On the public citation graph
Macrophages in spinal cord injury: Phenotypic and functional change from exposure to myelin debris
0 signed · 384 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/art.11237openalex-snapshot
Increased apoptotic neutrophils and macrophages and impaired macrophage phagocytic clearance of apoptotic neutrophils in systemic lupus erythematosus
inferredcites →https://doi.org/10.1002/cne.20517openalex-snapshot
Spinal cord injury is accompanied by chronic progressive demyelination
inferredcites →https://doi.org/10.1002/cne.20827openalex-snapshot
Comparative analysis of lesion development and intraspinal inflammation in four strains of mice following spinal contusion injury
inferredcites →https://doi.org/10.1002/cne.21149openalex-snapshot
Proinflammatory cytokine synthesis in the injured mouse spinal cord: Multiphasic expression pattern and identification of the cell types involved
inferredcites →https://doi.org/10.1002/glia.20611openalex-snapshot
Myelin‐phagocytosing macrophages in isolated sciatic and optic nerves reveal a unique reactive phenotype
inferredcites →https://doi.org/10.1002/glia.20713openalex-snapshot
Galectin‐3/MAC‐2, Ras and PI3K activate complement receptor‐3 and scavenger receptor‐AI/II mediated myelin phagocytosis in microglia
inferredcites →https://doi.org/10.1002/glia.20874openalex-snapshot
Microglia processes block the spread of damage in the brain and require functional chloride channels
inferredcites →https://doi.org/10.1002/glia.21062openalex-snapshot
The release of cytokines by macrophages is not affected by myelin ingestion
inferredcites →https://doi.org/10.1002/glia.22578openalex-snapshot
NMDA receptor couples Rac1-GEF Tiam1 to direct oligodendrocyte precursor cell migration
inferredcites →https://doi.org/10.1007/s13311-011-0033-5openalex-snapshot
Oligodendrocyte Fate after Spinal Cord Injury
inferredcites →https://doi.org/10.1016/0896-6273(94)90247-xopenalex-snapshot
Identification of myelin-associated glycoprotein as a major myelin-derived inhibitor of neurite growth
inferredcites →https://doi.org/10.1016/j.brainres.2008.04.025openalex-snapshot
Rosiglitazone, a PPAR gamma agonist, attenuates inflammation after surgical brain injury in rodents
inferredcites →https://doi.org/10.1016/j.cell.2006.01.007openalex-snapshot
Macrophages: Obligate Partners for Tumor Cell Migration, Invasion, and Metastasis
inferredcites →https://doi.org/10.1016/j.ejca.2006.01.003openalex-snapshot
Tumour-associated macrophages are a distinct M2 polarised population promoting tumour progression: Potential targets of anti-cancer therapy
inferredcites →https://doi.org/10.1016/j.expneurol.2007.02.009openalex-snapshot
The PPAR gamma agonist Pioglitazone improves anatomical and locomotor recovery after rodent spinal cord injury
inferredcites →https://doi.org/10.1016/j.gde.2008.07.016openalex-snapshot
Coordination of inflammation and metabolism by PPAR and LXR nuclear receptors
inferredcites →https://doi.org/10.1016/j.imbio.2010.05.020openalex-snapshot
Heme Oxygenase-1 expression in M-CSF-polarized M2 macrophages contributes to LPS-induced IL-10 release
inferredcites →https://doi.org/10.1016/j.immuni.2005.09.003openalex-snapshot
SHIP Represses the Generation of Alternatively Activated Macrophages
inferredcites →https://doi.org/10.1016/j.it.2004.09.015openalex-snapshot
The chemokine system in diverse forms of macrophage activation and polarization
inferredcites →https://doi.org/10.1016/j.neuron.2014.07.027openalex-snapshot
TNF and Increased Intracellular Iron Alter Macrophage Polarization to a Detrimental M1 Phenotype in the Injured Spinal Cord
inferredcites →https://doi.org/10.1016/s0079-6123(02)37019-5openalex-snapshot
Chapter 17 Spinal cord contusion models
inferredcites →https://doi.org/10.1016/s0092-8674(00)81683-9openalex-snapshot
The Hallmarks of Cancer
inferredcites →https://doi.org/10.1016/s0165-5728(96)00110-5openalex-snapshot
Macrophage phagocytosis of myelin in vitro determined by flow cytometry: phagocytosis is mediated by CR3 and induces production of tumor necrosis factor-α and nitric oxide
inferredcites →https://doi.org/10.1016/s1074-7613(03)00174-2openalex-snapshot
Blood Monocytes Consist of Two Principal Subsets with Distinct Migratory Properties
inferredcites →https://doi.org/10.1017/s1462399408000719openalex-snapshot
Galectins: structure, function and therapeutic potential
inferredcites →https://doi.org/10.1023/a:1022566121967openalex-snapshot
Phagocytosis of Myelin in Demyelinative Disease: A Review
inferredcites →https://doi.org/10.1038/35000219openalex-snapshot
Nogo-A is a myelin-associated neurite outgrowth inhibitor and an antigen for monoclonal antibody IN-1
inferredcites →https://doi.org/10.1038/emm.2006.40openalex-snapshot
Microglia, major player in the brain inflammation: their roles in the pathogenesis of Parkinson's disease
inferredcites →https://doi.org/10.1038/nature05894openalex-snapshot
Macrophage-specific PPARγ controls alternative activation and improves insulin resistance
inferredcites →https://doi.org/10.1038/nature07202openalex-snapshot
Integration of metabolism and inflammation by lipid-activated nuclear receptors
inferredcites →https://doi.org/10.1038/nn1426openalex-snapshot
High cholesterol level is essential for myelin membrane growth
inferredcites →https://doi.org/10.1038/nri1733openalex-snapshot
Monocyte and macrophage heterogeneity
inferredcites →https://doi.org/10.1038/nri2448openalex-snapshot
Exploring the full spectrum of macrophage activation
inferredcites →https://doi.org/10.1038/nri957openalex-snapshot
A blast from the past: clearance of apoptotic cells regulates immune responses
inferredcites →https://doi.org/10.1038/nrn3053openalex-snapshot
Repertoire of microglial and macrophage responses after spinal cord injury
inferredcites →https://doi.org/10.1038/sj.cdd.4400407openalex-snapshot
Apoptosis: The importance of being eaten
inferredcites →https://doi.org/10.1038/sj.jcbfm.9600182openalex-snapshot
Rosiglitazone and 15-deoxy-Δ12,14-prostaglandin J2 Cause Potent Neuroprotection after Experimental Stroke through Noncompletely Overlapping Mechanisms
inferredcites →https://doi.org/10.1046/j.1471-4159.1995.64020895.xopenalex-snapshot
Cholesterol for Synthesis of Myelin Is Made Locally, Not Imported into Brain
inferredcites →https://doi.org/10.1073/pnas.0911405106openalex-snapshot
Activation of innate and humoral immunity in the peripheral nervous system of ALS transgenic mice
inferredcites →https://doi.org/10.1089/neu.2009.1149openalex-snapshot
A Systematic Review of Non-Invasive Pharmacologic Neuroprotective Treatments for Acute Spinal Cord Injury
inferredcites →https://doi.org/10.1093/brain/awh707openalex-snapshot
Myelin-laden macrophages are anti-inflammatory, consistent with foam cells in multiple sclerosis
inferredcites →https://doi.org/10.1093/brain/awp322openalex-snapshot
Quantitative analysis of cellular inflammation after traumatic spinal cord injury: evidence for a multiphasic inflammatory response in the acute to chronic environment
inferredcites →https://doi.org/10.1096/fj.05-5007comopenalex-snapshot
Activation of cerebral peroxisome proliferator‐activated receptors gamma promotes neuroprotection by attenuation of neuronal cyclooxygenase‐2 overexpression after focal cerebral ischemia in rats
inferredcites →https://doi.org/10.1097/00041433-200310000-00006openalex-snapshot
Peroxisome proliferator-activated receptors: new targets for the pharmacological modulation of macrophage gene expression and function
inferredcites →https://doi.org/10.1124/jpet.106.113472openalex-snapshot
Thiazolidinedione Class of Peroxisome Proliferator-Activated Receptor γ Agonists Prevents Neuronal Damage, Motor Dysfunction, Myelin Loss, Neuropathic Pain, and Inflammation after Spinal Cord Injury in Adult Rats
inferredcites →https://doi.org/10.1126/science.1059344openalex-snapshot
Structural Mechanism for Statin Inhibition of HMG-CoA Reductase
inferredcites →https://doi.org/10.1128/mcb.20.11.4106-4114.2000openalex-snapshot
Analysis of Fractalkine Receptor CX3CR1 Function by Targeted Deletion and Green Fluorescent Protein Reporter Gene Insertion
inferredcites →https://doi.org/10.1146/annurev.neuro.30.051606.094354openalex-snapshot
Why Is Wallerian Degeneration in the CNS So Slow?
inferredcites →https://doi.org/10.1152/physrev.00005.2005openalex-snapshot
ATP-Binding Cassette Transporter A1: A Cell Cholesterol Exporter That Protects Against Cardiovascular Disease
inferredcites →https://doi.org/10.1155/2013/945034openalex-snapshot
Managing Inflammation after Spinal Cord Injury through Manipulation of Macrophage Function
inferredcites →https://doi.org/10.1158/0008-5472.can-09-2050openalex-snapshot
Folate Receptor β Is Expressed by Tumor-Associated Macrophages and Constitutes a Marker for M2 Anti-inflammatory/Regulatory Macrophages
inferredcites →https://doi.org/10.1158/0008-5472.can-11-3247openalex-snapshot
MIF Produced by Bone Marrow–Derived Macrophages Contributes to Teratoma Progression after Embryonic Stem Cell Transplantation
inferredcites →https://doi.org/10.1160/th11-05-0320openalex-snapshot
Differentiation factors and cytokines in the atherosclerotic plaque micro-environment as a trigger for macrophage polarisation
inferredcites →https://doi.org/10.1161/01.str.32.5.1208openalex-snapshot
Enhanced Expression of Iba1, Ionized Calcium-Binding Adapter Molecule 1, After Transient Focal Cerebral Ischemia In Rat Brain
inferredcites →https://doi.org/10.1161/atvbaha.108.179283openalex-snapshot
Role of HDL, ABCA1, and ABCG1 Transporters in Cholesterol Efflux and Immune Responses
inferredcites →https://doi.org/10.1172/jci31422openalex-snapshot
Altered macrophage differentiation and immune dysfunction in tumor development
inferredcites →https://doi.org/10.1172/jci8119openalex-snapshot
The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway
inferredcites →https://doi.org/10.1186/1471-2172-3-7openalex-snapshot
IL-4 dependent alternatively-activated macrophages have a distinctive in vivo gene expression phenotype
inferredcites →https://doi.org/10.1371/journal.pmed.1000113openalex-snapshot
Infiltrating Blood-Derived Macrophages Are Vital Cells Playing an Anti-inflammatory Role in Recovery from Spinal Cord Injury in Mice
inferredcites →https://doi.org/10.1371/journal.pone.0009380openalex-snapshot
Myelin Activates FAK/Akt/NF-κB Pathways and Provokes CR3-Dependent Inflammatory Response in Murine System
inferredcites →https://doi.org/10.1371/journal.pone.0013693openalex-snapshot
Selective Chemokine Receptor Usage by Central Nervous System Myeloid Cells in CCR2-Red Fluorescent Protein Knock-In Mice
inferredcites →https://doi.org/10.1371/journal.pone.0024795openalex-snapshot
Plexin-B2 Negatively Regulates Macrophage Motility, Rac, and Cdc42 Activation
inferredcites →https://doi.org/10.1371/journal.pone.0044998openalex-snapshot
Myelin-Derived Lipids Modulate Macrophage Activity by Liver X Receptor Activation
inferredcites →https://doi.org/10.1385/jmn:21:1:65openalex-snapshot
Microglia and Macrophage Activation and the Regulation of Complement-Receptor-3 (CR3/MAC-1)-Mediated Myelin Phagocytosis in Injury and Disease
inferredcites →https://doi.org/10.1523/jneurosci.3257-09.2009openalex-snapshot
Identification of Two Distinct Macrophage Subsets with Divergent Effects Causing either Neurotoxicity or Regeneration in the Injured Mouse Spinal Cord
inferredcites →https://doi.org/10.2174/1568010054022114openalex-snapshot
Neutrophil-Derived Cytokines: Potential Therapeutic Targets in Inflammation
inferredcites →https://doi.org/10.3171/spi-08/01/058openalex-snapshot
Delayed accumulation of activated macrophages and inhibition of remyelination after spinal cord injury in an adult rodent model
inferredcites →https://doi.org/10.3791/2698openalex-snapshot
Quantitative Assessment of Immune Cells in the Injured Spinal Cord Tissue by Flow Cytometry: a Novel Use for a Cell Purification Method
inferredcites →https://doi.org/10.3791/2698-vopenalex-snapshot
Quantitative Assessment of Immune Cells in the Injured Spinal Cord Tissue by Flow Cytometry: a Novel Use for a Cell Purification Method
inferredcites →https://doi.org/10.4049/jimmunol.1100421openalex-snapshot
The Fractalkine Receptor but Not CCR2 Is Present on Microglia from Embryonic Development throughout Adulthood
inferredcites →https://doi.org/10.4049/jimmunol.180.7.4978openalex-snapshot
Apoptotic Cells Protect Mice against Lipopolysaccharide-Induced Shock
inferredcites →https://doi.org/10.4049/jimmunol.181.11.8077openalex-snapshot
Sulfatide, A Major Lipid Component of Myelin Sheath, Activates Inflammatory Responses As an Endogenous Stimulator in Brain-Resident Immune Cells
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4704731openalex-extracted
Galectin-3 Inhibition Reduces Fibrotic Scarring and Promotes Functional Recovery after Spinal Cord Injury in Mice
inferred← citeshttps://doi.org/10.1002/adfm.202305325openalex-snapshot
Magnetotactic Bacteria‐Derived Mms6 Gene Helps M2 Macrophages to Form Magnetic Bio‐Nanoparticles to Prevent Ferroptosis and Promote Locomotor Functional Recovery after Spinal Cord Injury in Mice
inferred← citeshttps://doi.org/10.1002/adfm.202508435openalex-snapshot
Engineering Topographical Cues to Enhance Neural Regeneration in Spinal Cord Injury: Overcoming Challenges and Advancing Therapies
inferred← citeshttps://doi.org/10.1002/adhm.202100242openalex-snapshot
Rationally Designed, Self‐Assembling, Multifunctional Hydrogel Depot Repairs Severe Spinal Cord Injury
inferred← citeshttps://doi.org/10.1002/adma.202502795openalex-snapshot
Spatiotemporal Targeted Delivery of Biomimetic Bacterial Outer Membrane Nanoparticles for Enhanced Spinal Cord Injury Repair
inferred← citeshttps://doi.org/10.1002/advs.202405483openalex-snapshot
Pathophysiology‐Directed Engineering of a Combination Nanoanalgesic for Neuropathic Pain
inferred← citeshttps://doi.org/10.1002/advs.202414724openalex-snapshot
Engineering the Immune Response to Biomaterials
inferred← citeshttps://doi.org/10.1002/advs.202503269openalex-snapshot
A Myelin Debris Cleaner for Spinal Cord Injury Recovery: Polycaprolactone / Cell Membrane Assembled Scaffolds
inferred← citeshttps://doi.org/10.1002/advs.202513474openalex-snapshot
A Conjugation Delivery System of Macrophages and Platelet Pharmacytes Promotes Regeneration After Spinal Cord Injury
inferred← citeshttps://doi.org/10.1002/cns.71109openalex-snapshot
Lipid Metabolism in Central Nervous System Diseases: Pathological Mechanisms and Therapeutic Advances
inferred← citeshttps://doi.org/10.1002/glia.23021openalex-snapshot
Dynamic impact of brief electrical nerve stimulation on the neural immune axis—polarization of macrophages toward a pro‐repair phenotype in demyelinated peripheral nerve
inferred← citeshttps://doi.org/10.1002/glia.23132openalex-snapshot
E6020, a synthetic TLR4 agonist, accelerates myelin debris clearance, Schwann cell infiltration, and remyelination in the rat spinal cord
inferred← citeshttps://doi.org/10.1002/glia.23702openalex-snapshot
Myelin status and oligodendrocyte lineage cells over time after spinal cord injury: What do we know and what still needs to be unwrapped?
inferred← citeshttps://doi.org/10.1002/glia.24602openalex-snapshot
Myelin debris phagocytosis in demyelinating disease
inferred← citeshttps://doi.org/10.1002/glia.70048openalex-snapshot
Drebrin Upregulation Regulates Astrocyte Polarization and Supports Tissue Recovery After Spinal Cord Injury in Mice
inferred← citeshttps://doi.org/10.1002/jcp.30619openalex-snapshot
Taurolithocholic acid but not tauroursodeoxycholic acid rescues phagocytosis activity of bone marrow‐derived macrophages under inflammatory stress
inferred← citeshttps://doi.org/10.1002/jlb.3ma0721-007ropenalex-snapshot
High mobility group box-1 serves a pathogenic role in spinal cord injury via the promotion of pro-inflammatory cytokines
inferred← citeshttps://doi.org/10.1002/jlb.3ru0820-536ropenalex-snapshot
Functional consequences of a close encounter between microglia and brain-infiltrating monocytes during CNS pathology and repair
inferred← citeshttps://doi.org/10.1002/jnr.24114openalex-snapshot
Myelin as an inflammatory mediator: Myelin interactions with complement, macrophages, and microglia in spinal cord injury
inferred← citeshttps://doi.org/10.1002/jnr.24409openalex-snapshot
Melatonin improves functional recovery in female rats after acute spinal cord injury by modulating polarization of spinal microglial/macrophages
inferred← citeshttps://doi.org/10.1002/mabi.202100031openalex-snapshot
The Influence of Polysaccharides‐Based Material on Macrophage Phenotypes
inferred← citeshttps://doi.org/10.1002/smsc.202500260openalex-snapshot
Immunomodulatory Biomaterials for Bone and Soft Tissue Chronic Inflammation Diseases
inferred← citeshttps://doi.org/10.1002/sstr.202500875openalex-snapshot
Injectable Liposome‐Anchored Hydrogel Microspheres Promote Spinal Cord Injury Repair by Modulating the Inflammatory Microenvironment and Recruiting Endogenous Stem Cells
inferred← citeshttps://doi.org/10.1007/978-3-319-46293-6_19openalex-snapshot
Pathophysiology of Traumatic Spinal Cord Injury
inferred← citeshttps://doi.org/10.1007/978-981-99-4886-4_15openalex-snapshot
Microglia Lipid Droplets in Physiology and Neurodegeneration
inferred← citeshttps://doi.org/10.1007/s00018-022-04261-xopenalex-snapshot
Mitochondrial function in spinal cord injury and regeneration
inferred← citeshttps://doi.org/10.1007/s00401-019-01992-3openalex-snapshot
The origin, fate, and contribution of macrophages to spinal cord injury pathology
inferred← citeshttps://doi.org/10.1007/s10517-024-06095-yopenalex-snapshot
Exosomes Derived from Mesenchymal Stem Cells: Therapeutic Opportunities for Spinal Cord Injury
inferred← citeshttps://doi.org/10.1007/s10571-022-01203-wopenalex-snapshot
Myelin Debris Impairs Tight Junctions and Promotes the Migration of Microvascular Endothelial Cells in the Injured Spinal Cord
inferred← citeshttps://doi.org/10.1007/s11064-025-04347-5openalex-snapshot
Focusing on Formyl Peptide Receptors after Traumatic Spinal Cord Injury: from Immune Response to Neurogenesis
inferred← citeshttps://doi.org/10.1007/s12035-016-9709-5openalex-snapshot
The Effects of Co-transplantation of Olfactory Ensheathing Cells and Schwann Cells on Local Inflammation Environment in the Contused Spinal Cord of Rats
inferred← citeshttps://doi.org/10.1007/s12035-016-9787-4openalex-snapshot
Analysis of the Role of CX3CL1 (Fractalkine) and Its Receptor CX3CR1 in Traumatic Brain and Spinal Cord Injury: Insight into Recent Advances in Actions of Neurochemokine Agents
inferred← citeshttps://doi.org/10.1007/s12035-022-03052-6openalex-snapshot
Hematogenous Macrophages Contribute to Fibrotic Scar Formation After Optic Nerve Crush
inferred← citeshttps://doi.org/10.1007/s12035-024-03963-6openalex-snapshot
Janus Kinase Inhibitor Brepocitinib Rescues Myelin Phagocytosis Under Inflammatory Conditions: In Vitro Evidence from Microglia and Macrophage Cell Lines
inferred← citeshttps://doi.org/10.1007/s12035-025-05144-5openalex-snapshot
Quaking Protein in Myelin Maintenance and Regeneration in the Central Nervous System
inferred← citeshttps://doi.org/10.1007/s12264-025-01388-2openalex-snapshot
Histopathological Insights into Demyelination and Remyelination After Spinal Cord Injury in Non-human Primates
inferred← citeshttps://doi.org/10.1007/s13311-023-01376-2openalex-snapshot
The Promise of Niacin in Neurology
inferred← citeshttps://doi.org/10.1016/b978-0-12-818084-6.00008-8openalex-snapshot
Tissue engineering and regenerative medicine in spinal cord injury repair
inferred← citeshttps://doi.org/10.1016/j.aca.2023.341434openalex-snapshot
Quantitative biochemical phenotypic heterogeneity of macrophages after myelin debris phagocytosis at a single cell level by synchrotron radiation fourier transform infrared microspectroscopy
inferred← citeshttps://doi.org/10.1016/j.actbio.2018.06.038openalex-snapshot
Polycaprolactone/polysialic acid hybrid, multifunctional nanofiber scaffolds for treatment of spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.actbio.2022.01.028openalex-snapshot
Specific Labelling of Phagosome-Derived Vesicles in Macrophages with a Membrane Dye Delivered with Microfabricated Microparticles
inferred← citeshttps://doi.org/10.1016/j.autrev.2024.103578openalex-snapshot
Efferocytosis: Unveiling its potential in autoimmune disease and treatment strategies
inferred← citeshttps://doi.org/10.1016/j.bbi.2018.11.013openalex-snapshot
Reducing age-dependent monocyte-derived macrophage activation contributes to the therapeutic efficacy of NADPH oxidase inhibition in spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.bbi.2024.04.013openalex-snapshot
Targeting foamy macrophages by manipulating ABCA1 expression to facilitate lesion healing in the injured spinal cord
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.02.069openalex-snapshot
Astrocytes directly clear myelin debris through endocytosis pathways and followed by excessive gliosis after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.bioactmat.2021.01.029openalex-snapshot
A bioactive injectable self-healing anti-inflammatory hydrogel with ultralong extracellular vesicles release synergistically enhances motor functional recovery of spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.bioadv.2025.214627openalex-snapshot
Neutrophil-mimetic M2 macrophage extracellular vesicle for targeted spinal cord injury therapy
inferred← citeshttps://doi.org/10.1016/j.biopha.2018.08.005openalex-snapshot
Effects of miR-26a-5p on neuropathic pain development by targeting MAPK6 in in CCI rat models
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.112311openalex-snapshot
Exosomes-mediated phenotypic switch of macrophages in the immune microenvironment after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.biopha.2022.113500openalex-snapshot
Spatiotemporal dynamics of the cellular components involved in glial scar formation following spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115632openalex-snapshot
The role and mechanisms of mesenchymal stem cells regulating macrophage plasticity in spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2018.01.003openalex-snapshot
Quantitative analysis of lipid debris accumulation caused by cuprizone induced myelin degradation in different CNS areas
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2021.12.019openalex-snapshot
M1 macrophages impair tight junctions between endothelial cells after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2026.111823openalex-snapshot
SYK-dependent lipid handling in monocyte-derived macrophages governs functional recovery after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2026.112052openalex-snapshot
Lgals3high macrophages orchestrate neuroinflammation and extracellular matrix remodelling via NF-κB pathway in acute spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.canlet.2021.12.023openalex-snapshot
Osteosarcoma exocytosis of soluble LGALS3BP mediates macrophages toward a tumoricidal phenotype
inferred← citeshttps://doi.org/10.1016/j.carbon.2016.11.040openalex-snapshot
Poly(dopamine)-modified carbon nanotube multilayered film and its effects on macrophages
inferred← citeshttps://doi.org/10.1016/j.cej.2025.166727openalex-snapshot
A novel natural protein modulates foam macrophage formation: Implications for spinal cord injury intervention
inferred← citeshttps://doi.org/10.1016/j.cellimm.2022.104591openalex-snapshot
Consequences and mechanisms of myelin debris uptake and processing by cells in the central nervous system
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.06.018openalex-snapshot
Spinal Microgliosis Due to Resident Microglial Proliferation Is Required for Pain Hypersensitivity after Peripheral Nerve Injury
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117482openalex-snapshot
Elevated phagocytic capacity directs innate spinal cord repair
inferred← citeshttps://doi.org/10.1016/j.envres.2023.116563openalex-snapshot
Nanomedicine innovations in spinal cord injury management: Bridging the gap
inferred← citeshttps://doi.org/10.1016/j.expneurol.2019.112965openalex-snapshot
LINGO-1 deficiency promotes nerve regeneration through reduction of cell apoptosis, inflammation, and glial scar after spinal cord injury in mice
inferred← citeshttps://doi.org/10.1016/j.expneurol.2022.114114openalex-snapshot
Genetic deletion of the glucocorticoid receptor in Cx3cr1+ myeloid cells is neuroprotective and improves motor recovery after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2022.114273openalex-snapshot
Domino reaction of neurovascular unit in neuropathic pain after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2023.114367openalex-snapshot
Hydralazine plays an immunomodulation role of pro-regeneration in a mouse model of spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2024.114682openalex-snapshot
The acute spinal cord injury microenvironment and its impact on the homing of mesenchymal stem cells
inferred← citeshttps://doi.org/10.1016/j.expneurol.2024.114844openalex-snapshot
Repeated trans-spinal magnetic stimulation promotes microglial phagocytosis of myelin debris after spinal cord injury through LRP-1
inferred← citeshttps://doi.org/10.1016/j.expneurol.2024.114916openalex-snapshot
TRIM21-mediated ubiquitination of PLIN2 regulates neuronal lipid droplet accumulation after acute spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2024.114982openalex-snapshot
Genetic deletion of the apoptosis associated speck like protein containing a card in LysM+ macrophages attenuates spinal cord injury by regulating M1/M2 polarization through ASC-dependent inflammasome signaling axis
inferred← citeshttps://doi.org/10.1016/j.hest.2026.08.004openalex-snapshot
Decoding the spatiotemporal pleiotropy of CCL2-CCR2 signaling to guide staged therapies in central nervous system injury
inferred← citeshttps://doi.org/10.1016/j.it.2015.08.002openalex-snapshot
Immune Surveillance of the CNS following Infection and Injury
inferred← citeshttps://doi.org/10.1016/j.jconrel.2025.114308openalex-snapshot
Engineered lesion-homing liposomes encapsulating Rosuvastatin enhance spinal cord injury repair by preventing the formation of foamy macrophages
inferred← citeshttps://doi.org/10.1016/j.jcyt.2020.03.002openalex-snapshot
Transplantation of activated olfactory ensheathing cells by curcumin strengthens regeneration and recovery of function after spinal cord injury in rats
inferred← citeshttps://doi.org/10.1016/j.jot.2026.101049openalex-snapshot
Mitochondrial metabolism restoration via Tramiprosate suppresses mitochondrial ROS-driven foamy macrophage senescence post spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.mcn.2025.104054openalex-snapshot
The role of polarization dynamics in macrophages and microglia on the inflammatory microenvironment of spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.molimm.2019.09.022openalex-snapshot
Bisperoxovanadium induces M2-type macrophages and promotes functional recovery after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.mtbio.2025.102576openalex-snapshot
Engineering a targeted daphnetin delivery system to enhance spinal cord injury treatment effectiveness
inferred← citeshttps://doi.org/10.1016/j.mtbio.2026.103661openalex-snapshot
ROS-responsive hydrogel delivering liposomal indole-3-propionic acid promotes spinal cord injury repair by enhancing CX3CL1-CX3CR1 mediated neuron-microglia communication
inferred← citeshttps://doi.org/10.1016/j.nbd.2019.04.014openalex-snapshot
A hydrogel engineered to deliver minocycline locally to the injured cervical spinal cord protects respiratory neural circuitry and preserves diaphragm function
inferred← citeshttps://doi.org/10.1016/j.nbd.2021.105608openalex-snapshot
Myelin and non-myelin debris contribute to foamy macrophage formation after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.nbd.2023.106370openalex-snapshot
PI3K signaling promotes formation of lipid-laden foamy macrophages at the spinal cord injury site
inferred← citeshttps://doi.org/10.1016/j.neulet.2023.137345openalex-snapshot
Construction and optimization of a coculture system of mouse brain microvascular endothelial cells and myelin debris
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2024.11.074openalex-snapshot
Interaction of microglia with the microenvironment in spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.omtn.2018.03.009openalex-snapshot
Hydrogel-Assisted Antisense LNA Gapmer Delivery for In Situ Gene Silencing in Spinal Cord Injury
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2026.109122openalex-snapshot
Apolipoprotein E in spinal cord injury: mechanisms of lipid dysregulation, neuroinflammation, and opportunities for repair
inferred← citeshttps://doi.org/10.1016/j.phymed.2025.156396openalex-snapshot
Puerarin mitigates cognitive decline and white matter injury via CD36-Mediated microglial phagocytosis in chronic cerebral hypoperfusion
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2018.12.001openalex-snapshot
Macrophage biology in the peripheral nervous system after injury
inferred← citeshttps://doi.org/10.1016/j.prp.2023.154331openalex-snapshot
Conditioned medium from bone marrow mesenchymal stem cells relieves spinal cord injury through suppression of Gal-3/NLRP3 and M1 microglia/macrophage polarization
inferred← citeshttps://doi.org/10.1016/j.redox.2024.103469openalex-snapshot
Macropinocytosis enhances foamy macrophage formation and cholesterol crystallization to activate NLRP3 inflammasome after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.redox.2025.103857openalex-snapshot
GLP-1R activation restores Gas6-driven efferocytosis in senescent foamy macrophages to promote neural repair
inferred← citeshttps://doi.org/10.1016/j.regen.2019.100023openalex-snapshot
The role of the immune system during regeneration of the central nervous system
inferred← citeshttps://doi.org/10.1016/j.smim.2022.101629openalex-snapshot
Immune response after central nervous system injury
inferred← citeshttps://doi.org/10.1016/j.taap.2026.117839openalex-snapshot
Tetramethylpyrazine promotes spinal cord injury repair by modulating macrophage M1/M2 polarization via inhibition of the IL-6/JAK2/STAT3 pathway
inferred← citeshttps://doi.org/10.1016/j.tice.2019.07.002openalex-snapshot
Notch signaling regulates osteosarcoma proliferation and migration through Erk phosphorylation
inferred← citeshttps://doi.org/10.1016/j.xpro.2025.104029openalex-snapshot
Protocol to develop a preclinical severe contusive-compressive SCI mouse model for translational research
inferred← citeshttps://doi.org/10.1017/9781108917339.020openalex-snapshot
Acute Spinal Cord Injury and Spinal Trauma
inferred← citeshttps://doi.org/10.1021/acs.analchem.8b02682openalex-snapshot
Lipid Changes Associated with Traumatic Brain Injury Revealed by 3D MALDI-MSI
inferred← citeshttps://doi.org/10.1021/acs.analchem.9b02633openalex-snapshot
Matrix-Assisted Laser Desorption/Ionization-Mass Spectrometry Imaging of Lipids in Experimental Model of Traumatic Brain Injury Detecting Acylcarnitines as Injury Related Markers
inferred← citeshttps://doi.org/10.1021/acsami.5c13694openalex-snapshot
Nanovesicles Synergistically Regulate Ferroptosis Characteristic Macrophage-Induced Angiogenesis via Ferritin Heavy Chain 1/Glutathione Peroxidase 4 Pathway to Promote Peripheral Nerve Regeneration
inferred← citeshttps://doi.org/10.1038/s41392-023-01477-6openalex-snapshot
Spinal cord injury: molecular mechanisms and therapeutic interventions
inferred← citeshttps://doi.org/10.1038/s41419-017-0236-8openalex-snapshot
Plasma Hemopexin ameliorates murine spinal cord injury by switching microglia from the M1 state to the M2 state
inferred← citeshttps://doi.org/10.1038/s41419-022-04864-zopenalex-snapshot
Single-cell transcriptome analysis reveals the immune heterogeneity and the repopulation of microglia by Hif1α in mice after spinal cord injury
inferred← citeshttps://doi.org/10.1038/s41423-024-01204-3openalex-snapshot
GPR34 senses demyelination to promote neuroinflammation and pathologies
inferred← citeshttps://doi.org/10.1038/s41467-022-29496-xopenalex-snapshot
Long-term in vivo imaging of mouse spinal cord through an optically cleared intervertebral window
inferred← citeshttps://doi.org/10.1038/s41467-022-31797-0openalex-snapshot
Microglia coordinate cellular interactions during spinal cord repair in mice
inferred← citeshttps://doi.org/10.1038/s41593-018-0324-9openalex-snapshot
Microvascular endothelial cells engulf myelin debris and promote macrophage recruitment and fibrosis after neural injury
inferred← citeshttps://doi.org/10.1038/s41593-024-01847-5openalex-snapshot
Monocyte-derived macrophages act as reinforcements when microglia fall short in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1038/s41598-018-34518-0openalex-snapshot
3D MALDI mass spectrometry imaging reveals specific localization of long-chain acylcarnitines within a 10-day time window of spinal cord injury
inferred← citeshttps://doi.org/10.1038/s41598-020-75850-8openalex-snapshot
Key differences between olfactory ensheathing cells and Schwann cells regarding phagocytosis of necrotic cells: implications for transplantation therapies
inferred← citeshttps://doi.org/10.1038/s41598-021-85863-6openalex-snapshot
The effects of myelin on macrophage activation are phenotypic specific via cPLA2 in the context of spinal cord injury inflammation
inferred← citeshttps://doi.org/10.1038/s41598-024-84936-6openalex-snapshot
Cytosolic phospholipase A2 in infiltrating monocyte derived macrophages does not impair recovery after spinal cord injury in female mice
inferred← citeshttps://doi.org/10.1038/s41598-025-86991-zopenalex-snapshot
Glycosylated lysosomal membrane protein promotes tissue repair after spinal cord injury by reducing iron deposition and ferroptosis in microglia
inferred← citeshttps://doi.org/10.1038/s42003-023-04932-wopenalex-snapshot
Spinal muscular atrophy-like phenotype in a mouse model of acid ceramidase deficiency
inferred← citeshttps://doi.org/10.1038/s42003-025-09167-5openalex-snapshot
Lipid accumulation in foam cells drives C1q-dependent synaptic loss and impairs motor function recovery after spinal cord injury
inferred← citeshttps://doi.org/10.1039/d3bm01152fopenalex-snapshot
A multi-channel collagen conduit with aligned Schwann cells and endothelial cells for enhanced neuronal regeneration in spinal cord injury
inferred← citeshttps://doi.org/10.1039/d5tb02228bopenalex-snapshot
Injectable hydrogel-based localized delivery of IDO-galectin-3 mitigates neuroinflammation and promotes neuronal sparing after spinal cord contusion in rats
inferred← citeshttps://doi.org/10.1055/s-0041-1735854openalex-snapshot
Therapeutic Effects of Azithromycin on Spinal Cord Injury in Male Wistar Rats: A Role for Inflammatory Pathways
inferred← citeshttps://doi.org/10.1080/13510002.2026.2720356openalex-snapshot
Lipid droplets as redox-active organelles after spinal cord injury: lipid peroxidation, mitochondrial dysfunction, and neuroinflammation
inferred← citeshttps://doi.org/10.1080/14728222.2023.2235718openalex-snapshot
The role of the ATP-Binding Cassette A1 (ABCA1) in neurological disorders: a mechanistic review
inferred← citeshttps://doi.org/10.1080/21655979.2022.2073063openalex-snapshot
D-4F, an apolipoprotein A-I mimetic, promotes the clearance of myelin debris and the reduction of foamy macrophages after spinal cord injury
inferred← citeshttps://doi.org/10.1080/27694127.2025.2529196openalex-snapshot
The role of autophagy in the pathogenesis and treatment of multiple sclerosis
inferred← citeshttps://doi.org/10.1084/jem.20170686openalex-snapshot
γδ T cells provide the early source of IFN-γ to aggravate lesions in spinal cord injury
inferred← citeshttps://doi.org/10.1084/jem.20191660openalex-snapshot
Stearoyl-CoA desaturase-1 impairs the reparative properties of macrophages and microglia in the brain
inferred← citeshttps://doi.org/10.1084/jem.20210040openalex-snapshot
Single-cell analysis of the cellular heterogeneity and interactions in the injured mouse spinal cord
inferred← citeshttps://doi.org/10.1088/1741-2552/ad29d5openalex-snapshot
Local delivery of AdipoRon from self-assembled microparticles to inhibit myelin lipid uptake and to promote lipid efflux from rat macrophages
inferred← citeshttps://doi.org/10.1088/1748-605x/aa9bbbopenalex-snapshot
Biomaterial strategies for limiting the impact of secondary events following spinal cord injury
inferred← citeshttps://doi.org/10.1088/1748-605x/ac1d3copenalex-snapshot
Research advances of biomaterials-based microenvironment-regulation therapies for repair and regeneration of spinal cord injury
inferred← citeshttps://doi.org/10.1088/1748-605x/ad4079openalex-snapshot
Advances in electroactive bioscaffolds for repairing spinal cord injury
inferred← citeshttps://doi.org/10.1089/dna.2020.5647openalex-snapshot
Unexpected Role of Nonimmune Cells: Amateur Phagocytes
inferred← citeshttps://doi.org/10.1089/neu.2018.5783openalex-snapshot
Activating Adiponectin Signaling with Exogenous AdipoRon Reduces Myelin Lipid Accumulation and Suppresses Macrophage Recruitment after Spinal Cord Injury
inferred← citeshttps://doi.org/10.1089/neu.2019.6421openalex-snapshot
MIC-1/GDF15 Overexpression Is Associated with Increased Functional Recovery in Traumatic Spinal Cord Injury
inferred← citeshttps://doi.org/10.1089/neu.2019.6938openalex-snapshot
The Neuroprotective Role of Reactive Astrocytes after Central Nervous System Injury
inferred← citeshttps://doi.org/10.1089/neu.2020.7571openalex-snapshot
Intraspinal Administration of Netrin-1 Promotes Locomotor Recovery after Complete Spinal Cord Transection
inferred← citeshttps://doi.org/10.1089/neu.2021.0346openalex-snapshot
Fatty Acid-Binding Protein 4 Inhibition Promotes Locomotor and Autonomic Recovery in Rats following Spinal Cord Injury
inferred← citeshttps://doi.org/10.1089/ten.teb.2020.0188openalex-snapshot
Nanotechnology for the Treatment of Spinal Cord Injury
inferred← citeshttps://doi.org/10.1093/brain/awab250openalex-snapshot
Macrophage phagocytosis after spinal cord injury: when friends become foes
inferred← citeshttps://doi.org/10.1093/braincomms/fcad108openalex-snapshot
Nogo receptor-Fc delivered by haematopoietic cells enhances neurorepair in a multiple sclerosis model
inferred← citeshttps://doi.org/10.1093/burnst/tkab035openalex-snapshot
Deciphering glial scar after spinal cord injury
inferred← citeshttps://doi.org/10.1093/burnst/tkac054openalex-snapshot
Role of inflammation in neurological damage and regeneration following spinal cord injury and its therapeutic implications
inferred← citeshttps://doi.org/10.1093/hmg/ddac299openalex-snapshot
Upregulation of non-canonical and canonical inflammasome genes associates with pathological features in Krabbe disease and related disorders
inferred← citeshttps://doi.org/10.1093/hmg/ddz073openalex-snapshot
Docosahexaenoic acid reduces microglia phagocytic activity via miR-124 and induces neuroprotection in rodent models of spinal cord contusion injury
inferred← citeshttps://doi.org/10.1093/rb/rbv012openalex-snapshot
Bridging the lesion—engineering a permissive substrate for nerve regeneration
inferred← citeshttps://doi.org/10.1096/fj.201800754rropenalex-snapshot
Neuropathology of vitamin B 12 deficiency in the Cd320 −/− mouse
inferred← citeshttps://doi.org/10.1096/fj.202100081rropenalex-snapshot
Proteomics and bioinformatics reveal insights into neuroinflammation in the acute to subacute phases in rat models of spinal cord contusion injury
inferred← citeshttps://doi.org/10.1096/fj.202402891rropenalex-snapshot
Single‐Cell Transcriptomic Profiling of Brain Cells in Newborn Rats Following Hypoxic Ischemic Encephalopathy
inferred← citeshttps://doi.org/10.1097/br9.0000000000000036openalex-snapshot
The role of C-X3-C motif chemokine ligand 1/C-X3-C motif chemokine receptor 1 axis in spinal cord injury
inferred← citeshttps://doi.org/10.1097/js9.0000000000002955openalex-snapshot
Application and challenge of Schwann cell transplantation in spinal cord injury and clinical trial
inferred← citeshttps://doi.org/10.1097/wco.0000000000000783openalex-snapshot
Immunological mechanisms in poststroke dementia
inferred← citeshttps://doi.org/10.1101/2023.08.11.553038openalex-snapshot
Acute or chronic depletion of macrophages in the dorsal root ganglia induces neuropathic pain after unilateral cervical spinal cord injury
inferred← citeshttps://doi.org/10.1101/2025.03.19.643597openalex-snapshot
The concentration of myelin debris-like particles in the normal rat optic nerve
inferred← citeshttps://doi.org/10.1101/410258openalex-snapshot
Microglia limit lesion expansion and promote functional recovery after spinal cord injury in mice
inferred← citeshttps://doi.org/10.1111/bph.14193openalex-snapshot
Treatment with IL‐19 improves locomotor functional recovery after contusion trauma to the spinal cord
inferred← citeshttps://doi.org/10.1111/cns.14439openalex-snapshot
Inhibition of HDAC6 promotes microvascular endothelial cells to phagocytize myelin debris and reduces inflammatory response to accelerate the repair of spinal cord injury
inferred← citeshttps://doi.org/10.1111/cns.14642openalex-snapshot
Acetyl‐11‐keto‐beta‐boswellic acid modulates macrophage polarization and Schwann cell migration to accelerate spinal cord injury repair in rats
inferred← citeshttps://doi.org/10.1111/cns.70181openalex-snapshot
Interleukin‐3 Modulates Macrophage Phagocytic Activity and Promotes Spinal Cord Injury Repair
inferred← citeshttps://doi.org/10.1111/ejn.13190openalex-snapshot
Diffuse traumatic axonal injury in mice induces complex behavioural alterations that are normalized by neutralization of interleukin-1β
inferred← citeshttps://doi.org/10.1111/jcmm.13034openalex-snapshot
Macrophage polarization: a key event in the secondary phase of acute spinal cord injury
inferred← citeshttps://doi.org/10.1111/wrr.13006openalex-snapshot
Foamy macrophages potentially inhibit tuberculous wound healing by inhibiting the TLRs / NF‐κB signalling pathway
inferred← citeshttps://doi.org/10.1146/annurev-bioeng-103023-035352openalex-snapshot
Multimodal Toxicity of Acrolein and Associated Therapeutic Strategies in Central Nervous System Trauma and Disease
inferred← citeshttps://doi.org/10.1152/physiolgenomics.00078.2017openalex-snapshot
Chronic spinal cord changes in a high-fat diet-fed male rat model of thoracic spinal contusion
inferred← citeshttps://doi.org/10.1152/physrev.00017.2017openalex-snapshot
The Biology of Regeneration Failure and Success After Spinal Cord Injury
inferred← citeshttps://doi.org/10.1155/2022/9197940openalex-snapshot
Macrophage Extracellular Traps Exacerbate Secondary Spinal Cord Injury by Modulating Macrophage/Microglia Polarization via LL37/P2X7R/NF‐ κ B Signaling Pathway
inferred← citeshttps://doi.org/10.1155/np/6684089openalex-snapshot
Schwann Cells and Their Exosomes: Research Progress and Prospect in Spinal Cord Injury
inferred← citeshttps://doi.org/10.1155/sci/8841129openalex-snapshot
Exosome‐Loaded Bioscaffolds for Spinal Cord Injuries: A Review
inferred← citeshttps://doi.org/10.1161/strokeaha.120.029827openalex-snapshot
Reciprocal Interaction Between Pericytes and Macrophage in Poststroke Tissue Repair and Functional Recovery
inferred← citeshttps://doi.org/10.1167/iovs.65.10.22openalex-snapshot
Macrophages Modulate Optic Nerve Crush Injury Scar Formation and Retinal Ganglion Cell Function
inferred← citeshttps://doi.org/10.1172/jci.insight.174753openalex-snapshot
The immune system and metabolic products in epilepsy and glioma-associated epilepsy: emerging therapeutic directions
inferred← citeshttps://doi.org/10.1177/08977151251387696openalex-snapshot
Netrin-1 Therapy Restores Partial Hindlimb Movement in a Rat Model of High-Severity Chronic Spinal Cord Injury
inferred← citeshttps://doi.org/10.1177/2192568220950337openalex-snapshot
Immune and Metabolic Biomarkers in a Rodent Model of Spinal Cord Contusion
inferred← citeshttps://doi.org/10.1186/s12964-022-01036-6openalex-snapshot
Transplantation of A2 type astrocytes promotes neural repair and remyelination after spinal cord injury
inferred← citeshttps://doi.org/10.1186/s12967-024-05480-5openalex-snapshot
miR-223 accelerates lipid droplets clearance in microglia following spinal cord injury by upregulating ABCA1
inferred← citeshttps://doi.org/10.1186/s12974-015-0463-9openalex-snapshot
Cyclic AMP is a key regulator of M1 to M2a phenotypic conversion of microglia in the presence of Th2 cytokines
inferred← citeshttps://doi.org/10.1186/s12974-016-0736-yopenalex-snapshot
Multiple organ dysfunction and systemic inflammation after spinal cord injury: a complex relationship
inferred← citeshttps://doi.org/10.1186/s12974-020-01735-2openalex-snapshot
Macrophage MSR1 promotes the formation of foamy macrophage and neuronal apoptosis after spinal cord injury
inferred← citeshttps://doi.org/10.1186/s12974-020-01805-5openalex-snapshot
LncGBP9/miR-34a axis drives macrophages toward a phenotype conducive for spinal cord injury repair via STAT1/STAT6 and SOCS3
inferred← citeshttps://doi.org/10.1186/s12974-021-02161-8openalex-snapshot
Acute inflammatory profiles differ with sex and age after spinal cord injury
inferred← citeshttps://doi.org/10.1186/s12974-021-02292-yopenalex-snapshot
Macrophage-specific RhoA knockout delays Wallerian degeneration after peripheral nerve injury in mice
inferred← citeshttps://doi.org/10.1186/s12974-021-02353-2openalex-snapshot
Spleen tyrosine kinase facilitates neutrophil activation and worsens long-term neurologic deficits after spinal cord injury
inferred← citeshttps://doi.org/10.1186/s12974-021-02360-3openalex-snapshot
Citrullinated myelin induces microglial TNFα and inhibits endogenous repair in the cuprizone model of demyelination
inferred← citeshttps://doi.org/10.1186/s12974-022-02458-2openalex-snapshot
Macrophage-based delivery of interleukin-13 improves functional and histopathological outcomes following spinal cord injury
inferred← citeshttps://doi.org/10.1186/s12974-023-02833-7openalex-snapshot
Endothelial progenitor cell-derived exosomes promote anti-inflammatory macrophages via SOCS3/JAK2/STAT3 axis and improve the outcome of spinal cord injury
inferred← citeshttps://doi.org/10.1186/s12974-024-03089-5openalex-snapshot
Fascin-1 limits myosin activity in microglia to control mechanical characterization of the injured spinal cord
inferred← citeshttps://doi.org/10.1186/s12974-025-03379-6openalex-snapshot
Reawakening inflammation in the chronically injured spinal cord using lipopolysaccharide induces diverse microglial states
inferred← citeshttps://doi.org/10.1186/s12974-025-03411-9openalex-snapshot
Centripetal migration and prolonged retention of microglia promotes spinal cord injury repair
inferred← citeshttps://doi.org/10.1186/s12974-026-03743-0openalex-snapshot
FGF4 activates FGFR1 - PI3K/AKT signaling to enhance Clec10a-mediated intracellular myelin debris processing and promote spinal cord repair
inferred← citeshttps://doi.org/10.1186/s12974-026-03859-3openalex-snapshot
ABCA1-mediated lipid efflux restrains oxidative stress and neuroinflammation after spinal cord injury
inferred← citeshttps://doi.org/10.1186/s13024-016-0081-8openalex-snapshot
Reactive astrocytes undergo M1 microglia/macrohpages-induced necroptosis in spinal cord injury
inferred← citeshttps://doi.org/10.1186/s13041-016-0233-3openalex-snapshot
Rescuing macrophage normal function in spinal cord injury with embryonic stem cell conditioned media
inferred← citeshttps://doi.org/10.1186/s13287-021-02401-xopenalex-snapshot
SiRNA in MSC-derived exosomes silences CTGF gene for locomotor recovery in spinal cord injury rats
inferred← citeshttps://doi.org/10.1186/s13287-024-03914-xopenalex-snapshot
Progression of mesenchymal stem cell regulation on imbalanced microenvironment after spinal cord injury
inferred← citeshttps://doi.org/10.1186/s13578-024-01310-9openalex-snapshot
Galectin-3 inhibition reduces fibrotic scarring and promotes functional recovery after spinal cord injury in mice
inferred← citeshttps://doi.org/10.1186/s13578-025-01357-2openalex-snapshot
Trehalose enhances macrophage autophagy to promote myelin debris clearance after spinal cord injury
inferred← citeshttps://doi.org/10.1186/s40478-018-0628-8openalex-snapshot
The physiology of foamy phagocytes in multiple sclerosis
inferred← citeshttps://doi.org/10.1186/s40478-020-01016-2openalex-snapshot
Acute brain injuries trigger microglia as an additional source of the proteoglycan NG2
inferred← citeshttps://doi.org/10.1242/dev.204790openalex-snapshot
Mechanisms underpinning spontaneous spinal cord regeneration
inferred← citeshttps://doi.org/10.1371/journal.pone.0209733openalex-snapshot
Application of CNTF or FGF-2 increases the number of M2-like macrophages after optic nerve injury in adult Rana pipiens
inferred← citeshttps://doi.org/10.1371/journal.pone.0255196openalex-snapshot
Retinoic acid treatment recruits macrophages and increases axonal regeneration after optic nerve injury in the frog Rana pipiens
inferred← citeshttps://doi.org/10.14232/phd.10270openalex-snapshot
Mielinhüvely degradációt követő lipid törmelék eloszlás vizsgálata a központi idegrendszerben CARS mikroszkópiával és Agykérgi neurogliaform sejthálózat által kiváltott ionotróp és metabotróp gátló posztszinaptikus válaszok eltérő összegződése
inferred← citeshttps://doi.org/10.14670/hh-18-591openalex-snapshot
The significance of M1 macrophage should be highlighted in peripheral nerve regeneration.
showing the first 200 of 311 · page through all 311
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.