On the public citation graph

Eosinophil extracellular trap cell death–derived DNA traps: Their presence in secretions and functional attributes

https://doi.org/10.1016/j.jaci.2015.04.041
0 signed · 278 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1006/jmbi.1995.0498openalex-snapshot
Electrostatic Mechanism of Nucleosome Spacing
inferredcites →https://doi.org/10.1007/s00109-009-0481-0openalex-snapshot
Innate immunity turned inside-out: antimicrobial defense by phagocyte extracellular traps
inferredcites →https://doi.org/10.1016/0091-6749(88)90944-xopenalex-snapshot
A clinical and pathologic study of chronic sinusitis: The role of the eosinophil
inferredcites →https://doi.org/10.1016/j.anl.2010.11.016openalex-snapshot
Diagnostic criteria of eosinophilic otitis media, a newly recognized middle ear disease
inferredcites →https://doi.org/10.1016/j.chom.2012.05.015openalex-snapshot
Neutrophil Extracellular Traps Mediate a Host Defense Response to Human Immunodeficiency Virus-1
inferredcites →https://doi.org/10.1016/j.humpath.2003.10.024openalex-snapshot
Fungal sinusitis: histologic spectrum and correlation with culture
inferredcites →https://doi.org/10.1016/j.jaci.2009.11.029openalex-snapshot
Cysteinyl leukotrienes acting via granule membrane-expressed receptors elicit secretion from within cell-free human eosinophil granules
inferredcites →https://doi.org/10.1016/j.jcf.2011.09.008openalex-snapshot
Ultrastructural characterization of cystic fibrosis sputum using atomic force and scanning electron microscopy
inferredcites →https://doi.org/10.1016/j.sbi.2006.05.007openalex-snapshot
Structure of the ‘30nm’ chromatin fibre: A key role for the linker histone
inferredcites →https://doi.org/10.1016/s0092-8674(00)81958-3openalex-snapshot
Twenty-Five Years of the Nucleosome, Fundamental Particle of the Eukaryote Chromosome
inferredcites →https://doi.org/10.1038/cdd.2011.1openalex-snapshot
Dying for a cause: NETosis, mechanisms behind an antimicrobial cell death modality
inferredcites →https://doi.org/10.1038/nm.1855openalex-snapshot
Catapult-like release of mitochondrial DNA by eosinophils contributes to antibacterial defense
inferredcites →https://doi.org/10.1038/nrmicro1710openalex-snapshot
Beneficial suicide: why neutrophils die to make NETs
inferredcites →https://doi.org/10.1073/pnas.0804547105openalex-snapshot
Eosinophil granules function extracellularly as receptor-mediated secretory organelles
inferredcites →https://doi.org/10.1073/pnas.1005743107openalex-snapshot
Extracellular DNA traps promote thrombosis
inferredcites →https://doi.org/10.1073/pnas.94.12.6185openalex-snapshot
Ionic effects on the elasticity of single DNA molecules
inferredcites →https://doi.org/10.1074/jbc.270.24.14659openalex-snapshot
Intracellular Localization of 8-Oxo-dGTPase in Human Cells, with Special Reference to the Role of the Enzyme in Mitochondria
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.201006052openalex-snapshot
Neutrophil elastase and myeloperoxidase regulate the formation of neutrophil extracellular traps
inferredcites →https://doi.org/10.1111/j.1398-9995.2008.01871.xopenalex-snapshot
Soluble vascular cell adhesion molecule‐1 induces human eosinophil migration
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/trf.12700openalex-snapshot
Heme‐related molecules induce rapid production of neutrophil extracellular traps
inferredcites →https://doi.org/10.1126/science.1092385openalex-snapshot
Neutrophil Extracellular Traps Kill Bacteria
inferredcites →https://doi.org/10.1159/000126066openalex-snapshot
Chronic Rhinosinusitis: Risk Factors for the Recurrence of Chronic Rhinosinusitis Based on 5-Year Follow-Up after Endoscopic Sinus Surgery
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/10.1182/blood-2012-05-432088openalex-snapshot
Eosinophil extracellular DNA trap cell death mediates lytic release of free secretion-competent eosinophil granules in humans
inferredcites →https://doi.org/10.1371/journal.pone.0028526openalex-snapshot
Neutrophil Elastase Enhances Sputum Solubilization in Cystic Fibrosis Patients Receiving DNase Therapy
inferredcites →https://doi.org/10.1371/journal.ppat.1000639openalex-snapshot
Neutrophil Extracellular Traps Contain Calprotectin, a Cytosolic Protein Complex Involved in Host Defense against Candida albicans
inferredcites →https://doi.org/10.3389/fimmu.2013.00001openalex-snapshot
NET balancing: a problem in inflammatory lung diseases
inferredcites →https://doi.org/10.4049/jimmunol.181.11.7689openalex-snapshot
Retinoic Acids Are Potent Inhibitors of Spontaneous Human Eosinophil Apoptosis

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.4462311openalex-extracted
Exploring the Risk of Infection Events in Patients With Asthma Receiving Anti-IL-5 Monoclonal Antibodies: A Rapid Systematic Review and a Meta-Analysis
inferred← citeshttps://doi.org/10.1002/ana.26186openalex-snapshot
DNase Treatment Prevents Cerebrospinal Fluid Block in Early Experimental Pneumococcal Meningitis
inferred← citeshttps://doi.org/10.1002/art.41727openalex-snapshot
Eosinophil ETosis–Mediated Release of Galectin‐10 in Eosinophilic Granulomatosis With Polyangiitis
inferred← citeshttps://doi.org/10.1002/clt2.70175openalex-snapshot
Programmed Cell Death in Chronic Rhinosinusitis
inferred← citeshttps://doi.org/10.1002/jcp.28931openalex-snapshot
Reactive oxygen species are involved in eosinophil extracellular traps release and in airway inflammation in asthma
inferred← citeshttps://doi.org/10.1002/jcp.28966openalex-snapshot
Autophagy induces eosinophil extracellular traps formation and allergic airway inflammation in a murine asthma model
inferred← citeshttps://doi.org/10.1002/jlb.4mir1018-397rropenalex-snapshot
A STING to inflammation and autoimmunity
inferred← citeshttps://doi.org/10.1002/jlb.4mr1117-473ropenalex-snapshot
Eosinophils in fungal diseases: An overview
inferred← citeshttps://doi.org/10.1002/jlb.4ru0119-003ropenalex-snapshot
Subversion of host immune responses by otopathogens during otitis media
inferred← citeshttps://doi.org/10.1002/lary.26248openalex-snapshot
Predicting revision sinus surgery in allergic fungal and eosinophilic mucin chronic rhinosinusitis
inferred← citeshttps://doi.org/10.1002/ppul.26650openalex-snapshot
Eosinophilic plastic bronchitis: Case series and review of the literature
inferred← citeshttps://doi.org/10.1002/wjo2.138openalex-snapshot
Eosinophil extracellular traps in respiratory ailment: Pathogenic mechanisms and clinical translation
inferred← citeshttps://doi.org/10.1007/978-3-032-03370-3_18openalex-snapshot
Crowding and in-Cell Crystallization
inferred← citeshttps://doi.org/10.1007/s00259-026-07889-0openalex-snapshot
Al18F-FAPI PET/CT in hypereosinophilic syndrome with cardiac involvement and its potential association with eosinophil extracellular traps
inferred← citeshttps://doi.org/10.1007/s00535-018-1498-3openalex-snapshot
Epithelial-stromal crosstalk and fibrosis in eosinophilic esophagitis
inferred← citeshttps://doi.org/10.1007/s11239-018-1713-3openalex-snapshot
Elevated extracellular trap formation and contact system activation in acute leukemia
inferred← citeshttps://doi.org/10.1007/s11882-016-0634-5openalex-snapshot
Eosinophil ETosis and DNA Traps: a New Look at Eosinophilic Inflammation
inferred← citeshttps://doi.org/10.1007/s11882-017-0702-5openalex-snapshot
Eosinophilic Otitis Media: the Aftermath of Eosinophil Extracellular Trap Cell Death
inferred← citeshttps://doi.org/10.1007/s11882-019-0868-0openalex-snapshot
Charcot-Leyden Crystals in Eosinophilic Inflammation: Active Cytolysis Leads to Crystal Formation
inferred← citeshttps://doi.org/10.1007/s11882-023-01082-1openalex-snapshot
An Emerging Role of Extracellular Traps in Chronic Rhinosinusitis
inferred← citeshttps://doi.org/10.1007/s12070-020-01903-zopenalex-snapshot
Eosinophilic Otitis Media: Modern Aspects of Pathogenesis, Clinical Features, Diagnosis and Treatment
inferred← citeshttps://doi.org/10.1007/s12672-024-01513-zopenalex-snapshot
SPINK5 is a key regulator of eosinophil extracellular traps in head and neck squamous cell carcinoma
inferred← citeshttps://doi.org/10.1007/s13770-020-00241-zopenalex-snapshot
Extracellular Trap by Blood Cells: Clinical Implications
inferred← citeshttps://doi.org/10.1016/b978-0-08-102723-3.00200-6openalex-snapshot
Allergic Bronchopulmonary Aspergillosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-374279-7.03007-1openalex-snapshot
Eosinophils
inferred← citeshttps://doi.org/10.1016/b978-0-12-813755-0.00002-2openalex-snapshot
Eosinophil cell death
inferred← citeshttps://doi.org/10.1016/b978-0-12-813755-0.00003-4openalex-snapshot
Eosinophils as secretory cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-813755-0.00008-3openalex-snapshot
Eosinophil-associated diseases (EADs)
inferred← citeshttps://doi.org/10.1016/b978-0-12-813755-0.09990-1openalex-snapshot
References
inferred← citeshttps://doi.org/10.1016/b978-0-12-816388-7.00006-1openalex-snapshot
Immune Response and Tissue Damage
inferred← citeshttps://doi.org/10.1016/b978-0-128-24465-4.00102-2openalex-snapshot
Eosinophils – Role in Immunity
inferred← citeshttps://doi.org/10.1016/b978-0-323-44887-1.00008-0openalex-snapshot
Lung Defenses
inferred← citeshttps://doi.org/10.1016/b978-0-323-85415-3.00013-1openalex-snapshot
Asthma and autoimmunity
inferred← citeshttps://doi.org/10.1016/b978-0-323-85419-1.00005-0openalex-snapshot
Eosinophilic and noneosinophilic asthma: Beyond severe asthma
inferred← citeshttps://doi.org/10.1016/bs.ai.2018.03.001openalex-snapshot
Eosinophil Development, Disease Involvement, and Therapeutic Suppression
inferred← citeshttps://doi.org/10.1016/j.ajt.2026.01.028openalex-snapshot
Activation of donor-derived eosinophils during static storage contributes to primary graft dysfunction after lung transplantation
inferred← citeshttps://doi.org/10.1016/j.alit.2017.08.002openalex-snapshot
Mucus plugging in allergic bronchopulmonary aspergillosis: Implication of the eosinophil DNA traps
inferred← citeshttps://doi.org/10.1016/j.alit.2017.11.007openalex-snapshot
ETosis-derived DNA trap production in middle ear effusion is a common feature of eosinophilic otitis media
inferred← citeshttps://doi.org/10.1016/j.alit.2017.11.008openalex-snapshot
Recent advances in understanding the roles of blood platelets in the pathogenesis of allergic inflammation and bronchial asthma
inferred← citeshttps://doi.org/10.1016/j.alit.2018.12.004openalex-snapshot
Allergic bronchopulmonary aspergillosis in succession to chronic eosinophilic pneumonia
inferred← citeshttps://doi.org/10.1016/j.alit.2019.04.005openalex-snapshot
Comparison of CD16-negative selection vs. MACSxpress system for isolation of blood eosinophils
inferred← citeshttps://doi.org/10.1016/j.alit.2019.06.002openalex-snapshot
Cysteinyl leukotriene metabolism of human eosinophils in allergic disease
inferred← citeshttps://doi.org/10.1016/j.alit.2020.02.002openalex-snapshot
The roles of IL-5 and anti-IL-5 treatment in eosinophilic diseases: Asthma, eosinophilic granulomatosis with polyangiitis, and eosinophilic chronic rhinosinusitis
inferred← citeshttps://doi.org/10.1016/j.alit.2020.03.009openalex-snapshot
The impact of mepolizumab on the sputum level of eosinophil-derived protein in three cases of severe asthma
inferred← citeshttps://doi.org/10.1016/j.alit.2020.09.002openalex-snapshot
Eosinophils: Cells known for over 140 years with broad and new functions
inferred← citeshttps://doi.org/10.1016/j.alit.2020.10.002openalex-snapshot
How to detect eosinophil ETosis (EETosis) and extracellular traps
inferred← citeshttps://doi.org/10.1016/j.alit.2022.08.003openalex-snapshot
Neutrophil and eosinophil ETosis-mediated extracellular trap formation in a patient with chronic granulomatous disease
inferred← citeshttps://doi.org/10.1016/j.alit.2022.10.007openalex-snapshot
Differential role of mucus plugs in asthma: Effects of smoking and association with airway inflammation
inferred← citeshttps://doi.org/10.1016/j.alit.2023.10.002openalex-snapshot
Eosinophil extracellular trap formation in the giant papillae of atopic keratoconjunctivitis and vernal keratoconjunctivitis
inferred← citeshttps://doi.org/10.1016/j.alit.2024.03.002openalex-snapshot
Eosinophilic mucus diseases
inferred← citeshttps://doi.org/10.1016/j.alit.2026.05.002openalex-snapshot
Heparin-like compounds improve the biophysical properties of eosinophilic mucus
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2025.108017openalex-snapshot
Eosinophils from jennies form extracellular traps (EETs) in vitro in response to seminal plasma: A new perspective on uterine immune defense in donkeys
inferred← citeshttps://doi.org/10.1016/j.anl.2020.09.005openalex-snapshot
Effectiveness of myringoplasty in patients with eosinophilic otitis media
inferred← citeshttps://doi.org/10.1016/j.anl.2022.07.005openalex-snapshot
Intractable otitis media - Pathogenesis and treatment of Eosinophilic otitis media (EOM) and otitis media with Antineutrophil cytoplasmic antibody (ANCA) -associated vasculitis (OMAAV)
inferred← citeshttps://doi.org/10.1016/j.anl.2022.11.004openalex-snapshot
Eosinophilic otitis media; state-of-the-art diagnosis and treatment
inferred← citeshttps://doi.org/10.1016/j.anl.2025.05.009openalex-snapshot
Epithelial cell dynamics: Key drivers of type 2 inflammation in eosinophilic chronic rhinosinusitis
inferred← citeshttps://doi.org/10.1016/j.bcp.2020.113963openalex-snapshot
Eosinophil diversity in asthma
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.117655openalex-snapshot
The role and mechanism of extracellular traps in chronic rhinosinusitis
inferred← citeshttps://doi.org/10.1016/j.cell.2021.02.016openalex-snapshot
The basic immunology of asthma
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108621openalex-snapshot
Microfilariae Trigger Eosinophil Extracellular DNA Traps in a Dectin-1-Dependent Manner
inferred← citeshttps://doi.org/10.1016/j.chest.2019.08.2192openalex-snapshot
Meeting the Challenge of Identifying New Treatments for Type 2-Low Neutrophilic Asthma
inferred← citeshttps://doi.org/10.1016/j.chest.2020.01.021openalex-snapshot
Luminal Eosinophil Cell Death as a Biomarker for Loss of Asthma Control?
inferred← citeshttps://doi.org/10.1016/j.cyto.2016.08.013openalex-snapshot
The effect of hepatocyte growth factor on secretory functions in human eosinophils
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e23725openalex-snapshot
Exploring the risk of infection events in patients with asthma receiving anti-IL-5 monoclonal antibodies: A rapid systematic review and a meta-analysis
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.10.280openalex-snapshot
Phosphorothioate-linked guanine/cytosine-based stem-loop oligonucleotides induce the extracellular release of mitochondrial DNA from peritoneal B1a cells
inferred← citeshttps://doi.org/10.1016/j.ijmm.2024.151641openalex-snapshot
Signaling events driving Aspergillus fumigatus-induced eosinophil activation
inferred← citeshttps://doi.org/10.1016/j.jaci.2016.09.008openalex-snapshot
Advances in rhinitis and rhinosinusitis in 2015
inferred← citeshttps://doi.org/10.1016/j.jaci.2017.01.019openalex-snapshot
Extracellular eosinophilic traps in association with Staphylococcus aureus at the site of epithelial barrier defects in patients with severe airway inflammation
inferred← citeshttps://doi.org/10.1016/j.jaci.2017.01.044openalex-snapshot
Adhesion-induced eosinophil cytolysis requires the receptor-interacting protein kinase 3 (RIPK3)–mixed lineage kinase-like (MLKL) signaling pathway, which is counterregulated by autophagy
inferred← citeshttps://doi.org/10.1016/j.jaci.2017.05.047openalex-snapshot
Lytic eosinophils produce extracellular DNA traps as well as free eosinophil granules
inferred← citeshttps://doi.org/10.1016/j.jaci.2017.06.033openalex-snapshot
Sputum autoantibodies in patients with severe eosinophilic asthma
inferred← citeshttps://doi.org/10.1016/j.jaci.2017.07.048openalex-snapshot
Eosinophils release extracellular DNA traps in response to Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1016/j.jaci.2017.08.029openalex-snapshot
Advances in mechanisms of allergic disease in 2016
inferred← citeshttps://doi.org/10.1016/j.jaci.2017.09.009openalex-snapshot
Chronic rhinosinusitis in Asia
inferred← citeshttps://doi.org/10.1016/j.jaci.2021.03.024openalex-snapshot
Rethinking neutrophils and eosinophils in chronic rhinosinusitis
inferred← citeshttps://doi.org/10.1016/j.jaci.2023.11.925openalex-snapshot
Aggregated eosinophils and neutrophils characterize the properties of mucus in chronic rhinosinusitis
inferred← citeshttps://doi.org/10.1016/j.jaci.2023.12.030openalex-snapshot
Galectin-10 in serum extracellular vesicles reflects asthma pathophysiology
inferred← citeshttps://doi.org/10.1016/j.jaci.2025.11.004openalex-snapshot
Aberrant ceramide accumulation fuels eosinophilic inflammation by promoting eosinophil extracellular trap formation and release in chronic rhinosinusitis with nasal polyps
inferred← citeshttps://doi.org/10.1016/j.jaip.2025.11.028openalex-snapshot
Mucus Plugs and Eosinophilic Inflammation: Expanding the Paradigm to COPD
inferred← citeshttps://doi.org/10.1016/j.lfs.2021.119218openalex-snapshot
High chemokine ligand 11 levels in nasal lavage fluid: A potential predictor of and therapeutic target for murine eosinophilic chronic rhinosinusitis
inferred← citeshttps://doi.org/10.1016/j.lfs.2022.121191openalex-snapshot
Eosinophils: Focus on DNA extracellular traps
inferred← citeshttps://doi.org/10.1016/j.mimet.2017.03.015openalex-snapshot
A flow-cytometric method to evaluate eosinophil-mediated uptake of probiotic Lactobacillus reuteri
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2023.108445openalex-snapshot
Pathogenic helper T cells as the novel therapeutic targets for immune-mediated intractable diseases
inferred← citeshttps://doi.org/10.1016/j.rmcr.2019.100975openalex-snapshot
Endobronchial mucosal nodular lesions in allergic bronchopulmonary aspergillosis
inferred← citeshttps://doi.org/10.1016/j.rmcr.2020.101300openalex-snapshot
An unusual case of eosinophilic lung disease with multiple cyst formation
inferred← citeshttps://doi.org/10.1016/j.rmed.2022.107094openalex-snapshot
Quality over quantity; eosinophil activation status will deepen the insight into eosinophilic diseases
inferred← citeshttps://doi.org/10.1016/j.semcancer.2021.07.011openalex-snapshot
Neutrophil extracellular traps in cancer
inferred← citeshttps://doi.org/10.1016/j.tcb.2020.11.005openalex-snapshot
Programmed Cell Death: Central Player in Fungal Infections
inferred← citeshttps://doi.org/10.1016/j.tcb.2026.03.010openalex-snapshot
Eosinophil extracellular traps: heterogeneity of their stimuli, components, and functions
inferred← citeshttps://doi.org/10.1021/acsomega.7b01779openalex-snapshot
Selective Photoinduced Antibacterial Activity of Amoxicillin-Coated Gold Nanoparticles: From One-Step Synthesis to in Vivo Cytocompatibility
inferred← citeshttps://doi.org/10.1038/nri.2017.95openalex-snapshot
Functions of tissue-resident eosinophils
inferred← citeshttps://doi.org/10.1038/s12276-018-0136-8openalex-snapshot
Biological function of eosinophil extracellular traps in patients with severe eosinophilic asthma
inferred← citeshttps://doi.org/10.1038/s41467-024-45029-0openalex-snapshot
Cebp1 and Cebpβ transcriptional axis controls eosinophilopoiesis in zebrafish
inferred← citeshttps://doi.org/10.1038/s41467-025-64276-3openalex-snapshot
Eosinophil CD48 interactions with Candida albicans Als6 is protective in vitro and in mouse systemic candidiasis
inferred← citeshttps://doi.org/10.1038/s41577-024-01048-yopenalex-snapshot
Spatial adaptation of eosinophils and their emerging roles in homeostasis, infection and disease
inferred← citeshttps://doi.org/10.1038/s41577-025-01159-0openalex-snapshot
The immunology of asthma and chronic rhinosinusitis
inferred← citeshttps://doi.org/10.1038/s41581-019-0163-2openalex-snapshot
Extracellular DNA traps in inflammation, injury and healing
inferred← citeshttps://doi.org/10.1038/s41598-019-44627-zopenalex-snapshot
Eosinophil extracellular trap formation is closely associated with disease severity in chronic rhinosinusitis regardless of nasal polyp status
inferred← citeshttps://doi.org/10.1038/s41598-023-32246-8openalex-snapshot
Real-world efficacy of anti-IL-5 treatment in patients with allergic bronchopulmonary aspergillosis
inferred← citeshttps://doi.org/10.1038/s41598-025-24010-xopenalex-snapshot
Eosinophil extracellular traps formation is correlated with cancer prognosis by tumor microenvironment remodeling
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/10.1042/bsr20230410openalex-snapshot
Eosinophil extracellular traps in eosinophilic chronic rhinosinusitis induce Charcot–Leyden crystal formation and eosinophil recruitment
inferred← citeshttps://doi.org/10.1080/01902148.2021.1923864openalex-snapshot
Cysteinyl leukotriene induces eosinophil extracellular trap formation via cysteinyl leukotriene 1 receptor in a murine model of asthma
inferred← citeshttps://doi.org/10.1080/02770903.2024.2312429openalex-snapshot
Rapidly progressive mucus plugs in allergic bronchopulmonary mycosis
inferred← citeshttps://doi.org/10.1080/1744666x.2023.2200164openalex-snapshot
A review of current biomarkers in chronic rhinosinusitis with or without nasal polyps
inferred← citeshttps://doi.org/10.1080/2162402x.2017.1393134openalex-snapshot
Eosinophils: The unsung heroes in cancer?
inferred← citeshttps://doi.org/10.1084/jem.20221212openalex-snapshot
Type 2 inflammation and biological therapies in asthma: Targeted medicine taking flight
inferred← citeshttps://doi.org/10.1089/ars.2023.0329openalex-snapshot
Network of Extracellular Traps in the Pathogenesis of Sterile Chronic Inflammatory Diseases: Role of Oxidative Stress and Potential Clinical Applications
inferred← citeshttps://doi.org/10.1093/cei/uxac038openalex-snapshot
The regulatory role of eosinophils in viral, bacterial, and fungal infections
inferred← citeshttps://doi.org/10.1093/jleuko/qiad143openalex-snapshot
Role of immune cells in the pathogenesis of myocarditis
inferred← citeshttps://doi.org/10.1093/jleuko/qiae010openalex-snapshot
Ally, adversary, or arbitrator? The context-dependent role of eosinophils in vaccination for respiratory viruses and subsequent breakthrough infections
inferred← citeshttps://doi.org/10.1093/jleuko/qiae173openalex-snapshot
Eosinophils as modulators of host defense during parasitic, fungal, bacterial, and viral infections
inferred← citeshttps://doi.org/10.1093/mrcr/rxae046openalex-snapshot
A case of eosinophilic granulomatosis with polyangiitis preceded by allergic bullous lesions
inferred← citeshttps://doi.org/10.1096/fj.201800691ropenalex-snapshot
Peptidylarginine deiminase 4: a nuclear button triggering neutrophil extracellular traps in inflammatory diseases and aging
inferred← citeshttps://doi.org/10.1097/aci.0000000000000588openalex-snapshot
Th2 inflammatory responses in the development of nasal polyps and chronic rhinosinusitis
inferred← citeshttps://doi.org/10.1097/aci.0000000000000956openalex-snapshot
Interaction of eosinophilic and neutrophilic inflammation in patients with chronic rhinosinusitis
inferred← citeshttps://doi.org/10.1097/mao.0000000000004739openalex-snapshot
Eosinophil Extracellular Trap Remnants as Potential Biomarkers for the Diagnosis and Activity Assessment of Otitis Media Associated With Eosinophilic Granulomatosis With Polyangiitis and Eosinophilic Otitis Media
inferred← citeshttps://doi.org/10.1097/md.0000000000039361openalex-snapshot
Plastic bronchitis linked to human bocavirus 1 identified through high-throughput next-generation sequencing: A case report
inferred← citeshttps://doi.org/10.1101/2022.11.15.22282331openalex-snapshot
Aggregated eosinophils characterize airway mucus properties
inferred← citeshttps://doi.org/10.1111/1346-8138.16656openalex-snapshot
Presence of eosinophil extracellular trap cell death in the affected skin of eosinophilic granulomatosis with polyangiitis
inferred← citeshttps://doi.org/10.1111/all.12851openalex-snapshot
sCD48 is anti-inflammatory inStaphylococcus aureusEnterotoxin B-induced eosinophilic inflammation
inferred← citeshttps://doi.org/10.1111/all.13997openalex-snapshot
Eosinophil extracellular traps activate type 2 innate lymphoid cells through stimulating airway epithelium in severe asthma
inferred← citeshttps://doi.org/10.1111/all.14450openalex-snapshot
Lysophosphatidylserine induces eosinophil extracellular trap formation and degranulation: Implications in severe asthma
inferred← citeshttps://doi.org/10.1111/all.14620openalex-snapshot
Adult‐onset eosinophilic airway diseases
inferred← citeshttps://doi.org/10.1111/all.15884openalex-snapshot
Eosinophils—from cradle to grave
inferred← citeshttps://doi.org/10.1111/all.16687openalex-snapshot
Fungal‐Driven Airways Dis‐Immunity From Asthma to Allergic Bronchopulmonary Aspergillosis: Dissecting Similarities and Differences. An EAACI Task Force Report
inferred← citeshttps://doi.org/10.1111/cea.14220openalex-snapshot
Airway autoimmunity, asthma exacerbations, and response to biologics
inferred← citeshttps://doi.org/10.1111/cea.70235openalex-snapshot
Prognostic Significance of Eosinophil Extracellular Traps in Chronic Rhinosinusitis and Innovative Nanosheets‐Based Clearance Therapy
inferred← citeshttps://doi.org/10.1111/myc.13705openalex-snapshot
High attenuation mucus in bronchi with allergic bronchopulmonary mycosis
inferred← citeshttps://doi.org/10.1111/odi.13434openalex-snapshot
Sialodochitis fibrinosa: Salivary duct obstruction by eosinophil extracellular traps?
inferred← citeshttps://doi.org/10.1124/pharmrev.120.000090openalex-snapshot
The Emerging Role of the Innate Immune Response in Idiosyncratic Drug Reactions
inferred← citeshttps://doi.org/10.1146/annurev-pathmechdis-012419-032756openalex-snapshot
Contributions of Eosinophils to Human Health and Disease
inferred← citeshttps://doi.org/10.1146/annurev-pathol-042220-015902openalex-snapshot
The Pathology of Asthma: What Is Obstructing Our View?
inferred← citeshttps://doi.org/10.1160/th17-09-0630openalex-snapshot
The Pathophysiological Role of Neutrophil Extracellular Traps in Inflammatory Diseases
inferred← citeshttps://doi.org/10.1164/rccm.202012-4374imopenalex-snapshot
Charcot–Leyden Crystals in Rapidly Progressing Plastic Bronchitis
inferred← citeshttps://doi.org/10.1165/rcmb.2023-0438ocopenalex-snapshot
Characteristics and Regulation of Human Eosinophil ETosis In Vitro
inferred← citeshttps://doi.org/10.1172/jci127963openalex-snapshot
Allergen presensitization drives an eosinophil-dependent arrest in lung-specific helminth development
inferred← citeshttps://doi.org/10.1172/jci141594openalex-snapshot
Extracellular traps released by antimicrobial TH17 cells contribute to host defense
inferred← citeshttps://doi.org/10.1172/jci84538openalex-snapshot
Neutrophil extracellular traps — the dark side of neutrophils
inferred← citeshttps://doi.org/10.1177/1945892419860646openalex-snapshot
Predictive Significance of Charcot–Leyden Crystals for Eosinophilic Chronic Rhinosinusitis With Nasal Polyps
inferred← citeshttps://doi.org/10.1177/1945892420961964openalex-snapshot
Surgery in Nasal Polyp Patients: Outcome After a Minimum Observation of 10 Years
inferred← citeshttps://doi.org/10.1182/blood-2018-04-842260openalex-snapshot
Charcot-Leyden crystal formation is closely associated with eosinophil extracellular trap cell death
inferred← citeshttps://doi.org/10.1182/bloodadvances.2022009432openalex-snapshot
Lack of eosinophil extracellular trap formation due to failure of plasma membrane breakdown in the absence of elastase
inferred← citeshttps://doi.org/10.1183/13993003.00452-2026openalex-snapshot
Targeting eosinophil extracellular traps in asthma: a new axis for biologic intervention
inferred← citeshttps://doi.org/10.1183/13993003.00470-2019openalex-snapshot
In vivoobservations provide insight into roles of eosinophils and epithelial cells in asthma
inferred← citeshttps://doi.org/10.1183/2312508x.10010216openalex-snapshot
Nasal polyposis and asthma: a mechanistic paradigm focusing on Staphylococcus aureus
inferred← citeshttps://doi.org/10.1183/2312508x.10030020openalex-snapshot
Allergic fungal diseases in the upper and lower airways
inferred← citeshttps://doi.org/10.1183/2312508x.10030720openalex-snapshot
Eosinophils as potential mediators of autoimmunity in eosinophilic lung disease
inferred← citeshttps://doi.org/10.1183/2312508x.10030920openalex-snapshot
Future prospects of translational and clinical eosinophil research
inferred← citeshttps://doi.org/10.1186/s12931-023-02504-4openalex-snapshot
Eosinophil extracellular traps in asthma: implications for pathogenesis and therapy
inferred← citeshttps://doi.org/10.1186/s12931-024-02923-xopenalex-snapshot
The role of extracellular traps released by neutrophils, eosinophils, and macrophages in asthma
inferred← citeshttps://doi.org/10.1186/s12964-025-02217-9openalex-snapshot
Accumulation of long-chain unsaturated fatty acids in the airway inflammatory microenvironment drives eosinophil etosis and corticosteroid resistance
inferred← citeshttps://doi.org/10.1186/s12986-018-0260-4openalex-snapshot
A leukocyte activation test identifies food items which induce release of DNA by innate immune peripheral blood leucocytes
inferred← citeshttps://doi.org/10.1186/s13075-023-03057-zopenalex-snapshot
Expression of S100A8 protein on B cells is associated with disease activity in patients with systemic lupus erythematosus
inferred← citeshttps://doi.org/10.12688/f1000research.11133.1openalex-snapshot
Recent advances in understanding eosinophil biology
inferred← citeshttps://doi.org/10.1371/journal.pone.0152865openalex-snapshot
Proteomic Characterization of Middle Ear Fluid Confirms Neutrophil Extracellular Traps as a Predominant Innate Immune Response in Chronic Otitis Media
inferred← citeshttps://doi.org/10.17116/rosrino201826241openalex-snapshot
The modern trends in the diagnostic search for and the treatment of chronic rhinosinusitis with nasal polyps
inferred← citeshttps://doi.org/10.2147/copd.s115969openalex-snapshot
Evidence of eosinophil extracellular trap cell death in COPD: does it represent the trigger that switches on the disease?
inferred← citeshttps://doi.org/10.2169/internalmedicine.4386-24openalex-snapshot
Allergic Bronchopulmonary Aspergillosis/Mycosis: An Allergic Disease or an Eosinophilic Disease?
inferred← citeshttps://doi.org/10.2169/internalmedicine.7523-26openalex-snapshot
Eosinophils in the immunologic spectrum of Eosinophilic Granulomatosis with Polyangiitis: From Fundamental Pathobiology to Emerging Therapeutic Strategies and Future Perspectives
inferred← citeshttps://doi.org/10.2169/internalmedicine.9339-22openalex-snapshot
Measurement of Blood Eosinophils in Asthma and Chronic Obstructive Pulmonary Disease
inferred← citeshttps://doi.org/10.2169/naika.111.2102openalex-snapshot
IV. Allergic Bronchopulmonary Aspergillosis
inferred← citeshttps://doi.org/10.22263/2312-4156.2019.5.26openalex-snapshot
Eosinophil extracellular traps: their role in health and disease
inferred← citeshttps://doi.org/10.2468/jbes.70.320openalex-snapshot
Eosinophilic Diseases in Otorhinolaryngology
inferred← citeshttps://doi.org/10.2468/jbes.70.341openalex-snapshot
Systemic Eosinophilic Diseases
inferred← citeshttps://doi.org/10.25587/2587-5590-2024-2-17-29openalex-snapshot
EOSINOPHILIC SIALODOCHITIS: DESCRIPTION OF TWO CASES AND LITERATURE REVIEW
inferred← citeshttps://doi.org/10.31579/2693-2156/030openalex-snapshot
Severe Neutrophilic Asthma: Pathogenesis and Treatment
inferred← citeshttps://doi.org/10.33590/emj/htiq1028openalex-snapshot
The Role of IL-5 in Type 2 Inflammatory Diseases
inferred← citeshttps://doi.org/10.3388/jspaci.33.346openalex-snapshot
ETosis
inferred← citeshttps://doi.org/10.3389/falgy.2024.1448007openalex-snapshot
Eosinophil extracellular vesicles and DNA traps in allergic inflammation
inferred← citeshttps://doi.org/10.3389/falgy.2025.1548338openalex-snapshot
Antiviral roles of eosinophils in asthma and respiratory viral infection
inferred← citeshttps://doi.org/10.3389/fimmu.2017.01538openalex-snapshot
Identification of Secretory Leukoprotease Inhibitor As an Endogenous Negative Regulator in Allergic Effector Cells
inferred← citeshttps://doi.org/10.3389/fimmu.2018.02346openalex-snapshot
Allergic Bronchopulmonary Aspergillosis–A Luminal Hypereosinophilic Disease With Extracellular Trap Cell Death
inferred← citeshttps://doi.org/10.3389/fimmu.2018.02763openalex-snapshot
Eosinophil Extracellular Traps and Inflammatory Pathologies—Untangling the Web!
inferred← citeshttps://doi.org/10.3389/fimmu.2019.02767openalex-snapshot
Relevance of Macrophage Extracellular Traps in C. albicans Killing
inferred← citeshttps://doi.org/10.3389/fimmu.2020.594520openalex-snapshot
Host Immunity and Inflammation to Pulmonary Helminth Infections
inferred← citeshttps://doi.org/10.3389/fimmu.2021.621311openalex-snapshot
Multiple Origins of Extracellular DNA Traps
inferred← citeshttps://doi.org/10.3389/fimmu.2021.715766openalex-snapshot
Eosinophils and Neutrophils Eliminate Migrating Strongyloides ratti Larvae at the Site of Infection in the Context of Extracellular DNA Trap Formation
inferred← citeshttps://doi.org/10.3389/fimmu.2021.801897openalex-snapshot
Increased Circulating Cell-Free DNA in Eosinophilic Granulomatosis With Polyangiitis: Implications for Eosinophil Extracellular Traps and Immunothrombosis
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.2022.915392openalex-snapshot
Unveiling Leukocyte Extracellular Traps in Inflammatory Responses of the Central Nervous System
inferred← citeshttps://doi.org/10.3389/fimmu.2022.938691openalex-snapshot
In Vivo ETosis of Human Eosinophils: The Ultrastructural Signature Captured by TEM in Eosinophilic Diseases
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1253964openalex-snapshot
Neutrophil extracellular traps regulating tumorimmunity in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1295921openalex-snapshot
Neutrophil extracellular traps in upper respiratory tract secretions: insights into infectious and allergic rhinitis
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1533407openalex-snapshot
Inhibition of EETosis with an anti-citrullinated histone antibody: a novel therapeutic approach for eosinophilic inflammatory disorders
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1574314openalex-snapshot
Eosinophils as predictive biomarkers in anti-programmed cell death 1 monotherapy for non-small cell lung cancer
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1870612openalex-snapshot
Innate airway immune response to fungal allergens
inferred← citeshttps://doi.org/10.3389/fmicb.2021.633696openalex-snapshot
Structural and Signaling Events Driving Aspergillus fumigatus-Induced Human Eosinophil Extracellular Trap Release
inferred← citeshttps://doi.org/10.3389/fmicb.2021.634043openalex-snapshot
Neutrophil and Eosinophil DNA Extracellular Trap Formation: Lessons From Pathogenic Fungi
inferred← citeshttps://doi.org/10.3389/fmicb.2022.798853openalex-snapshot
Role of Extracellular Trap Release During Bacterial and Viral Infection
inferred← citeshttps://doi.org/10.3389/fonc.2022.869706openalex-snapshot
Extracellular DNA Traps: Origin, Function and Implications for Anti-Cancer Therapies
inferred← citeshttps://doi.org/10.3389/fped.2026.1814321openalex-snapshot
Plastic bronchitis: a narrative review of the classification methods and pathogenesis
inferred← citeshttps://doi.org/10.3390/allergies2040012openalex-snapshot
Proposal for Structured Histopathology of Nasal Secretions for Endotyping Chronic Rhinosinusitis: An Exploratory Study
inferred← citeshttps://doi.org/10.3390/biom12101385openalex-snapshot
Galectin-10 as a Potential Biomarker for Eosinophilic Diseases
inferred← citeshttps://doi.org/10.3390/biomedicines10020431openalex-snapshot
Neutrophil Extracellular Traps, Angiogenesis and Cancer
inferred← citeshttps://doi.org/10.3390/cancers17193250openalex-snapshot
Eosinophil ETosis and Cancer: Ultrastructural Evidence and Oncological Implications
inferred← citeshttps://doi.org/10.3390/cells10030528openalex-snapshot
Interleukin-1α Is a Critical Mediator of the Response of Human Bronchial Fibroblasts to Eosinophilic Inflammation
inferred← citeshttps://doi.org/10.3390/cells10081891openalex-snapshot
The Immune System Throws Its Traps: Cells and Their Extracellular Traps in Disease and Protection
inferred← citeshttps://doi.org/10.3390/cells11213521openalex-snapshot
Neutrophil Extracellular Traps in Asthma: Friends or Foes?
inferred← citeshttps://doi.org/10.3390/cells12232746openalex-snapshot
The Neutralization of the Eosinophil Peroxidase Antibody Accelerates Eosinophilic Mucin Decomposition
showing the first 200 of 248
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.