreatits in Children

Zarembo, E., Eņģelis, A., Zviedre, A., & Pētersons, A. (2012) · Acta Chirurgica Latviensis · doi:10.2478/v10163-012-0013-9

hippocampus after transient cerebral ischemia: a comparative study of two rat strains using stereological tools

Kelsen, J., Larsen, M. H., Sørensen, J. C. H., Møller, A., Frøkiær, J., Nielsen, S. U., Nyengaard, J. R., Mikkelsen, J. D., & Christian, L. (2010)

Dissertação para obtenção do Grau de Mestre em Genética Molecular e Biomedicina

Filipa, A., & de Oliveira, M. I. P. (2011)

Trajectories of Recovery and Dysfunction after Acute Illness, with Implications for Clinical Trial Design

Jt, J., & Mh, S. (2012)

Tumour necrosis FA cTor - ALPHA mediAT ed mecHAnisms oF cogniT ive dysF unc Tion 1 Discipline of Psychiatry, School of Medicine,

Baune, B. T., Camara, M.-L., Eyre, H. A., Jawahar, M. C., Anscomb, H., & Körner, H. (2012)

Synaptic Plasticity in Mammalian Brain Resting Microglial Motility Is Independent of

MacVicar, B. A., Dissing‐Olesen, L., LeDue, J. M., Rungta, R. L., Hefendehl, J. K., Choi, H. B., Wu, L., Madry, C., & Attwell, D. (2015)

Microglial clearance function: dependence on phenotypes

Oliveira, A. F. (2011) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

Severe Head Trauma and Omega-3 Fatty Acids

Lewis, M. D. (2014) · Springer eBooks · doi:10.1007/978-1-4614-8503-2_114-1

The role of alpha-synuclein phosphorylation in synucleinopathies

Basso, E. (2014) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

EFECTO ANTIOXIDANTE DEL EXTRACTO HIDROALCOHÓLICO DE TILIA PLATYPHYLLOS SCOPOLI "TILO DE HOJA ANCHA" EN ISQUEMIA-REPERFUSIÓN CEREBRAL EXPERIMENTAL EN RATAS

Quispe, L. E. C., & Sevillano, O. E. P. (2016) · Dialnet (Universidad de la Rioja)

Potential neuroprotective effects of fermented rooibos herbal tea in a rat model of ischemic brain injury

Akinrinmade, O. A. (2015) · University of the Western Cape Electronic Theses and Dissertations Repository (University of the Western Cape)

Neuregulin’s role in regulating the anti-inflammatory pathway

Nash, M. M. (2009) · UWSpace (University of Waterloo)

Utilization of Fish Oil for the Prevention and Treatment of Traumatic Brain Injury

Lewis, M. D. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802844-5.00027-0

The Function of Cytokines in Ischemic Stroke

Leonardo, C. C., & Pennypacker, K. R. (2016) · Springer series in translational stroke research · doi:10.1007/978-3-319-32337-4_15

Development of Stable Long‐term Electrode Tissue Interfaces for Recording and Stimulation

Schouenborg, J. (2016) · Wiley eBooks · doi:10.1002/9781118816028.ch2

Mammalian and bacterial toxicity of nanoparticles used in hazardous waste treatment and environmental remediation

Long, T. C. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/cfym-p630

Pathophysiology of the Blood–Brain Barrier in Neuroinflammatory Diseases

Majerová, P., & Kováč, A. (2017) · Springer eBooks · doi:10.1007/978-3-319-45514-3_4

Inflammatory pathology in neurodegenerative dementias

Niedermayer, G. (2014)

Sex Differences in Morphine Analgesia and the Role of Microglia in the Periaqueductal Gray of the Rat

Doyle, H. H. (2022) · Digital Archive @ GSU · doi:10.57709/10165308

Inflammation-Mediated Neurodegeneration: Models, Mechanisms, and Therapeutic Interventions for Neurodegenerative Diseases

Gao, H., Gao, Y., Tu, D., Liu, Y., Zhou, H., & Hong, J. (2017) · Wiley-VCH eBooks · doi:10.1002/9783527692156.ch48

The Role of A3 Adenosine Receptors in Opioid Analgesic Tolerance

Xu, Y. (2017) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/28315

Terapia génica y reprogramación celular en modelos animales de envejecimiento cerebral

Pardo, J. (2017) · El Servicio de Difusión de la Creación Intelectual (National University of La Plata) · doi:10.35537/10915/64088

Commentary on interactions between neurotropic pathogens, neuroinflammatory pathways, and autophagic neural cell death

Cellina, M. I., & Orsi, M. (2018) · Neuroimmunology and Neuroinflammation · doi:10.20517/2347-8659.2018.15

Neurological effects of ambient air pollution

Waaijenberg, C. M. (2012) · Utrecht University Repository (Utrecht University)

Le virus herpes simplex de type 1 : résistance aux antiviraux et réponse inflammatoire cérébrale

Sergerie, Y. (2007) · Corpus Université Laval (Université Laval)

Molecular inflection points in the aging human brainPreprint

Deng, E. Z. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/455105

Terapia celular y génica con timulina E IGF-1 en modelos animales de neuroinflamación

Villar, M. F. Z. (2018) · El Servicio de Difusión de la Creación Intelectual (National University of La Plata) · doi:10.35537/10915/71572

Relationship between central cholinergic system and neuroinflammation a molecular pharmacological approach

Tyagi, E. (2011) · Shodhganga

ANTI-INFLAMMATORY EFFECTS OF POLYPHENOL-ENRICHED EXTRACTS AND THEIR GUT MICROBIAL METABOLITES

DaSilva, N. A. (2019) · Digital Commons - URI (University of Rhode Island) · doi:10.23860/diss-dasilva-nicholas-2019

Investigating anti-neuroinflammatory mechanism of orientin in lipopolysaccharide-induced BV2 microglia cells

Gan, P. H., Ling, A. P. K., Voon, K., Koh, R. Y., & Wong, Y. P. (2019) · Asia-Pacific Journal of Molecular Biology and Biotechnology · doi:10.35118/apjmbb.2019.027.2.11

Atypical gene expression of neuroinflammatory and steroid related genes following injury in the photoperiodic Japanese quail

Arndtsen, C., Ballon, J., Blackshear, K., Corbett, C. B., Lee, K. M., Peyer, J., Holloway, K. S., & Duncan, K. A. (2019) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2019.113361

Cellular and Proteolytic Studies of Alzheimer's Disease Amyloid Beta Peptide with Microglia, Stem Cells and Mmp9

Njie, E. G. (2010) · University of Florida Digital Collections (University of Florida)

Cerebrospinal fluid biomarkers of Parkinson's disease: an update

Nagao, K. J., & LeWitt, P. A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-815946-0.00021-1

Neuroinflammation and Chronic Pelvic Pain Syndrome

Crupi, R., Cordaro, M., & Cuzzocrea, S. (2020) · Urodynamics, neurourology and pelvic floor dysfunctions · doi:10.1007/978-3-030-56387-5_3

MICROGLYOCYTES MORPHOLOGY AFTER FOCAL ISCHEMIC STROKE IN A MOUSE BRAIN

Гиганова, А. А., Ананьина, Т. В., Kisel, A. A., & Ходанович, М. Ю. (2020) · Международная Звенигородская конференция по физике плазмы и управляемому термоядерному синтезу · doi:10.37539/vt187.2020.56.18.005

Positron emission tomography imaging agents for evaluating the pathologic features of Alzheimer's disease and drug development

Huang, Y. H., Jia, H., & Bao, W. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-816475-4.00013-6

Longitudinal Examination of Peripheral Blood Biomarkers in Healthy Athletes: Implications for Concussion

Watling, S. E. (2019) · TSpace (University of Toronto)

Insulin signaling and microglia in the young and aged brain

Haas, C. B. (2021) · doi:10.33612/diss.183132348

Neuroinflammatory mechanisms and translational approaches in environmental neurotoxicity models

Jeffrey, C. E. (2012) · doi:10.31274/etd-180810-2851

Management of Athletes’ Medications

Gore, A. D. (2009) · OhioLink ETD Center (Ohio Library and Information Network)

Metabotropic Glutamate Receptor 5 Negative Allosteric Modulation Effects on Microglia Phenotype

Curtis, N. (2021) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2021-14640

The Hypothalamus in Alzheimer’s Disease: A Golgi and Electron and Microscope Study

Balogiannis, S., Mavroudis, I. A., Mitilineos, D., Baloyannis, I. S., & Costa, V. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.75887

White matter integrity of the frontal brain and its relevance for catatonia and executive function

Arinrad, S. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8974

Studies on the Involvement of the Immune system in Alzheimer's disease

Marcello, A. (2010) · doi:10.53846/goediss-3277

The role of the novel small molecule QUIN-A in suppressing neuroinflammation and its target

Wang, J., Yang, Y., Li, W., Wu, S., & Han, C. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.108651

Abstracts and Citations

Kaniecki, R. G., Taylor, F. R., & Stillman, M. J. (2010) · Headache The Journal of Head and Face Pain · doi:10.1111/j.1526-4610.2010.01614.x

Faculty Opinions recommendation of Persistent Toxoplasma Infection of the Brain Induced Neurodegeneration Associated with Activation of Complement and Microglia.

Yap, G. S., & Nasuhidehnavi, A. (2021) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735972270.793588180

Severe Head Trauma and Omega-3 Fatty Acids

Lewis, M. D. (2015) · Springer eBooks · doi:10.1007/978-1-4614-7836-2_114

The action of maternal separation on glutamate receptors and neuroinflammation

Ganguly, P. (2018) · Digital Repository Service (Northeastern University) · doi:10.17760/d20316401

Processus neurodégénératifs et inflammation

Véga, C. (2022) · Elsevier eBooks · doi:10.1016/b978-2-294-76331-1.00001-x

Melatonin ameliorates cisplatin-induced neurodegeneration in medulla oblongata through the expressions of Aqp-1,-4, inflammation, and apoptosis pathway genes.

Öztopuz, Ö. (2022) · PubMed Central · doi:10.3906/biy-2110-90

Spatio-temporal dynamics of microglia phenotype in human and murine cSVD: impact of acute and chronic hypertensive statesPreprint

Morton, L., Arndt, P., Garza, A. P., Henneicke, S., Mattern, H., Gonzalez, M., Dityatev, A. E., Yilmazer‐Hanke, D., Schreiber, S., & Dunay, I. R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.15.553403

Regulatory Role of PKR in Systemic Inflammation-Triggered Neuroinflammation and its Modulation of Glucose Metabolism and Cognitive Functions in Cholinergic NeuronsPreprint

Cheng, W., Lee, X.-Z., Lai, M. S., Ho, J. Y. S., & Chang, R. C. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.10.561630

Reprogramación celular y rejuvenecimiento: aplicación en el cerebro senil

Canatelli-Mallat, M. (2023) · El Servicio de Difusión de la Creación Intelectual (National University of La Plata) · doi:10.35537/10915/160047

Docking Sites of Indole Derivative on Mitogen-Activated Protein Kinase (MAPK) Inhibitor (PDB ID- 1A9U) against Inflammation

Bhor, R. J., Agale, A. C., Gaikwad, M. S., Navnath, M. D., & Sunil, W. S. (2023) · International Journal of Pharmaceutical Investigation · doi:10.5530/ijpi.14.1.22

The inflammatory injury of microglia involved in Tourette syndrome development

Hu, M. (2024) · MedScien · doi:10.61173/hex2ak76

Rat primary cortical cell tri-culture to study effects of amyloid-beta on microglia functionPreprint

Kim, H., Le, B., Goshi, N., Zhu, K., Grodzki, A. C., Lein, P. J., Zhao, M., & Şeker, E. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.15.584736

In the afterglow: Immune dysfunction in schizophrenia spectrum disorders

Gangadin, S. S. (2024) · doi:10.33612/diss.939086872

Immunobiology and Immunotherapies in Huntington's Disease

Pal, A., Kumari, G., & Kumar, S. (2024) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815238754124010007

Trazodone exerts cytoprotective effects in human activated microglial cells by modulating inflammatory pathwaysPreprint

Chelucci, E., Daniele, S., Vergassola, M., Ceccarelli, L., Zucchi, S., Boltri, L., & Martini, C. (2024) · doi:10.22541/au.172449918.83105698/v1

Neuroprotective Potential of Andrographolide (AG) and its Structural Analogs in Alzheimer’s Disease

Vishnusai, B., Reddy, A. G., Chinnappan, S., Rajangam, J., Sundaramoorthy, A. P., Bhattacharya, V., Mishra, N., Mayasa, V., & Nelson, V. K. (2024) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815256567124010010

Neuroinflammation and Cognitive Function

Sharma, K., & Veena, N. (2025) · Advances in medical diagnosis, treatment, and care (AMDTC) book series · doi:10.4018/979-8-3693-7432-0.ch009

Down Syndrome: Progress in Defining Pathogenesis and Treatments for Neurodevelopmental Deficits and Alzheimer’s Disease

Bartesaghi, R., Chen, X., Johnstone, A. D., Das, U., & Mobley, W. C. (2025) · Springer eBooks · doi:10.1007/978-3-031-89307-0_19

Bidirectional Mediation of Cognition by DNA Methylation and Lean Body Mass in Chinese Monozygotic Twins

Li, H., Wang, T., Tian, X., Zhang, D., & Wang, W. (2025) · Twin Research and Human Genetics · doi:10.1017/thg.2025.10014

Sport concussion in female athletes: a systematic reviewPreprint

Westhead, R., & Sigala, N. (2025) · medRxiv · doi:10.1101/2025.09.29.25336877

ACETATO: MECANISMOS CELULARES E POTENCIAL TERAPÊUTICO EM DOENÇAS NEUROIMUNOLÓGICAS E NEURODEGENERATIVAS

Lopes, L. K. D., Maranduba, C. M. D. C., Trevizani, M., & Silva, F. D. S. (2025) · LUMEN ET VIRTUS · doi:10.56238/levv16n53-008

Neuroinflammatory effects of magnetic fields: insights into glia-mediated secondary cascades and mechanisms

Luo, Y., Zhao, C., Ren, J., Tian, L., & Pan, Y. (2025) · Life Sciences · doi:10.1016/j.lfs.2025.124061 · Cited by 1

Preventive Effect of Epigallocatechin-3-Gallate on Postoperative Cognitive Dysfunction in Aged Rats via Modulation of Microglial Differentiation: An Experimental Animal Study

Hong, S., Piao, L., Cho, E.-H., Seo, E., & Kim, S. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262311326

Neurological aging and neurodegenerative disease in humans and great apes

Edler, M. K., Hearn, C. J., Guevara, E. E., Mhatre‐Winters, I., Varghese, M., Freire‐Cobo, C., Sherwood, C. C., Richardson, J. R., Raghanti, M. A., & Hof, P. R. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-27380-3.00074-9

Additional file 2 of Interleukin-4 from curcumin-activated OECs emerges as a central modulator for increasing M2 polarization of microglia/macrophage in OEC anti-inflammatory activity for functional repair of spinal cord injury

Guo, J., Tang, X., Deng, P., Hui, H., Chen, B., An, J., Zhang, G., Shi, K., Wang, J., He, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25357964

Additional file 8 of Herpes simplex virus 1 accelerates the progression of Alzheimer’s disease by modulating microglial phagocytosis and activating NLRP3 pathway

Wang, Z., Liu, J., Han, J., Zhang, T., Li, S., Hou, Y., Su, H., Han, F., & Zhang, C. (2024) · Figshare · doi:10.6084/m9.figshare.26751314

Additional file 8 of Spatio-temporal dynamics of microglia phenotype in human and murine cSVD: impact of acute and chronic hypertensive states

Morton, L., Arndt, P., Garza, A. P., Henneicke, S., Mattern, H., Gonzalez, M., Dityatev, A. E., Yilmazer‐Hanke, D., Schreiber, S., & Dunay, I. R. (2024) · Figshare · doi:10.6084/m9.figshare.26656204

Additional file 3 of Herpes simplex virus 1 accelerates the progression of Alzheimer’s disease by modulating microglial phagocytosis and activating NLRP3 pathway

Wang, Z., Liu, J., Han, J., Zhang, T., Li, S., Hou, Y., Su, H., Han, F., & Zhang, C. (2024) · Figshare · doi:10.6084/m9.figshare.26751299

Additional file 1 of Chronic neuroinflammation during aging leads to cholinergic neurodegeneration in the mouse medial septum

Gamage, R. V., Rossetti, I., Niedermayer, G., Münch, G. W., Buskila, Y., & Gyengési, E. (2024) · Figshare · doi:10.6084/m9.figshare.26626864

Additional file 2 of Herpes simplex virus 1 accelerates the progression of Alzheimer’s disease by modulating microglial phagocytosis and activating NLRP3 pathway

Wang, Z., Liu, J., Han, J., Zhang, T., Li, S., Hou, Y., Su, H., Han, F., & Zhang, C. (2024) · Figshare · doi:10.6084/m9.figshare.26751296

Additional file 1 of Microglial burden, activation and dystrophy patterns in frontotemporal lobar degeneration

Woollacott, I., Toomey, C. E., Strand, C., Courtney, R. J., Benson, B. C., Rohrer, J. D., & Lashley, T. (2020) · Figshare · doi:10.6084/m9.figshare.12788931

Additional file 4 of Spatio-temporal dynamics of microglia phenotype in human and murine cSVD: impact of acute and chronic hypertensive states

Morton, L., Arndt, P., Garza, A. P., Henneicke, S., Mattern, H., Gonzalez, M., Dityatev, A. E., Yilmazer‐Hanke, D., Schreiber, S., & Dunay, I. R. (2024) · Figshare · doi:10.6084/m9.figshare.26656192

Additional file 1 of Spatio-temporal dynamics of microglia phenotype in human and murine cSVD: impact of acute and chronic hypertensive states

Morton, L., Arndt, P., Garza, A. P., Henneicke, S., Mattern, H., Gonzalez, M., Dityatev, A. E., Yilmazer‐Hanke, D., Schreiber, S., & Dunay, I. R. (2024) · Figshare · doi:10.6084/m9.figshare.26656183

Additional file 2 of Spatio-temporal dynamics of microglia phenotype in human and murine cSVD: impact of acute and chronic hypertensive states

Morton, L., Arndt, P., Garza, A. P., Henneicke, S., Mattern, H., Gonzalez, M., Dityatev, A. E., Yilmazer‐Hanke, D., Schreiber, S., & Dunay, I. R. (2023) · Figshare · doi:10.6084/m9.figshare.26656186

Additional file 5 of Herpes simplex virus 1 accelerates the progression of Alzheimer’s disease by modulating microglial phagocytosis and activating NLRP3 pathway

Wang, Z., Liu, J., Han, J., Zhang, T., Li, S., Hou, Y., Su, H., Han, F., & Zhang, C. (2024) · Figshare · doi:10.6084/m9.figshare.26751305

Microglia-mediated neuroinflammation in neurodegenerative diseases

Subhramanyam, C. S., Wang, C., Hu, Q., & Dheen, S. T. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.05.004 · Cited by 897

[The Role of Microglia in Neuroinflammation].

Suzumura, A. (2017) · PubMed · doi:10.11477/mf.1416200857 · Cited by 7

Microglia Mediated Neuroinflammation: A Silent Contributor to Alzheimer’s DiseasePreprint

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