On the public citation graph

Role of macrophages in Wallerian degeneration and axonal regeneration after peripheral nerve injury

https://doi.org/10.1007/s00401-015-1482-4

0 signed · 655 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.

Claim with ORCID

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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1097-4547(19980715)53:2<260::aid-jnr15>3.0.co;2-aopenalex-snapshot

Monocyte chemoattractant protein 1 is responsible for macrophage recruitment following injury to sciatic nerve

inferredcites →https://doi.org/10.1002/bies.950140610openalex-snapshot

Role of macrophages in peripheral nerve degeneration and repair

inferredcites →https://doi.org/10.1002/dneu.20384openalex-snapshot

Inhibiting effect of minocycline on the regeneration of peripheral nerves

inferredcites →https://doi.org/10.1002/glia.20766openalex-snapshot

Interactions between Schwann cells and macrophages in injury and inherited demyelinating disease

inferredcites →https://doi.org/10.1002/glia.20894openalex-snapshot

Proteasome inhibition suppresses Schwann cell dedifferentiation in vitro and in vivo

inferredcites →https://doi.org/10.1002/glia.22382openalex-snapshot

Local production of serum amyloid a is implicated in the induction of macrophage chemoattractants in Schwann cells during wallerian degeneration of peripheral nerves

inferredcites →https://doi.org/10.1002/jnr.21166openalex-snapshot

Macrophage depletion alters the blood–nerve barrier without affecting Schwann cell function after neural injury

inferredcites →https://doi.org/10.1002/mus.880120803openalex-snapshot

The blood–nerve barrier in Wallerian degeneration: A sequential long‐term study

inferredcites →https://doi.org/10.1002/neu.480270203openalex-snapshot

Changes in the macrophage population of the rat superior cervical ganglion after postganglionic nerve injury

inferredcites →https://doi.org/10.1006/exnr.1996.0142openalex-snapshot

Reduced Hyperalgesia in Nerve-Injured WLD Mice: Relationship to Nerve Fiber Phagocytosis, Axonal Degeneration, and Regeneration in Normal Mice

inferredcites →https://doi.org/10.1007/bf00307696openalex-snapshot

Anti-macrophage CR3 antibody blocks myelin phagocytosis by macrophages in vitro

inferredcites →https://doi.org/10.1007/bf00686796openalex-snapshot

Myelin phagocytosis in Wallerian degeneration

inferredcites →https://doi.org/10.1007/bf01195557openalex-snapshot

Responses of macrophages in rat dorsal root ganglia following peripheral nerve injury

inferredcites →https://doi.org/10.1007/bf02150231openalex-snapshot

Myelin-stimulated macrophages release neurotrophic factors for adult dorsal root ganglion neurons in culture

inferredcites →https://doi.org/10.1007/s00018-009-0205-1openalex-snapshot

Platelets and innate immunity

inferredcites →https://doi.org/10.1007/s00401-014-1369-9openalex-snapshot

Collagen VI regulates peripheral nerve regeneration by modulating macrophage recruitment and polarization

inferredcites →https://doi.org/10.1007/s004010050611openalex-snapshot

The dynamics of macrophage recruitment after nerve transection

inferredcites →https://doi.org/10.1007/s10753-013-9621-3openalex-snapshot

The Adenosine-Dependent Angiogenic Switch of Macrophages to an M2-Like Phenotype is Independent of Interleukin-4 Receptor Alpha (IL-4Rα) Signaling

inferredcites →https://doi.org/10.1016/0006-8993(86)90289-1openalex-snapshot

Myelin phagocytosis in Wallerian degeneration of peripheral nerves depends on silica-sensitive,bg/bg-negative and Fc-positive monocytes

inferredcites →https://doi.org/10.1016/0022-510x(91)90162-zopenalex-snapshot

The role of complement in myelin phagocytosis during PNS wallerian degeneration

inferredcites →https://doi.org/10.1016/0165-5728(92)90085-yopenalex-snapshot

TNF-α suppresses CR3-mediated myelin removal by macrophages

inferredcites →https://doi.org/10.1016/0197-4580(96)00105-4openalex-snapshot

Unusual aspects of inflammation in the nervous system: Wallerian degeneration

inferredcites →https://doi.org/10.1016/b978-0-12-407704-1.00001-4openalex-snapshot

Role of Macrophage Polarization in Tumor Angiogenesis and Vessel Normalization

inferredcites →https://doi.org/10.1016/j.aanat.2011.02.011openalex-snapshot

Wallerian degeneration and peripheral nerve conditions for both axonal regeneration and neuropathic pain induction

inferredcites →https://doi.org/10.1016/j.bbi.2014.10.016openalex-snapshot

Stromal cell-derived CCL2 drives neuropathic pain states through myeloid cell infiltration in injured nerve

inferredcites →https://doi.org/10.1016/j.bbrc.2005.04.105openalex-snapshot

Expression of Reg/PAP family members during motor nerve regeneration in rat

inferredcites →https://doi.org/10.1016/j.biomaterials.2012.02.034openalex-snapshot

Macrophage polarization: An opportunity for improved outcomes in biomaterials and regenerative medicine

inferredcites →https://doi.org/10.1016/j.biomaterials.2012.08.050openalex-snapshot

Effect of modulating macrophage phenotype on peripheral nerve repair

inferredcites →https://doi.org/10.1016/j.brainresrev.2005.11.004openalex-snapshot

Immune and inflammatory mechanisms in neuropathic pain

inferredcites →https://doi.org/10.1016/j.ccell.2015.02.015openalex-snapshot

Macrophages and Therapeutic Resistance in Cancer

inferredcites →https://doi.org/10.1016/j.ccr.2010.11.009openalex-snapshot

HRG Inhibits Tumor Growth and Metastasis by Inducing Macrophage Polarization and Vessel Normalization through Downregulation of PlGF

inferredcites →https://doi.org/10.1016/j.cell.2010.03.014openalex-snapshot

Macrophage Diversity Enhances Tumor Progression and Metastasis

inferredcites →https://doi.org/10.1016/j.cell.2010.08.039openalex-snapshot

EphB Signaling Directs Peripheral Nerve Regeneration through Sox2-Dependent Schwann Cell Sorting

inferredcites →https://doi.org/10.1016/j.cell.2015.07.021openalex-snapshot

Macrophage-Induced Blood Vessels Guide Schwann Cell-Mediated Regeneration of Peripheral Nerves

inferredcites →https://doi.org/10.1016/j.cyto.2013.09.019openalex-snapshot

Epigenetic upregulation of CCL2 and CCL3 via histone modifications in infiltrating macrophages after peripheral nerve injury

inferredcites →https://doi.org/10.1016/j.expneurol.2004.02.004openalex-snapshot

Blocking of up-regulated ICAM-1 does not prevent macrophage infiltration during Wallerian degeneration of peripheral nerve

inferredcites →https://doi.org/10.1016/j.expneurol.2009.09.007openalex-snapshot

A role for galectin-1 in the immune response to peripheral nerve injury

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.jim.2015.03.013openalex-snapshot

Interleukin-10 conjugated electrospun polycaprolactone (PCL) nanofibre scaffolds for promoting alternatively activated (M2) macrophages around the peripheral nerve in vivo

inferredcites →https://doi.org/10.1016/j.lfs.2013.10.005openalex-snapshot

Contribution of macrophages to peripheral neuropathic pain pathogenesis

inferredcites →https://doi.org/10.1016/j.molimm.2008.08.269openalex-snapshot

CCR7-specific migration to CCL19 and CCL21 is induced by PGE2 stimulation in human monocytes: Involvement of EP2/EP4 receptors activation

inferredcites →https://doi.org/10.1016/j.nbd.2013.01.003openalex-snapshot

Deletion of Nrf2 impairs functional recovery, reduces clearance of myelin debris and decreases axonal remyelination after peripheral nerve injury

inferredcites →https://doi.org/10.1016/j.neures.2004.01.004openalex-snapshot

Enhanced production of monocyte chemoattractant protein-1 in the dorsal root ganglia in a rat model of neuropathic pain: possible involvement in the development of neuropathic pain

inferredcites →https://doi.org/10.1016/j.neuron.2011.11.031openalex-snapshot

A Central Role for the ERK-Signaling Pathway in Controlling Schwann Cell Plasticity and Peripheral Nerve Regeneration In Vivo

inferredcites →https://doi.org/10.1016/j.neuron.2012.06.021openalex-snapshot

c-Jun Reprograms Schwann Cells of Injured Nerves to Generate a Repair Cell Essential for Regeneration

inferredcites →https://doi.org/10.1016/j.neuron.2014.06.016openalex-snapshot

Diminished Schwann Cell Repair Responses Underlie Age-Associated Impaired Axonal Regeneration

inferredcites →https://doi.org/10.1016/j.neuroscience.2014.09.027openalex-snapshot

The neuroimmunology of degeneration and regeneration in the peripheral nervous system

inferredcites →https://doi.org/10.1016/j.pain.2013.06.042openalex-snapshot

P-selectin is required for neutrophils and macrophage infiltration into injured site and contributes to generation of behavioral hypersensitivity following peripheral nerve injury in mice

inferredcites →https://doi.org/10.1016/j.pain.2013.12.006openalex-snapshot

Prostacyclin mediates neuropathic pain through interleukin 1β-expressing resident macrophages

inferredcites →https://doi.org/10.1016/j.pain.2014.08.013openalex-snapshot

Nox2-dependent signaling between macrophages and sensory neurons contributes to neuropathic pain hypersensitivity

inferredcites →https://doi.org/10.1016/j.pneurobio.2015.05.003openalex-snapshot

Alternatively activated microglia and macrophages in the central nervous system

inferredcites →https://doi.org/10.1016/s0002-9440(10)63070-2openalex-snapshot

Rapid Response of Identified Resident Endoneurial Macrophages to Nerve Injury

inferredcites →https://doi.org/10.1016/s0006-8993(97)01327-9openalex-snapshot

Painful mononeuropathy in C57BL/Wld mice with delayed Wallerian degeneration: differential effects of cytokine production and nerve regeneration on thermal and mechanical hypersensitivity

inferredcites →https://doi.org/10.1016/s0092-8674(03)00422-7openalex-snapshot

Apoptotic Cells Induce Migration of Phagocytes via Caspase-3-Mediated Release of a Lipid Attraction Signal

inferredcites →https://doi.org/10.1016/s0165-5728(00)00343-xopenalex-snapshot

The chemokine receptor CCR2 is involved in macrophage recruitment to the injured peripheral nervous system

inferredcites →https://doi.org/10.1016/s0167-5699(97)01002-5openalex-snapshot

A role for secretory phospholipase A2 and C-reactive protein in the removal of injured cells

inferredcites →https://doi.org/10.1016/s0304-3959(99)00306-1openalex-snapshot

Depletion of macrophages reduces axonal degeneration and hyperalgesia following nerve injury

inferredcites →https://doi.org/10.1016/s1471-4906(02)02302-5openalex-snapshot

Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes

inferredcites →https://doi.org/10.1038/ki.2014.216openalex-snapshot

The calcium-binding protein complex S100A8/A9 has a crucial role in controlling macrophage-mediated renal repair following ischemia/reperfusion

inferredcites →https://doi.org/10.1038/nature13989openalex-snapshot

Tissue-resident macrophages originate from yolk-sac-derived erythro-myeloid progenitors

inferredcites →https://doi.org/10.1038/ncb1507openalex-snapshot

Tumour-mediated upregulation of chemoattractants and recruitment of myeloid cells predetermines lung metastasis

inferredcites →https://doi.org/10.1038/ncb1794openalex-snapshot

The S100A8–serum amyloid A3–TLR4 paracrine cascade establishes a pre-metastatic phase

inferredcites →https://doi.org/10.1038/ni.1889openalex-snapshot

Revised map of the human progenitor hierarchy shows the origin of macrophages and dendritic cells in early lymphoid development

inferredcites →https://doi.org/10.1038/ni.2109openalex-snapshot

Phenotypic and functional plasticity of cells of innate immunity: macrophages, mast cells and neutrophils

inferredcites →https://doi.org/10.1038/nm.3337openalex-snapshot

CSF-1R inhibition alters macrophage polarization and blocks glioma progression

inferredcites →https://doi.org/10.1038/nri1733openalex-snapshot

Monocyte and macrophage heterogeneity

inferredcites →https://doi.org/10.1038/nrn3722openalex-snapshot

Microglia and brain macrophages in the molecular age: from origin to neuropsychiatric disease

inferredcites →https://doi.org/10.1046/j.1432-1327.1999.00657.xopenalex-snapshot

Serum amyloid A, the major vertebrate acute‐phase reactant

inferredcites →https://doi.org/10.1046/j.1471-4159.1995.64051996.xopenalex-snapshot

Fibroblasts that Reside in Mouse and Frog Injured Peripheral Nerves Produce Apolipoproteins

inferredcites →https://doi.org/10.1055/s-0032-1333314openalex-snapshot

FK506 and Nerve Regeneration: Past, Present, and Future

inferredcites →https://doi.org/10.1055/s-0032-1333316openalex-snapshot

Nerve Repair by Means of Tubulization: Past, Present, Future

inferredcites →https://doi.org/10.1073/pnas.1001948107openalex-snapshot

Endogenous antibodies promote rapid myelin clearance and effective axon regeneration after nerve injury

inferredcites →https://doi.org/10.1073/pnas.76.2.888openalex-snapshot

Regulation of macrophage migration by products of the complement system.

inferredcites →https://doi.org/10.1073/pnas.83.4.1130openalex-snapshot

Nerve injury stimulates the secretion of apolipoprotein E by nonneuronal cells.

inferredcites →https://doi.org/10.1074/jbc.m114.622316openalex-snapshot

The Calcium-binding Proteins S100A8 and S100A9 Initiate the Early Inflammatory Program in Injured Peripheral Nerves

inferredcites →https://doi.org/10.1083/jcb.200310079openalex-snapshot

Peritoneal macrophages express both P-selectin and PSGL-1

inferredcites →https://doi.org/10.1084/jem.165.4.1218openalex-snapshot

The macrophage response to central and peripheral nerve injury. A possible role for macrophages in regeneration.

inferredcites →https://doi.org/10.1089/wound.2011.0307openalex-snapshot

Regulation of Macrophage Polarization and Wound Healing

inferredcites →https://doi.org/10.1093/brain/awh407openalex-snapshot

Involvement of monocyte chemoattractant protein-1, macrophage inflammatory protein-1 and interleukin-1 in Wallerian degeneration

inferredcites →https://doi.org/10.1093/glycob/cwp077openalex-snapshot

Galectin-1 stimulates monocyte chemotaxis via the p44/42 MAP kinase pathway and a pertussis toxin-sensitive pathway

inferredcites →https://doi.org/10.1093/hmg/ddh029openalex-snapshot

Expression of complement components in the peripheral nervous system

inferredcites →https://doi.org/10.1093/jnen/60.1.85openalex-snapshot

Matrix Metalloproteinase Expression and Inhibition After Sciatic Nerve Axotomy

inferredcites →https://doi.org/10.1096/fj.13-239533openalex-snapshot

Collagen VI regulates peripheral nerve myelination and function

inferredcites →https://doi.org/10.1097/00001756-200103050-00034openalex-snapshot

Monocyte chemoattractant protein (MCP)-1 is rapidly expressed by sympathetic ganglion neurons following axonal injury

inferredcites →https://doi.org/10.1097/00005072-199311000-00001openalex-snapshot

Macrophage Systems in Peripheral Nerves. A Review

inferredcites →https://doi.org/10.1097/01.lab.0000056993.28149.bfopenalex-snapshot

Macrophage Response to Peripheral Nerve Injury: The Quantitative Contribution of Resident and Hematogenous Macrophages

inferredcites →https://doi.org/10.1097/aln.0b013e31820b8b1eopenalex-snapshot

Inflammation Confers Dual Effects on Nociceptive Processing in Chronic Neuropathic Pain Model

inferredcites →https://doi.org/10.1097/j.pain.0000000000000097openalex-snapshot

Peripheral interleukin-4 ameliorates inflammatory macrophage-dependent neuropathic pain

inferredcites →https://doi.org/10.1097/wco.0b013e32834c208dopenalex-snapshot

Inflammation and axon regeneration

inferredcites →https://doi.org/10.1111/j.1085-9489.2003.03021.xopenalex-snapshot

Effects of FK506 on regeneration and macrophages in injured rat sciatic nerve

inferredcites →https://doi.org/10.1111/j.1460-9568.1997.tb01373.xopenalex-snapshot

Adhesion Molecules Involved in Macrophage Responses to Wallerian Degeneration in the Murine Peripheral Nervous System

inferredcites →https://doi.org/10.1111/j.1750-3639.1997.tb01060.xopenalex-snapshot

The Role of Macrophages in Wallerian Degeneration

inferredcites →https://doi.org/10.1111/j.1750-3639.1999.tb00229.xopenalex-snapshot

Nerve Injury, Axonal Degeneration and Neural Regeneration: Basic Insights

inferredcites →https://doi.org/10.1124/mol.105.022103openalex-snapshot

Serum Amyloid A Induces Contrary Immune Responses via Formyl Peptide Receptor-Like 1 in Human Monocytes

inferredcites →https://doi.org/10.1124/mol.106.024737openalex-snapshot

Antioxidant Down-Regulates Interleukin-18 Expression in Asthma

inferredcites →https://doi.org/10.1126/science.1118313openalex-snapshot

Glial Membranes at the Node of Ranvier Prevent Neurite Outgrowth

inferredcites →https://doi.org/10.1146/annurev.neuro.30.051606.094337openalex-snapshot

Peripheral Regeneration

inferredcites →https://doi.org/10.1155/2013/828354openalex-snapshot

S100A8 and S100A9: DAMPs at the Crossroads between Innate Immunity, Traditional Risk Factors, and Cardiovascular Disease

inferredcites →https://doi.org/10.1155/2015/676473openalex-snapshot

Parthenolide Relieves Pain and Promotes M2 Microglia/Macrophage Polarization in Rat Model of Neuropathy

inferredcites →https://doi.org/10.1159/000292020openalex-snapshot

Molecular Inflammatory Mediators in Peripheral Nerve Degeneration and Regeneration

inferredcites →https://doi.org/10.1161/atvbaha.111.222745openalex-snapshot

Apolipoprotein E Induces Antiinflammatory Phenotype in Macrophages

inferredcites →https://doi.org/10.1161/circulationaha.107.695189openalex-snapshot

Chemokine Fractalkine Mediates Leukocyte Recruitment to Inflammatory Endothelial Cells in Flowing Whole Blood

inferredcites →https://doi.org/10.1172/jci200519229openalex-snapshot

Human intestinal macrophages display profound inflammatory anergy despite avid phagocytic and bacteriocidal activity

inferredcites →https://doi.org/10.1179/016164110x12714125204353openalex-snapshot

Dynamic changes of ICAM-1 expression in peripheral nervous system following sciatic nerve injury

inferredcites →https://doi.org/10.1186/1742-2094-8-109openalex-snapshot

Wallerian degeneration: the innate-immune response to traumatic nerve injury

inferredcites →https://doi.org/10.1186/1742-2094-8-110openalex-snapshot

Wallerian degeneration: gaining perspective on inflammatory events after peripheral nerve injury

inferredcites →https://doi.org/10.1186/1742-2094-9-176openalex-snapshot

Acute injury in the peripheral nervous system triggers an alternative macrophage response

inferredcites →https://doi.org/10.1186/1744-8069-7-74openalex-snapshot

Toll-Like Receptor 2 Contributes to Chemokine Gene Expression and Macrophage Infiltration in the Dorsal Root Ganglia after Peripheral Nerve Injury

inferredcites →https://doi.org/10.1189/jlb.1008647openalex-snapshot

The endogenous Toll–like receptor 4 agonist S100A8/S100A9 (calprotectin) as innate amplifier of infection, autoimmunity, and cancer

inferredcites →https://doi.org/10.12703/p6-13openalex-snapshot

The M1 and M2 paradigm of macrophage activation: time for reassessment

inferredcites →https://doi.org/10.1371/journal.pone.0033664openalex-snapshot

The MMP-9/TIMP-1 Axis Controls the Status of Differentiation and Function of Myelin-Forming Schwann Cells in Nerve Regeneration

inferredcites →https://doi.org/10.1523/jneurosci.0023-06.2006openalex-snapshot

Pancreatitis-Associated Protein-III Is a Novel Macrophage Chemoattractant Implicated in Nerve Regeneration

inferredcites →https://doi.org/10.1523/jneurosci.1372-04.2005openalex-snapshot

Degeneration of Myelinated Efferent Fibers Prompts Mitosis in Remak Schwann Cells of Uninjured C-Fiber Afferents

inferredcites →https://doi.org/10.1523/jneurosci.1447-08.2008openalex-snapshot

Requirement of Myeloid Cells for Axon Regeneration

inferredcites →https://doi.org/10.1523/jneurosci.18-17-06713.1998openalex-snapshot

Complement Depletion Reduces Macrophage Infiltration and Activation during Wallerian Degeneration and Axonal Regeneration

inferredcites →https://doi.org/10.1523/jneurosci.22-08-03052.2002openalex-snapshot

The cytokine network of Wallerian degeneration: tumor necrosis factor-alpha, interleukin-1alpha, and interleukin-1beta.

inferredcites →https://doi.org/10.1523/jneurosci.22-15-06696.2002openalex-snapshot

Denervated Schwann Cells Attract Macrophages by Secretion of Leukemia Inhibitory Factor (LIF) and Monocyte Chemoattractant Protein-1 in a Process Regulated by Interleukin-6 and LIF

inferredcites →https://doi.org/10.1523/jneurosci.23-34-10892.2003openalex-snapshot

Caught in the Act:In VivoMapping of Macrophage Infiltration in Nerve Injury by Magnetic Resonance Imaging

inferredcites →https://doi.org/10.1523/jneurosci.2840-11.2011openalex-snapshot

Functional Recovery after Peripheral Nerve Injury is Dependent on the Pro-Inflammatory Cytokines IL-1β and TNF: Implications for Neuropathic Pain

inferredcites →https://doi.org/10.1523/jneurosci.3027-07.2007openalex-snapshot

Toll-Like Receptor Signaling Is Critical for Wallerian Degeneration and Functional Recovery after Peripheral Nerve Injury

inferredcites →https://doi.org/10.1523/jneurosci.3319-12.2013openalex-snapshot

A Critical Role for Macrophages Near Axotomized Neuronal Cell Bodies in Stimulating Nerve Regeneration

inferredcites →https://doi.org/10.1523/jneurosci.3558-14.2015openalex-snapshot

The Role of G-Protein Receptor 84 in Experimental Neuropathic Pain

inferredcites →https://doi.org/10.1523/jneurosci.4483-03.2004openalex-snapshot

Oxidized Galectin-1 Stimulates Macrophages to Promote Axonal Regeneration in Peripheral Nerves after Axotomy

inferredcites →https://doi.org/10.1523/jneurosci.5225-11.2012openalex-snapshot

In Vivo Nerve–Macrophage Interactions Following Peripheral Nerve Injury

inferredcites →https://doi.org/10.2353/ajpath.2008.070660openalex-snapshot

Soluble Complement Receptor 1 Protects the Peripheral Nerve from Early Axon Loss after Injury

inferredcites →https://doi.org/10.2741/2692openalex-snapshot

Macrophage activation and polarization

inferredcites →https://doi.org/10.4049/jimmunol.1202002openalex-snapshot

Cyclooxygenase-2 Deficiency in Macrophages Leads to Defective p110γ PI3K Signaling and Impairs Cell Adhesion and Migration

inferredcites →https://doi.org/10.4049/jimmunol.1302821openalex-snapshot

CCL2 Shapes Macrophage Polarization by GM-CSF and M-CSF: Identification of CCL2/CCR2-Dependent Gene Expression Profile

inferredcites →https://doi.org/10.4049/jimmunol.181.6.4332openalex-snapshot

Serum Amyloid A Induces CCL2 Production via Formyl Peptide Receptor-Like 1-Mediated Signaling in Human Monocytes

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.3945933openalex-extracted

Inhibition of Nav1.8 Transport Promotes Axon Regeneration Via Regulating Dynamic Changes in Macrophage Phenotype after Sciatic Nerve Injury

inferred← citeshttps://doi.org/10.1002/2211-5463.13859openalex-snapshot

Ficus carica L. (Fig) promotes nerve regeneration in a mouse model of sciatic nerve crush

inferred← citeshttps://doi.org/10.1002/9781119432463.ch11openalex-snapshot

Molecular Mechanisms Regulating Wallerian Degeneration

inferred← citeshttps://doi.org/10.1002/adbi.202200033openalex-snapshot

Schwann Cells in Peripheral Cancers: Bystanders or Promoters?

inferred← citeshttps://doi.org/10.1002/adhm.202201596openalex-snapshot

Biomechanically‐Adapted Immunohydrogels Reconstructing Myelin Sheath for Peripheral Nerve Regeneration

inferred← citeshttps://doi.org/10.1002/adhm.202302994openalex-snapshot

Bredigite‐Based Bioactive Nerve Guidance Conduit for Pro‐Healing Macrophage Polarization and Peripheral Nerve Regeneration

inferred← citeshttps://doi.org/10.1002/adhm.202501123openalex-snapshot

Light‐Responsive Oxygen Generation from Chlorella Hydrogels for Facial Nerve Injury Recovery: Crosstalk between M1/M2 Macrophages and Schwann Cells

inferred← citeshttps://doi.org/10.1002/adhm.202504185openalex-snapshot

Self‐Assembling Biohybrid Bands of Büngner for Axonal Regeneration in the Peripheral Nervous System

inferred← citeshttps://doi.org/10.1002/adma.202202513openalex-snapshot

Modulation of the Crosstalk between Schwann Cells and Macrophages for Nerve Regeneration: A Therapeutic Strategy Based on a Multifunctional Tetrahedral Framework Nucleic Acids System

inferred← citeshttps://doi.org/10.1002/adma.202311264openalex-snapshot

In Situ‐Sprayed Bioinspired Adhesive Conductive Hydrogels for Cavernous Nerve Repair

inferred← citeshttps://doi.org/10.1002/admi.202000225openalex-snapshot

Functional Polymer‐Based Nerve Guide Conduits to Promote Peripheral Nerve Regeneration

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.202512592openalex-snapshot

Near‐Infrared Switch‐Driven Macrophage Dynamically Reprogramming for Anti‐Infection and Tissue Healing on Polyetheretherketone Implants

inferred← citeshttps://doi.org/10.1002/advs.202520323openalex-snapshot

Schwann Cell Synthesized Cholesterol Orchestrates Peripheral Nerve Regeneration via Structural and IGF1‐Dependent Signaling Mechanisms

inferred← citeshttps://doi.org/10.1002/brb3.1400openalex-snapshot

Miconazole alleviates peripheral nerve crush injury by mediating a macrophage phenotype change through the NF‐κB pathway

inferred← citeshttps://doi.org/10.1002/brb3.1747openalex-snapshot

Intra and inter: Alterations in functional brain resting‐state networks after peripheral nerve injury

inferred← citeshttps://doi.org/10.1002/brb3.659openalex-snapshot

Patterns of production of collagen‐rich deposits in peripheral nerves in response to injury: A pilot study in a rabbit model

inferred← citeshttps://doi.org/10.1002/cbin.10796openalex-snapshot

Bone marrow‐derived cells response in proximal regions of nerves after peripheral nerve injury

inferred← citeshttps://doi.org/10.1002/exp.20230098openalex-snapshot

Decoding the regulatory role of ATP synthase inhibitory factor 1 (ATPIF1) in Wallerian degeneration and peripheral nerve regeneration

inferred← citeshttps://doi.org/10.1002/glia.23204openalex-snapshot

Siglec‐H is a microglia‐specific marker that discriminates microglia from CNS‐associated macrophages and CNS‐infiltrating monocytes

inferred← citeshttps://doi.org/10.1002/glia.23705openalex-snapshot

Prostaglandin D2 synthase modulates macrophage activity and accumulation in injured peripheral nerves

inferred← citeshttps://doi.org/10.1002/glia.24220openalex-snapshot

Transforming growth factor‐beta signaling modulates perineurial glial bridging following peripheral spinal motor nerve injury in zebrafish

inferred← citeshttps://doi.org/10.1002/glia.24309openalex-snapshot

Electrical stimulation accelerates Wallerian degeneration and promotes nerve regeneration after sciatic nerve injury

inferred← citeshttps://doi.org/10.1002/glia.24568openalex-snapshot

Myelinated peripheral axons are more vulnerable to mechanical trauma in a model of enlarged axonal diameters

inferred← citeshttps://doi.org/10.1002/j.2769-2795.2017.tb00011.xopenalex-snapshot

Gene expression profiles in the spinal cord following transected injury

inferred← citeshttps://doi.org/10.1002/jat.3710openalex-snapshot

Evaluation of neurobehavioral impairment in methylmercury‐treated KK‐Ay mice by dynamic weight‐bearing test

inferred← citeshttps://doi.org/10.1002/jbm.a.36090openalex-snapshot

A novel technique for decellularization of allogenic nerves and in vivo study of their use for peripheral nerve reconstruction

inferred← citeshttps://doi.org/10.1002/jbm.a.38008openalex-snapshot

Adipose‐Derived Stem Cell‐Loaded Fish‐ GelMA / CMC Hydrogel Accelerates Wound Healing via Macrophage Polarization Suppression and Promoting Angiogenesis

inferred← citeshttps://doi.org/10.1002/jcb.27105openalex-snapshot

FGF9 modulates Schwann cell myelination in developing nerves and induces a pro‐inflammatory environment during injury

inferred← citeshttps://doi.org/10.1002/jcp.27446openalex-snapshot

Transcriptional landscape of alternative splicing during peripheral nerve injury

inferred← citeshttps://doi.org/10.1002/jcp.28815openalex-snapshot

Regulation of adult mammalian intrinsic axonal regeneration by NF‐κB/STAT3 signaling cascade

inferred← citeshttps://doi.org/10.1002/jnr.24738openalex-snapshot

Adipose tissue stem cells in peripheral nerve regeneration— In vitro and in vivo

inferred← citeshttps://doi.org/10.1002/lary.27572openalex-snapshot

Time Course of Recovery of Iatrogenic Vocal Fold Paralysis

inferred← citeshttps://doi.org/10.1002/mabi.202300476openalex-snapshot

Nerve Guide Conduits Integrated with Fisetin‐Loaded Chitosan Hydrogels for Reducing Oxidative Stress, Inflammation, and Nerve Regeneration

inferred← citeshttps://doi.org/10.1002/mco2.71019openalex-snapshot

Myelination and Remyelination in Peripheral Nerve Injury: Mechanisms, Regulation, and Therapeutic Perspectives

inferred← citeshttps://doi.org/10.1002/mus.25225openalex-snapshot

Gene expression analysis at multiple time-points identifies key genes for nerve regeneration

inferred← citeshttps://doi.org/10.1002/mus.26097openalex-snapshot

Monitoring of macrophage recruitment enhanced by Toll‐like receptor 4 activation with MR imaging in nerve injury

inferred← citeshttps://doi.org/10.1002/mus.26862openalex-snapshot

Magnetic resonance imaging of enhanced nerve repair with mesenchymal stem cells combined with microenvironment immunomodulation in neurotmesis

inferred← citeshttps://doi.org/10.1002/mus.28336openalex-snapshot

FK506 Enhancement of Neuromuscular Junction Recovery After Nerve Injury Is Macrophage‐Dependent

inferred← citeshttps://doi.org/10.1002/sen2.70009openalex-snapshot

Secretome Profiling in Axon Regeneration: Emerging Techniques and Therapeutic Translation

inferred← citeshttps://doi.org/10.1002/stem.2534openalex-snapshot

Secreted Ectodomain of Sialic Acid-Binding Ig-Like Lectin-9 and Monocyte Chemoattractant Protein-1 Synergistically Regenerate Transected Rat Peripheral Nerves by Altering Macrophage Polarity

inferred← citeshttps://doi.org/10.1002/syn.22191openalex-snapshot

CCR2 downregulation attenuates spinal cord injury by suppressing inflammatory monocytes

inferred← citeshttps://doi.org/10.1007/978-3-030-06217-0_1-1openalex-snapshot

The History of Nerve Repair

inferred← citeshttps://doi.org/10.1007/978-3-030-06217-0_1-2openalex-snapshot

The History of Nerve Repair

inferred← citeshttps://doi.org/10.1007/978-3-030-06217-0_14-1openalex-snapshot

Basic Nerve Histology and Histological Analyses Following Peripheral Nerve Repair and Regeneration

inferred← citeshttps://doi.org/10.1007/978-3-030-06217-0_16-1openalex-snapshot

Drug Therapies for Peripheral Nerve Injuries

inferred← citeshttps://doi.org/10.1007/978-3-030-21052-6_1openalex-snapshot

The History of Nerve Repair

inferred← citeshttps://doi.org/10.1007/978-3-030-21052-6_14openalex-snapshot

Basic Nerve Histology and Histological Analyses Following Peripheral Nerve Repair and Regeneration

inferred← citeshttps://doi.org/10.1007/978-3-030-21052-6_16openalex-snapshot

Drug Therapies for Peripheral Nerve Injuries

inferred← citeshttps://doi.org/10.1007/978-3-030-80662-0_32openalex-snapshot

Nanobioelectronics for Noninvasive Neural Therapy

inferred← citeshttps://doi.org/10.1007/978-3-030-98256-0_14openalex-snapshot

Regenerative Medicine Procedures Under Ultrasound Guidance

inferred← citeshttps://doi.org/10.1007/978-3-031-32005-7_1openalex-snapshot

Decision-Making in Reconstructive Surgery

inferred← citeshttps://doi.org/10.1007/978-3-031-72079-6_17openalex-snapshot

Neuroimmune Interactions in Chronic Pain: Focus on Mononuclear Phagocytes

inferred← citeshttps://doi.org/10.1007/978-3-032-18296-8_11openalex-snapshot

Histological Analysis of Nervous Tissue: Methodologies, Pathological Insights, and Applications in Neurodegenerative Disease Research

inferred← citeshttps://doi.org/10.1007/978-3-319-52319-4_10openalex-snapshot

Peripheral Nerve Tissue Engineering: An Outlook on Experimental Concepts

inferred← citeshttps://doi.org/10.1007/978-981-15-3258-0_12openalex-snapshot

Fundamentals and Current Strategies for Peripheral Nerve Repair and Regeneration

inferred← citeshttps://doi.org/10.1007/s00011-026-02207-8openalex-snapshot

Balancing inflammation and regeneration: immune cell dynamics in nerve repair: a comprehensive review

inferred← citeshttps://doi.org/10.1007/s00262-018-02296-3openalex-snapshot

Schwann cells shape the neuro-immune environs and control cancer progression

inferred← citeshttps://doi.org/10.1007/s00383-019-04602-1openalex-snapshot

The incidence of neuropathic pain after intercostal cryoablation during the Nuss procedure

inferred← citeshttps://doi.org/10.1007/s10561-021-09920-0openalex-snapshot

Schwann-like cell conditioned medium promotes angiogenesis and nerve regeneration

inferred← citeshttps://doi.org/10.1007/s10571-023-01395-9openalex-snapshot

PGC-1α Inhibits Schwann Cell Dedifferentiation and Delays Peripheral Nerve Degeneration by Targeting PON1

inferred← citeshttps://doi.org/10.1007/s10571-023-01431-8openalex-snapshot

Genetic Features of Young and Aged Animals After Peripheral Nerve Injury: Implications for Diminished Regeneration Capacity

inferred← citeshttps://doi.org/10.1007/s10571-023-01442-5openalex-snapshot

Roles of Macrophages and Their Interactions with Schwann Cells After Peripheral Nerve Injury

inferred← citeshttps://doi.org/10.1007/s10753-026-02453-2openalex-snapshot

CXCL12 Promotes Peripheral Nerve Injury Repair by Inhibiting the Ferroptosis-Inflammation Axis via the ERK/Nrf2 Pathway

inferred← citeshttps://doi.org/10.1007/s11064-018-2670-0openalex-snapshot

Runx2 was Correlated with Neurite Outgrowth and Schwann Cell Differentiation, Migration After Sciatic Nerve Crush

inferred← citeshttps://doi.org/10.1007/s11064-022-03721-xopenalex-snapshot

Effect of Azithromycin on Sciatic Nerve Injury in the Wistar Rats

inferred← citeshttps://doi.org/10.1007/s11064-024-04198-6openalex-snapshot

Exogenous NT-3 Promotes Phenotype Switch of Resident Macrophages and Improves Sciatic Nerve Injury through AMPK/NF-κB Signaling Pathway

inferred← citeshttps://doi.org/10.1007/s11248-018-0062-5openalex-snapshot

EGFP transgene: a useful tool to track transplanted bone marrow mononuclear cell contribution to peripheral remyelination

inferred← citeshttps://doi.org/10.1007/s12015-023-10609-yopenalex-snapshot

Potential Application of Orofacial MSCs in Tissue Engineering Nerve Guidance for Peripheral Nerve Injury Repair

inferred← citeshttps://doi.org/10.1007/s12017-017-8450-1openalex-snapshot

Functional and Molecular Characterization of a Novel Traumatic Peripheral Nerve–Muscle Injury Model

inferred← citeshttps://doi.org/10.1007/s12035-021-02607-3openalex-snapshot

SIRT6 Negatively Regulates Schwann Cells Dedifferentiation via Targeting c-Jun During Wallerian Degeneration After Peripheral Nerve Injury

inferred← citeshttps://doi.org/10.1007/s12035-022-03090-0openalex-snapshot

Transcriptional Control of Peripheral Nerve Regeneration

inferred← citeshttps://doi.org/10.1007/s12035-023-03590-7openalex-snapshot

Unleashing Axonal Regeneration Capacities: Neuronal and Non-neuronal Changes After Injuries to Dorsal Root Ganglion Neuron Central and Peripheral Axonal Branches

inferred← citeshttps://doi.org/10.1007/s12035-026-05732-zopenalex-snapshot

Macrophage-Derived Amphiregulin Enhances Schwann Cell Phagocytosis Through the EGFR/CTSS Signaling Pathway

inferred← citeshttps://doi.org/10.1007/s12264-025-01564-4openalex-snapshot

Aging-Related Changes in the Injury Response of the Peripheral Nervous System

inferred← citeshttps://doi.org/10.1007/s13311-021-01125-3openalex-snapshot

Lessons from Injury: How Nerve Injury Studies Reveal Basic Biological Mechanisms and Therapeutic Opportunities for Peripheral Nerve Diseases

inferred← citeshttps://doi.org/10.1007/s13365-017-0529-9openalex-snapshot

An oral form of methylglyoxal-bis-guanylhydrazone reduces monocyte activation and traffic to the dorsal root ganglia in a primate model of HIV-peripheral neuropathy

inferred← citeshttps://doi.org/10.1007/s40883-020-00174-yopenalex-snapshot

Copolymer Surfactant Poloxamer 188 Accelerates Post-axonotemetic Sciatic Nerve Regeneration

inferred← citeshttps://doi.org/10.1007/s40883-024-00361-1openalex-snapshot

Macrophages’ Functions in the Central and Peripheral Nervous Regeneration

inferred← citeshttps://doi.org/10.1007/s42765-026-00677-3openalex-snapshot

Aligned Fiber Nerve Conduit Filled with Chiral Poly(Amino Acid) Hydrogel for Immunomodulation-Driven Repair of Peripheral Nerve Injury

inferred← citeshttps://doi.org/10.1016/b978-0-08-101745-6.00016-5openalex-snapshot

3D conduits for peripheral nerve regeneration

inferred← citeshttps://doi.org/10.1016/b978-0-12-820661-4.00007-8openalex-snapshot

The roles and functions of macrophages in endometriosis

inferred← citeshttps://doi.org/10.1016/b978-0-443-15580-2.00004-7openalex-snapshot

Staining reagents for neuronal degeneration and axon regeneration studies

inferred← citeshttps://doi.org/10.1016/bs.ctdb.2017.08.005openalex-snapshot

The Composition, Development, and Regeneration of Neuromuscular Junctions

inferred← citeshttps://doi.org/10.1016/bs.irn.2024.10.002openalex-snapshot

Molecular mechanisms of neuropathic pain

inferred← citeshttps://doi.org/10.1016/j.actbio.2019.02.034openalex-snapshot

Macroporous nanofiber wraps promote axonal regeneration and functional recovery in nerve repair by limiting fibrosis

inferred← citeshttps://doi.org/10.1016/j.actbio.2023.02.004openalex-snapshot

Injectable hydrogel encapsulated with VEGF-mimetic peptide-loaded nanoliposomes promotes peripheral nerve repair in vivo

inferred← citeshttps://doi.org/10.1016/j.actbio.2025.11.052openalex-snapshot

Electrowritten topographical conduit integrated with 4-octyl itaconate for peripheral nerve immunomodulation and regeneration

inferred← citeshttps://doi.org/10.1016/j.addr.2019.01.006openalex-snapshot

Nanotechnology in peripheral nerve repair and reconstruction

inferred← citeshttps://doi.org/10.1016/j.ajpath.2026.04.012openalex-snapshot

Proteolipid Protein 1 Homeostatically Regulates Schwann and Endothelial Cell Function and Communication in Peripheral Nerve Repair

inferred← citeshttps://doi.org/10.1016/j.apmt.2020.100870openalex-snapshot

Graphene-based conductive fibrous scaffold boosts sciatic nerve regeneration and functional recovery upon electrical stimulation

inferred← citeshttps://doi.org/10.1016/j.bbcan.2026.189687openalex-snapshot

Macrophages as central mediators of perineural invasion in cancer: Implications for pain and prognosis

inferred← citeshttps://doi.org/10.1016/j.bbi.2018.08.013openalex-snapshot

The impact of mouse strain-specific spatial and temporal immune responses on the progression of neuropathic pain

inferred← citeshttps://doi.org/10.1016/j.bbih.2022.100548openalex-snapshot

CD206+/MHCII− macrophage accumulation at nerve injury site correlates with attenuation of allodynia in TASTPM mouse model of Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/j.bbrc.2026.153878openalex-snapshot

Macrophages are dispensable for taste bud regeneration upon nerve injury repair

inferred← citeshttps://doi.org/10.1016/j.bioactmat.2021.02.016openalex-snapshot

Biopolymer-nanotube nerve guidance conduit drug delivery for peripheral nerve regeneration: In vivo structural and functional assessment

inferred← citeshttps://doi.org/10.1016/j.bioactmat.2021.04.019openalex-snapshot

Anisotropic scaffolds for peripheral nerve and spinal cord regeneration

inferred← citeshttps://doi.org/10.1016/j.bioactmat.2023.05.013openalex-snapshot

Li–Mg–Si bioceramics provide a dynamic immuno-modulatory and repair-supportive microenvironment for peripheral nerve regeneration

inferred← citeshttps://doi.org/10.1016/j.bioactmat.2025.01.031openalex-snapshot

Dental pulp stem cells alleviate Schwann cell pyroptosis via mitochondrial transfer to enhance facial nerve regeneration

inferred← citeshttps://doi.org/10.1016/j.bioactmat.2026.08.023openalex-snapshot

Metabolic targeting by a small extracellular vesicle-based cellulose-GelMA hydrogel restores neurovascular regeneration in diabetic nerve injury

inferred← citeshttps://doi.org/10.1016/j.biocel.2017.03.002openalex-snapshot

Combined Wharton’s jelly derived mesenchymal stem cells and nerve guidance conduit: A potential promising therapy for peripheral nerve injuries

inferred← citeshttps://doi.org/10.1016/j.biocel.2021.105921openalex-snapshot

Exosomes produced by adipose-derived stem cells inhibit schwann cells autophagy and promote the regeneration of the myelin sheath

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2017.01.014openalex-snapshot

Long-term usability and bio-integration of polyimide-based intra-neural stimulating electrodes

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2021.120692openalex-snapshot

Spider silk nerve graft promotes axonal regeneration on long distance nerve defect in a sheep model

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2021.121251openalex-snapshot

BMSC-derived extracellular matrix better optimizes the microenvironment to support nerve regeneration

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2023.122207openalex-snapshot

Gelatin nanofiber-reinforced decellularized amniotic membrane promotes axon regeneration and functional recovery in the surgical treatment of peripheral nerve injury

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2026.124063openalex-snapshot

Macrophages: Redefining extracellular matrix architecture through phenotypic switches as therapeutic targets

inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116645openalex-snapshot

Advances of Schwann cells in peripheral nerve regeneration: From mechanism to cell therapy

inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116769openalex-snapshot

Lactobacillus Plantarum intake mitigates neuropathic pain behavior via enhancing macrophage M2 polarization in a rat model of peripheral neuropathy

inferred← citeshttps://doi.org/10.1016/j.bjps.2016.08.016openalex-snapshot

Development of a decellularization method to produce nerve allografts using less invasive detergents and hyper/hypotonic solutions

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2019.06.011openalex-snapshot

FGF9 alters the Wallerian degeneration process by inhibiting Schwann cell transformation and accelerating macrophage infiltration

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2020.04.005openalex-snapshot

Immunomodulation by dimethyl fumarate treatment improves mouse sciatic nerve regeneration

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2021.06.001openalex-snapshot

TNF-mimetic peptide mixed with fibrin glue improves peripheral nerve regeneration

inferred← citeshttps://doi.org/10.1016/j.cclet.2025.112205openalex-snapshot

Electroactive biomaterials in neural regeneration: Advances and therapeutic mechanisms

inferred← citeshttps://doi.org/10.1016/j.cej.2024.159075openalex-snapshot

Immune regulated fibrous membrane loaded FK506 enhances peripheral nerve regeneration

inferred← citeshttps://doi.org/10.1016/j.cej.2025.161831openalex-snapshot

Bioactive Peptide-MOF based nanogel for peripheral nerve repair through remodeling the regenerative microenvironment

inferred← citeshttps://doi.org/10.1016/j.cej.2025.162045openalex-snapshot

Low-frequency ultrasound-driven piezoelectric films repair neuro-immune circuits in diabetic wound healing

inferred← citeshttps://doi.org/10.1016/j.cej.2026.179316openalex-snapshot

Aligned-to-random bilayered collagen nerve conduit enhances pain relief and nerve repair following surgical decompression in diabetic entrapment neuropathy

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.cellimm.2025.104934openalex-snapshot

Divergent impact of endotoxin priming and endotoxin tolerance on macrophage responses to cancer cells

inferred← citeshttps://doi.org/10.1016/j.celrep.2018.08.004openalex-snapshot

Macrophages Regulate Schwann Cell Maturation after Nerve Injury

inferred← citeshttps://doi.org/10.1016/j.celrep.2018.12.081openalex-snapshot

RETRACTED: Macrophage-Derived Slit3 Controls Cell Migration and Axon Pathfinding in the Peripheral Nerve Bridge

inferred← citeshttps://doi.org/10.1016/j.colsurfb.2023.113672openalex-snapshot

Progress and mechanism of graphene oxide-composited materials in application of peripheral nerve repair

inferred← citeshttps://doi.org/10.1016/j.ejphar.2023.175955openalex-snapshot

Potential role of Schwann cells in neuropathic pain

inferred← citeshttps://doi.org/10.1016/j.ejphar.2024.176346openalex-snapshot

The role of olfactory ensheathing cells in the repair of nerve injury

inferred← citeshttps://doi.org/10.1016/j.expneurol.2018.03.011openalex-snapshot

Transcriptional networks of progressive diabetic peripheral neuropathy in the db/db mouse model of type 2 diabetes: An inflammatory story

inferred← citeshttps://doi.org/10.1016/j.expneurol.2022.114069openalex-snapshot

New insights into peripheral nerve regeneration: The role of secretomes

inferred← citeshttps://doi.org/10.1016/j.expneurol.2022.114139openalex-snapshot

Exosomes from LPS-preconditioned bone marrow MSCs accelerated peripheral nerve regeneration via M2 macrophage polarization: Involvement of TSG-6/NF-κB/NLRP3 signaling pathway

inferred← citeshttps://doi.org/10.1016/j.expneurol.2024.114882openalex-snapshot

The role of exosomes derived from stem cells in nerve regeneration: A contribution to neurological repair

inferred← citeshttps://doi.org/10.1016/j.expneurol.2025.115194openalex-snapshot

Macrophage-myofibroblast transition contributes to the macrophage elimination and functional regeneration in the late stage of nerve injury

inferred← citeshttps://doi.org/10.1016/j.gendis.2023.02.016openalex-snapshot

Structure, ligands, and roles of GPR126/ADGRG6 in the development and diseases

inferred← citeshttps://doi.org/10.1016/j.ibneur.2024.12.013openalex-snapshot

Molecular and cellular mechanisms underlying peripheral nerve injury-induced cellular ecological shifts: Implications for neuroregeneration

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2026.154152openalex-snapshot

A gelatin methacryloyl (GelMA)-based biomimetic melatonin/vascular endothelial growth factor-encoding plasmid (pVEGF) nerve conduit regulates the early redox-angiogenic microenvironment for long-gap peripheral nerve repair

inferred← citeshttps://doi.org/10.1016/j.immuni.2019.05.009openalex-snapshot

A Subset of Skin Macrophages Contributes to the Surveillance and Regeneration of Local Nerves

inferred← citeshttps://doi.org/10.1016/j.intimp.2022.109026openalex-snapshot

Research progress of targeting NLRP3 inflammasome in peripheral nerve injury and pain

inferred← citeshttps://doi.org/10.1016/j.intimp.2023.110711openalex-snapshot

IL-33 promotes sciatic nerve regeneration in mice by modulating macrophage polarization

inferred← citeshttps://doi.org/10.1016/j.intimp.2024.112452openalex-snapshot

The protective effect of erythropoietin and its novel derived peptides in peripheral nerve injury

inferred← citeshttps://doi.org/10.1016/j.intimp.2025.114833openalex-snapshot

IL-33 alleviates corneal nerve damage in herpes simplex keratitis

inferred← citeshttps://doi.org/10.1016/j.intimp.2026.116474openalex-snapshot

Lactate drive M2 polarization via OXPHOS and Cebpb and accelerate peripheral nerve regeneration

inferred← citeshttps://doi.org/10.1016/j.intimp.2026.116636openalex-snapshot

Perineural invasion: A neuroimmune axis mediating immunotherapy resistance across malignancies

inferred← citeshttps://doi.org/10.1016/j.isci.2021.103434openalex-snapshot

STING regulates peripheral nerve regeneration and colony stimulating factor 1 receptor (CSF1R) processing in microglia

inferred← citeshttps://doi.org/10.1016/j.isci.2023.107264openalex-snapshot

SnRNA-seq reveals the heterogeneity of spinal ventral horn and mechanism of motor neuron axon regeneration

inferred← citeshttps://doi.org/10.1016/j.it.2021.02.004openalex-snapshot

Context-Dependent Glioblastoma–Macrophage/Microglia Symbiosis and Associated Mechanisms

inferred← citeshttps://doi.org/10.1016/j.jare.2026.07.045openalex-snapshot

Chiral MoS2-based nanozymes co-delivering indole-3-propionic acid synergistically inhibit ferroptosis and reprogram metabolism for enhanced peripheral nerve regeneration

inferred← citeshttps://doi.org/10.1016/j.jbc.2024.108146openalex-snapshot

Angiogenesis-promoting effect of SKP-SC-EVs-derived miRNA-30a-5p in peripheral nerve regeneration by targeting LIF and ANGPT2

inferred← citeshttps://doi.org/10.1016/j.jconrel.2019.01.013openalex-snapshot

Aligned microchannel polymer-nanotube composites for peripheral nerve regeneration: Small molecule drug delivery

inferred← citeshttps://doi.org/10.1016/j.jconrel.2019.11.021openalex-snapshot

Functional polymeric nerve guidance conduits and drug delivery strategies for peripheral nerve repair and regeneration

inferred← citeshttps://doi.org/10.1016/j.jconrel.2026.114797openalex-snapshot

Ultrasound-guided nanocomposite hydrogel injection to enhance nerve repair via temporal delivery of a colony-stimulating factor 1 receptor inhibitor

inferred← citeshttps://doi.org/10.1016/j.jep.2020.113063openalex-snapshot

Augmented Buyang Huanwu Decoction facilitates axonal regeneration after peripheral nerve transection through the regulation of inflammatory cytokine production

inferred← citeshttps://doi.org/10.1016/j.jff.2024.106424openalex-snapshot

Astaxanthin promotes nerve repair by regulating the M1/M2 ratio of microglia and promoting angiogenesis

inferred← citeshttps://doi.org/10.1016/j.jhsa.2021.08.023openalex-snapshot

Evaluation of the Induced Membrane for Neurotrophic Factors

inferred← citeshttps://doi.org/10.1016/j.jhsg.2023.07.014openalex-snapshot

Histological Comparison of Porcine Small Intestine Submucosa and Bovine Type-I Collagen Conduit for Nerve Repair in a Rat Model

inferred← citeshttps://doi.org/10.1016/j.jhsg.2025.100784openalex-snapshot

Hyaluronate-Alginate Gel-Coated Porcine Small Intestine Submucosa for Nerve Protection Minimizes Extraneural Collagen Deposition in a Preclinical Model

inferred← citeshttps://doi.org/10.1016/j.jhsg.2025.100816openalex-snapshot

Protecting the Nerve Coaptation: Connector-Assisted Nerve Repair in Complex Injuries

inferred← citeshttps://doi.org/10.1016/j.jma.2024.05.011openalex-snapshot

The immunomodulatory effects and mechanisms of magnesium-containing implants in bone regeneration: A review

inferred← citeshttps://doi.org/10.1016/j.jneumeth.2020.108981openalex-snapshot

Liposomes embedded within fibrin gels facilitate localized macrophage manipulations within nerve

inferred← citeshttps://doi.org/10.1016/j.jneuroim.2020.577423openalex-snapshot

Macrophage-specific deletion of BACE1 does not enhance macrophage recruitment to the injured peripheral nerve

inferred← citeshttps://doi.org/10.1016/j.joen.2022.10.012openalex-snapshot

Determination of the Severity of Pulpitis by Immunohistological Analysis and Comparison with the Clinical Picture

inferred← citeshttps://doi.org/10.1016/j.jor.2020.03.026openalex-snapshot

Tobacco use and neurogenesis: A theoretical review of pathophysiological mechanism affecting the outcome of peripheral nerve regeneration

inferred← citeshttps://doi.org/10.1016/j.jshs.2019.07.004openalex-snapshot

Impacts of exercise interventions on different diseases and organ functions in mice

inferred← citeshttps://doi.org/10.1016/j.jss.2023.03.017openalex-snapshot

Evaluation of the Aging Effect on Peripheral Nerve Regeneration: A Systematic Review

inferred← citeshttps://doi.org/10.1016/j.jtos.2025.07.001openalex-snapshot

Early myeloid cell infiltration and subset-specific macrophage responses in murine corneal nerve injury

inferred← citeshttps://doi.org/10.1016/j.labinv.2025.104193openalex-snapshot

Lacking TRPA1 Cation Channel Impairs Primary Closure of a Stromal Incision Injury in a Mouse Cornea

inferred← citeshttps://doi.org/10.1016/j.lfs.2020.117459openalex-snapshot

Schwann cells apoptosis is induced by high glucose in diabetic peripheral neuropathy

inferred← citeshttps://doi.org/10.1016/j.lfs.2020.117959openalex-snapshot

Resveratrol regulates the recovery of rat sciatic nerve crush injury by promoting the autophagy of Schwann cells

inferred← citeshttps://doi.org/10.1016/j.lfs.2021.119422openalex-snapshot

Minocycline alleviates peripheral nerve adhesion by promoting regulatory macrophage polarization via the TAK1 and its downstream pathway

inferred← citeshttps://doi.org/10.1016/j.matdes.2026.115779openalex-snapshot

Peripheral nerve regeneration: From molecular mechanisms to biomaterial design strategies

inferred← citeshttps://doi.org/10.1016/j.matdes.2026.116891openalex-snapshot

Piezoelectric materials: a new dawn in neural injury repair

inferred← citeshttps://doi.org/10.1016/j.mattod.2021.09.014openalex-snapshot

Functional nanomaterials in peripheral nerve regeneration: Scaffold design, chemical principles and microenvironmental remodeling

inferred← citeshttps://doi.org/10.1016/j.molcel.2018.09.011openalex-snapshot

Mixed Lineage Kinase Domain-like Protein MLKL Breaks Down Myelin following Nerve Injury

inferred← citeshttps://doi.org/10.1016/j.molcel.2018.10.025openalex-snapshot

MLKL Reveals Its Friendly Face: A Role in Nerve Regeneration

inferred← citeshttps://doi.org/10.1016/j.molimm.2020.03.003openalex-snapshot

Improved mouse sciatic nerve regeneration following lymphocyte cell therapy

inferred← citeshttps://doi.org/10.1016/j.molimm.2024.03.006openalex-snapshot

CXCL1-CXCR2 axis mediates inflammatory response after sciatic nerve injury by regulating macrophage infiltration

inferred← citeshttps://doi.org/10.1016/j.mtbio.2025.101808openalex-snapshot

Regulation of nanomaterials in peripheral nerve regeneration from a microenvironmental perspective: biological effects and mechanisms

inferred← citeshttps://doi.org/10.1016/j.mtbio.2026.102780openalex-snapshot

Injectable anti-inflammatory, antioxidant supramolecular nanofiber hydrogel for peripheral nerve injury repair and neuropathic pain relief

inferred← citeshttps://doi.org/10.1016/j.mtbio.2026.103041openalex-snapshot

Conductive ionic liquid hydrogel filled anti-inflammatory nerve conduit repairs peripheral nerve defect

inferred← citeshttps://doi.org/10.1016/j.nbd.2026.107262openalex-snapshot

Multi-omics analysis identifies mitochondrial dysfunction in CD83+ macrophages as a key event in diabetic peripheral neuropathy progression

inferred← citeshttps://doi.org/10.1016/j.neuint.2021.104984openalex-snapshot

Arginase-1 deficiency in neural cells does not contribute to neurodevelopment or functional outcomes after sciatic nerve injury

inferred← citeshttps://doi.org/10.1016/j.neuint.2025.105940openalex-snapshot

Temporal and spatial expression of Phosphodiesterase-4B after sciatic nerve compression in rats and its mechanism of action on sciatic nerve repair

inferred← citeshttps://doi.org/10.1016/j.neulet.2018.09.041openalex-snapshot

miR-1b overexpression suppressed proliferation and migration of RSC96 and increased cell apoptosis

inferred← citeshttps://doi.org/10.1016/j.neulet.2021.136391openalex-snapshot

Curcumin enhances the proliferation and myelinization of Schwann cells through Runx2 to repair sciatic nerve injury

inferred← citeshttps://doi.org/10.1016/j.neulet.2024.137813openalex-snapshot

OTULIN of exosomes derived from Schwann cells promotes peripheral nerve injury repair by regulating macrophage polarization via deubiquitination of ERBB2

inferred← citeshttps://doi.org/10.1016/j.neulet.2024.138112openalex-snapshot

Nasal mucosal mesenchymal stem cells promote repair of sciatic nerve injury in rats by modulating the inflammatory microenvironment

inferred← citeshttps://doi.org/10.1016/j.neulet.2026.138751openalex-snapshot

Neural mobilization combined with a polylactic acid conduit enhances functional and morphological recovery following median nerve repair

inferred← citeshttps://doi.org/10.1016/j.neures.2021.11.001openalex-snapshot

Neuroinflammation: Breaking barriers and bridging gaps

inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2017.01.006openalex-snapshot

AlphaB-crystallin expression correlates with aging deficits in the peripheral nervous system

inferred← citeshttps://doi.org/10.1016/j.neuropharm.2024.110169openalex-snapshot

Inhibition of KIF5b-mediated Nav1.8 transport by ropivacaine contributes to axonal regeneration following sciatic nerve injury in rats

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2018.04.018openalex-snapshot

Schwann Cell Plasticity is Regulated by a Weakened Intrinsic Antioxidant Defense System in Acute Peripheral Nerve Injury

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2019.09.023openalex-snapshot

Inosine Accelerates the Regeneration and Anticipates the Functional Recovery after Sciatic Nerve Crush Injury in Mice

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2021.05.033openalex-snapshot

Rapamycin Accelerates Axon Regeneration Through Schwann Cell-mediated Autophagy Following Inferior Alveolar Nerve Transection in Rats

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2022.05.003openalex-snapshot

Proteomics Reveals the Key Molecules Involved in Curcumin-induced Protection Against Sciatic Nerve Injury in Rats

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2025.03.039openalex-snapshot

Mutual inhibitory interaction between M1 macrophages and Schwann cells in the myelin sheath of auditory nerves

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2020.107581openalex-snapshot

Chemokines in chronic pain: cellular and molecular mechanisms and therapeutic potential

inferred← citeshttps://doi.org/10.1016/j.phymed.2026.158214openalex-snapshot

Hyperoside accelerates myelin debris clearance by inhibiting signal transducer and activator of transcription 3 phosphorylation in peripheral nerve injury

inferred← citeshttps://doi.org/10.1016/j.pneurobio.2020.101970openalex-snapshot

Macrophagic and microglial complexity after neuronal injury

inferred← citeshttps://doi.org/10.1016/j.pneurobio.2021.102172openalex-snapshot

Neuroimmune interactions and immunoengineering strategies in peripheral nerve repair

inferred← citeshttps://doi.org/10.1016/j.preteyeres.2022.101105openalex-snapshot

Neuroimmune crosstalk in the cornea: The role of immune cells in corneal nerve maintenance during homeostasis and inflammation

inferred← citeshttps://doi.org/10.1016/j.reth.2024.08.018openalex-snapshot

ADSCs encapsulated in Gelatin methacrylate substrate promotes the repair of peripheral nerve injury by SIRT6/PGC-1α pathway

inferred← citeshttps://doi.org/10.1016/j.sopen.2020.11.002openalex-snapshot

Scalpel edge roughness affects post-transection peripheral nerve regeneration

inferred← citeshttps://doi.org/10.1016/j.tice.2024.102379openalex-snapshot

Enhancing sciatic nerve regeneration with osteopontin-loaded acellular nerve allografts in rats: Effects on macrophage polarization

showing the first 200 of 526

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.