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Barrier function of the nasal mucosa in health and type‐2 biased airway diseases

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

inferredcites →https://doi.org/10.1001/archotol.129.6.665openalex-snapshot

Expression Patterns of Galectin-1 and Galectin-3 in Nasal Polyps and Middle and Inferior Turbinates in Relation to Growth Regulation and Immunosuppression

inferredcites →https://doi.org/10.1001/jama.2015.19330openalex-snapshot

Effect of Subcutaneous Dupilumab on Nasal Polyp Burden in Patients With Chronic Sinusitis and Nasal Polyposis

inferredcites →https://doi.org/10.1002/lary.22398openalex-snapshot

Microbiome complexity and Staphylococcus aureus in chronic rhinosinusitis

inferredcites →https://doi.org/10.1016/0091-6749(84)90403-2openalex-snapshot

Human respiratory mucus

inferredcites →https://doi.org/10.1016/0091-6749(89)90418-1openalex-snapshot

Major basic protein and eosinophil-derived neurotoxin concentrations in nasal-lavage fluid after antigen challenge: Effect of systemic corticosteroids and relationship to eosinophil influx

inferredcites →https://doi.org/10.1016/j.anl.2008.02.001openalex-snapshot

Toll-like receptor 2, 3, 4, 5 ligands and interleukin-4 synergistically induce TARC production in nasal polyp fibroblasts

inferredcites →https://doi.org/10.1016/j.autrev.2008.11.009openalex-snapshot

The immunological potential of galectin-1 and -3

inferredcites →https://doi.org/10.1016/j.bbrc.2007.08.065openalex-snapshot

Epithelial Na+ channel and ion transport in human nasal polyp and paranasal sinus mucosa

inferredcites →https://doi.org/10.1016/j.clim.2014.09.007openalex-snapshot

Increased ILC2s in the eosinophilic nasal polyp endotype are associated with corticosteroid responsiveness

inferredcites →https://doi.org/10.1016/j.coi.2012.08.010openalex-snapshot

Eosinophil extracellular DNA traps: molecular mechanisms and potential roles in disease

inferredcites →https://doi.org/10.1016/j.immuni.2011.12.020openalex-snapshot

Lung Natural Helper Cells Are a Critical Source of Th2 Cell-Type Cytokines in Protease Allergen-Induced Airway Inflammation

inferredcites →https://doi.org/10.1016/j.immuni.2013.08.021openalex-snapshot

SnapShot: Innate Lymphoid Cells

inferredcites →https://doi.org/10.1016/j.jaci.2009.11.045openalex-snapshot

Evidence for diminished levels of epithelial psoriasin and calprotectin in chronic rhinosinusitis

inferredcites →https://doi.org/10.1016/j.jaci.2010.12.1103openalex-snapshot

Eosinophil and neutrophil extracellular DNA traps in human allergic asthmatic airways

inferredcites →https://doi.org/10.1016/j.jaci.2011.04.060openalex-snapshot

Reduced diversity of the intestinal microbiota during infancy is associated with increased risk of allergic disease at school age

inferredcites →https://doi.org/10.1016/j.jaci.2011.05.038openalex-snapshot

Defective epithelial barrier function in asthma

inferredcites →https://doi.org/10.1016/j.jaci.2011.07.049openalex-snapshot

Pathogenesis of chronic rhinosinusitis: Inflammation

inferredcites →https://doi.org/10.1016/j.jaci.2011.07.056openalex-snapshot

Mepolizumab, a humanized anti–IL-5 mAb, as a treatment option for severe nasal polyposis

inferredcites →https://doi.org/10.1016/j.jaci.2012.03.010openalex-snapshot

The interpersonal and intrapersonal diversity of human-associated microbiota in key body sites

inferredcites →https://doi.org/10.1016/j.jaci.2012.05.052openalex-snapshot

Defective epithelial barrier in chronic rhinosinusitis: The regulation of tight junctions by IFN-γ and IL-4

inferredcites →https://doi.org/10.1016/j.jaci.2012.07.047openalex-snapshot

Omalizumab is effective in allergic and nonallergic patients with nasal polyps and asthma

inferredcites →https://doi.org/10.1016/j.jaci.2014.06.024openalex-snapshot

Enhanced innate type 2 immune response in peripheral blood from patients with asthma

inferredcites →https://doi.org/10.1016/j.jaci.2015.01.043openalex-snapshot

Oncostatin M promotes mucosal epithelial barrier dysfunction, and its expression is increased in patients with eosinophilic mucosal disease

inferredcites →https://doi.org/10.1016/j.meegid.2013.03.013openalex-snapshot

Staphylococcus aureus toxins – Their functions and genetics

inferredcites →https://doi.org/10.1016/j.nano.2013.11.002openalex-snapshot

Antimicrobial protein rBPI21-induced surface changes on Gram-negative and Gram-positive bacteria

inferredcites →https://doi.org/10.1016/j.oraloncology.2010.04.008openalex-snapshot

AG013, a mouth rinse formulation of Lactococcus lactis secreting human Trefoil Factor 1, provides a safe and efficacious therapeutic tool for treating oral mucositis

inferredcites →https://doi.org/10.1016/j.otohns.2007.01.025openalex-snapshot

Sinonasal Surfactant Protein A1, A2, and D Gene Expression in Cystic Fibrosis: A Preliminary Report

inferredcites →https://doi.org/10.1016/j.pupt.2010.12.009openalex-snapshot

TLR agonist mediated suppression of allergic responses is associated with increased innate inflammation in the airways

inferredcites →https://doi.org/10.1016/j.virol.2008.07.024openalex-snapshot

Enhanced expression of murine β-defensins (MBD-1, -2,- 3, and -4) in upper and lower airway mucosa of influenza virus infected mice

inferredcites →https://doi.org/10.1016/s0149-2918(97)80115-4openalex-snapshot

The effect of fluticasone propionate aqueous nasal spray on eosinophils and cytokines in nasal secretions of patients with ragweed allergic rhinitis

inferredcites →https://doi.org/10.1016/s0194-5998(98)70235-9openalex-snapshot

Assessment by Nasal Biopsy of Long‐Term Use of Mometasone Furoate Aqueous Nasal Spray (Nasonex) in the Treatment of Perennial Rhinitis

inferredcites →https://doi.org/10.1016/s1081-1206(10)61503-7openalex-snapshot

Lysozyme levels in the nasal secretions of patients with perennial allergic rhinitis and recurrent sinusitis

inferredcites →https://doi.org/10.1021/bi060176zopenalex-snapshot

Human Pulmonary Surfactant Protein D Binds the Extracellular Domains of Toll-like Receptors 2 and 4 through the Carbohydrate Recognition Domain by a Mechanism Different from Its Binding to Phosphatidylinositol and Lipopolysaccharide

inferredcites →https://doi.org/10.1034/j.1398-9995.2003.00180.xopenalex-snapshot

Human β‐defensins and toll‐like receptors in the upper airway

inferredcites →https://doi.org/10.1038/ni.2104openalex-snapshot

Human IL-25- and IL-33-responsive type 2 innate lymphoid cells are defined by expression of CRTH2 and CD161

inferredcites →https://doi.org/10.1038/ni.2534openalex-snapshot

Human type 1 innate lymphoid cells accumulate in inflamed mucosal tissues

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/nm1638openalex-snapshot

Mrp8 and Mrp14 are endogenous activators of Toll-like receptor 4, promoting lethal, endotoxin-induced shock

inferredcites →https://doi.org/10.1056/nejmoa021481openalex-snapshot

Endogenous Antimicrobial Peptides and Skin Infections in Atopic Dermatitis

inferredcites →https://doi.org/10.1056/nejmoa1402895openalex-snapshot

Effects of an Anti-TSLP Antibody on Allergen-Induced Asthmatic Responses

inferredcites →https://doi.org/10.1056/nejmoa1411776openalex-snapshot

Allergen-Induced Asthmatic Responses Modified by a GATA3-Specific DNAzyme

inferredcites →https://doi.org/10.1056/nejmra0910061openalex-snapshot

Airway Mucus Function and Dysfunction

inferredcites →https://doi.org/10.1073/pnas.0702130104openalex-snapshot

Human β-defensin-3 activates professional antigen-presenting cells via Toll-like receptors 1 and 2

inferredcites →https://doi.org/10.1074/jbc.m309388200openalex-snapshot

Design of Chimeric Receptor Mimics with Different TcRVβ Isoforms

inferredcites →https://doi.org/10.1080/00016480500475625openalex-snapshot

Blocking of protease allergens with inhibitors reduces allergic responses in allergic rhinitis and other allergic diseases

inferredcites →https://doi.org/10.1084/jem.20062027openalex-snapshot

Eosinophil-derived neurotoxin acts as an alarmin to activate the TLR2–MyD88 signal pathway in dendritic cells and enhances Th2 immune responses

inferredcites →https://doi.org/10.1097/00005537-200303000-00023openalex-snapshot

Distribution of Respiratory Mucin Proteins in Human Nasal Mucosa

inferredcites →https://doi.org/10.1097/01.mlg.0000243196.75418.6fopenalex-snapshot

Surfactant Protein D Expression in Chronic Rhinosinusitis Patients and Immune Responses In Vitro to Aspergillus and Alternaria in a Nasal Explant Model

inferredcites →https://doi.org/10.1097/aci.0000000000000120openalex-snapshot

Role of the bitter taste receptor T2R38 in upper respiratory infection and chronic rhinosinusitis

inferredcites →https://doi.org/10.1097/moo.0b013e3283533632openalex-snapshot

Role of innate immunity in the pathogenesis of allergic rhinitis

inferredcites →https://doi.org/10.1100/2012/474020openalex-snapshot

Galectin-10 Is Released in the Nasal Lavage Fluid of Patients with Aspirin-Sensitive Respiratory Disease

inferredcites →https://doi.org/10.1111/all.12374openalex-snapshot

Decreased diversity of nasal microbiota and their secreted extracellular vesicles in patients with chronic rhinosinusitis based on a metagenomic analysis

inferredcites →https://doi.org/10.1111/all.12440openalex-snapshot

Association between Group 2 Innate Lymphoid Cells enrichment, nasal polyps and allergy in Chronic Rhinosinusitis

inferredcites →https://doi.org/10.1111/all.12570openalex-snapshot

Active eosinophilic esophagitis is characterized by epithelial barrier defects and eosinophil extracellular trap formation

inferredcites →https://doi.org/10.1111/all.12627openalex-snapshot

Th2 cytokines impair innate immune responses to rhinovirus in respiratory epithelial cells

inferredcites →https://doi.org/10.1111/cea.12253openalex-snapshot

Low gut microbiota diversity in early infancy precedes asthma at school age

inferredcites →https://doi.org/10.1111/cea.12422openalex-snapshot

The CD48 receptor mediates Staphylococcus aureus human and murine eosinophil activation

inferredcites →https://doi.org/10.1111/cea.12462openalex-snapshot

Group 2 innate lymphoid cells ( ILC 2s) are increased in chronic rhinosinusitis with nasal polyps or eosinophilia

inferredcites →https://doi.org/10.1111/j.1365-2796.2012.02559.xopenalex-snapshot

Chronic rhinosinusitis and asthma: novel understanding of the role of IgE ‘above atopy’

inferredcites →https://doi.org/10.1111/j.1398-9995.2005.00958.xopenalex-snapshot

Pen ch 13 allergen induces secretion of mediators and degradation of occludin protein of human lung epithelial cells

inferredcites →https://doi.org/10.1111/j.1398-9995.2009.02313.xopenalex-snapshot

Staphylococcus aureus enterotoxin B augments granulocyte migration and survival via airway epithelial cell activation

inferredcites →https://doi.org/10.1111/j.1398-9995.2010.02498.xopenalex-snapshot

Alternatively activated macrophages and impaired phagocytosis of S. aureus in chronic rhinosinusitis

inferredcites →https://doi.org/10.1111/j.1398-9995.2011.02598.xopenalex-snapshot

Pollen proteases compromise the airway epithelial barrier through degradation of transmembrane adhesion proteins and lung bioactive peptides

inferredcites →https://doi.org/10.1111/j.1398-9995.2011.02637.xopenalex-snapshot

The association between bacterial colonization and inflammatory pattern in Chinese chronic rhinosinusitis patients with nasal polyps

inferredcites →https://doi.org/10.1111/j.1398-9995.2012.02848.xopenalex-snapshot

Reduced expression of antimicrobial PLUNC proteins in nasal polyp tissues of patients with chronic rhinosinusitis

inferredcites →https://doi.org/10.1111/j.1398-9995.2012.02868.xopenalex-snapshot

Thymic stromal lymphopoietin stimulates the formation of eosinophil extracellular traps

inferredcites →https://doi.org/10.1111/j.1574-695x.2008.00444.xopenalex-snapshot

Differentiated S100A7 expression in infected tonsils and tonsils from allergic individuals

inferredcites →https://doi.org/10.1126/science.1075565openalex-snapshot

Toll-Like Receptor 4-Dependent Activation of Dendritic Cells by β-Defensin 2

inferredcites →https://doi.org/10.1126/science.1152449openalex-snapshot

Metal Chelation and Inhibition of Bacterial Growth in Tissue Abscesses

inferredcites →https://doi.org/10.1126/science.1242255openalex-snapshot

Staphylococcus aureus Degrades Neutrophil Extracellular Traps to Promote Immune Cell Death

inferredcites →https://doi.org/10.1128/iai.72.12.7275-7281.2004openalex-snapshot

Antifungal Immune Reactivity in Nasal Polyposis

inferredcites →https://doi.org/10.1128/iai.73.6.3609-3617.2005openalex-snapshot

Antimicrobial Activity of Murine Lung Cells against Staphylococcus aureus Is Increased In Vitro and In Vivo after Elafin Gene Transfer

inferredcites →https://doi.org/10.1136/thoraxjnl-2011-200750openalex-snapshot

Regulation of inflammatory responses by the commensal microbiota: Figure 1

inferredcites →https://doi.org/10.1146/annurev.pathol.4.110807.092135openalex-snapshot

Epithelial Barriers in Homeostasis and Disease

inferredcites →https://doi.org/10.1155/2013/947072openalex-snapshot

Regulation of Tight Junctions in Upper Airway Epithelium

inferredcites →https://doi.org/10.1164/rccm.201010-1574ocopenalex-snapshot

Dysregulation of Allergic Airway Inflammation in the Absence of Microbial Colonization

inferredcites →https://doi.org/10.1164/rccm.201212-2227ocopenalex-snapshot

IL-33–Responsive Innate Lymphoid Cells Are an Important Source of IL-13 in Chronic Rhinosinusitis with Nasal Polyps

inferredcites →https://doi.org/10.1164/rccm.201406-1039ocopenalex-snapshot

IL-33–Dependent Type 2 Inflammation during Rhinovirus-induced Asthma Exacerbations In Vivo

inferredcites →https://doi.org/10.1165/rcmb.2006-0035sfopenalex-snapshot

Regulation of Mucin Genes in Chronic Inflammatory Airway Diseases

inferredcites →https://doi.org/10.1165/rcmb.2006-0064ocopenalex-snapshot

Epithelial Ion Transport of Human Nasal Polyp and Paranasal Sinus Mucosa

inferredcites →https://doi.org/10.1172/jci64240openalex-snapshot

T2R38 taste receptor polymorphisms underlie susceptibility to upper respiratory infection

inferredcites →https://doi.org/10.1177/147323000803600426openalex-snapshot

Rosiglitazone Attenuates Allergic Inflammation and Inhibits Expression of Galectin-3 in a Mouse Model of Allergic Rhinitis

inferredcites →https://doi.org/10.1183/13993003.00159-2015openalex-snapshot

Differential release and deposition of S100A8/A9 proteins in inflamed upper airway tissue

inferredcites →https://doi.org/10.1186/1465-9921-13-2openalex-snapshot

Diminished levels of nasal S100A7 (psoriasin) in seasonal allergic rhinitis: an effect mediated by Th2 cytokines

inferredcites →https://doi.org/10.1186/1465-9921-6-118openalex-snapshot

Psoriasin, one of several new proteins identified in nasal lavage fluid from allergic and non-allergic individuals using 2-dimensional gel electrophoresis and mass spectrometry

inferredcites →https://doi.org/10.1186/1465-9921-9-29openalex-snapshot

Comprehensive evaluation of genetic variation in S100A7 suggests an association with the occurrence of allergic rhinitis

inferredcites →https://doi.org/10.1189/jlb.0609382openalex-snapshot

Human defensins and LL-37 in mucosal immunity

inferredcites →https://doi.org/10.1371/journal.pone.0024418openalex-snapshot

Microbiological and Molecular Assessment of Bacteriophage ISP for the Control of Staphylococcus aureus

inferredcites →https://doi.org/10.1371/journal.pone.0039875openalex-snapshot

Herpes Simplex Virus Type 1 Infection Facilitates Invasion of Staphylococcus aureus into the Nasal Mucosa and Nasal Polyp Tissue

inferredcites →https://doi.org/10.1371/journal.pone.0082373openalex-snapshot

The Development of Nasal Polyp Disease Involves Early Nasal Mucosal Inflammation and Remodelling

inferredcites →https://doi.org/10.1590/s1808-86942010000200011openalex-snapshot

Expressão dos genes que codificam as proteínas anexina-1 e galectina-1 nos pólipos rinossinusais e sua modulação pelo glicocorticoide

inferredcites →https://doi.org/10.2174/138920108784567236openalex-snapshot

Eosinophil-Derived Neurotoxin / RNase 2: Connecting the Past, the Present and the Future

inferredcites →https://doi.org/10.2500/ajr.2007.21.2997openalex-snapshot

Sinonasal Epithelial Cell Expression of Toll-Like Receptor 9 is Decreased in Chronic Rhinosinusitis with Polyps

inferredcites →https://doi.org/10.2500/ajr.2008.22.3136openalex-snapshot

Th2 Cytokines associated with Chronic Rhinosinusitis with Polyps Down-Regulate the Antimicrobial Immune Function of Human Sinonasal Epithelial Cells

inferredcites →https://doi.org/10.2500/ajra.2009.23.3367openalex-snapshot

Detection of Staphylococcus Aureus in Nasal Tissue with Peptide Nucleic Acid–Fluorescence in Situ Hybridization

inferredcites →https://doi.org/10.2500/ajra.2010.24.3446openalex-snapshot

Treatment-Recalcitrant Chronic Rhinosinusitis with Polyps is Associated with Altered Epithelial Cell Expression of Interleukin-33

inferredcites →https://doi.org/10.2500/ajra.2012.26.3716openalex-snapshot

Acquired Cilia Dysfunction in Chronic Rhinosinusitis

inferredcites →https://doi.org/10.2500/ajra.2014.28.3971openalex-snapshot

Staphylococcus Enterotoxin a Induces Muc5B Expression Via Toll-Like Receptor 2, Extracellular Signal–Regulated Kinase 1/2, and P38 Mitogen-Activated Protein Kinase in Human Airway Epithelial Cells

inferredcites →https://doi.org/10.2500/ajra.2014.28.4024openalex-snapshot

The Importance of Local Eosinophilia in the Surgical Outcome of Chronic Rhinosinusitis: A 3-Year Prospective Observational Study

inferredcites →https://doi.org/10.3109/08830180903197498openalex-snapshot

Modulation of Gut-Associated Lymphoid Tissue Functions with Genetically ModifiedLactococcus lactis

inferredcites →https://doi.org/10.3109/9781420014020-14openalex-snapshot

Staphylococcus aureus Enterotoxins as Immune Stimulants in Chronic Rhinosinusitis

inferredcites →https://doi.org/10.3389/fimmu.2012.00131openalex-snapshot

An Insight into the Diverse Roles of Surfactant Proteins, SP-A and SP-D in Innate and Adaptive Immunity

inferredcites →https://doi.org/10.3389/fimmu.2015.00147openalex-snapshot

Airway Epithelium Interactions with Aeroallergens: Role of Secreted Cytokines and Chemokines in Innate Immunity

inferredcites →https://doi.org/10.4049/jimmunol.1003020openalex-snapshot

The Danger Signal, Extracellular ATP, Is a Sensor for an Airborne Allergen and Triggers IL-33 Release and Innate Th2-Type Responses

inferredcites →https://doi.org/10.4168/aair.2015.7.4.367openalex-snapshot

TMEM16A-Mediated Mucin Secretion in IL-13-Induced Nasal Epithelial Cells From Chronic Rhinosinusitis Patients

inferredcites →https://doi.org/10.4193/rhin15.213openalex-snapshot

Th2 biased upper airway inflammation is associated with an impaired response to viral infection with Herpes simplex virus

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Neutrophils are a major source of the epithelial barrier disrupting cytokine oncostatin M in patients with mucosal airways disease

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Etiology of epithelial barrier dysfunction in patients with type 2 inflammatory diseases

inferred← citeshttps://doi.org/10.1016/j.jaci.2018.05.035openalex-snapshot

Staphylococcus aureus impairs sinonasal epithelial repair: Effects in patients with chronic rhinosinusitis with nasal polyps and control subjects

inferred← citeshttps://doi.org/10.1016/j.jaci.2018.11.021openalex-snapshot

Staphylococcus aureus, epithelial disruption, and nasal polyps: Are we one step ahead in combatting this foe?

inferred← citeshttps://doi.org/10.1016/j.jaci.2019.07.042openalex-snapshot

MUC1 deficiency promotes nasal epithelial barrier dysfunction in subjects with allergic rhinitis

inferred← citeshttps://doi.org/10.1016/j.jaci.2020.06.037openalex-snapshot

Proteomic analysis of nasal mucus samples of healthy patients and patients with chronic rhinosinusitis

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.2021.07.037openalex-snapshot

IL-17A–producing sinonasal MAIT cells in patients with chronic rhinosinusitis with nasal polyps

inferred← citeshttps://doi.org/10.1016/j.jaci.2022.02.016openalex-snapshot

Mechanisms and pathogenesis of chronic rhinosinusitis

inferred← citeshttps://doi.org/10.1016/j.jaci.2022.11.031openalex-snapshot

Alterations of nasal microbiome in eosinophilic chronic rhinosinusitis

inferred← citeshttps://doi.org/10.1016/j.jconrel.2023.02.011openalex-snapshot

Recent advances in respiratory immunization: A focus on COVID-19 vaccines

inferred← citeshttps://doi.org/10.1016/j.jep.2024.118041openalex-snapshot

Mahuang Fuzi Xixin decoction alleviates allergic rhinitis by inhibiting NLRP3/Caspase-1/GSDMD-N-mediated pyroptosis

inferred← citeshttps://doi.org/10.1016/j.jhin.2021.03.023openalex-snapshot

BNT 13b2 Pfizer vaccine protects against SARS-CoV-2 respiratory mucosal colonization even after prolonged exposure to positive family members

inferred← citeshttps://doi.org/10.1016/j.mucimm.2025.08.002openalex-snapshot

Leukotriene B4 regulates T cell recognition and control of MCMV in mucosal tissues

inferred← citeshttps://doi.org/10.1016/j.nbd.2021.105561openalex-snapshot

SARS-CoV-2 deregulates the vascular and immune functions of brain pericytes via Spike protein

inferred← citeshttps://doi.org/10.1016/j.reval.2021.02.001openalex-snapshot

Mechanism of modified Yupingfeng naristillae in protecting the nasal mucosal epithelial barrier during allergic rhinitis

inferred← citeshttps://doi.org/10.1021/acs.jcim.4c00613openalex-snapshot

Breaking Down the Bottlebrush: Atomically Detailed Structural Dynamics of Mucins

inferred← citeshttps://doi.org/10.1021/acssensors.2c01507openalex-snapshot

Bioelectrical Nose Platform Using Odorant-Binding Protein as a Molecular Transporter Mimicking Human Mucosa for Direct Gas Sensing

inferred← citeshttps://doi.org/10.1038/nrmicro.2017.104openalex-snapshot

The commensal lifestyle of Staphylococcus aureus and its interactions with the nasal microbiota

inferred← citeshttps://doi.org/10.1038/s41385-020-00359-2openalex-snapshot

The central role of the nasal microenvironment in the transmission, modulation, and clinical progression of SARS-CoV-2 infection

inferred← citeshttps://doi.org/10.1038/s41541-022-00485-xopenalex-snapshot

Towards the future exploration of mucosal mRNA vaccines against emerging viral diseases; lessons from existing next-generation mucosal vaccine strategies

inferred← citeshttps://doi.org/10.1038/s41572-020-00218-1openalex-snapshot

Adult chronic rhinosinusitis

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/s41598-022-13818-6openalex-snapshot

Construction and analysis of a ceRNA network and patterns of immune infiltration in chronic rhinosinusitis with nasal polyps: based on data mining and experimental verification

inferred← citeshttps://doi.org/10.1080/14656566.2018.1527904openalex-snapshot

Chronic rhinosinusitis: pathogenesis, therapy options, and more

inferred← citeshttps://doi.org/10.1080/1744666x.2019.1601556openalex-snapshot

Epithelial physical barrier defects in chronic rhinosinusitis

inferred← citeshttps://doi.org/10.1080/21688370.2017.1367458openalex-snapshot

Airway epithelial barrier dysfunction in the pathogenesis and prognosis of respiratory tract diseases in childhood and adulthood

inferred← citeshttps://doi.org/10.1088/2516-1091/ad776copenalex-snapshot

A comprehensive review on organ-on-chips as powerful preclinical models to study tissue barriers

inferred← citeshttps://doi.org/10.1093/femsre/fuab041openalex-snapshot

Staphylococcal trafficking and infection—from ‘nose to gut’ and back

inferred← citeshttps://doi.org/10.1093/intimm/dxae002openalex-snapshot

Recent advances in the epithelial barrier theory

inferred← citeshttps://doi.org/10.1097/md.0000000000049863openalex-snapshot

E-cigarette or vaping product use–associated lung injury without pulmonary symptoms: A case report and literature review

inferred← citeshttps://doi.org/10.1111/ahe.70067openalex-snapshot

Descriptive Histology and Anatomy of the Nasal Cavity and Its Associated Sensory Organs in the European Hedgehog ( Erinaceus europaeus ) Based on Four Standardised Transverse Sections

inferred← citeshttps://doi.org/10.1111/all.13489openalex-snapshot

Th2 cytokines orchestrate the secretion of MUC 5 AC and MUC 5B in IL ‐5‐positive chronic rhinosinusitis with nasal polyps

inferred← citeshttps://doi.org/10.1111/all.13824openalex-snapshot

Direct assessment of skin epithelial barrier by electrical impedance spectroscopy

inferred← citeshttps://doi.org/10.1111/all.14044openalex-snapshot

Novel findings in immunopathophysiology of chronic rhinosinusitis and their role in a model of precision medicine

inferred← citeshttps://doi.org/10.1111/all.14067openalex-snapshot

Recent developments and highlights in allergic rhinitis

inferred← citeshttps://doi.org/10.1111/all.16600openalex-snapshot

Dupilumab Treatment Is Associated With Clinical Improvement and a Shift Toward a Health‐Associated Nasal Passage Microbiota in Diffuse Type 2 Chronic Rhinosinusitis

inferred← citeshttps://doi.org/10.1146/annurev-pathol-052016-100401openalex-snapshot

Immunopathogenesis of Chronic Rhinosinusitis and Nasal Polyposis

inferred← citeshttps://doi.org/10.1155/2018/9095275openalex-snapshot

Eosinophils from Physiology to Disease: A Comprehensive Review

inferred← citeshttps://doi.org/10.1165/rcmb.2016-0024ocopenalex-snapshot

Wnt Signaling in Chronic Rhinosinusitis with Nasal Polyps

inferred← citeshttps://doi.org/10.1165/rcmb.2016-0325ocopenalex-snapshot

Potential Involvement of the Epidermal Growth Factor Receptor Ligand Epiregulin and Matrix Metalloproteinase-1 in Pathogenesis of Chronic Rhinosinusitis

inferred← citeshttps://doi.org/10.1172/jci124608openalex-snapshot

Epithelial barrier repair and prevention of allergy

inferred← citeshttps://doi.org/10.1177/0003489419843143openalex-snapshot

The pH Value as a Factor Modifying Bacterial Colonization of Sinonasal Mucosa in Healthy Persons

inferred← citeshttps://doi.org/10.1177/1945892419839538openalex-snapshot

Asian Sand Dust Regulates IL-32 Production in Airway Epithelial Cells: Inhibitory Effect of Glucocorticoids

inferred← citeshttps://doi.org/10.1177/1945892419868588openalex-snapshot

Contribution of Epithelial Cell Dysfunction to the Pathogenesis of Chronic Rhinosinusitis with Nasal Polyps

inferred← citeshttps://doi.org/10.1177/1945892419871795openalex-snapshot

Microarray Assay Reveals Ciliary Abnormalities of the Allergic Nasal Mucosa

inferred← citeshttps://doi.org/10.1177/1945892420983646openalex-snapshot

LPCAT2 Methylation, a Novel Biomarker for the Severity of Cedar Pollen Allergic Rhinitis in Japan

inferred← citeshttps://doi.org/10.1177/19458924211004006openalex-snapshot

Urban Particulate Matters May Affect Endoplasmic Reticulum Stress and Tight Junction Disruption in Nasal Epithelial Cells

inferred← citeshttps://doi.org/10.1177/19458924221090050openalex-snapshot

Chronic Rhinosinusitis and the Increased Incidence of Atopic Dermatitis

inferred← citeshttps://doi.org/10.1177/19458924231154061openalex-snapshot

New Concepts in Barrier Dysfunction in CRSwNP and Emerging Roles of Tezepelumab and Dupilumab

inferred← citeshttps://doi.org/10.1177/19458924231184741openalex-snapshot

Cigarette Smoke Mediates Nasal Epithelial Barrier Dysfunction via TNF-α

inferred← citeshttps://doi.org/10.1183/2312508x.10010016openalex-snapshot

Nasal polyposis and asthma: the otorhinolaryngologist's view

inferred← citeshttps://doi.org/10.1183/2312508x.10010216openalex-snapshot

Nasal polyposis and asthma: a mechanistic paradigm focusing on Staphylococcus aureus

inferred← citeshttps://doi.org/10.1186/s40168-025-02088-9openalex-snapshot

Porcine nasal organoids to model interactions between the swine nasal microbiota and the host

inferred← citeshttps://doi.org/10.1186/s40168-026-02357-1openalex-snapshot

Dysbiosis of the nasal microbiome is associated with prospective acute exacerbation of COPD

inferred← citeshttps://doi.org/10.1186/s43163-026-01057-9openalex-snapshot

Efficacy of nasal steroid irrigation in chronic rhinosinusitis after sinus surgery: a meta-analysis study

inferred← citeshttps://doi.org/10.13201/j.issn.2096-7993.2020.11.024openalex-snapshot

[The role of epithelial cells in the formation and development of nasal polyps].

inferred← citeshttps://doi.org/10.1371/journal.pone.0157058openalex-snapshot

Diesel Exhaust Particles Upregulate Interleukins IL-6 and IL-8 in Nasal Fibroblasts

inferred← citeshttps://doi.org/10.1371/journal.pone.0328241openalex-snapshot

Single cell transcriptomic analysis reveals transcriptome differences of different cells between eosinophilic chronic rhinosinusitis with nasal polyps and non-eosinophilic chronic rhinosinusitis with nasal polyps

inferred← citeshttps://doi.org/10.14639/0392-100x-2361openalex-snapshot

Multiple gene expression profiling suggests epithelial dysfunction in polypoid chronic rhinosinusitis

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/10.20538/1682-0363-2017-2-32-46openalex-snapshot

The role of barrier function of mucous membranes in allergic diseases and sublingual allergen-specific immunotherapy

inferred← citeshttps://doi.org/10.2147/jaa.s535065openalex-snapshot

Inhibition of LOXL2 Suppresses Nasal Mucosal Inflammation and Remodeling in Allergic Rhinitis

inferred← citeshttps://doi.org/10.2147/jaa.s542695openalex-snapshot

PP2A Promotes Epithelial-Mesenchymal Transition in Chronic Rhinosinusitis with Nasal Polyps via Wnt/β-Catenin Pathway: A Novel Insight

inferred← citeshttps://doi.org/10.2147/jir.s345664openalex-snapshot

EGF Protects Epithelial Cells from Barrier Damage in Chronic Rhinosinusitis with Nasal Polyps

inferred← citeshttps://doi.org/10.2147/jir.s567454openalex-snapshot

Association of Increased Nasal Fluids-Serum Concordance of Protein Profile with Prognosis in Nasal Polyps

inferred← citeshttps://doi.org/10.2174/9789815324570125010005openalex-snapshot

Nasal Vaccination: Breaking New Ground in Immune Response

inferred← citeshttps://doi.org/10.22529/me.2017.2(1)02openalex-snapshot

Mecanismos de la conexión nariz-pulmón

inferred← citeshttps://doi.org/10.22541/au.170664764.47596455/v1openalex-snapshot

The effect of MG53 for modulating TGF-β1/Smad pathway in the nasal epithelial repair of nasal polyps.

inferred← citeshttps://doi.org/10.23866/brnrev:2017-0049openalex-snapshot

Cigarette Smoke Exposure Alters Bacterial-Host Interactions in the Respiratory Tract to Promote Disease

inferred← citeshttps://doi.org/10.23866/brnrev:2017-m0049openalex-snapshot

Cigarette Smoke Exposure Alters Bacterial-Host Interactions in the Respiratory Tract to Promote Disease

inferred← citeshttps://doi.org/10.24875/brn.m17000016openalex-snapshot

Cigarette Smoke Exposure Alters Bacterial-Host Interactions in the Respiratory Tract to Promote Disease

inferred← citeshttps://doi.org/10.3233/adr-170017openalex-snapshot

Genetic, Transcriptome, Proteomic, and Epidemiological Evidence for Blood-Brain Barrier Disruption and Polymicrobial Brain Invasion as Determinant Factors in Alzheimer’s Disease

inferred← citeshttps://doi.org/10.3389/falgy.2024.1387774openalex-snapshot

Genetic correlation between chronic sinusitis and autoimmune diseases

inferred← citeshttps://doi.org/10.3389/fimmu.2022.879575openalex-snapshot

H1N1 Influenza Virus-Infected Nasal Mucosal Epithelial Progenitor Cells Promote Dendritic Cell Recruitment and Maturation

inferred← citeshttps://doi.org/10.3389/fimmu.2023.1224129openalex-snapshot

Recent advances in understanding the effects of T lymphocytes on mucosal barrier function in allergic rhinitis

inferred← citeshttps://doi.org/10.3389/fimmu.2024.1354556openalex-snapshot

The last step to achieve barrier damage control

inferred← citeshttps://doi.org/10.3389/fped.2026.1931883openalex-snapshot

Advances and mechanisms in the application and treatment of functionalized stem cells and their derivatives in allergic rhinitis

inferred← citeshttps://doi.org/10.3390/biology12091223openalex-snapshot

Exploring the Immune Response against RSV and SARS-CoV-2 Infection in Children

inferred← citeshttps://doi.org/10.3390/biomedicines12020408openalex-snapshot

A Novel Bionebulizer Approach to Study the Effects of Natural Mineral Water on a 3D In Vitro Nasal Model from Allergic Rhinitis Patients

inferred← citeshttps://doi.org/10.3390/diagnostics13040808openalex-snapshot

Airway Epithelium: A Neglected but Crucial Cell Type in Asthma Pathobiology

inferred← citeshttps://doi.org/10.3390/ijerph18189905openalex-snapshot

Effects of Air Pollutants on Airway Diseases

inferred← citeshttps://doi.org/10.3390/jpm14010098openalex-snapshot

The Relationship between Fine Particle Matter (PM2.5) Exposure and Upper Respiratory Tract Diseases

inferred← citeshttps://doi.org/10.3390/life13051088openalex-snapshot

The Protecting Activity of RIPACUT®: A New Therapeutic Approach Preserving Epithelial Health Based on the Combination of Iceland Lichen Extract, Silver Salt, and Sodium Hyaluronate

inferred← citeshttps://doi.org/10.3390/liquids5020011openalex-snapshot

Enhancing Physiological Realism in Nasal Spray Deposition Studies: Synthetic Mucus Properties and Interactions with Saline Solutions and Stereolithography Resin

inferred← citeshttps://doi.org/10.3390/microorganisms9091965openalex-snapshot

Respiratory and Neurological Disease across Different Ethnic Groups Is Influenced by the Microbiome

inferred← citeshttps://doi.org/10.3390/pathogens8030106openalex-snapshot

Airway Epithelial Derived Cytokines and Chemokines and Their Role in the Immune Response to Respiratory Syncytial Virus Infection

inferred← citeshttps://doi.org/10.3390/reports8020066openalex-snapshot

Unilateral Palpebral Edema as a Central Sign of Acute Enterobacter-Associated Rhinosinusitis in a 5-Year-Old: A Rare Pediatric Case

inferred← citeshttps://doi.org/10.33920/med-12-2601-01openalex-snapshot

The effect of local anthropogenic pollution of a metropolis on refractory chronic rhinosinusitis

inferred← citeshttps://doi.org/10.34883/pi.2025.15.4.029openalex-snapshot

Эпидемиология полипозного риносинусита в условиях урбанизации мегаполиса с развитой тяжелой индустрией

inferred← citeshttps://doi.org/10.4081/ejh.2020.3079openalex-snapshot

Can the AGE/RAGE/ERK signalling pathway and the epithelial-to-mesenchymal transition interact in the pathogenesis of chronic rhinosinusitis with nasal polyps?

inferred← citeshttps://doi.org/10.4081/mrm.2023.939openalex-snapshot

Local allergic rhinitis: considerations

inferred← citeshttps://doi.org/10.4110/in.2017.17.1.60openalex-snapshot

Immune Cell Responses and Mucosal Barrier Disruptions in Chronic Rhinosinusitis

inferred← citeshttps://doi.org/10.4168/aair.2017.9.4.299openalex-snapshot

Emerging Endotypes of Chronic Rhinosinusitis and Its Application to Precision Medicine

inferred← citeshttps://doi.org/10.4168/aair.2021.13.6.850openalex-snapshot

The Impact of Environmental Pollutants on Barrier Dysfunction in Respiratory Disease

inferred← citeshttps://doi.org/10.4168/aair.2023.15.4.512openalex-snapshot

Predictive Significance of Claudin-3 for Epithelial Barrier Dysfunction in Chronic Rhinosinusitis With Nasal Polyps

inferred← citeshttps://doi.org/10.4168/aair.2025.17.2.212openalex-snapshot

Platelet-Activating Factor Disrupts the Nasal Epithelial Barrier Independently of the Platelet-Activating Factor Receptor Pathway

inferred← citeshttps://doi.org/10.4193/rhin18.128openalex-snapshot

Novel roles for nasal epithelium in the pathogenesis of chronic rhinosinusitis with nasal polyps

inferred← citeshttps://doi.org/10.4193/rhin20.034openalex-snapshot

Scoping review of chronic rhinosinusitis proteomics

inferred← citeshttps://doi.org/10.4193/rhin21.046openalex-snapshot

Differences and similarities between the upper and lower airway: focusing on innate immunity

inferred← citeshttps://doi.org/10.4193/rhin21.287openalex-snapshot

Association between the use of electronic cigarettes and the prevalence of chronic rhinosinusitis and allergic rhinitis: a nationwide cross-sectional study

inferred← citeshttps://doi.org/10.4274/turkderm.galenos.2022.90132openalex-snapshot

Evaluation of COVID-19 risk in patients on systemic retinoid therapy

inferred← citeshttps://doi.org/10.53846/goediss-8336openalex-snapshot

Occurence and characteristics of allergic rhinitis in 195 patients with chronic rhinosinusitis

inferred← citeshttps://doi.org/10.7287/peerj.9834v0.1/reviews/1openalex-snapshot

Peer Review #1 of "Zonula occludens and nasal epithelial barrier integrity in allergic rhinitis (v0.1)"

inferred← citeshttps://doi.org/10.7717/peerj.9834openalex-snapshot

Zonula occludens and nasal epithelial barrier integrity in allergic rhinitis

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.