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Classical ROS-dependent and early/rapid ROS-independent release of Neutrophil Extracellular Traps triggered by Leishmania parasites
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00281-013-0384-6openalex-snapshot
Molecular mechanisms regulating NETosis in infection and disease
inferredcites →https://doi.org/10.1016/0006-291x(89)92506-0openalex-snapshot
Generation of nitric oxide by human neutrophils
inferredcites →https://doi.org/10.1016/0006-291x(92)91594-gopenalex-snapshot
Co-purification of 130 KD nitric oxide synthase and A 22 KD link protein from human neutrophils
inferredcites →https://doi.org/10.1016/j.bbrc.2013.12.007openalex-snapshot
Uric acid induces NADPH oxidase-independent neutrophil extracellular trap formation
inferredcites →https://doi.org/10.1016/j.fsi.2013.02.010openalex-snapshot
Carp neutrophilic granulocytes form extracellular traps via ROS-dependent and independent pathways
inferredcites →https://doi.org/10.1016/j.niox.2010.01.001openalex-snapshot
Nitric oxide donors release extracellular traps from human neutrophils by augmenting free radical generation
inferredcites →https://doi.org/10.1016/s0006-291x(87)80039-6openalex-snapshot
A new enzymatic pathway of citrullinogenesis in murine hemopoietic cells
inferredcites →https://doi.org/10.1016/s0166-6851(02)00021-xopenalex-snapshot
Detection of iNOS gene expression in cutaneous leishmaniasis biopsy tissue
inferredcites →https://doi.org/10.1021/bi00367a011openalex-snapshot
Mechanism of inactivation of human leukocyte elastase by a chloromethyl ketone: kinetic and solvent isotope effect studies
inferredcites →https://doi.org/10.1021/bi061180dopenalex-snapshot
Inhibitors and Inactivators of Protein Arginine Deiminase 4: Functional and Structural Characterization ,
inferredcites →https://doi.org/10.1038/cdd.2011.75openalex-snapshot
Peculiarities of cell death mechanisms in neutrophils
inferredcites →https://doi.org/10.1038/labinvest.2013.53openalex-snapshot
Methods for defining distinct bioenergetic profiles in platelets, lymphocytes, monocytes, and neutrophils, and the oxidative burst from human blood
inferredcites →https://doi.org/10.1038/sj.cdd.4401320openalex-snapshot
Functional characterization of mitochondria in neutrophils: a role restricted to apoptosis
inferredcites →https://doi.org/10.1042/bj2900041openalex-snapshot
Studies on the inhibitory mechanism of iodonium compounds with special reference to neutrophil NADPH oxidase
inferredcites →https://doi.org/10.1042/bj3210503openalex-snapshot
Mechanism of inactivation of myeloperoxidase by 4-aminobenzoic acid hydrazide
inferredcites →https://doi.org/10.1046/j.1471-4159.2001.00548.xopenalex-snapshot
ΔΨ m ‐Dependent and ‐independent production of reactive oxygen species by rat brain mitochondria
inferredcites →https://doi.org/10.1073/pnas.0900226106openalex-snapshot
Leishmania amazonensis promastigotes induce and are killed by neutrophil extracellular traps
inferredcites →https://doi.org/10.1074/jbc.m115.640094openalex-snapshot
A Metabolic Shift toward Pentose Phosphate Pathway Is Necessary for Amyloid Fibril- and Phorbol 12-Myristate 13-Acetate-induced Neutrophil Extracellular Trap (NET) Formation
inferredcites →https://doi.org/10.1083/jcb.200606027openalex-snapshot
Novel cell death program leads to neutrophil extracellular traps
inferredcites →https://doi.org/10.1083/jcb.200806072openalex-snapshot
Histone hypercitrullination mediates chromatin decondensation and neutrophil extracellular trap formation
inferredcites →https://doi.org/10.1083/jcb.201006052openalex-snapshot
Neutrophil elastase and myeloperoxidase regulate the formation of neutrophil extracellular traps
inferredcites →https://doi.org/10.1084/jem.20100239openalex-snapshot
PAD4 is essential for antibacterial innate immunity mediated by neutrophil extracellular traps
inferredcites →https://doi.org/10.1111/j.1365-3024.2011.01343.xopenalex-snapshot
Comparative study of the in situ immune response in oral and nasal mucosal leishmaniasis
inferredcites →https://doi.org/10.1111/j.1365-4632.2007.03047.xopenalex-snapshot
Diagnostic approach and significance of inducible nitric oxide positivity in human cutaneous leishmaniasis caused by leishmania tropica
inferredcites →https://doi.org/10.1111/j.1462-5822.2005.00659.xopenalex-snapshot
Neutrophil extracellular traps capture and kill Candida albicans yeast and hyphal forms
inferredcites →https://doi.org/10.1111/j.1476-5381.1990.tb14151.xopenalex-snapshot
Characterization of three inhibitors of endothelial nitric oxide synthase in vitro and in vivo
inferredcites →https://doi.org/10.1126/science.1092385openalex-snapshot
Neutrophil Extracellular Traps Kill Bacteria
inferredcites →https://doi.org/10.1128/iai.70.8.4638-4642.2002openalex-snapshot
Expression of Inducible Nitric Oxide Synthase in Skin Lesions of Patients with American Cutaneous Leishmaniasis
inferredcites →https://doi.org/10.1152/ajplung.90522.2008openalex-snapshot
Participation of mitochondrial respiratory complex III in neutrophil activation and lung injury
inferredcites →https://doi.org/10.1155/2012/849136openalex-snapshot
The Impact of Various Reactive Oxygen Species on the Formation of Neutrophil Extracellular Traps
inferredcites →https://doi.org/10.1155/2012/929743openalex-snapshot
ETosis: A Microbicidal Mechanism beyond Cell Death
inferredcites →https://doi.org/10.1155/2015/478039openalex-snapshot
Xanthine Oxidase Inhibitor, Allopurinol, Prevented Oxidative Stress, Fibrosis, and Myocardial Damage in Isoproterenol Induced Aged Rats
inferredcites →https://doi.org/10.1159/000444256openalex-snapshot
Modulating Innate and Adaptive Immunity by (R)-Roscovitine: Potential Therapeutic Opportunity in Cystic Fibrosis
inferredcites →https://doi.org/10.1161/circresaha.109.214601openalex-snapshot
Therapeutic Targeting of Mitochondrial Superoxide in Hypertension
inferredcites →https://doi.org/10.1164/rccm.200710-1602ocopenalex-snapshot
Mitochondrial Respiratory Complex I Regulates Neutrophil Activation and Severity of Lung Injury
inferredcites →https://doi.org/10.1172/jci112190openalex-snapshot
Activation of the human neutrophil nicotinamide adenine dinucleotide phosphate (NADPH)-oxidase by protein kinase C.
inferredcites →https://doi.org/10.1182/blood-2008-07-171629openalex-snapshot
Impaired neutrophil extracellular trap (NET) formation: a novel innate immune deficiency of human neonates
inferredcites →https://doi.org/10.1182/blood-2009-05-221606openalex-snapshot
Restoration of NET formation by gene therapy in CGD controls aspergillosis
inferredcites →https://doi.org/10.1182/blood-2010-06-290171openalex-snapshot
Myeloperoxidase is required for neutrophil extracellular trap formation: implications for innate immunity
inferredcites →https://doi.org/10.1182/blood-2013-04-457671openalex-snapshot
NETosis: how vital is it?
inferredcites →https://doi.org/10.1189/jlb.1010549openalex-snapshot
Rac2 is required for the formation of neutrophil extracellular traps
inferredcites →https://doi.org/10.1189/jlb.1211601openalex-snapshot
Requirements for NADPH oxidase and myeloperoxidase in neutrophil extracellular trap formation differ depending on the stimulus
inferredcites →https://doi.org/10.1371/journal.pone.0022043openalex-snapshot
PAD4-Mediated Neutrophil Extracellular Trap Formation Is Not Required for Immunity against Influenza Infection
inferredcites →https://doi.org/10.1371/journal.pone.0025590openalex-snapshot
Impact of the Genome on the Epigenome Is Manifested in DNA Methylation Patterns of Imprinted Regions in Monozygotic and Dizygotic Twins
inferredcites →https://doi.org/10.1371/journal.pone.0042984openalex-snapshot
Influences of Chloride and Hypochlorite on Neutrophil Extracellular Trap Formation
inferredcites →https://doi.org/10.1371/journal.pone.0133063openalex-snapshot
Are Neutrophil Extracellular Traps Playing a Role in the Parasite Control in Active American Tegumentary Leishmaniasis Lesions?
inferredcites →https://doi.org/10.3389/fimmu.2012.00424openalex-snapshot
Reactive oxidants and myeloperoxidase and their involvement in neutrophil extracellular traps
inferredcites →https://doi.org/10.3390/molecules18032821openalex-snapshot
Apocynin: Chemical and Biophysical Properties of a NADPH Oxidase Inhibitor
inferredcites →https://doi.org/10.4049/jimmunol.1000675openalex-snapshot
A Novel Mechanism of Rapid Nuclear Neutrophil Extracellular Trap Formation in Response to Staphylococcus aureus
inferredcites →https://doi.org/10.4049/jimmunol.1000893openalex-snapshot
Leishmania donovani Promastigotes Evade the Antimicrobial Activity of Neutrophil Extracellular Traps
inferredcites →https://doi.org/10.4049/jimmunol.1201167openalex-snapshot
A SerpinB1 Regulatory Mechanism Is Essential for Restricting Neutrophil Extracellular Trap Generation
inferredcites →https://doi.org/10.4049/jimmunol.1202671openalex-snapshot
An Extracellular Matrix–Based Mechanism of Rapid Neutrophil Extracellular Trap Formation in Response to Candida albicans
inferredcites →https://doi.org/10.4049/jimmunol.180.3.1895openalex-snapshot
Histone Deimination As a Response to Inflammatory Stimuli in Neutrophils
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ddr.22169openalex-snapshot
Neutrophil hitchhiking: Riding the drug delivery wave to treat diseases
inferred← citeshttps://doi.org/10.1002/jcp.30029openalex-snapshot
Neutrophils and Visceral Leishmaniasis: Impact on innate immune response and cross‐talks with macrophages and dendritic cells
inferred← citeshttps://doi.org/10.1002/jlb.2a0520-334ropenalex-snapshot
CD200R1L is a functional evolutionary conserved activating receptor in human neutrophils
inferred← citeshttps://doi.org/10.1002/jlb.3vma0918-374ropenalex-snapshot
Adenosine from a biologic source regulates neutrophil extracellular traps (NETs)
inferred← citeshttps://doi.org/10.1002/jlb.4mr0521-849rropenalex-snapshot
Neutrophils vs. amoebas: Immunity against the protozoan parasiteEntamoeba histolytica
inferred← citeshttps://doi.org/10.1002/mco2.70101openalex-snapshot
The emerging role of neutrophil extracellular traps in autoimmune and autoinflammatory diseases
inferred← citeshttps://doi.org/10.1002/med.21958openalex-snapshot
Fast and furious: The neutrophil and its armamentarium in health and disease
inferred← citeshttps://doi.org/10.1002/yea.3842openalex-snapshot
Release of neutrophil extracellular traps in response to Candida albicans yeast, as a secondary defense mechanism activated by phagocytosis
inferred← citeshttps://doi.org/10.1007/978-1-0716-1162-3_9openalex-snapshot
Visualization and Quantification of Neutrophil Extracellular Traps
inferred← citeshttps://doi.org/10.1007/978-3-031-24355-4_14openalex-snapshot
Vaccine Development for Human Leishmaniasis
inferred← citeshttps://doi.org/10.1007/978-3-032-21135-4_17openalex-snapshot
NOX2 and Neutrophil Extracellular Traps
inferred← citeshttps://doi.org/10.1007/978-3-319-72386-0_5openalex-snapshot
Immunological and Immunopathological Aspects
inferred← citeshttps://doi.org/10.1007/978-981-13-8763-0_13openalex-snapshot
Oxidative Stress and Antioxidants in Host Defense in Leishmaniasis
inferred← citeshttps://doi.org/10.1007/978-981-13-8763-0_16openalex-snapshot
Role of Reactive Oxygen Species in Infection by the Intracellular Leishmania Parasites
inferred← citeshttps://doi.org/10.1007/978-981-99-6999-9_14openalex-snapshot
Understanding the Heterogeneity in Mast Cell Role in Host Defence During Leishmaniasis
inferred← citeshttps://doi.org/10.1007/s00011-025-01994-wopenalex-snapshot
Mitochondrial dysfunction is a major cause of thromboinflammation and inflammatory cell death in critical illnesses
inferred← citeshttps://doi.org/10.1007/s00210-025-03921-6openalex-snapshot
Role of platelets and NETs in arterial thrombosis
inferred← citeshttps://doi.org/10.1007/s00281-019-00760-5openalex-snapshot
Towards a pro-resolving concept in systemic lupus erythematosus
inferred← citeshttps://doi.org/10.1007/s00436-022-07755-6openalex-snapshot
Trichomonas gallinae induces heterophil extracellular trap formation in pigeons
inferred← citeshttps://doi.org/10.1007/s00580-025-03708-4openalex-snapshot
Oral neutrophils and cancer: a molecular battle in the oral cavity
inferred← citeshttps://doi.org/10.1007/s10067-026-08384-5openalex-snapshot
NETs mediate neuropathic pain in PSS-PN by participating in inflammatory injury to the vasa nervorum
inferred← citeshttps://doi.org/10.1007/s10753-018-0903-7openalex-snapshot
IRF-1 Intervention in the Classical ROS-Dependent Release of NETs during LPS-Induced Acute Lung Injury in Mice
inferred← citeshttps://doi.org/10.1007/s10753-021-01526-8openalex-snapshot
Characteristics and Role of Neutrophil Extracellular Traps in Asthma
inferred← citeshttps://doi.org/10.1007/s10753-025-02327-zopenalex-snapshot
Mac-1 Promotes Neutrophil Extracellular Traps Formation via ERK Phosphorylation in Renal Ischemia-Reperfusion Injury
inferred← citeshttps://doi.org/10.1016/b978-0-12-811436-0.00006-xopenalex-snapshot
Insect-Borne Pathogens and Skin Interface
inferred← citeshttps://doi.org/10.1016/b978-0-323-85730-7.00054-0openalex-snapshot
The NET response to biofilm infections
inferred← citeshttps://doi.org/10.1016/b978-0-443-18566-3.00039-6openalex-snapshot
Maternal and fetal issues in COVID-19-mediated thromboinflammation
inferred← citeshttps://doi.org/10.1016/j.apjtb.2017.01.022openalex-snapshot
Caffeic acid and quercetin exert caspases-independent apoptotic effects on Leishmania major promastigotes, and reactivate the death of infected phagocytes derived from BALB/c mice
inferred← citeshttps://doi.org/10.1016/j.bbagen.2020.129561openalex-snapshot
The action of Echis carinatus and Naja naja venoms on human neutrophils; an emphasis on NETosis
inferred← citeshttps://doi.org/10.1016/j.biocel.2026.106957openalex-snapshot
Quorum sensing regulated neutrophil extracellular traps (NETs) dysregulation in chronic obstructive pulmonary disease (COPD): Host-pathogen interplay in Pseudomonas aeruginosa infection
inferred← citeshttps://doi.org/10.1016/j.biochi.2023.12.003openalex-snapshot
Leishmania donovani mevalonate kinase regulates host actin for inducing phagocytosis
inferred← citeshttps://doi.org/10.1016/j.biochi.2025.01.004openalex-snapshot
Neutrophils and purinergic signaling: Partners in the crime against Leishmania parasites?
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106624openalex-snapshot
Next generation of selenocyanate and diselenides with upgraded leishmanicidal activity
inferred← citeshttps://doi.org/10.1016/j.bvth.2025.100086openalex-snapshot
Epigenetic metabolite lipid nanoparticles alleviate venous thrombosis via bone marrow reprogramming
inferred← citeshttps://doi.org/10.1016/j.cca.2016.05.029openalex-snapshot
NETosis markers: Quest for specific, objective, and quantitative markers
inferred← citeshttps://doi.org/10.1016/j.cellimm.2021.104449openalex-snapshot
Protective immune response mediated by neutrophils in experimental visceral leishmaniasis is enhanced by IL-32γ
inferred← citeshttps://doi.org/10.1016/j.cellimm.2022.104640openalex-snapshot
Neutrophil extracellular traps: Modulation mechanisms by pathogens
inferred← citeshttps://doi.org/10.1016/j.cyto.2024.156503openalex-snapshot
Alpha 1-acid glycoprotein is upregulated in severe COVID-19 patients and decreases neutrophil NETs in SARS-CoV-2 infection
inferred← citeshttps://doi.org/10.1016/j.cytox.2020.100041openalex-snapshot
Macrophages as host, effector and immunoregulatory cells in leishmaniasis: Impact of tissue micro-environment and metabolism
inferred← citeshttps://doi.org/10.1016/j.dci.2025.105430openalex-snapshot
Extracellular traps release by coelomocytes in Eisenia andrei earthworm are involved in encapsulation process
inferred← citeshttps://doi.org/10.1016/j.dsx.2018.07.010openalex-snapshot
Neutrophil extracellular traps: The core player in vascular complications of diabetes mellitus
inferred← citeshttps://doi.org/10.1016/j.ebiom.2023.104499openalex-snapshot
Neutrophil extracellular traps as a unique target in the treatment of chemotherapy-induced peripheral neuropathy
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2018.02.080openalex-snapshot
Squamocin induce histological and ultrastructural changes in the midgut cells of Anticarsia gemmatalis (Lepidoptera: Noctuidae)
inferred← citeshttps://doi.org/10.1016/j.ejphar.2026.178822openalex-snapshot
Neutrophil extracellular traps (NETs) extrusion in infection and diseases: A hallway for diagnosis and prognosis
inferred← citeshttps://doi.org/10.1016/j.ekir.2018.11.005openalex-snapshot
Clinical Implications of Excessive Neutrophil Extracellular Trap Formation in Renal Autoimmune Diseases
inferred← citeshttps://doi.org/10.1016/j.exppara.2022.108459openalex-snapshot
Effect of Leishmania RNA virus 2 on virulence factors and cytokines gene expression in a human macrophage infected with Leishmania major: A preliminary study
inferred← citeshttps://doi.org/10.1016/j.fsi.2020.01.040openalex-snapshot
Chromatin extracellular trap release in rainbow trout, Oncorhynchus mykiss (Walbaum, 1792)
inferred← citeshttps://doi.org/10.1016/j.imlet.2016.05.015openalex-snapshot
Fine-tuning neutrophil activation: Strategies and consequences
inferred← citeshttps://doi.org/10.1016/j.imlet.2025.106991openalex-snapshot
Neutrophil extracellular traps and reactive oxygen species: Predictors of prognosis in bladder cancer
inferred← citeshttps://doi.org/10.1016/j.intimp.2021.108400openalex-snapshot
Exploring the paradox of defense between host and Leishmania parasite
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.110100openalex-snapshot
Entamoeba histolytica induced NETosis and the dual role of NETs in amoebiasis
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.114934openalex-snapshot
Pathological roles of NETs-platelet synergy in thrombotic diseases: From molecular mechanisms to therapeutic targeting
inferred← citeshttps://doi.org/10.1016/j.jaci.2020.02.038openalex-snapshot
The role of neutrophils in host defense and disease
inferred← citeshttps://doi.org/10.1016/j.jdermsci.2016.07.001openalex-snapshot
Neutrophil extracellular traps in dermatology: Caught in the NET
inferred← citeshttps://doi.org/10.1016/j.jri.2021.103306openalex-snapshot
Polymicrobial stimulation of human fetal membranes induce neutrophil activation and neutrophil extracellular trap release
inferred← citeshttps://doi.org/10.1016/j.lfs.2025.123779openalex-snapshot
Under pressure: Updated insights into the mechanisms of Leishmania's defense in response to oxidative stress
inferred← citeshttps://doi.org/10.1016/j.lfs.2025.124122openalex-snapshot
Unraveling the signaling mechanisms behind Histoplasma capsulatum-induced neutrophil NETosis
inferred← citeshttps://doi.org/10.1016/j.mam.2025.101419openalex-snapshot
The crosstalk of neutrophil extracellular trap-inflammasome and their roles in disease progression
inferred← citeshttps://doi.org/10.1016/j.micinf.2023.105261openalex-snapshot
Chick heterophils release DNA extracellular traps (DETs) in vitro and in vivo upon Aspergillus fumigatus conidia exposure
inferred← citeshttps://doi.org/10.1016/j.micpath.2021.105066openalex-snapshot
Multi-facets of neutrophil extracellular trap in infectious diseases: Moving beyond immunity
inferred← citeshttps://doi.org/10.1016/j.molimm.2022.09.008openalex-snapshot
Signal inhibitory receptor on leukocytes-1 regulates the formation of the neutrophil extracellular trap in rheumatoid arthritis
inferred← citeshttps://doi.org/10.1016/j.parint.2020.102178openalex-snapshot
Natural nodular worm infection in goats induces eosinophil extracellular DNA trap (EET) formation
inferred← citeshttps://doi.org/10.1016/j.pt.2016.02.003openalex-snapshot
Different Leishmania Species Drive Distinct Neutrophil Functions
inferred← citeshttps://doi.org/10.1016/j.redox.2019.101344openalex-snapshot
Activation leads to a significant shift in the intracellular redox homeostasis of neutrophil-like cells
inferred← citeshttps://doi.org/10.1016/j.redox.2021.102225openalex-snapshot
Mitochondria in human neutrophils mediate killing of Staphylococcus aureus
inferred← citeshttps://doi.org/10.1016/j.semcancer.2021.07.011openalex-snapshot
Neutrophil extracellular traps in cancer
inferred← citeshttps://doi.org/10.1016/j.surg.2019.10.009openalex-snapshot
Early intravenous administration of tranexamic acid ameliorates intestinal barrier injury induced by neutrophil extracellular traps in a rat model of trauma/hemorrhagic shock
inferred← citeshttps://doi.org/10.1016/j.thromres.2026.109613openalex-snapshot
Mechanisms of cerebral venous sinus thrombosis due to essential thrombocythemia: Current status and future perspectives
inferred← citeshttps://doi.org/10.1016/j.tips.2024.05.008openalex-snapshot
Targeting extranuclear histones to alleviate acute and chronic inflammation
inferred← citeshttps://doi.org/10.1016/j.vetpar.2021.109502openalex-snapshot
Trypanosoma evansi triggered neutrophil extracellular traps formation dependent on myeloperoxidase, neutrophil elastase, and extracellular signal-regulated kinase 1/2 signaling pathways
inferred← citeshttps://doi.org/10.1016/j.virusres.2016.11.033openalex-snapshot
Understanding the molecular mechanisms of NETs and their role in antiviral innate immunity
inferred← citeshttps://doi.org/10.1017/erm.2024.41openalex-snapshot
Understanding Sex-biases in Kinetoplastid Infections: Leishmaniasis and Trypanosomiasis
inferred← citeshttps://doi.org/10.1017/s0031182019001707openalex-snapshot
Besnoitia besnoitibradyzoite stages induce suicidal- and rapid vital-NETosis
inferred← citeshttps://doi.org/10.1038/nm.4294openalex-snapshot
An emerging role for neutrophil extracellular traps in noninfectious disease
inferred← citeshttps://doi.org/10.1038/nrgastro.2017.183openalex-snapshot
Neutrophils and neutrophil extracellular traps in the liver and gastrointestinal system
inferred← citeshttps://doi.org/10.1038/nri.2016.72openalex-snapshot
Cutaneous leishmaniasis: immune responses in protection and pathogenesis
inferred← citeshttps://doi.org/10.1038/s41385-018-0045-0openalex-snapshot
Neutrophil extracellular traps prevent HIV infection in the female genital tract
inferred← citeshttps://doi.org/10.1038/s41418-023-01124-1openalex-snapshot
Moonlighting chromatin: when DNA escapes nuclear control
inferred← citeshttps://doi.org/10.1038/s41419-025-07857-wopenalex-snapshot
Exploring the involvement of serine proteases in neutrophil extracellular traps: a review of mechanisms and implications
inferred← citeshttps://doi.org/10.1038/s41598-017-06901-wopenalex-snapshot
Differential Signalling and Kinetics of Neutrophil Extracellular Trap Release Revealed by Quantitative Live Imaging
inferred← citeshttps://doi.org/10.1038/s41598-017-17561-1openalex-snapshot
cfDNA correlates with endothelial damage after cardiac surgery with prolonged cardiopulmonary bypass and amplifies NETosis in an intracellular TLR9-independent manner
inferred← citeshttps://doi.org/10.1038/s41598-018-32576-yopenalex-snapshot
Respiratory Syncytial Virus induces the classical ROS-dependent NETosis through PAD-4 and necroptosis pathways activation
inferred← citeshttps://doi.org/10.1038/s41598-018-36070-3openalex-snapshot
Bovine neutrophils form extracellular traps in response to the gastrointestinal parasite Ostertagia ostertagi
inferred← citeshttps://doi.org/10.1038/s41598-024-59854-2openalex-snapshot
Resveratrol prevents the release of neutrophil extracellular traps (NETs) by controlling hydrogen peroxide levels and nuclear elastase migration
inferred← citeshttps://doi.org/10.1038/s41598-025-91425-xopenalex-snapshot
Candida albicans aspartyl protease (Sap6) inhibits neutrophil function via a “Trojan horse” mechanism
inferred← citeshttps://doi.org/10.1038/srep41749openalex-snapshot
Transcriptional firing helps to drive NETosis
inferred← citeshttps://doi.org/10.1042/bsr20180916openalex-snapshot
The state of art of neutrophil extracellular traps in protozoan and helminthic infections
inferred← citeshttps://doi.org/10.1055/s-0039-1678529openalex-snapshot
Fibrin Modulates Shear-Induced NETosis in Sterile Occlusive Thrombi Formed under Haemodynamic Flow
inferred← citeshttps://doi.org/10.1080/08830185.2018.1540616openalex-snapshot
Many Ways–One Destination: Different Types of Neutrophils Death
inferred← citeshttps://doi.org/10.1080/08830185.2021.1921174openalex-snapshot
Neutrophil extracellular trap-associated molecules: a review on their immunophysiological and inflammatory roles
inferred← citeshttps://doi.org/10.1080/09537104.2020.1718631openalex-snapshot
Platelets and extracellular traps in infections
inferred← citeshttps://doi.org/10.1080/20477724.2016.1232042openalex-snapshot
Pro- and anti-inflammatory cytokines in cutaneous leishmaniasis: a review
inferred← citeshttps://doi.org/10.1089/ars.2023.0304openalex-snapshot
Modulation of Innate Immune Memory Dynamics by Subcellular Reactive Oxygen Species
inferred← citeshttps://doi.org/10.1093/cvr/cvz084openalex-snapshot
Novel findings in neutrophil biology and their impact on cardiovascular disease
inferred← citeshttps://doi.org/10.1093/infdis/jiae317openalex-snapshot
Contrasting Phenotypes of Neutrophils During Asymptomatic Versus Symptomatic Leishmania braziliensis Infection
inferred← citeshttps://doi.org/10.1093/jleuko/qiae196openalex-snapshot
Leishmania amazonensis-derived extracellular vesicles (EVs) induce neutrophil extracellular traps (NETs)
inferred← citeshttps://doi.org/10.1096/fj.202201904ropenalex-snapshot
Peripheral nervous system is injured by neutrophil extracellular traps ( NETs ) elicited by nonstructural ( NS ) protein‐1 from Zika virus
inferred← citeshttps://doi.org/10.1097/bor.0000000000000450openalex-snapshot
Neutrophil extracellular traps in vasculitis, friend or foe?
inferred← citeshttps://doi.org/10.1098/rsos.210090openalex-snapshot
A model of the innate immune response to SARS-CoV-2 in the alveolar epithelium
inferred← citeshttps://doi.org/10.1101/2024.03.04.583250openalex-snapshot
Addressing anemia severity in antimony-resistant Leishmania donovani infection at the nexus of oxidative outburst and iron transit
inferred← citeshttps://doi.org/10.1111/aji.70269openalex-snapshot
The Effects of Sex Hormones and Aging on the Mucosal Immune System in the Human Female Reproductive Tract and Implications for HIV Acquisition
inferred← citeshttps://doi.org/10.1111/bph.70202openalex-snapshot
Indian cobra ( Naja naja ) venom‐induced neutrophil extracellular trap (NET) formation: The role of cytotoxins and calcium flux
inferred← citeshttps://doi.org/10.1111/imm.13325openalex-snapshot
Cell death as part of innate immunity: Cause or consequence?
inferred← citeshttps://doi.org/10.1111/jmi.12620openalex-snapshot
Independent trafficking of flavocytochrome b558 and myeloperoxidase to phagosomes during phagocytosis visualised by energy‐filtering and energy‐dispersive spectroscopy‐scanning transmission electron microscopy
inferred← citeshttps://doi.org/10.1111/jth.13907openalex-snapshot
Hemodynamic force triggers rapid NETosis within sterile thrombotic occlusions
inferred← citeshttps://doi.org/10.1111/pim.12572openalex-snapshot
Ovine vital neutrophil extracellular traps bind and impair Haemonchus contortus L3 in a breed‐dependent manner
inferred← citeshttps://doi.org/10.1111/pim.12610openalex-snapshot
Mouse neutrophils release extracellular traps in response to Naegleria fowleri
inferred← citeshttps://doi.org/10.1128/iai.00605-19openalex-snapshot
During the Early Stages of Staphylococcus aureus Biofilm Formation, Induced Neutrophil Extracellular Traps Are Degraded by Autologous Thermonuclease
inferred← citeshttps://doi.org/10.1128/mbio.01980-23openalex-snapshot
Mechanisms regulating host cell death during Leishmania infection
inferred← citeshttps://doi.org/10.1134/s1990519x19050055openalex-snapshot
Stearylamine Causes the Formation of Neutrophil Extracellular Traps Independently of Reactive Oxygen Species
inferred← citeshttps://doi.org/10.1134/s2635167623601080openalex-snapshot
Sphingosine and Other Amine-Containing Compounds Induce Rapid NOX-Independent NETosis
inferred← citeshttps://doi.org/10.1155/2016/5898074openalex-snapshot
Far beyond Phagocytosis: Phagocyte-Derived Extracellular Traps Act Efficiently against Protozoan ParasitesIn VitroandIn Vivo
inferred← citeshttps://doi.org/10.1155/2019/3638562openalex-snapshot
Programmed Cell Death Pathways in the Pathogenesis of Systemic Lupus Erythematosus
inferred← citeshttps://doi.org/10.1155/2019/7198484openalex-snapshot
Optimization of Experimental Settings for the Assessment of Reactive Oxygen Species Production by Human Blood
inferred← citeshttps://doi.org/10.1155/2019/7816491openalex-snapshot
Neutrophil Extracellular Trap Components Associate with Infarct Size, Ventricular Function, and Clinical Outcome in STEMI
inferred← citeshttps://doi.org/10.1155/2023/7022337openalex-snapshot
The Formation of NETs and Their Mechanism of Promoting Tumor Metastasis
inferred← citeshttps://doi.org/10.11606/t.17.2022.tde-03022023-110423openalex-snapshot
Ativação do inflamassoma: a importância na leishmaniose, na influenza e na COVID-19
inferred← citeshttps://doi.org/10.1161/circresaha.116.309692openalex-snapshot
Neutrophil Extracellular Traps in Atherosclerosis and Atherothrombosis
inferred← citeshttps://doi.org/10.1177/1753425918821168openalex-snapshot
Glycoconjugates of Gram-negative bacteria and parasitic protozoa – are they similar in orchestrating the innate immune response?
inferred← citeshttps://doi.org/10.1183/23120541.00596-2021openalex-snapshot
Enhanced neutrophil extracellular trap formation in COVID-19 is inhibited by the protein kinase C inhibitor ruboxistaurin
inferred← citeshttps://doi.org/10.1186/s12866-024-03270-zopenalex-snapshot
Neutrophil extracellular traps formation: effect of Leishmania major promastigotes and salivary gland homogenates of Phlebotomus papatasi in human neutrophil culture
inferred← citeshttps://doi.org/10.1186/s12964-020-0515-3openalex-snapshot
F0F1 ATP synthase regulates extracellular calcium influx in human neutrophils by interacting with Cav2.3 and modulates neutrophil accumulation in the lipopolysaccharide-challenged lung
inferred← citeshttps://doi.org/10.1186/s12964-026-02947-4openalex-snapshot
Mast cells release DNA Extracellular Traps (DETs) in response to SARS-CoV-2 and its spike protein
inferred← citeshttps://doi.org/10.1186/s13058-019-1237-6openalex-snapshot
Neutrophil extracellular traps in breast cancer and beyond: current perspectives on NET stimuli, thrombosis and metastasis, and clinical utility for diagnosis and treatment
inferred← citeshttps://doi.org/10.1186/s13071-016-1540-3openalex-snapshot
The site of the bite: Leishmania interaction with macrophages, neutrophils and the extracellular matrix in the dermis
inferred← citeshttps://doi.org/10.1186/s13071-025-06956-zopenalex-snapshot
Neutrophil extracellular traps induced by Haemonchus contortus excretory–secretory proteins varies among goats, gerbils, and mice
inferred← citeshttps://doi.org/10.1186/s13567-021-00920-2openalex-snapshot
Innate immune response in bovine neutrophils stimulated with Mycoplasma bovis
inferred← citeshttps://doi.org/10.1186/s40164-025-00670-3openalex-snapshot
Exploring neutrophil extracellular traps: mechanisms of immune regulation and future therapeutic potential
inferred← citeshttps://doi.org/10.1186/s43556-025-00337-9openalex-snapshot
Neutrophil Extracellular Traps (NETs) in health and disease
inferred← citeshttps://doi.org/10.1189/jlb.4a0615-261rropenalex-snapshot
Neutrophil extracellular traps release induced by Leishmania : role of PI3Kγ, ERK, PI3Kσ, PKC, and [Ca2+]
inferred← citeshttps://doi.org/10.13070/mm.en.9.2714openalex-snapshot
Extracellular Traps – NETosis and METosis
inferred← citeshttps://doi.org/10.1371/journal.pntd.0008167openalex-snapshot
Epigenetic regulation of defense genes by histone deacetylase1 in human cell line-derived macrophages promotes intracellular survival of Leishmania donovani
inferred← citeshttps://doi.org/10.1371/journal.pone.0159031openalex-snapshot
Conservative Mechanisms of Extracellular Trap Formation by Annelida Eisenia andrei: Serine Protease Activity Requirement
inferred← citeshttps://doi.org/10.1371/journal.pone.0171850openalex-snapshot
Enhanced survival of Leishmania major in neutrophil granulocytes in the presence of apoptotic cells
inferred← citeshttps://doi.org/10.1371/journal.pone.0226396openalex-snapshot
Murine lupus is neutrophil elastase-independent in the MRL.Faslpr model
inferred← citeshttps://doi.org/10.1371/journal.ppat.1012592openalex-snapshot
Functional plasticity shapes neutrophil response to Leishmania major infection in susceptible and resistant strains of mice
inferred← citeshttps://doi.org/10.1371/journal.ppat.1012858openalex-snapshot
Oxidative stress-driven enhanced iron production and scavenging through Ferroportin reorientation worsens anemia in antimony-resistant Leishmania donovani infection
inferred← citeshttps://doi.org/10.15252/embr.201948779openalex-snapshot
Nuclear envelope rupture and NET formation is driven by PKCα‐mediated lamin B disassembly
inferred← citeshttps://doi.org/10.2147/jir.s460333openalex-snapshot
Targeting Neutrophil Extracellular Traps in Gouty Arthritis: Insights into Pathogenesis and Therapeutic Potential
inferred← citeshttps://doi.org/10.21608/puj.2021.95583.1132openalex-snapshot
Perceptions on therapeutic modalities regarding the virulence and immunity of cutaneous leishmaniasis
inferred← citeshttps://doi.org/10.2174/0115748855295089240322081903openalex-snapshot
Innate Immune Effectors and Leishmania: an Overview of Complexities
inferred← citeshttps://doi.org/10.22271/oral.2021.v7.i1d.1138openalex-snapshot
Neutrophil extracellular traps-periodontal implications of netosis: A literature review
inferred← citeshttps://doi.org/10.23880/ijbp-16000222openalex-snapshot
Revisiting Pyronin Y, A Classical Photostable Xanthene Dye useful for Cost Effective Multimodal Fluorescence Microscopy
inferred← citeshttps://doi.org/10.29245/2578-3009/2018/5.1161openalex-snapshot
Emerging Evidence Supports the Hypothesis that Neutrophil Extracellular Traps are a Major Factor in Genesis and Progression of Chronic Obstructive Pulmonary Disease
inferred← citeshttps://doi.org/10.32657/10356/160631openalex-snapshot
Mechanisms of enterococcus faecalis-mediated Immunomodulation
inferred← citeshttps://doi.org/10.33263/briac132.135openalex-snapshot
Activity of Benzimidazole Derivatives and their N-Heterocyclic Carbene Silver Complexes Against Leishmania major Promastigotes and Amastigotes
inferred← citeshttps://doi.org/10.3384/diss.diva-132327openalex-snapshot
The Contribution of Innate Immunity to the Pathogenesis of ANCA-associated Vasculitis
inferred← citeshttps://doi.org/10.3389/fcimb.2017.00104openalex-snapshot
Understanding the Entanglement: Neutrophil Extracellular Traps (NETs) in Cystic Fibrosis
inferred← citeshttps://doi.org/10.3389/fcimb.2017.00159openalex-snapshot
Influence of Microbes on Neutrophil Life and Death
inferred← citeshttps://doi.org/10.3389/fcimb.2017.00414openalex-snapshot
Aspartic Proteases and Major Cell Wall Components in Candida albicans Trigger the Release of Neutrophil Extracellular Traps
inferred← citeshttps://doi.org/10.3389/fcimb.2018.00184openalex-snapshot
Entamoeba histolytica Trophozoites Induce a Rapid Non-classical NETosis Mechanism Independent of NOX2-Derived Reactive Oxygen Species and PAD4 Activity
inferred← citeshttps://doi.org/10.3389/fcimb.2018.00226openalex-snapshot
Entamoeba histolytica Induce Signaling via Raf/MEK/ERK for Neutrophil Extracellular Trap (NET) Formation
inferred← citeshttps://doi.org/10.3389/fcimb.2021.639768openalex-snapshot
Salmonella Typhimurium Triggers Extracellular Traps Release in Murine Macrophages
inferred← citeshttps://doi.org/10.3389/fcimb.2021.681030openalex-snapshot
Extracellular Nucleic Acids Present in the Candida albicans Biofilm Trigger the Release of Neutrophil Extracellular Traps
inferred← citeshttps://doi.org/10.3389/fcimb.2021.710006openalex-snapshot
Neutrophil Activation: Influence of Antimony Tolerant and Susceptible Clinical Strains of L. (V.) panamensis and Meglumine Antimoniate
inferred← citeshttps://doi.org/10.3389/fcimb.2023.1326521openalex-snapshot
The immune response in canine and human leishmaniasis and how this influences the diagnosis- a review and assessment of recent research
inferred← citeshttps://doi.org/10.3389/fimmu.2016.00256openalex-snapshot
Neutrophil Extracellular Traps in ANCA-Associated Vasculitis
inferred← citeshttps://doi.org/10.3389/fimmu.2016.00261openalex-snapshot
Inhibitors of Serine Proteases in Regulating the Production and Function of Neutrophil Extracellular Traps
inferred← citeshttps://doi.org/10.3389/fimmu.2016.00363openalex-snapshot
Neutrophil Integrins and Matrix Ligands and NET Release
inferred← citeshttps://doi.org/10.3389/fimmu.2016.00565openalex-snapshot
Multimodal Regulation of NET Formation in Pregnancy: Progesterone Antagonizes the Pro-NETotic Effect of Estrogen and G-CSF
inferred← citeshttps://doi.org/10.3389/fimmu.2017.01354openalex-snapshot
Interleukin-4 Receptor Alpha: From Innate to Adaptive Immunity in Murine Models of Cutaneous Leishmaniasis
inferred← citeshttps://doi.org/10.3389/fimmu.2017.01558openalex-snapshot
Survival Mechanisms Used by Some Leishmania Species to Escape Neutrophil Killing
inferred← citeshttps://doi.org/10.3389/fimmu.2017.01849openalex-snapshot
Alkaline pH Promotes NADPH Oxidase-Independent Neutrophil Extracellular Trap Formation: A Matter of Mitochondrial Reactive Oxygen Species Generation and Citrullination and Cleavage of Histone
inferred← citeshttps://doi.org/10.3389/fimmu.2018.00178openalex-snapshot
Pathogenic Bacterium Acinetobacter baumannii Inhibits the Formation of Neutrophil Extracellular Traps by Suppressing Neutrophil Adhesion
inferred← citeshttps://doi.org/10.3389/fimmu.2018.01182openalex-snapshot
Protein Deiminase 4 and CR3 Regulate Aspergillus fumigatus and β-Glucan-Induced Neutrophil Extracellular Trap Formation, but Hyphal Killing Is Dependent Only on CR3
inferred← citeshttps://doi.org/10.3389/fimmu.2018.02529openalex-snapshot
Macrophage Polarization in Leishmaniasis: Broadening Horizons
inferred← citeshttps://doi.org/10.3389/fimmu.2018.02854openalex-snapshot
Streptococcus Suis Serotype 2 Stimulates Neutrophil Extracellular Traps Formation via Activation of p38 MAPK and ERK1/2
inferred← citeshttps://doi.org/10.3389/fimmu.2018.03040openalex-snapshot
Resistance of Leishmania (Viannia) Panamensis to Meglumine Antimoniate or Miltefosine Modulates Neutrophil Effector Functions
inferred← citeshttps://doi.org/10.3389/fimmu.2019.02190openalex-snapshot
Detrimental Effect of Type I IFNs During Acute Lung Infection With Pseudomonas aeruginosa Is Mediated Through the Stimulation of Neutrophil NETosis
inferred← citeshttps://doi.org/10.3389/fimmu.2020.00145openalex-snapshot
Placental Protein 13 (Galectin-13) Polarizes Neutrophils Toward an Immune Regulatory Phenotype
inferred← citeshttps://doi.org/10.3389/fimmu.2020.610696openalex-snapshot
Insights Into Immunothrombosis: The Interplay Among Neutrophil Extracellular Trap, von Willebrand Factor, and ADAMTS13
inferred← citeshttps://doi.org/10.3389/fimmu.2021.635188openalex-snapshot
Neutrophil Extracellular Traps: A Potential Therapeutic Target in MPO-ANCA Associated Vasculitis?
inferred← citeshttps://doi.org/10.3389/fimmu.2021.660760openalex-snapshot
β2 Integrin Regulation of Neutrophil Functional Plasticity and Fate in the Resolution of Inflammation
inferred← citeshttps://doi.org/10.3389/fimmu.2021.728848openalex-snapshot
The Paradox of a Phagosomal Lifestyle: How Innate Host Cell-Leishmania amazonensis Interactions Lead to a Progressive Chronic Disease
inferred← citeshttps://doi.org/10.3389/fimmu.2021.788976openalex-snapshot
Neutrophil-Mediated Immunopathology and Matrix Metalloproteinases in Central Nervous System – Tuberculosis
inferred← citeshttps://doi.org/10.3389/fimmu.2022.1022380openalex-snapshot
The role of extracellular traps in ischemia reperfusion injury
inferred← citeshttps://doi.org/10.3389/fimmu.2022.1075260openalex-snapshot
No NETs no TIME: Crosstalk between neutrophil extracellular traps and the tumor immune microenvironment
inferred← citeshttps://doi.org/10.3389/fimmu.2022.842482openalex-snapshot
Glycolysis, monocarboxylate transport, and purinergic signaling are key events in Eimeria bovis-induced NETosis
inferred← citeshttps://doi.org/10.3389/fimmu.2022.921077openalex-snapshot
Neutrophil Extracellular Traps Are Found in Bronchoalveolar Lavage Fluids of Horses With Severe Asthma and Correlate With Asthma Severity
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1127277openalex-snapshot
The transient receptor potential channels in rheumatoid arthritis: Need to pay more attention
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1206529openalex-snapshot
Mycobacterium tuberculosis PE/PPE proteins enhance the production of reactive oxygen species and formation of neutrophil extracellular traps
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1282278openalex-snapshot
Human neutrophil extracellular traps do not impair in vitro Toxoplasma gondii infection
inferred← citeshttps://doi.org/10.3389/fimmu.2024.1295168openalex-snapshot
Complexation of fungal extracellular nucleic acids by host LL-37 peptide shapes neutrophil response to Candida albicans biofilm
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1498453openalex-snapshot
Bibliometric analysis of neutrophil extracellular traps induced by protozoan and helminth parasites (2008–2024)
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1547559openalex-snapshot
The hypoxic microenvironment of Candida albicans biofilms shapes neutrophil responses
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1573151openalex-snapshot
IL-1beta expressing neutrophil extracellular traps in Legionella pneumophila infection
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1589329openalex-snapshot
Neutrophil extracellular traps in diseases of the female reproductive organs
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1599956openalex-snapshot
A new insight: crosstalk between neutrophil extracellular traps and the gut-liver axis for nonalcoholic fatty liver disease
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1638314openalex-snapshot
Neutrophil extracellular traps in tumor microenvironment for radiotherapy: friend or foe?
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1731687openalex-snapshot
Interactions between neutrophil extracellular traps and macrophages: the key to inflammatory diseases
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1808191openalex-snapshot
Neutrophil extracellular traps are found at epithelial barriers in canine sinonasal aspergillosis
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1873341openalex-snapshot
Leishmania infantum eukaryotic initiation factor 4A modulates in vitro functional activity of human neutrophils
inferred← citeshttps://doi.org/10.3389/fmed.2020.00155openalex-snapshot
G-CSF Infusion for Stem Cell Mobilization Transiently Increases Serum Cell-Free DNA and Protease Concentrations
inferred← citeshttps://doi.org/10.3389/fmed.2023.1076690openalex-snapshot
Spontaneous NETosis in diabetes: A role of hyperglycemia mediated ROS and autophagy
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