Neuroinflammation in amyotrophic lateral sclerosis: role of glial activation in motor neuron disease

The chemokine system in diverse forms of macrophage activation and polarization

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Astrocytes: Biology and pathology

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

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Mechanisms underlying inflammation in neurodegeneration

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Excitatory Amino Acids as a Final Common Pathway for Neurologic Disorders

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Local self-renewal can sustain CNS microglia maintenance and function throughout adult life

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Onset and Progression in Inherited ALS Determined by Motor Neurons and Microglia

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β-Lactam antibiotics offer neuroprotection by increasing glutamate transporter expression

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Selective loss of glial glutamate transporter GLT‐1 in amyotrophic lateral sclerosis

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ALS-Linked SOD1 Mutant G85R Mediates Damage to Astrocytes and Promotes Rapidly Progressive Disease with SOD1-Containing Inclusions

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Kaempferol and kaempferide against amyotrophic lateral sclerosis

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The Role of the human microbiome in neurodegenerative diseases: A Perspective

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Single-nucleus transcriptomics of an engineered pig model reveals microglia–T cell interactions driving Huntington’s disease neurodegeneration

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Immune imbalance between T helper 1, T helper 17 and regulatory T cells fuels amyotrophic lateral sclerosis pathogenesis: disease trajectory, diagnosis and therapeutic implications

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Nanomedicine for neuroinflammation modulation: Next-generation nano-immunotherapies for neurodegenerative disorders

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Toll-like receptors 2 and 4 influence neuronal survival and glial reactions following ventral root crush injury in mice

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Neuroaxonal Degeneration as a Converging Mechanism in Motor Neuron Diseases (MNDs): Molecular Insights into RNA Dysregulation and Emerging Therapeutic Targets

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Chitosan-Based Biomaterials for Tissue Engineering of Glial Cells

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Elucidation of the role of microglia‐macrophage‐based neuroinflammation in neurological diseases

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Exploring the Causal Association Between 91 Circulating Inflammatory Proteins and Neurodegenerative Diseases: A Bidirectional Two‐Sample Mendelian Randomization and Bioinformatics Analysis

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The Role of Osteopontin in Amyotrophic Lateral Sclerosis: A Systematic Review

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EARLY CHANGES IN THE REACTIVE PROFILE OF MOUSE HIPPOCAMPAL GLIAL CELLS IN RESPONSE TO LIPOPOLYSACCHARIDE

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Cyclo (His-Pro) Protects SOD1G93A Microglial Cells from Paraquat–Induced Toxicity

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Diseases of Motor Neurons and Neuromuscular Junctions

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Theme 7 Pre-clinical therapeutic strategies

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ACTH (Acthar Gel) Reduces Toxic SOD1 Protein Linked to Amyotrophic Lateral Sclerosis in Transgenic Mice: A Novel Observation

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Preclinical testing of potential therapeutics for Amyotrophic Lateral Sclerosis

Kaneb, H. (2012) · Spiral (Imperial College London) · doi:10.25560/9606 · Cited by 3

BTK inhibition suppresses neuroinflammation and neurodegeneration in amyotrophic lateral sclerosis

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Elevated plasma sTREM2 reflects microglial activation but lacks diagnostic and clinical relevance in amyotrophic lateral sclerosis

Senerchia, G., Iuzzolino, V. V., Spisto, M., Panico, F., Polito, C., Aruta, L., Fiorenza, M., Sirica, R., Terracciano, D., & Dubbioso, R. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2026.107430 · Cited by 2

Motoneuron Diseases

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A Systematic review of Inflammatory biomarkers, Clinical significance, Detection, and their therapeutic agents

Vadlapudi, V., & Kulkarni, S. (2024) · World Journal of Biology Pharmacy and Health Sciences · doi:10.30574/wjbphs.2024.17.3.0137 · Cited by 2

Spinal TNF-α receptor 1 is differentially required for phrenic long-term facilitation (pLTF) over the course of motor neuron death in adult rats

Lewis, R. D., Keilholz, A. N., Smith, C. L., Burd, E. A., & Nichols, N. L. (2024) · Frontiers in Physiology · doi:10.3389/fphys.2024.1488951 · Cited by 3

Physicochemical properties of N,N'-(1,4-phenylene)bis(2,2,2-trifluoroacetamide), the bis(trifluoromethyl) derivative of N,N′-diacetyl-p-phenylenediamine

Akers, P. C., & Shell, T. A. (2025) · Total Chemistry · doi:10.1016/j.totche.2025.100001 · Cited by 2

Diseases of Motor Neurons and Neuromuscular Junctions

Sontheimer, H. W. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800244-5.00006-9 · Cited by 2

Amyotrophic Lateral Sclerosis and Primary Biliary Cirrhosis Overlap Syndrome: Two Cases Report

Zhang, H., Liu, Y., Li, Z., Liang, N., Zhou, X., Nie, X., Zhang, T., & Qi, W. (2019) · Frontiers in Neurology · doi:10.3389/fneur.2019.00890 · Cited by 3

Neuroinflammation in Neurological Disorders

Kira, J. (2013) · Advances in neurobiology · doi:10.1007/978-1-4614-8313-7_2 · Cited by 2

The role of astrocytes with genetic mutations linked to amyotrophic lateral sclerosis

Brash-Arias, D., Aranda-Abreu, G. E., Rojas-Durán, F., Hernández‐Aguilar, M. E., Toledo‐Cárdenas, M. R., Pérez-Estudillo, C. A., Ortega, A., & Chi-Castañeda, D. (2023) · Neurology Perspectives · doi:10.1016/j.neurop.2023.100117 · Cited by 3

Sampling methods and biomarkers for early detection of neurodegenerative disorders

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Metal Toxicity and Brain-Liver Axis

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Amyotrophic Lateral Sclerosis

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Exploring motor neuron degeneration in ALS - prevention by glycoursodeoxycholic acid and signaling to microglia

Cunha, J. C. M. (2012) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · Cited by 2

Neuroimmunology of Amyotrophic Lateral Sclerosis

Henkel-Tigges, J., Beers, D. R., Zhao, W., & Appel, S. H. (2014) · doi:10.1002/9781118406557.ch8 · Cited by 2

Pharmakologische Inhibition von Rho-Kinase im Mausmodell der Amyotrophen Lateralsklerose

Günther, R. (2015) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5125 · Cited by 2

Zebrafish C9orf72 loss-of-function models of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia

Rounding, N. (2018) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York) · Cited by 2

Evidence for a Growing Involvement of Glia in Amyotrophic Lateral Sclerosis

Radford, R. A. W., Vidal-Itriago, A., Scherer, N. M., Lee, A., Graeber, M. B., Chung, R. S., & Morsch, M. (2021) · Wiley eBooks · doi:10.1002/9781119745532.ch7 · Cited by 3

Non-Coding Genetic Analysis Implicates Interleukin 18 Receptor Accessory Protein 3′UTR in Amyotrophic Lateral SclerosisPreprint

Eitan, C., Siany, A., Barkan, E., Olender, T., van Eijk, K. R., Moisse, M., Farhan, S. M. K., Danino, Y. M., Yanowski, E., Marmor-Kollet, H., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.06.03.446863 · Cited by 2

Exosome-shuttled miRNAs contribute to the modulation of the neuroinflammatory microglia phenotype by mesenchymal stem cells. Implication for amyotrophic lateral sclerosisPreprint

Giunti, D., Marini, C., Parodi, B., Usai, C., Milanese, M., Bonanno, G., de Rosbo, N. K., & Uccelli, A. (2019) · doi:10.21203/rs.2.17858/v1 · Cited by 2

Loss of Nuclear TDP-43 Impairs Lipid Metabolism in Microglia-Like CellsPreprint

Kabra, K., Dressman, D., Talcoff, R., Yidenk, M., Rifai, O. M., Hoover, B. N., Shneider, N. A., Elyaman, W., Área-Gómez, E., & Bradshaw, E. M. (2025) · Research Square · doi:10.1101/2025.09.17.676815 · Cited by 2

Spinal Muscular Atrophy in Blonde D'Aquitaine Calves Is Not Associated With FVT1 Gene Mutation

Cagnotti, G., Cantile, C., Chessa, S., Sacchi, P., D’Angelo, A., & Bellino, C. (2020) · Frontiers in Veterinary Science · doi:10.3389/fvets.2020.00348 · Cited by 1

Recent updates on immunotherapy in neurodegenerative diseases

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Immunotherapy for Neurodegenerative Movement Disorders

Mosley, R. L., Saleh, M., & Olson, K. E. (2024) · Springer eBooks · doi:10.1007/978-3-031-68237-7_52 · Cited by 1

Is TREM2 a Stretch: Implications of TREM2 Along Spinal Cord Circuits in Health, Aging, Injury, and Disease

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Accelerated brain aging in amyotrophic lateral sclerosis and its prognostic associations: a cohort study

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Decoding the Gut Microbiome in Neuromuscular Diseases: a Review of Fundamental Mechanisms and Condition-Specific Evidence

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Secretory leukocyte protease inhibitor (SLPI) attenuates TLR4/NF-κB-mediated neuroinflammation in amyotrophic lateral sclerosis: a candidate molecule associated with neuro-pathology

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Microglia, Calcification and Neurodegenerative Diseases

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Reactive Oxygen and Nitrogen Species – A Driving Force in Amyotrophic Lateral Sclerosis

Henkel-Tigges, J., Beers, D. R., Zhao, W., & Appel, S. H. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_131 · Cited by 1

An Autopsy Case of Amyotrophic Lateral Sclerosis with Neuroinflammatory change

Ha, S. H., Baek, W., Kim, H., Noh, M., Hwang, S. J., & Kim, S. H. (2012) · Journal of the Korean Neurological Association · Cited by 1

REVISTA MEXICANA DE NEUROCIENCIA MAYO 2018

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The Beneficial Role of Natural Antioxidants in Alleviating Neuroinflammatory Disorders Including Neurodegeneration

Das, M., & Devi, K. P. (2022) · Reference series in phytochemistry · doi:10.1007/978-3-030-78160-6_31 · Cited by 1

Amyotrophic Lateral Sclerosis: From Mechanisms to Current, Emerging, and Alternative Therapeutics

Kioutchoukova, I. P. (2023) · Med Discoveries · doi:10.52768/2993-1142/1059 · Cited by 1

Three-dimensional magnetic resonance neurography aids in detection of brachial plexus nerve root signal and size alterations in patients with amyotrophic lateral sclerosis: a case-control study

Wang, S., Man, X., Chen, Y., Gong, T., Gao, F., Chen, W., Wang, G., Zhao, B., & Chhabra, A. B. (2023) · Quantitative Imaging in Medicine and Surgery · doi:10.21037/qims-23-833 · Cited by 1

Differential response of injured and healthy retinas to syngeneic and allogeneic transplantation of a clonal cell line of immortalized olfactory ensheathing glia: a double-edged sword

Norte‐Muñoz, M., Portela-Lomba, M., Sobrado‐Calvo, P., Simón, D., Pierdomenico, J. D., Gallego‐Ortega, A., Pérez, M., Cabrera‐Maqueda, J. M., Sierra, J., Vidal‐Sanz, M., et al. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01631 · Cited by 2

Astrocyte-Neuron Interactions Contributing to Amyotrophic Lateral Sclerosis Progression

Jensen, B. K. (2024) · Advances in neurobiology · doi:10.1007/978-3-031-64839-7_12 · Cited by 1

Recent advances in neurodegenerative disease research

Singh, E., & Dilawari, R. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-28822-7.00014-3 · Cited by 1

In Vivo Imaging in Neurodegenerative Diseases

Wang, X., Arbel‐Ornath, M., Wegmann, S., Kastanenka, K. V., & Bacskai, B. J. (2014) · Springer eBooks · doi:10.1007/978-94-017-9361-2_3 · Cited by 1

Glial pathology in amyotrophic lateral sclerosis

Yamanaka, K. (2011) · Rinsho Shinkeigaku · doi:10.5692/clinicalneurol.51.1192 · Cited by 1

Editorial on the original article entitled "Genetic validation of a therapeutic target in a mouse model of ALS" published in the Science Translational Medicine on August 6, 2014.

Silani, V. (2015) · PubMed · doi:10.3978/j.issn.2305-5839.2015.02.23 · Cited by 1

Effekte der präsymptomatischen Applikation der Rho-Kinase-Inhibitoren Fasudil und Y-27632 im SOD1-(G93A)-Mausmodell der Amyotrophen Lateralsklerose

Suhr, M. E. H. (2017) · doi:10.53846/goediss-6146 · Cited by 1

Einfluss der Rho-Kinase-Hemmung auf Mikrogliazellen im SOD1-G93A-Mausmodell der Amyotrophen Lateralsklerose

Jansen, J. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6353

Neuroinflammation

Gullett, J. M. (2019) · Springer eBooks · doi:10.1007/978-3-319-69892-2_675-1 · Cited by 1

Amyotrophic Lateral Sclerosis

Turner, M. R. (2014) · Springer eBooks · doi:10.1007/978-3-642-54307-4_29 · Cited by 1

Transplanted Haematopoietic Cells Populate The Murine CNS In The Absence Of Irradiation

Manning, J. (2013) · Summit (Simon Fraser University)

The Astrocytic Contribution in ALS: Inflammation and Excitotoxicity

Staats, K. A., & Bosch, L. V. D. (2012) · InTech eBooks · doi:10.5772/30965

Molecular and Electrical Abnormalities in the Mouse Model of Amyotrophic Lateral Sclerosis

Katharina, A., Sherif, M., & Heckm, C. J. (2012) · InTech eBooks · doi:10.5772/32715

Understanding the gender-based mechanism of MSO treatment in ALS mice: A metabolic characterization of the SOD1-G93A mouse model

Bame, M. (2012)

Caracterização celular e molecular da influência do astrócito na degeneração do neurônio motor no modelo in vitro da esclerose lateral amiotrófica utilizando camundongos trangênicos para SOD1 humana mutante

Scorisa, J. M. (2013) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2013.tde-14082013-153550

Fisiopatologia de l'esclerosi lateral amiotròfica

Toda, M. T. (2015) · Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona)

Estudos dos produtos da oxidação não enzimática do ácido docosahexaenoico como possíveis biomarcadores para doenças neurodegenerativas

Derogis, P. B. M. C. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.46.2014.tde-20012015-075520

E-NTPDase 1 modulation of neuronal and astrocytic activity in the CNS

Rocha, A. (2014) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-14214

Traces of disease in amyotrophic lateral sclerosis

Verstraete, E. (2012) · Utrecht University Repository (Utrecht University)

Análise da influência da microglia mutante na sobrevida do neurônio motor no modelo in vitro da esclerose lateral amiotrófica utilizando camundongos transgênicos para SOD1 humana

Duobles, T. (2013) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2013.tde-09082013-140206

Notch-1 signaaltransductie en oligodendrocyten dysfunctie in amyotrofe laterale sclerose

Geneeskunde, F., & Wetenschappen, B. (2013)

Glia-Motoneuron dialogue in ALS onset and progression in SOD1G93A-mice model

Santos, C. D. P. P. (2014) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

ENDOTHELIN-1 IS OVER-EXPRESSED IN AMYOTROPHIC LATERAL SCLEROSIS AND INDUCES MOTOR NEURON CELL DEATH

Nazionale, C., & Ricerche, D. (2013)

Is "Non-Cell Autonomous" neuron death common to neurodegenerative diseases?

Yamanaka, K. (2012) · Rinsho Shinkeigaku · doi:10.5692/clinicalneurol.52.1329

Blood-spinal cord barrier breakdown and pericyte reductions in amyotrophic lateral sclerosis Ethan A. WinklerJesse D. SengilloJohn S. Sullivan • Jenny S. HenkelStanley H. AppelBerislav V. Zlokovic

Sullivan, S. M., Zloković, B. V., & Appel, H. (2013)

The role of humoral immune response in the aetiopathogenesis of amyotrophic lateral sclerosis

Milosevic, M. M. (2012) · doi:10.2298/bg20120928milosevic

Neuroimaging in Amyotrophic Lateral Sclerosis

Cistaro, A. (2016) · Springer eBooks · doi:10.1007/978-3-319-31614-7_14

The role of ALS associated genes and c-Jun in neurodegeneration

Acosta‐Saltos, A. (2016) · UCL Discovery (University College London)

Autonomous and motor disorders

Pietropaolo, S., Sluyter, F., & Crusio, W. E. (2014) · Cambridge University Press eBooks · doi:10.1017/cbo9781107360556.005

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

Effect of elevated calcium level and calcium binding proteins in acute and chronic degeneration of motor neurons

Patai, R. (2017) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.4041

Intraspinal Delivery of Recombinant AAV-Mediated Interleukin-10 Modifies Disease in ALS Mice

Chakrabarty, P., & Ayers, J. I. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809813-4.00011-9

Esclerosis Lateral Amiotrófica y Embarazo, una asociación poco común

Macías, J. I. C., Vázquez, G. S., Departamento de Medicina y Nutrición, U. D. G., Campos, M. O. D., Departamento de Medicina y Nutrición, U. D. G., Aldana, I. Q., Departamento de Medicina y Nutrición, U. D. G., & García-Cazares, R. (2018) · Revista de Fomento Social · doi:10.31190/rmn.2018.19.3.95.102

Applications of mass spectrometry imaging and top-down proteomic techniques for clinical and biomedical research

Rawlins (2018) · Digital Repository Service (Northeastern University) · doi:10.17760/d20292916

Establishing the therapeutic potential of the P2X7 receptor ion channel in amyotrophic lateral sclerosis

Dongol, A. (2018) · Research Online (University of Wollongong)

The Beneficial Role of Natural Antioxidants in Alleviating Neuroinflammatory Disorders Including Neurodegeneration

Das, M., & Devi, K. P. (2020) · Reference series in phytochemistry · doi:10.1007/978-3-030-45299-5_31-1

Immunity and inflammation in amyotrophic lateral sclerosis : an epidemiological approach

Cui, C. (2021) · Figshare

Investigations into the accumulation of hematopoietic cells in the spinal cord in a murine model of motor neuron disease

Lewis, C. B. (2011) · Summit (Simon Fraser University)

Neuroinflammation

Gullett, J. M. (2021) · Springer eBooks · doi:10.1007/978-3-030-22009-9_675

Polypyrimidine Tract-binding Protein 2 is a Potential Treated Target in Tg(SOD1*G93A)1Gur MicePreprint

Xiong, Z., Li, X., Yang, D., Xiong, C., & Zhou, Q. (2022) · Research Square · doi:10.21203/rs.3.rs-1470191/v1

Motor disorders

Gordon, D., & Talbot, K. (2014) · Cambridge University Press eBooks · doi:10.1017/cbo9781107360556.008

The Beneficial Role of Natural Antioxidants in Alleviating Neuroinflammatory Disorders Including Neurodegeneration

Das, M., & Devi, K. P. (2020) · Reference series in phytochemistry · doi:10.1007/978-3-030-45299-5_31-2

THEME 9IN VIVOEXPERIMENTAL MODELS

(2013) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.3109/21678421.2013.838424

Evaluating the roles spinal plasticity and an accessory inspiratory muscle have in a rodent model of respiratory motor neuron death

Borkowski, L. F. (2021) · doi:10.32469/10355/90984

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ИЗМЕНЕНИЯ РЕАКТИВНОГО ПРОФИЛЯ АСТРОЦИТОВ ПЕРЕДНЕГО КОРТИКАЛЬНОГО ЯДРА АМИГДАЛЫ У КРЫС C АБСАНСНОЙ ЭПИЛЕПСИЕЙ В ОТВЕТ НА ГОНАДЭКТОМИЮ

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