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Benzo(a)pyrene facilitates dermatophagoides group 1 (Der f 1)‐induced epithelial cytokine release through aryl hydrocarbon receptor in asthma
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ajim.20887openalex-snapshot
The IARC october 2009 evaluation of benzene carcinogenicity was incomplete and needs to be reconsidered
inferredcites →https://doi.org/10.1002/jat.3308openalex-snapshot
Low‐dose benzo[a]pyrene aggravates allergic airway inflammation in mice
inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/398_2017_3openalex-snapshot
A Global Perspective of Fine Particulate Matter Pollution and Its Health Effects
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Role of the Aryl Hydrocarbon Receptor in the Pathogenesis of Chronic Rhinosinusitis with Nasal Polyps
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Diesel Exhaust Particle-Exposed Human Bronchial Epithelial Cells Induce Dendritic Cell Maturation and Polarization via Thymic Stromal Lymphopoietin
inferredcites →https://doi.org/10.1016/j.cdtm.2018.04.001openalex-snapshot
Effects of particulate matter on allergic respiratory diseases
inferredcites →https://doi.org/10.1016/j.clim.2012.03.001openalex-snapshot
Dynamic role of epithelium-derived cytokines in asthma
inferredcites →https://doi.org/10.1016/j.coi.2015.02.001openalex-snapshot
Epithelial cytokines and pulmonary allergic inflammation
inferredcites →https://doi.org/10.1016/j.ecoenv.2018.01.038openalex-snapshot
Use of GLM approach to assess the responses of tropical trees to urban air pollution in relation to leaf functional traits and tree characteristics
inferredcites →https://doi.org/10.1016/j.envint.2017.01.021openalex-snapshot
Air pollution, PM 2.5 composition, source factors, and respiratory symptoms in asthmatic and nonasthmatic children in Santiago, Chile
inferredcites →https://doi.org/10.1016/j.envres.2018.02.039openalex-snapshot
Plasticizer, di(2-ethylhexyl)phthalate (DEHP) enhances cockroach allergen extract-driven airway inflammation by enhancing pulmonary Th2 as well as Th17 immune responses in mice
inferredcites →https://doi.org/10.1016/j.febslet.2005.01.081openalex-snapshot
ERK‐dependent induction of TNFα expression by the environmental contaminant benzo(a)pyrene in primary human macrophages
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2017.08.020openalex-snapshot
Elimination of dysfunctional mitochondria through mitophagy suppresses benzo[a]pyrene-induced apoptosis
inferredcites →https://doi.org/10.1016/j.immuni.2017.12.012openalex-snapshot
Regulation of the Immune Response by the Aryl Hydrocarbon Receptor
inferredcites →https://doi.org/10.1016/j.jaci.2008.09.022openalex-snapshot
Cigarette smoke extract induces thymic stromal lymphopoietin expression, leading to TH2-type immune responses and airway inflammation
inferredcites →https://doi.org/10.1016/j.jaci.2013.07.036openalex-snapshot
Measures of gene expression in sputum cells can identify TH2-high and TH2-low subtypes of asthma
inferredcites →https://doi.org/10.1016/j.jaci.2013.10.047openalex-snapshot
A mouse model links asthma susceptibility to prenatal exposure to diesel exhaust
inferredcites →https://doi.org/10.1016/j.jaci.2014.04.002openalex-snapshot
Diesel exhaust particle exposure during pregnancy promotes development of asthma and atopy
inferredcites →https://doi.org/10.1016/j.jaci.2014.11.043openalex-snapshot
Exposure to allergen and diesel exhaust particles potentiates secondary allergen-specific memory responses, promoting asthma susceptibility
inferredcites →https://doi.org/10.1016/j.jaci.2017.06.013openalex-snapshot
Functional role of kynurenine and aryl hydrocarbon receptor axis in chronic rhinosinusitis with nasal polyps
inferredcites →https://doi.org/10.1016/j.jaci.2018.04.042openalex-snapshot
Vitamin D supplementation attenuates asthma development following traffic-related particulate matter exposure
inferredcites →https://doi.org/10.1016/j.jaci.2018.08.023openalex-snapshot
Ras homolog family member A/Rho-associated protein kinase 1 signaling modulates lineage commitment of mesenchymal stem cells in asthmatic patients through lymphoid enhancer–binding factor 1
inferredcites →https://doi.org/10.1016/j.tox.2004.02.029openalex-snapshot
The ex vivo study of synergistic effects of polycyclic aromatic hydrocarbon, benzo(a)pyrene with ovalbumin on systemic immune responses by oral route
inferredcites →https://doi.org/10.1016/j.tox.2011.10.012openalex-snapshot
Alleviation of lung injury by glycyrrhizic acid in benzo(a)pyrene exposed rats: Probable role of soluble epoxide hydrolase and thioredoxin reductase
inferredcites →https://doi.org/10.1016/j.toxlet.2005.01.002openalex-snapshot
The cumulative activity of benzo(a)pyrene on systemic immune responses with mite allergen extract after intranasal instillation and ex vivo response to ovalbumin in mice
inferredcites →https://doi.org/10.1016/j.vph.2005.09.005openalex-snapshot
Lysophosphatidylcholine-induced elevation of asymmetric dimethylarginine level by the NADPH oxidase pathway in endothelial cells
inferredcites →https://doi.org/10.1016/s0140-6736(14)60617-6openalex-snapshot
Outdoor air pollution and asthma
inferredcites →https://doi.org/10.1021/acs.est.5b03709openalex-snapshot
Ambient Air Pollution Exposure Estimation for the Global Burden of Disease 2013
inferredcites →https://doi.org/10.1021/ol101040popenalex-snapshot
Intramolecular Fe(II)-Catalyzed N−O or N−N Bond Formation from Aryl Azides
inferredcites →https://doi.org/10.1021/tx7001965openalex-snapshot
The Search for Endogenous Activators of the Aryl Hydrocarbon Receptor
inferredcites →https://doi.org/10.1038/36285openalex-snapshot
Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
inferredcites →https://doi.org/10.1038/nature06880openalex-snapshot
Control of Treg and TH17 cell differentiation by the aryl hydrocarbon receptor
inferredcites →https://doi.org/10.1038/nature06881openalex-snapshot
The aryl hydrocarbon receptor links TH17-cell-mediated autoimmunity to environmental toxins
inferredcites →https://doi.org/10.1038/nature13323openalex-snapshot
Aryl hydrocarbon receptor control of a disease tolerance defence pathway
inferredcites →https://doi.org/10.1038/nature13684openalex-snapshot
AhR sensing of bacterial pigments regulates antibacterial defence
inferredcites →https://doi.org/10.1038/ni.2617openalex-snapshot
TH2, allergy and group 2 innate lymphoid cells
inferredcites →https://doi.org/10.1038/s41590-018-0107-1openalex-snapshot
Apoptotic cell–induced AhR activity is required for immunological tolerance and suppression of systemic lupus erythematosus in mice and humans
inferredcites →https://doi.org/10.1042/bsr20171577openalex-snapshot
Identification of abnormally expressed lncRNAs induced by PM2.5 in human bronchial epithelial cells
inferredcites →https://doi.org/10.1046/j.1365-2222.2000.00845.xopenalex-snapshot
Der p 1 and Der f 1, the highly related and major allergens from house dust mites, are differentially affected by a plant cystatin
inferredcites →https://doi.org/10.1074/jbc.m601192200openalex-snapshot
Aryl Hydrocarbon Receptor- and Calcium-dependent Induction of the Chemokine CCL1 by the Environmental Contaminant Benzo[a]pyrene
inferredcites →https://doi.org/10.1084/jem.20090560openalex-snapshot
Aryl hydrocarbon receptor in combination with Stat1 regulates LPS-induced inflammatory responses
inferredcites →https://doi.org/10.1093/eep/dvy020openalex-snapshot
Diesel exhaust and house dust mite allergen lead to common changes in the airway methylome and hydroxymethylome
inferredcites →https://doi.org/10.1111/all.12593openalex-snapshot
IL ‐33 drives airway hyper‐responsiveness through IL ‐13‐mediated mast cell: airway smooth muscle crosstalk
inferredcites →https://doi.org/10.1111/all.13462openalex-snapshot
Aryl hydrocarbon receptor activation by diesel exhaust particles mediates epithelium‐derived cytokines expression in severe allergic asthma
inferredcites →https://doi.org/10.1111/all.13784openalex-snapshot
Benzo(a)pyrene facilitates dermatophagoides group 1 (Der f 1)‐induced epithelial cytokine release through aryl hydrocarbon receptor in asthma
inferredcites →https://doi.org/10.1111/cea.12200openalex-snapshot
Diesel exhaust particle exposure increases severity of allergic asthma in young mice
inferredcites →https://doi.org/10.1111/j.0022-202x.2005.23910.xopenalex-snapshot
Cutaneous, But Not Airway, Latex Exposure Induces Allergic Lung Inflammation and Airway Hyperreactivity in Mice
inferredcites →https://doi.org/10.1111/j.1365-2567.2009.03054.xopenalex-snapshot
The aryl hydrocarbon receptor: a perspective on potential roles in the immune system
inferredcites →https://doi.org/10.1111/j.1399-3038.2010.01034.xopenalex-snapshot
Intrauterine exposure to polycyclic aromatic hydrocarbons, fine particulate matter and early wheeze. Prospective birth cohort study in 4-year olds
inferredcites →https://doi.org/10.1124/mol.112.083303openalex-snapshot
Aryl Hydrocarbon Receptor Modulates NADPH Oxidase Activity via Direct Transcriptional Regulation of p40phox Expression
inferredcites →https://doi.org/10.1126/scitranslmed.3006135openalex-snapshot
CaMKII Is Essential for the Proasthmatic Effects of Oxidation
inferredcites →https://doi.org/10.1126/scitranslmed.aaf1938openalex-snapshot
Combinatorial targeting of TSLP, IL-25, and IL-33 in type 2 cytokine–driven inflammation and fibrosis
inferredcites →https://doi.org/10.1128/iai.00575-16openalex-snapshot
The Aryl Hydrocarbon Receptor Modulates Production of Cytokines and Reactive Oxygen Species and Development of Myocarditis during Trypanosoma cruzi Infection
inferredcites →https://doi.org/10.1146/annurev.pa.35.040195.001515openalex-snapshot
The ARYL Hydrocarbon Receptor Complex
inferredcites →https://doi.org/10.1152/ajplung.00208.2006openalex-snapshot
Nonhematopoietic NADPH oxidase regulation of lung eosinophilia and airway hyperresponsiveness in experimentally induced asthma
inferredcites →https://doi.org/10.1155/2014/591479openalex-snapshot
Aryl Hydrocarbon Receptor (AhR) Modulates Cockroach Allergen-Induced Immune Responses through Active TGFβ1 Release
inferredcites →https://doi.org/10.1164/ajrccm.156.3.9606031openalex-snapshot
Noninvasive Measurement of Airway Responsiveness in Allergic Mice Using Barometric Plethysmography
inferredcites →https://doi.org/10.1164/rccm.201211-1987ocopenalex-snapshot
In-Home Air Pollution Is Linked to Respiratory Morbidity in Former Smokers with Chronic Obstructive Pulmonary Disease
inferredcites →https://doi.org/10.1164/rccm.201410-1852ocopenalex-snapshot
Ozone, Fine Particulate Matter, and Chronic Lower Respiratory Disease Mortality in the United States
inferredcites →https://doi.org/10.1165/rcmb.2013-0519ocopenalex-snapshot
Mitochondrial-Targeted Antioxidant Therapy Decreases Transforming Growth Factor-β–Mediated Collagen Production in a Murine Asthma Model
inferredcites →https://doi.org/10.1172/jci.insight.88297openalex-snapshot
Mitochondrial CaMKII inhibition in airway epithelium protects against allergic asthma
inferredcites →https://doi.org/10.1172/jci.insight.90139openalex-snapshot
Oxidized CaMKII promotes asthma through the activation of mast cells
inferredcites →https://doi.org/10.1177/0960327116650009openalex-snapshot
Amelioration of Benzo[a]pyrene-induced oxidative stress and pulmonary toxicity by Naringenin in Wistar rats: A plausible role of COX-2 and NF-κB
inferredcites →https://doi.org/10.1182/blood-2012-08-453597openalex-snapshot
Aryl hydrocarbon receptor controls murine mast cell homeostasis
inferredcites →https://doi.org/10.1186/1465-9921-11-7openalex-snapshot
Mouse models to unravel the role of inhaled pollutants on allergic sensitization and airway inflammation
inferredcites →https://doi.org/10.1186/1743-8977-7-41openalex-snapshot
Diesel exhaust particles induce CYP1A1 and pro-inflammatory responses via differential pathways in human bronchial epithelial cells
inferredcites →https://doi.org/10.1186/1745-6673-4-17openalex-snapshot
Airborne particulate matter PM2.5 from Mexico City affects the generation of reactive oxygen species by blood neutrophils from asthmatics: an in vitro approach
inferredcites →https://doi.org/10.1371/journal.pone.0051268openalex-snapshot
Neutralization of TSLP Inhibits Airway Remodeling in a Murine Model of Allergic Asthma Induced by Chronic Exposure to House Dust Mite
inferredcites →https://doi.org/10.21037/jtd.2017.01.05openalex-snapshot
Recent developments in the role of reactive oxygen species in allergic asthma
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/10.3892/mmr.2018.8998openalex-snapshot
Overexpression of Annexin A1 protects against benzo[a]pyrene‑induced bronchial epithelium injury
inferredcites →https://doi.org/10.4049/jimmunol.1000719openalex-snapshot
Diesel Exhaust Particle-Treated Human Bronchial Epithelial Cells Upregulate Jagged-1 and OX40 Ligand in Myeloid Dendritic Cells via Thymic Stromal Lymphopoietin
inferredcites →https://doi.org/10.4049/jimmunol.1701167openalex-snapshot
miR-155 Modulates Cockroach Allergen– and Oxidative Stress–Induced Cyclooxygenase-2 in Asthma
inferredcites →https://doi.org/10.4049/jimmunol.174.12.8183openalex-snapshot
Thymic Stromal Lymphopoietin Expression Is Increased in Asthmatic Airways and Correlates with Expression of Th2-Attracting Chemokines and Disease Severity
inferredcites →https://doi.org/10.4049/jimmunol.1800709openalex-snapshot
Bronchial Allergen Challenge of Patients with Atopic Asthma Triggers an Alarmin (IL-33, TSLP, and IL-25) Response in the Airways Epithelium and Submucosa
inferredcites →https://doi.org/10.4049/jimmunol.181.4.2790openalex-snapshot
Expression and Cellular Provenance of Thymic Stromal Lymphopoietin and Chemokines in Patients with Severe Asthma and Chronic Obstructive Pulmonary Disease
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.4816437openalex-extracted
Gene Expression Profiles to Clarify the Effect of Low-Dose Benzo(A)Pyrene on Crystalline Silica Induced Acute Lung Injury
inferred← citeshttps://doi.org/10.1002/jat.4017openalex-snapshot
Activation of aryl hydrocarbon receptor by benzo[a]pyrene increases interleukin 33 expression and eosinophil infiltration in a mouse model of allergic airway inflammation
inferred← citeshttps://doi.org/10.1002/jat.4458openalex-snapshot
Biological impact of sequential exposures to allergens and ultrafine particle‐rich combustion aerosol on human bronchial epithelial BEAS‐2B cells at the air liquid interface
inferred← citeshttps://doi.org/10.1002/tox.23907openalex-snapshot
Wogonin alleviates BaP‐induced DNA damage and oxidative stress in human airway epithelial cells by dual inhibiting CYP1A1 activity and expression
inferred← citeshttps://doi.org/10.1002/tox.23957openalex-snapshot
2,2′,4,4′‐Tetrabromodiphenyl ether and cadmium co‐exposure activates aryl hydrocarbon receptor pathway to induce ROS and GSDME ‐dependent pyroptosis in renal tubular epithelial cells
inferred← citeshttps://doi.org/10.1007/s10565-022-09706-4openalex-snapshot
Transcriptomic analysis in zebrafish larvae identifies iron-dependent mitochondrial dysfunction as a possible key event of NAFLD progression induced by benzo[a]pyrene/ethanol co-exposure
inferred← citeshttps://doi.org/10.1016/j.cbi.2022.109845openalex-snapshot
Ligand-independent activation of AhR by hydroquinone mediates benzene-induced hematopoietic toxicity
inferred← citeshttps://doi.org/10.1016/j.cellimm.2023.104694openalex-snapshot
Fine particulate matter (PM2.5) induces inhibitory memory alveolar macrophages through the AhR/IL-33 pathway
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.125356openalex-snapshot
Maternal 1-nitropyrene exposure during pregnancy increases susceptibility of allergic asthma in adolescent offspring
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2021.112570openalex-snapshot
miR-122–5p regulates hepatocytes damage caused by BaP and DBP co-exposure through SOCS1/STAT3 signaling in vitro
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2021.113138openalex-snapshot
Ticlopidine induces cardiotoxicity in zebrafish embryos through AHR-mediated oxidative stress signaling pathway
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.113833openalex-snapshot
Autocrine TGF-alpha is associated with Benzo(a)pyrene-induced mucus production and MUC5AC expression during allergic asthma
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.117095openalex-snapshot
Chrysene contribution to bronchial asthma: Activation of TRPA1 disrupts bronchial epithelial barrier via ERK pathway
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2026.120415openalex-snapshot
Benzo(a)pyrene aggregating lung inflammation via inducing IL1R1 expression in asthma: Insights from network toxicology, single-cell transcriptomics, and Mendelian randomization
inferred← citeshttps://doi.org/10.1016/j.envint.2022.107209openalex-snapshot
Alkyl organophosphate flame retardants (OPFRs) induce lung inflammation and aggravate OVA-simulated asthmatic response via the NF-кB signaling pathway
inferred← citeshttps://doi.org/10.1016/j.envint.2026.110557openalex-snapshot
Benzo[a]pyrene and bisphenol A interact to induce combined pulmonary toxicity through an integrated transcriptomic-metabolomic network
inferred← citeshttps://doi.org/10.1016/j.envpol.2024.124580openalex-snapshot
Gene expression profiles to clarify the effect of low-dose benzo(a)pyrene on crystalline silica induced acute lung injury in mice
inferred← citeshttps://doi.org/10.1016/j.envpol.2025.127557openalex-snapshot
Benzo(a)pyrene exposure aggravates airway remodeling in asthma by activating AhR-GDF15 pathway in epithelial cells
inferred← citeshttps://doi.org/10.1016/j.etap.2021.103782openalex-snapshot
The impact of benzo[a]pyrene on murine allergic airway inflammation via epigenetic remodeling
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e38029openalex-snapshot
NOX2 mediates NLRP3/ROS facilitating nasal mucosal epithelial inflammation in chronic rhinosinusitis with nasal polyps
inferred← citeshttps://doi.org/10.1016/j.jaci.2019.10.008openalex-snapshot
Particulate matter of 2.5 μm or less in diameter disturbs the balance of TH17/regulatory T cells by targeting glutamate oxaloacetate transaminase 1 and hypoxia-inducible factor 1α in an asthma model
inferred← citeshttps://doi.org/10.1016/j.jaci.2020.08.033openalex-snapshot
CaMKII oxidation regulates cockroach allergen–induced mitophagy in asthma
inferred← citeshttps://doi.org/10.1016/j.jaci.2024.01.016openalex-snapshot
Impact of climate change on immune responses and barrier defense
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Qufeng Xuanbi Formula inhibited benzo[a]pyrene-induced aggravated asthma airway mucus secretion by AhR/ROS/ERK pathway
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2021.126069openalex-snapshot
Detrimental effects of microplastic exposure on normal and asthmatic pulmonary physiology
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.135542openalex-snapshot
Coke oven emissions exacerbate allergic asthma by promoting ferroptosis in airway epithelial cells
inferred← citeshttps://doi.org/10.1016/j.jphs.2021.09.006openalex-snapshot
L-type amino acid transporter 1 as a target for inflammatory disease and cancer immunotherapy
inferred← citeshttps://doi.org/10.1016/j.jtauto.2022.100177openalex-snapshot
Effect of polycyclic aromatic hydrocarbons on immunity
inferred← citeshttps://doi.org/10.1016/j.mam.2021.101026openalex-snapshot
Molecular mechanisms of oxidative stress in asthma
inferred← citeshttps://doi.org/10.1016/j.mvr.2021.104179openalex-snapshot
Benzo(α)pyrene induces oxidative stress and inflammation in human vascular endothelial cells through AhR and NF-κB pathways
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.135097openalex-snapshot
AHR-mediated ROS production contributes to the cardiac developmental toxicity of PM2.5 in zebrafish embryos
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.148029openalex-snapshot
The aggravation of allergic airway inflammation with dibutyl phthalate involved in Nrf2-mediated activation of the mast cells
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.151965openalex-snapshot
Benzo(a)pyrene induces airway epithelial injury through Wnt5a-mediated non-canonical Wnt-YAP/TAZ signaling
inferred← citeshttps://doi.org/10.1016/j.tox.2021.152965openalex-snapshot
AHR/ROS-mediated mitochondria apoptosis contributes to benzo[a]pyrene-induced heart defects and the protective effects of resveratrol
inferred← citeshttps://doi.org/10.1021/acsomega.1c02929openalex-snapshot
Biological Response-Enhancing Activity with Antigens in A549 Cells Exposed to Representative Polycyclic Aromatic Hydrocarbons
inferred← citeshttps://doi.org/10.1038/s41598-023-46455-8openalex-snapshot
Identification of genetic biomarkers, drug targets and agents for respiratory diseases utilising integrated bioinformatics approaches
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PIP-seq identifies novel heterogeneous lung innate lymphocyte population activation after combustion product exposure
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Involvement of autophagy in exacerbation of eosinophilic airway inflammation in a murine model of obese asthma
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Aryl hydrocarbon receptor: Linking environment to aging process in elderly patients with asthma
inferred← citeshttps://doi.org/10.1097/mcp.0000000000000644openalex-snapshot
Asthma and air pollution: recent insights in pathogenesis and clinical implications
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Role of IL‐25, IL‐33, and TSLP in triggering united airway diseases toward type 2 inflammation
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Advances and recent developments in asthma in 2020
inferred← citeshttps://doi.org/10.1111/all.70489openalex-snapshot
Epithelial AhR – NKX3 ‐1–Senescence Axis Drives Barrier Function and Inflammation in Allergic Rhinitis
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Mechanisms of Formation and Persistence of IgE Products and Potential Innovative Means of Therapy for Allergic Pathologies
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Adjuvant Effect of Benzo(a)pyrene on Specific IgE Production and B-Cell Subpopulations in Lungs, Regional Lymph Nodes, and Spleen in Mouse Allergy Model
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The Role and Potential Pathogenic Mechanism of Particulate Matter in Childhood Asthma: A Review and Perspective
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Benzo[a]pyrene aggravates atopic dermatitis-like skin lesions in mice
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Association between polycyclic aromatic hydrocarbons exposure and current asthma: a population-based study
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Potential role of polycyclic aromatic hydrocarbons in air pollution-induced non-malignant respiratory diseases
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Fine particulate matter contributes to COPD-like pathophysiology: experimental evidence from rats exposed to diesel exhaust particles
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Inhaled tea polyphenol-loaded nanoparticles coated with platelet membranes largely attenuate asthmatic inflammation
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Evaluation of the Impact of BaP Exposure on the Gut Microbiota and Allergic Responses in an OVA-Sensitized Mouse Model
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The Effects and Pathogenesis of PM2.5 and Its Components on Chronic Obstructive Pulmonary Disease
inferred← citeshttps://doi.org/10.2147/jaa.s288052openalex-snapshot
Impact of Annual Exposure to Polycyclic Aromatic Hydrocarbons on Acute Exacerbation Frequency in Asthmatic Patients
inferred← citeshttps://doi.org/10.28940/terra.v41i0.1719openalex-snapshot
Importancia del Benzo(a)pireno en los sistemas biológicos y su biodegradación
inferred← citeshttps://doi.org/10.29413/abs.2025-10.1.4openalex-snapshot
In regards to lipoxins as lipid mediators for the resolution of inflammation using the example of asthma
inferred← citeshttps://doi.org/10.31857/s0132342324060106openalex-snapshot
The adjuvant effect of benzo(a)pyrene on specific IgE production is linked with the accumulation of germinal center B cells within the spleen and extrafollicular b-cells ativation within the lungs
inferred← citeshttps://doi.org/10.31857/s0555109923060028openalex-snapshot
Mechanisms of Formation and Persistence of Ige Products and Potential Innovative Means of Therapy for Allergic Pathologies
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The role of the triad of respiratory epithelial cell-derived cytokines in the pathogenesis of allergic rhinitis
inferred← citeshttps://doi.org/10.3389/fimmu.2019.02787openalex-snapshot
Environmental Exposures and Asthma Development: Autophagy, Mitophagy, and Cellular Senescence
inferred← citeshttps://doi.org/10.3389/fimmu.2021.643260openalex-snapshot
Benzo(a)pyrene Enhanced Dermatophagoides Group 1 (Der f 1)-Induced TGFβ1 Signaling Activation Through the Aryl Hydrocarbon Receptor–RhoA Axis in Asthma
inferred← citeshttps://doi.org/10.3389/fimmu.2021.767508openalex-snapshot
Epithelial Aryl Hydrocarbon Receptor Protects From Mucus Production by Inhibiting ROS-Triggered NLRP3 Inflammasome in Asthma
inferred← citeshttps://doi.org/10.3389/fimmu.2022.1099509openalex-snapshot
Vanadium exposure exacerbates allergic airway inflammation and remodeling through triggering reactive oxidative stress
inferred← citeshttps://doi.org/10.3389/fimmu.2022.964575openalex-snapshot
Type II alveolar epithelial cell aryl hydrocarbon receptor protects against allergic airway inflammation through controlling cell autophagy
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1099509openalex-snapshot
Vanadium exposure exacerbates allergic airway inflammation and remodeling through triggering reactive oxidative stress
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1156493openalex-snapshot
Transcriptomic signatures reveal a shift towards an anti-inflammatory gene expression profile but also the induction of type I and type II interferon signaling networks through aryl hydrocarbon receptor activation in murine macrophages
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1699886openalex-snapshot
Benzo[a]pyrene exacerbates allergen-induced airway inflammation through NLRP3-dependent dendritic cell activation and pathogenic T helper cell polarization
inferred← citeshttps://doi.org/10.3389/fmed.2021.783720openalex-snapshot
Proximity to Heavy Traffic Roads and Patient Characteristics of Late of Onset Asthma in an Urban Asthma Center
inferred← citeshttps://doi.org/10.3389/fonc.2022.1009508openalex-snapshot
Inhibition of RNF182 mediated by Bap promotes non-small cell lung cancer progression
inferred← citeshttps://doi.org/10.3390/atmos12070898openalex-snapshot
Air Pollution and the Airways: Lessons from a Century of Human Urbanization
inferred← citeshttps://doi.org/10.3390/ijms21228797openalex-snapshot
The Aryl Hydrocarbon Receptor in Asthma: Friend or Foe?
inferred← citeshttps://doi.org/10.3390/ijms23031516openalex-snapshot
The Aryl Hydrocarbon Receptor (AHR): A Novel Therapeutic Target for Pulmonary Diseases?
inferred← citeshttps://doi.org/10.3390/ijms23126719openalex-snapshot
Aryl Hydrocarbon Receptor in Oxidative Stress as a Double Agent and Its Biological and Therapeutic Significance
inferred← citeshttps://doi.org/10.3390/molecules25225384openalex-snapshot
Biseugenol Exhibited Anti-Inflammatory and Anti-Asthmatic Effects in an Asthma Mouse Model of Mixed-Granulocytic Asthma
inferred← citeshttps://doi.org/10.3390/molecules26113127openalex-snapshot
Lycopene Inhibits Toll-Like Receptor 4-Mediated Expression of Inflammatory Cytokines in House Dust Mite-Stimulated Respiratory Epithelial Cells
inferred← citeshttps://doi.org/10.3892/mmr.2020.11617openalex-snapshot
Differentially expressed circular RNAs in a murine asthma model
inferred← citeshttps://doi.org/10.6084/m9.figshare.26660732openalex-snapshot
Additional file 1 of Fine particulate matter contributes to COPD-like pathophysiology: experimental evidence from rats exposed to diesel exhaust particles
inferred← citeshttps://doi.org/10.70675/1a09963fzaa28z454cz91c3zb9dedffddc20openalex-snapshot
Impact d'une exposition aux nanoparticules de carbone couplées au benzo(a)pyrène sur la réponse inflammatoire dans des modèles expérimentaux d'asthme
inferred← citeshttps://doi.org/10.7150/thno.75100openalex-snapshot
XBP1 is required in Th2 polarization induction in airway allergy
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