On the public citation graph

Airway Remodelling in Asthma: From Benchside to Clinical Practice

https://doi.org/10.1155/2010/318029

0 signed · 431 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1007/s11882-004-0054-9openalex-snapshot

Airway smooth muscle and fibroblasts in the pathogenesis of asthma

inferredcites →https://doi.org/10.1016/0014-2999(94)00679-2openalex-snapshot

Effects of glucocorticoids and β-adrenoceptor agonists on the proliferation of airway smooth muscle

inferredcites →https://doi.org/10.1016/0091-6749(91)90160-popenalex-snapshot

Eosinophils, T-lymphocytes, mast cells, neutrophils, and macrophages in bronchial biopsy specimens from atopic subjects with asthma: Comparison with biopsy specimens from atopic subjects without asthma and normal control subjects and relationship to bronchial hyperresponsiveness

inferredcites →https://doi.org/10.1016/0091-6749(92)90079-hopenalex-snapshot

Nasal beclomethasone prevents the seasonal increase in bronchial responsiveness in patients with allergic rhinitis and asthma

inferredcites →https://doi.org/10.1016/0091-6749(93)90301-uopenalex-snapshot

Treatment of allergic rhinitis with intranasal corticosteroids in patients with mild asthma: Effect on lower airway responsiveness

inferredcites →https://doi.org/10.1016/j.jaci.2003.09.047openalex-snapshot

Allergic rhinitis

inferredcites →https://doi.org/10.1016/j.jaci.2003.11.001openalex-snapshot

Amb a 1–immunostimulatory oligodeoxynucleotide conjugate immunotherapy decreases the nasal inflammatory response

inferredcites →https://doi.org/10.1016/j.jaci.2007.02.018openalex-snapshot

Connective tissue growth factor expression is regulated by histamine in lung fibroblasts: Potential role of histamine in airway remodeling

inferredcites →https://doi.org/10.1016/j.tice.2004.12.002openalex-snapshot

Attachment of columnar airway epithelial cells in asthma

inferredcites →https://doi.org/10.1016/s0091-6749(00)90070-8openalex-snapshot

IL-11 expression is increased in severe asthma: Association with epithelial cells and eosinophils

inferredcites →https://doi.org/10.1016/s0091-6749(03)01634-8openalex-snapshot

Airway structural alterations selectively associated with severe asthma

inferredcites →https://doi.org/10.1016/s0091-6749(99)70370-2openalex-snapshot

Perennial rhinitis: An independent risk factor for asthma in nonatopic subjects☆☆☆★Results from the European Community Respiratory Health Survey

inferredcites →https://doi.org/10.1016/s0091-6749(99)70379-9openalex-snapshot

Inhaled corticosteroids decrease subepithelial collagen deposition by modulation of the balance between matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 expression in asthma☆☆☆

inferredcites →https://doi.org/10.1016/s0091-6749(99)70460-4openalex-snapshot

Relationships between duration of asthma and asthma severity among children in the Childhood Asthma Management Program (CAMP)

inferredcites →https://doi.org/10.1016/s0091-6749(99)70469-0openalex-snapshot

Increase in IL-8, IL-10, IL-13, and RANTES mRNA levels (in situ hybridization) in the nasal mucosa after nasal allergen provocation

inferredcites →https://doi.org/10.1016/s0140-6736(00)03496-6openalex-snapshot

Effects of an interleukin-5 blocking monoclonal antibody on eosinophils, airway hyper-responsìveness, and the late asthmatic response

inferredcites →https://doi.org/10.1016/s0140-6736(89)90067-6openalex-snapshot

SUBEPITHELIAL FIBROSIS IN THE BRONCHI OF ASTHMATICS

inferredcites →https://doi.org/10.1016/s0954-6111(03)00136-7openalex-snapshot

Airway inflammation and basement membrane tenascin in newly diagnosed atopic and nonatopic asthma

inferredcites →https://doi.org/10.1016/s1094-5539(03)00068-3openalex-snapshot

Concentration-dependent effects of mometasone furoate and dexamethasone on foetal lung fibroblast functions involved in airway inflammation and remodeling

inferredcites →https://doi.org/10.1016/s1357-2725(02)00058-4openalex-snapshot

Correlation between airway responsiveness and proteoglycan production by bronchial fibroblasts from normal and asthmatic subjects

inferredcites →https://doi.org/10.1034/j.1398-9995.1999.00957.xopenalex-snapshot

Cellular infiltration and cytokine mRNA expression in perennial allergic rhinitis

inferredcites →https://doi.org/10.1034/j.1399-3003.1999.14a12.xopenalex-snapshot

Asymptomatic airway hyperresponsiveness: relationships with airway inflammation and remodelling

inferredcites →https://doi.org/10.1038/emm.2006.14openalex-snapshot

The effects of low dose leukotriene receptor antagonist therapy on airway remodeling and cysteinyl leukotriene expression in a mouse asthma model

inferredcites →https://doi.org/10.1046/j.1365-2222.1997.600864.xopenalex-snapshot

The measurement of reticular basement membrane and submucosal collagen in the asthmatic airway

inferredcites →https://doi.org/10.1046/j.1365-2222.2001.00964.xopenalex-snapshot

Effects of monotherapy with intra-nasal corticosteroid or combined oral histamine and leukotriene receptor antagonists in seasonal allergic rhinitis

inferredcites →https://doi.org/10.1046/j.1365-2222.2001.01160.xopenalex-snapshot

An open audit of montelukast, a leukotriene receptor antagonist, in nasal polyposis associated with asthma

inferredcites →https://doi.org/10.1046/j.1365-2222.2003.01785.xopenalex-snapshot

Regulation of procollagen I (α1) by interleukin‐4 in human bronchial fibroblasts: a possible role in airway remodelling in asthma

inferredcites →https://doi.org/10.1046/j.1440-1681.2001.03426.xopenalex-snapshot

Annual Scientific Meeting of ASCEPT, 1999 Role Of Human Airway Smooth Muscle In Altered Extracellular Matrix Production In Asthma

inferredcites →https://doi.org/10.1056/nejm199409153311103openalex-snapshot

Effects of Reducing or Discontinuing Inhaled Budesonide in Patients with Mild Asthma

inferredcites →https://doi.org/10.1056/nejm199810223391703openalex-snapshot

A 15-Year Follow-up Study of Ventilatory Function in Adults with Asthma

inferredcites →https://doi.org/10.1056/nejm199912233412603openalex-snapshot

Treatment of Allergic Asthma with Monoclonal Anti-IgE Antibody

inferredcites →https://doi.org/10.1056/nejm200010123431501openalex-snapshot

Long-Term Effects of Budesonide or Nedocromil in Children with Asthma

inferredcites →https://doi.org/10.1056/nejmoa064707openalex-snapshot

Asthma Control during the Year after Bronchial Thermoplasty

inferredcites →https://doi.org/10.1067/mai.2001.111928openalex-snapshot

Expression of vascular endothelial growth factor, basic fibroblast growth factor, and angiogenin immunoreactivity in asthmatic airways and its relationship to angiogenesis

inferredcites →https://doi.org/10.1067/mai.2001.112027openalex-snapshot

Grass pollen immunotherapy for seasonal rhinitis and asthma: A randomized, controlled trial

inferredcites →https://doi.org/10.1067/mai.2001.117929openalex-snapshot

IL-17 is increased in asthmatic airways and induces human bronchial fibroblasts to produce cytokines

inferredcites →https://doi.org/10.1067/mai.2001.118891openalex-snapshot

Allergic Rhinitis and Its Impact on Asthma

inferredcites →https://doi.org/10.1067/mai.2002.121701openalex-snapshot

Rhinitis as an independent risk factor for adult-onset asthma

inferredcites →https://doi.org/10.1067/mai.2002.129371openalex-snapshot

CpG-oligodeoxynucleotides inhibit airway remodeling in a murine model of chronic asthma

inferredcites →https://doi.org/10.1067/mai.2002.129429openalex-snapshot

Airway smooth muscle: An immunomodulatory cell

inferredcites →https://doi.org/10.1067/mai.2003.1414openalex-snapshot

Polarized in vivo expression of IL-11 and IL-17 between acute and chronic skin lesions

inferredcites →https://doi.org/10.1067/mai.2003.1464openalex-snapshot

Subepithelial basement membrane immunoreactivity for matrix metalloproteinase 9: Association with asthma severity, neutrophilic inflammation, and wound repair

inferredcites →https://doi.org/10.1067/mai.2003.1557openalex-snapshot

Airway remodeling-associated mediators in moderate to severe asthma: Effect of steroids on TGF-β, IL-11, IL-17, and type I and type III collagen expression

inferredcites →https://doi.org/10.1081/jas-100105868openalex-snapshot

Matrix Metalloproteinases and Tissue lnhibitors of Matrix Metalloproteinases in Sputum from Patients with Bronchial Asthma

inferredcites →https://doi.org/10.1084/jem.172.3.921openalex-snapshot

Generation of interleukin 4 (IL-4)-producing cells in vivo and in vitro: IL-2 and IL-4 are required for in vitro generation of IL-4-producing cells.

inferredcites →https://doi.org/10.1093/oxfordjournals.bmb.a072537openalex-snapshot

Pathology of asthma

inferredcites →https://doi.org/10.1097/01.lab.0000035023.53893.b6openalex-snapshot

Airway Obstruction Correlates with Collagenase-2 (MMP-8) Expression and Activation in Bronchial Asthma

inferredcites →https://doi.org/10.1097/01.wox.0000301298.92527.81openalex-snapshot

Antiproliferative and anti remodelling effect of beclomethasone dipropionate, formoterol and salbutamol alone or in combination in primary human bronchial fibroblasts

inferredcites →https://doi.org/10.1097/aci.0b013e328013d61bopenalex-snapshot

The role of epithelial injury and repair in the origins of asthma

inferredcites →https://doi.org/10.1097/mcp.0b013e3282f333c8openalex-snapshot

New interventions in asthma including bronchial thermoplasty

inferredcites →https://doi.org/10.1111/j.1398-9995.2007.01582.xopenalex-snapshot

Anti‐proliferative and anti‐remodelling effect of beclomethasone dipropionate, formoterol and salbutamol alone or in combination in primary human bronchial fibroblasts

inferredcites →https://doi.org/10.1111/j.1476-5381.1995.tb15127.xopenalex-snapshot

The effect of glucocorticoids on proliferation of human cultured airway smooth muscle

inferredcites →https://doi.org/10.1111/j.1476-5381.1996.tb15744.xopenalex-snapshot

Corticosteroid modulation of Na +‐K+ pump‐mediated relaxation in maturing airway smooth muscle

inferredcites →https://doi.org/10.1124/jpet.103.053819openalex-snapshot

Inhibition of Inflammation and Remodeling by Roflumilast and Dexamethasone in Murine Chronic Asthma

inferredcites →https://doi.org/10.1136/thorax.57.3.247openalex-snapshot

High resolution computed tomographic assessment of airway wall thickness in chronic asthma: reproducibility and relationship with lung function and severity

inferredcites →https://doi.org/10.1136/thorax.57.4.309openalex-snapshot

Airway inflammation, basement membrane thickening and bronchial hyperresponsiveness in asthma

inferredcites →https://doi.org/10.1136/thx.17.1.69openalex-snapshot

The Shedding of the Mucosa of the Bronchial Tree in Asthma

inferredcites →https://doi.org/10.1136/thx.47.7.499openalex-snapshot

The site of disruption of the bronchial epithelium in asthmatic and non-asthmatic subjects.

inferredcites →https://doi.org/10.1136/thx.51.5.496openalex-snapshot

Relationship between the inflammatory infiltrate in bronchial biopsy specimens and clinical severity of asthma in patients treated with inhaled steroids.

inferredcites →https://doi.org/10.1136/thx.52.4.310openalex-snapshot

Airway wall remodelling in asthma

inferredcites →https://doi.org/10.1136/thx.53.1.21openalex-snapshot

Expression of growth factors and remodelling of the airway wall in bronchial asthma

inferredcites →https://doi.org/10.1152/ajplung.1993.265.4.l360openalex-snapshot

Corticosteroids differentially regulate secretion of IL-6, IL-8, and G-CSF by a human bronchial epithelial cell line

inferredcites →https://doi.org/10.1152/ajplung.1999.276.3.l412openalex-snapshot

Modulation of human airway smooth muscle proliferation by type 3 phosphodiesterase inhibition

inferredcites →https://doi.org/10.1152/ajplung.1999.277.6.l1109openalex-snapshot

Autocrine production of matrix metalloproteinase-2 is required for human airway smooth muscle proliferation

inferredcites →https://doi.org/10.1152/jappl.2001.91.3.1035openalex-snapshot

On the functional consequences of bronchial basement membrane thickening

inferredcites →https://doi.org/10.1152/japplphysiol.00662.2001openalex-snapshot

Relationship of airway narrowing, compliance, and cartilage in isolated bronchial segments

inferredcites →https://doi.org/10.1152/physrev.1997.77.4.1033openalex-snapshot

Mast cells

inferredcites →https://doi.org/10.1155/2004/271362openalex-snapshot

Adult Asthma Consensus Guidelines Update 2003

inferredcites →https://doi.org/10.1159/000070434openalex-snapshot

Immunological and Clinical Changes in Allergic Asthmatics following Treatment with Omalizumab

inferredcites →https://doi.org/10.1159/000452828openalex-snapshot

Successful Treatment of a Bullous Pemphigoid Patient with Rituximab Who Was Refractory to Corticosteroid and Omalizumab Treatments

inferredcites →https://doi.org/10.1161/01.atv.0000100402.69997.c3openalex-snapshot

Matrix Metalloproteinase-2 and −9 Differentially Regulate Smooth Muscle Cell Migration and Cell-Mediated Collagen Organization

inferredcites →https://doi.org/10.1161/01.res.0000111527.42357.62openalex-snapshot

Matrix Metalloproteinase-9 Is Required for Adequate Angiogenic Revascularization of Ischemic Tissues

inferredcites →https://doi.org/10.1164/ajrccm.150.1.8025745openalex-snapshot

Placebo-Controlled Immunopathologic Study of Four Months of Inhaled Corticosteroids in Asthma

inferredcites →https://doi.org/10.1164/ajrccm.151.6.7767539openalex-snapshot

Immunomodulation by Theophylline in Asthma. Demonstration by Withdrawal of Therapy

inferredcites →https://doi.org/10.1164/ajrccm.153.2.8564096openalex-snapshot

Prednisolone Treatment in Asthma. Reduction in the Numbers of Eosinophils, T Cells, Tryptase-Only Positive Mast Cells, and Modulation of IL-4, IL-5, and Interferon-Gamma Cytokine Gene Expression Within the Bronchial Mucosa

inferredcites →https://doi.org/10.1164/ajrccm.155.6.9196087openalex-snapshot

Effect of Short-Term Treatment With Low-Dose Inhaled Fluticasone Propionate on Airway Inflammation and Remodeling in Mild Asthma: A Placebo-Controlled Study

inferredcites →https://doi.org/10.1164/ajrccm.156.1.9607066openalex-snapshot

Increased Vascularity of the Bronchial Mucosa in Mild Asthma

inferredcites →https://doi.org/10.1164/ajrccm.156.3.9610084openalex-snapshot

Tenascin Is Increased in Airway Basement Membrane of Asthmatics and Decreased by an Inhaled Steroid

inferredcites →https://doi.org/10.1164/ajrccm.158.6.9803014openalex-snapshot

Sputum Metalloproteinase-9/Tissue Inhibitor of Metalloproteinase-1 Ratio Correlates with Airflow Obstruction in Asthma and Chronic Bronchitis

inferredcites →https://doi.org/10.1164/ajrccm.159.3.9712144openalex-snapshot

Morphometric Analysis of Bronchial Cartilage in Chronic Obstructive Pulmonary Disease and Bronchial Asthma

inferredcites →https://doi.org/10.1164/ajrccm.159.4.9708080openalex-snapshot

Contribution of 92 kDa Gelatinase/Type IV Collagenase in Bronchial Inflammation during Status Asthmaticus

inferredcites →https://doi.org/10.1164/ajrccm.159.4.9806052openalex-snapshot

Clinical Control and Histopathologic Outcome of Asthma when Using Airway Hyperresponsiveness as an Additional Guide to Long-Term Treatment

inferredcites →https://doi.org/10.1164/ajrccm.160.2.9809040openalex-snapshot

Enhanced Proteoglycan Deposition in the Airway Wall of Atopic Asthmatics

inferredcites →https://doi.org/10.1164/ajrccm.160.6.9808146openalex-snapshot

Interleukin-4 Receptor in Moderate Atopic Asthma: A Phase I/II Randomized, Placebo-controlled Trial

inferredcites →https://doi.org/10.1164/ajrccm.160.6.9812100openalex-snapshot

Risk Factors for Growth and Decline of Lung Function in Asthmatic Individuals up to Age 42 years: A 30-year Follow-up Study

inferredcites →https://doi.org/10.1164/ajrccm.161.supplement_2.a1q4-4openalex-snapshot

Airway Remodeling in Asthma: Unanswered Questions

inferredcites →https://doi.org/10.1164/ajrccm.162.4.9910051openalex-snapshot

Airway Hyperresponsiveness, Inflammation, and Subepithelial Collagen Deposition in Recently Diagnosed versus Long-standing Mild Asthma

inferredcites →https://doi.org/10.1164/ajrccm.162.6.2001041openalex-snapshot

Epithelial Desquamation in Asthma

inferredcites →https://doi.org/10.1164/ajrccm.164.1.2006003openalex-snapshot

Effect of a Long-acting β2-Agonist over Three Months on Airway Wall Vascular Remodeling in Asthma

inferredcites →https://doi.org/10.1164/ajrccm.164.10.2103013openalex-snapshot

Apoptosis of Airway Epithelial Cells Induced by Corticosteroids

inferredcites →https://doi.org/10.1164/ajrccm.165.1.2105051openalex-snapshot

A Role for Cysteinyl Leukotrienes in Airway Remodeling in a Mouse Asthma Model

inferredcites →https://doi.org/10.1164/ajrccm/140.6.1745openalex-snapshot

Bronchial Biopsies in Asthma: An Ultrastructural, Quantitative Study and Correlation with Hyperreactivity

inferredcites →https://doi.org/10.1164/ajrccm/143.2.423openalex-snapshot

Eosinophilic Airway Inflammation during Exacerbation of Asthma and Its Treatment with Inhaled Corticosteroid

inferredcites →https://doi.org/10.1164/ajrccm/145.3.669openalex-snapshot

Effect of an Inhaled Corticosteroid on Airway Inflammation and Symptoms in Asthma

inferredcites →https://doi.org/10.1164/ajrccm/147.2.405openalex-snapshot

The Structure of Large and Small Airways in Nonfatal and Fatal Asthma

inferredcites →https://doi.org/10.1164/arrd.1985.131.4.599openalex-snapshot

Damage of the Airway Epithelium and Bronchial Reactivity in Patients with Asthma

inferredcites →https://doi.org/10.1164/rccm.200205-414ocopenalex-snapshot

Early Thickening of the Reticular Basement Membrane in Children with Difficult Asthma

inferredcites →https://doi.org/10.1164/rccm.200205-455ocopenalex-snapshot

In Vivo and In Vitro Effects of SAR 943, a Rapamycin Analogue, on Airway Inflammation and Remodeling

inferredcites →https://doi.org/10.1164/rccm.200206-509ocopenalex-snapshot

Effects of Montelukast and Budesonide on Airway Responses and Airway Inflammation in Asthma

inferredcites →https://doi.org/10.1164/rccm.200209-1030ocopenalex-snapshot

Airway Structural Alterations Selectively Associated with Severe Asthma

inferredcites →https://doi.org/10.1164/rccm.200306-727ocopenalex-snapshot

Increased Airway Vascularity in Newly Diagnosed Asthma Using a High-magnification Bronchovideoscope

inferredcites →https://doi.org/10.1164/rccm.200312-1651ocopenalex-snapshot

Effects of Treatment with Anti-immunoglobulin E Antibody Omalizumab on Airway Inflammation in Allergic Asthma

inferredcites →https://doi.org/10.1164/rccm.200507-1162ocopenalex-snapshot

Bronchial Thermoplasty for Asthma

inferredcites →https://doi.org/10.1164/rccm.200704-571ocopenalex-snapshot

Safety and Efficacy of Bronchial Thermoplasty in Symptomatic, Severe Asthma

inferredcites →https://doi.org/10.1164/rccm.2108069openalex-snapshot

The Relationship of Reticular Basement Membrane Thickness to Airway Wall Remodeling in Asthma

inferredcites →https://doi.org/10.1164/rccm.2109012openalex-snapshot

Interleukin-2–induced Increased Airway Responsiveness and Lung Th2 Cytokine Expression Occur after Antigen Challenge through the Leukotriene Pathway

inferredcites →https://doi.org/10.1165/ajrcmb.17.3.2733openalex-snapshot

Eosinophil-associated TGF-β1 mRNA Expression and Airways Fibrosis in Bronchial Asthma

inferredcites →https://doi.org/10.1165/ajrcmb.17.5.2562openalex-snapshot

Increased Release of Matrix Metalloproteinase-9 in Bronchoalveolar Lavage Fluid and by Alveolar Macrophages of Asthmatics

inferredcites →https://doi.org/10.1165/ajrcmb.23.2.3999openalex-snapshot

Airway Subepithelial Fibrosis in a Murine Model of Atopic Asthma: Suppression by Dexamethasone or Anti–Interleukin-5 Antibody

inferredcites →https://doi.org/10.1172/jci17974openalex-snapshot

Anti-IL-5 treatment reduces deposition of ECM proteins in the bronchial subepithelial basement membrane of mild atopic asthmatics

inferredcites →https://doi.org/10.1172/jci5809openalex-snapshot

Regulation of TH1- and TH2-type cytokine expression and action in atopic asthmatic sensitized airway smooth muscle

inferredcites →https://doi.org/10.1172/jci8124openalex-snapshot

Airway remodeling in asthma

inferredcites →https://doi.org/10.1177/000992280104000513openalex-snapshot

Long-Term Effects of Budesonide or Nedocromil in Children with Asthma

inferredcites →https://doi.org/10.1183/09031936.00019906openalex-snapshot

Tools used to measure airway remodelling in research

inferredcites →https://doi.org/10.1183/09031936.93.05080945openalex-snapshot

Inhaled beclomethasone improves the course of asthma and COPD

inferredcites →https://doi.org/10.1183/09031936.94.07030519openalex-snapshot

Pulmonary immune cells in health and disease: the eosinophil leucocyte (Part I)

inferredcites →https://doi.org/10.1183/09031936.94.07040743openalex-snapshot

Pulmonary immune cells in health and disease: the eosinophil leucocyte (Part II)

inferredcites →https://doi.org/10.1378/chest.101.4.916openalex-snapshot

Marked Goblet Cell Hyperplasia with Mucus Accumulation in the Airways of Patients Who Died of Severe Acute Asthma Attack

inferredcites →https://doi.org/10.1378/chest.108.5.1228openalex-snapshot

Effect of Early vs Late Intervention With Inhaled Corticosteroids in Asthma

inferredcites →https://doi.org/10.1378/chest.111.4.852openalex-snapshot

Airways Remodeling Is a Distinctive Feature of Asthma and Is Related to Severity of Disease

inferredcites →https://doi.org/10.1378/chest.112.1.45openalex-snapshot

Bronchial Subepithelial Fibrosis Correlates With Airway Responsiveness to Methacholine

inferredcites →https://doi.org/10.1378/chest.122.5.1543openalex-snapshot

Matrix Metalloproteinase-9 Expression in Asthma

inferredcites →https://doi.org/10.1378/chest.122.5.1553openalex-snapshot

Matrix Metalloproteinase-9, but not Tissue Inhibitor of Matrix Metalloproteinase-1, Increases in the Sputum from Allergic Asthmatic Patients After Allergen Challenge

inferredcites →https://doi.org/10.1378/chest.124.1.32openalex-snapshot

Histopathology of Severe Childhood Asthma

inferredcites →https://doi.org/10.1378/chest.130.3.741openalex-snapshot

Montelukast Treatment Attenuates the Increase in Myofibroblasts Following Low-Dose Allergen Challenge

inferredcites →https://doi.org/10.1590/s0100-879x2006000200016openalex-snapshot

Protective effects of phosphodiesterase inhibitors on lung function and remodeling in a murine model of chronic asthma

inferredcites →https://doi.org/10.2500/108854194778816634openalex-snapshot

Long-Term Risk Factors for Developing Asthma and Allergic Rhinitis: A 23-Year Follow-Up Study of College Students

inferredcites →https://doi.org/10.2500/108854195778771435openalex-snapshot

Inhaled Corticosteroid Treatment for Asthma

inferredcites →https://doi.org/10.4049/jimmunol.136.7.2348openalex-snapshot

Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins.

inferredcites →https://doi.org/10.4049/jimmunol.145.11.3796openalex-snapshot

IL-4 directs the development of Th2-like helper effectors.

inferredcites →https://doi.org/10.4049/jimmunol.164.2.1086openalex-snapshot

Soluble IL-4 Receptor Inhibits Airway Inflammation Following Allergen Challenge in a Mouse Model of Asthma

inferredcites →https://doi.org/10.4049/jimmunol.165.10.5906openalex-snapshot

CpG Oligodeoxynucleotides Can Reverse Th2-Associated Allergic Airway Responses and Alter the B7.1/B7.2 Expression in a Murine Model of Asthma

inferredcites →https://doi.org/10.4049/jimmunol.166.9.5792openalex-snapshot

A Murine IL-4 Receptor Antagonist That Inhibits IL-4- and IL-13-Induced Responses Prevents Antigen-Induced Airway Eosinophilia and Airway Hyperresponsiveness

inferredcites →https://doi.org/10.4049/jimmunol.175.4.2702openalex-snapshot

CCR3 Expression and Function in Asthmatic Airway Smooth Muscle Cells

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.4096591openalex-extracted

Targeting the Semaphorin3E/PlexinD1 in Allergic Asthma

inferred← citeshttps://doi.org/10.1002/alr.21135openalex-snapshot

Steroid‐independent upregulation of matrix metalloproteinase 9 in chronic rhinosinusitis patients with radiographic evidence of osteitis

inferred← citeshttps://doi.org/10.1002/alr.21611openalex-snapshot

Asthma treatments: new and emerging therapies

inferred← citeshttps://doi.org/10.1002/alr.21754openalex-snapshot

Clinical implications of mucosal remodeling from chronic rhinosinusitis

inferred← citeshttps://doi.org/10.1002/cphy.c200027openalex-snapshot

Lung Pericytes in Pulmonary Vascular Physiology and Pathophysiology

inferred← citeshttps://doi.org/10.1002/cphy.c220011openalex-snapshot

From Beneath the Skin to the Airway Wall: Understanding the Pathological Role of Adipose Tissue in Comorbid Asthma‐Obesity

inferred← citeshttps://doi.org/10.1002/dvdy.24541openalex-snapshot

Epithelial–mesenchymal transition, a spectrum of states: Role in lung development, homeostasis, and disease

inferred← citeshttps://doi.org/10.1002/j.2040-4603.2021.tb00178.xopenalex-snapshot

Lung Pericytes in Pulmonary Vascular Physiology and Pathophysiology

inferred← citeshttps://doi.org/10.1002/j.2040-4603.2023.tb00252.xopenalex-snapshot

From Beneath the Skin to the Airway Wall: Understanding the Pathological Role of Adipose Tissue in Comorbid Asthma‐Obesity

inferred← citeshttps://doi.org/10.1002/j.2040-4603.2023.tb00284.xopenalex-snapshot

Mechanosensitive Channels in Lung Health and Disease

inferred← citeshttps://doi.org/10.1002/ppul.71800openalex-snapshot

Pediatric Mild Asthma: Bridging Current Gaps to Improve Future Care

inferred← citeshttps://doi.org/10.1002/ptr.7874openalex-snapshot

The molecular mechanisms underlying anti‐inflammatory effects of galangin in different diseases

inferred← citeshttps://doi.org/10.1007/164_2016_61openalex-snapshot

Pathogenesis of COPD and Asthma

inferred← citeshttps://doi.org/10.1007/5584_2021_633openalex-snapshot

Effects of Inhalation of STIM-Orai Antagonist SKF 96365 on Ovalbumin-Induced Airway Remodeling in Guinea Pigs

inferred← citeshttps://doi.org/10.1007/978-3-031-40858-8_97-1openalex-snapshot

Innovations in Asthma Care: Efficacy of Mobile App-Assisted Patient Education in Promoting Asthma Self-Management

inferred← citeshttps://doi.org/10.1007/978-3-031-64828-1_20openalex-snapshot

Lymphatic System and Immune Cell-Based Response

inferred← citeshttps://doi.org/10.1007/978-3-031-93455-1_22openalex-snapshot

Basics and Epidemiology of Asthma

inferred← citeshttps://doi.org/10.1007/978-3-662-67757-5_29openalex-snapshot

Fall 29 – Thorax-CT

inferred← citeshttps://doi.org/10.1007/978-981-16-4392-7_17openalex-snapshot

Targeted Micellar Systems for Pulmonary Disease Intervention

inferred← citeshttps://doi.org/10.1007/978-981-99-3505-5_1openalex-snapshot

Introduction to Pulmonary Diseases and OMICS Approaches

inferred← citeshttps://doi.org/10.1007/s00011-015-0913-yopenalex-snapshot

Glycomacropeptide administration attenuates airway inflammation and remodeling associated to allergic asthma in rat

inferred← citeshttps://doi.org/10.1007/s00210-023-02704-1openalex-snapshot

Baicalin and lung diseases

inferred← citeshttps://doi.org/10.1007/s00441-019-03117-4openalex-snapshot

The equine asthma model of airway remodeling: from a veterinary to a human perspective

inferred← citeshttps://doi.org/10.1007/s10753-026-02460-3openalex-snapshot

Mast Cell Chymase and Human Lung Fibroblast Interaction: Mechanisms and Implications for Asthma

inferred← citeshttps://doi.org/10.1007/s11033-020-05439-xopenalex-snapshot

The differential effects of commercial specialized media on cell growth and transforming growth factor beta 1-induced epithelial-mesenchymal transition in bronchial epithelial cells

inferred← citeshttps://doi.org/10.1007/s11302-018-9625-4openalex-snapshot

P2X4R promotes airway remodeling by acting on the phenotype switching of bronchial smooth muscle cells in rats

inferred← citeshttps://doi.org/10.1007/s12016-018-8720-1openalex-snapshot

Mast Cell-Mediated Orchestration of the Immune Responses in Human Allergic Asthma: Current Insights

inferred← citeshttps://doi.org/10.1016/b978-0-12-801496-7.00018-6openalex-snapshot

Leveraging genomics to uncover the genetic, environmental and age-related factors leading to asthma

inferred← citeshttps://doi.org/10.1016/b978-0-12-813832-8.00002-9openalex-snapshot

The Hypoxic Adenosine Response and Inflammation in Lung Disease

inferred← citeshttps://doi.org/10.1016/b978-0-12-823931-5.00018-9openalex-snapshot

Epigenetics of the pathogenic myofibroblast in lung disease

inferred← citeshttps://doi.org/10.1016/b978-0-443-15502-4.00007-0openalex-snapshot

Association between T-helper cell-mediated immune response and airway remodeling in allergic asthma

inferred← citeshttps://doi.org/10.1016/b978-0-443-27345-2.00006-0openalex-snapshot

3D printing, bioprinting, and drug delivery: the new frontier of respiratory care

inferred← citeshttps://doi.org/10.1016/bs.ai.2017.06.003openalex-snapshot

β2-Adrenoceptor Function in Asthma

inferred← citeshttps://doi.org/10.1016/j.amjoto.2019.03.014openalex-snapshot

Histopathologic analysis in chronic rhinosinusitis: Impact on quality of life outcomes

inferred← citeshttps://doi.org/10.1016/j.anai.2012.12.015openalex-snapshot

Role of vascular endothelial growth factor antagonism on airway remodeling in asthma

inferred← citeshttps://doi.org/10.1016/j.anai.2023.03.015openalex-snapshot

Sputum inflammatory, neural, and remodeling mediators in eosinophilic and noneosinophilic asthma

inferred← citeshttps://doi.org/10.1016/j.arbres.2024.09.007openalex-snapshot

Airway Remodeling in Asthma: Mechanisms, Diagnosis, Treatment, and Future Directions

inferred← citeshttps://doi.org/10.1016/j.bcp.2023.115839openalex-snapshot

Catch your breath: The protective role of the angiotensin AT2 receptor for the treatment of idiopathic pulmonary fibrosis

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2018.08.043openalex-snapshot

3D culture models for studying branching morphogenesis in the mammary gland and mammalian lung

inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105409openalex-snapshot

Synthesis and in vitro evaluation of anti-inflammatory, antioxidant, and anti-fibrotic effects of new 8-aminopurine-2,6-dione-based phosphodiesterase inhibitors as promising anti-asthmatic agents

inferred← citeshttps://doi.org/10.1016/j.ceca.2019.01.005openalex-snapshot

ORAI channels in cellular remodeling of cardiorespiratory disease

inferred← citeshttps://doi.org/10.1016/j.cellimm.2021.104425openalex-snapshot

Caspase-11 regulates lung inflammation in response to house dust mites

inferred← citeshttps://doi.org/10.1016/j.chemosphere.2022.134277openalex-snapshot

Elevated serum periostin levels among arsenic-exposed individuals and their associations with the features of asthma

inferred← citeshttps://doi.org/10.1016/j.chest.2024.11.035openalex-snapshot

Promoting Prevention and Targeting Remission of Asthma

inferred← citeshttps://doi.org/10.1016/j.cyto.2017.09.002openalex-snapshot

Connective tissue growth factor regulates transition of primary bronchial fibroblasts to myofibroblasts in asthmatic subjects

inferred← citeshttps://doi.org/10.1016/j.drudis.2011.09.005openalex-snapshot

New perspectives in pharmacological treatment of mild persistent asthma

inferred← citeshttps://doi.org/10.1016/j.ebiom.2023.104717openalex-snapshot

Cellular senescence in asthma: from pathogenesis to therapeutic challenges

inferred← citeshttps://doi.org/10.1016/j.eclinm.2025.103163openalex-snapshot

Association between BMI and asthma in adults over 45 years of age: analysis of Global Burden of Disease 2021, China Health and Retirement Longitudinal Study, and National Health and Nutrition Examination Survey data

inferred← citeshttps://doi.org/10.1016/j.ejphar.2017.01.011openalex-snapshot

An orally active geranyl acetophenone attenuates airway remodeling in a murine model of chronic asthma

inferred← citeshttps://doi.org/10.1016/j.ejphar.2019.172779openalex-snapshot

Novel phosphodiesterases inhibitors from the group of purine-2,6-dione derivatives as potent modulators of airway smooth muscle cell remodelling

inferred← citeshttps://doi.org/10.1016/j.ejphar.2022.175450openalex-snapshot

The anti-asthmatic potential of Rho-kinase inhibitor hydroxyfasudil in the model of experimentally induced allergic airway inflammation

inferred← citeshttps://doi.org/10.1016/j.forsciint.2016.11.001openalex-snapshot

Postmortem serum levels of IgE and mast cell tryptase in fatal asthma

inferred← citeshttps://doi.org/10.1016/j.intimp.2020.107116openalex-snapshot

Riparin II potentials the effect of ephedrine on inflammation and remodelling in the airway of rats suffering from asthma by regulating transforming growth factor-β/Smad3 signalling pathway

inferred← citeshttps://doi.org/10.1016/j.intimp.2022.108808openalex-snapshot

Ouabain modulates airway remodeling caused by Th2-high asthma in mice

inferred← citeshttps://doi.org/10.1016/j.jaci.2011.04.047openalex-snapshot

Remodeling in asthma

inferred← citeshttps://doi.org/10.1016/j.jaci.2018.09.029openalex-snapshot

Mucosal bromodomain-containing protein 4 mediates aeroallergen-induced inflammation and remodeling

inferred← citeshttps://doi.org/10.1016/j.jaci.2019.09.035openalex-snapshot

Shared genetic and experimental links between obesity-related traits and asthma subtypes in UK Biobank

inferred← citeshttps://doi.org/10.1016/j.jaci.2020.07.006openalex-snapshot

Network study of nasal transcriptome profiles reveals master regulator genes of asthma

inferred← citeshttps://doi.org/10.1016/j.jaci.2021.12.765openalex-snapshot

Recent advances in the immunopathogenesis of severe asthma

inferred← citeshttps://doi.org/10.1016/j.jaci.2023.09.035openalex-snapshot

Airway wall extracellular matrix changes induced by bronchial thermoplasty in severe asthma

inferred← citeshttps://doi.org/10.1016/j.jacig.2022.04.001openalex-snapshot

Novel potential treatable traits in asthma: Where is the research taking us?

inferred← citeshttps://doi.org/10.1016/j.jaip.2023.05.011openalex-snapshot

The Unified Airway Hypothesis: Evidence From Specific Intervention With Anti–IL-5 Biologic Therapy

inferred← citeshttps://doi.org/10.1016/j.jep.2018.06.011openalex-snapshot

Mahuang decoction mitigates airway inflammation and regulates IL-21/STAT3 signaling pathway in rat asthma model

inferred← citeshttps://doi.org/10.1016/j.jim.2019.03.002openalex-snapshot

Experimental protocol for development of adjuvant-free murine chronic model of allergic asthma

inferred← citeshttps://doi.org/10.1016/j.jphs.2024.10.004openalex-snapshot

Targeting TMEM16A ion channels suppresses airway hyperreactivity, inflammation, and remodeling in an experimental Guinea pig asthma model

inferred← citeshttps://doi.org/10.1016/j.mce.2023.112087openalex-snapshot

Estrogen receptors differentially modifies lamellipodial and focal adhesion dynamics in airway smooth muscle cell migration

inferred← citeshttps://doi.org/10.1016/j.micron.2012.04.014openalex-snapshot

Grape seed extract attenuates lung parenchyma pathology in ovalbumin-induced mouse asthma model: An ultrastructural study

inferred← citeshttps://doi.org/10.1016/j.molimm.2023.04.008openalex-snapshot

House dust mite allergy: The importance of house dust mite allergens for diagnosis and immunotherapy

inferred← citeshttps://doi.org/10.1016/j.opresp.2024.100384openalex-snapshot

Airway Remodeling in Asthma

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2014.11.010openalex-snapshot

Asthma is not only an airway disease, but also a vascular disease

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2018.02.004openalex-snapshot

Serelaxin as a novel therapeutic opposing fibrosis and contraction in lung diseases

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2023.108351openalex-snapshot

Targeting the Semaphorin3E-plexinD1 complex in allergic asthma

inferred← citeshttps://doi.org/10.1016/j.phrs.2020.105045openalex-snapshot

MicroRNAs in chronic airway diseases: Clinical correlation and translational applications

inferred← citeshttps://doi.org/10.1016/j.pupt.2017.10.007openalex-snapshot

The leukotriene receptor antagonist pranlukast attenuates airway remodeling by suppressing TGF-β signaling

inferred← citeshttps://doi.org/10.1016/j.resp.2012.03.009openalex-snapshot

The message in the air: Hydrogen sulfide metabolism in chronic respiratory diseases

inferred← citeshttps://doi.org/10.1016/j.rmed.2018.10.002openalex-snapshot

Clinical and economic burden of severe asthma: A French cohort study

inferred← citeshttps://doi.org/10.1016/j.rmed.2023.107117openalex-snapshot

Epidermal growth factor receptor in asthma: A promising therapeutic target?

inferred← citeshttps://doi.org/10.1016/j.slasd.2022.02.001openalex-snapshot

Epithelial 3D-spheroids as a tool to study air pollutant-induced lung pathology

inferred← citeshttps://doi.org/10.1038/s41598-017-09414-8openalex-snapshot

Fluticasone/salmeterol reduces remodelling and neutrophilic inflammation in severe equine asthma

inferred← citeshttps://doi.org/10.1038/s41598-018-24574-xopenalex-snapshot

A 4-Week Model of House Dust Mite (HDM) Induced Allergic Airways Inflammation with Airway Remodeling

inferred← citeshttps://doi.org/10.1038/s41598-018-34847-0openalex-snapshot

The geranyl acetophenone tHGA attenuates human bronchial smooth muscle proliferation via inhibition of AKT phosphorylation

inferred← citeshttps://doi.org/10.1038/s41598-019-42981-6openalex-snapshot

Glucagon reduces airway hyperreactivity, inflammation, and remodeling induced by ovalbumin

inferred← citeshttps://doi.org/10.1038/s41598-020-66617-2openalex-snapshot

Transient Receptor Potential Vanilloid channel regulates fibroblast differentiation and airway remodeling by modulating redox signals through NADPH Oxidase 4

inferred← citeshttps://doi.org/10.1038/s41598-023-45640-zopenalex-snapshot

Lignosus rhinocerotis extract ameliorates airway inflammation and remodelling via attenuation of TGF-β1 and Activin A in a prolonged induced allergic asthma model

inferred← citeshttps://doi.org/10.1039/c4tx00096jopenalex-snapshot

Dibutyl phthalate induced oxidative stress does not lead to a significant adjuvant effect on a mouse asthma model

inferred← citeshttps://doi.org/10.1042/cs20191309openalex-snapshot

Bidirectional interaction of airway epithelial remodeling and inflammation in asthma

inferred← citeshttps://doi.org/10.1042/cs20230792openalex-snapshot

Airway-associated adipose tissue accumulation is increased in a kisspeptin receptor knockout mouse model

inferred← citeshttps://doi.org/10.1080/01902148.2016.1207727openalex-snapshot

Effect of tranilast in comparison with beclomethasone in chronic murine model of asthma

inferred← citeshttps://doi.org/10.1080/01902148.2017.1339141openalex-snapshot

Effect of nintedanib on airway inflammation and remodeling in a murine chronic asthma model

inferred← citeshttps://doi.org/10.1080/01902148.2020.1753853openalex-snapshot

The roles of dipeptidyl peptidase-4 and its inhibitors in the regulation of airway epithelial-mesenchymal transition

inferred← citeshttps://doi.org/10.1080/02770903.2016.1244828openalex-snapshot

Evaluation of inflammatory markers interleukin-6 (IL-6) and matrix metalloproteinase-9 (MMP-9) in asthma

inferred← citeshttps://doi.org/10.1080/02770903.2017.1292282openalex-snapshot

Asthma causes inflammation of human pulmonary arteries and decreases vasodilatation induced by prostaglandin I 2 analogs

inferred← citeshttps://doi.org/10.1080/02770903.2020.1771727openalex-snapshot

Augmented angiogenic transcription factor, SOX18, is associated with asthma exacerbation

inferred← citeshttps://doi.org/10.1080/02770903.2022.2034850openalex-snapshot

Consensus on mild asthma management: results of a modified Delphi study

inferred← citeshttps://doi.org/10.1080/02770903.2026.2633352openalex-snapshot

Association between pan-immune-inflammation value and asthma all-cause-mortality in American adults: NHANES 1999–2018

inferred← citeshttps://doi.org/10.1080/08916934.2021.1998895openalex-snapshot

LncRNA RP5-857K21.7 inhibits PDGF-BB-induced proliferation and migration of airway smooth muscle cells through the miR-508-3p/PI3K/AKT/mTOR axis

inferred← citeshttps://doi.org/10.1080/13543784.2018.1427729openalex-snapshot

Targeted anti-IL-13 therapies in asthma: current data and future perspectives

inferred← citeshttps://doi.org/10.1080/13543784.2018.1432592openalex-snapshot

Fevipiprant in the treatment of asthma

inferred← citeshttps://doi.org/10.1080/13880209.2020.1871374openalex-snapshot

Evodiamine protects against airway remodelling and inflammation in asthmatic rats by modulating the HMGB1/NF-κB/TLR-4 signalling pathway

inferred← citeshttps://doi.org/10.1080/14656566.2018.1540589openalex-snapshot

An evaluation of fevipiprant for the treatment of asthma: a promising new therapy?

inferred← citeshttps://doi.org/10.1080/14728222.2019.1667976openalex-snapshot

COPD: preclinical models and emerging therapeutic targets

inferred← citeshttps://doi.org/10.1080/14728222.2022.2035720openalex-snapshot

Novel regulators of airway epithelial barrier function during inflammation: potential targets for drug repurposing

inferred← citeshttps://doi.org/10.1080/14789450.2021.1931130openalex-snapshot

Evolution of proteomics technologies for understanding respiratory syncytial virus pathogenesis

inferred← citeshttps://doi.org/10.1080/17476348.2018.1526677openalex-snapshot

Therapeutic targets for inflammation-mediated airway remodeling in chronic lung disease

inferred← citeshttps://doi.org/10.1080/17476348.2019.1578211openalex-snapshot

Mechanisms how mucosal innate immunity affects progression of allergic airway disease

inferred← citeshttps://doi.org/10.1080/17476348.2024.2449079openalex-snapshot

Interactions between epithelial mesenchymal plasticity, barrier dysfunction and innate immune pathways shape the genesis of allergic airway disease

inferred← citeshttps://doi.org/10.1080/19490976.2025.2457489openalex-snapshot

The role of the early-life gut microbiome in childhood asthma

inferred← citeshttps://doi.org/10.1080/21645515.2020.1753440openalex-snapshot

Mabs for treating asthma: omalizumab, mepolizumab, reslizumab, benralizumab, dupilumab

inferred← citeshttps://doi.org/10.1089/ped.2012.0176openalex-snapshot

The Role of Small Airways in Childhood Asthma

inferred← citeshttps://doi.org/10.1096/fj.201801085ropenalex-snapshot

TRPC1 intensifies house dust mite–induced airway remodeling by facilitating epithelial‐to‐mesenchymal transition and STAT3/NF‐κB signaling

inferred← citeshttps://doi.org/10.1096/fj.201802307ropenalex-snapshot

iPSC‐ and mesenchymoangioblast‐derived mesenchymal stem cells provide greater protection against experimental chronic allergic airways disease compared with a clinically used corticosteroid

inferred← citeshttps://doi.org/10.1096/fj.202502055rropenalex-snapshot

Sema3E ‐ plexinD1 Axis Is a Modulator of Foxp3 + Regulatory T‐Cells in House Dust Mite Model of Asthma

inferred← citeshttps://doi.org/10.1097/aci.0000000000000887openalex-snapshot

Regulatory T-cells in asthma

inferred← citeshttps://doi.org/10.1097/jom.0000000000001814openalex-snapshot

Is There An Explanation for How An Irritant Causes A Nonallergic Asthmatic Disorder Such as Reactive Airways Dysfunction Syndrome (RADS)?

inferred← citeshttps://doi.org/10.1097/mcp.0000000000000007openalex-snapshot

Monoclonal antibodies for the treatment of refractory asthma

inferred← citeshttps://doi.org/10.1097/mcp.0b013e32835b10ecopenalex-snapshot

Asthma phenotypes and endotypes

inferred← citeshttps://doi.org/10.1101/2023.01.17.524257openalex-snapshot

Bromodomain-containing Protein 4 Regulates Innate Inflammation in Airway Epithelial Cells via Modulation of Alternative Splicing

inferred← citeshttps://doi.org/10.1101/2023.09.11.557276openalex-snapshot

PlexinD1 deficiency in CD11c+ dendritic cells exacerbates airway hyperresponsiveness and enhances IgE and mucus production in allergic asthma

inferred← citeshttps://doi.org/10.1101/735969openalex-snapshot

Single Cell RNAseq Reveals A Critical Role of Chloride Channels in Airway Development

inferred← citeshttps://doi.org/10.1111/all.12275openalex-snapshot

EAACI position statement on asthma exacerbations and severe asthma

inferred← citeshttps://doi.org/10.1111/all.13258openalex-snapshot

Asthma in the elderly and late‐onset adult asthma

inferred← citeshttps://doi.org/10.1111/all.14406openalex-snapshot

iTRAQ‐based proteomic analysis reveals potential serum biomarkers of allergic and nonallergic asthma

inferred← citeshttps://doi.org/10.1111/apm.13103openalex-snapshot

Human rhinovirus 16 induces antiviral and inflammatory response in the human vascular endothelium

inferred← citeshttps://doi.org/10.1111/bph.12318openalex-snapshot

AVE 0991, a non‐peptide mimic of angiotensin‐(1–7) effects, attenuates pulmonary remodelling in a model of chronic asthma

inferred← citeshttps://doi.org/10.1111/cea.12481openalex-snapshot

Resistin‐like molecule‐β ( RELM ‐β) targets airways fibroblasts to effect remodelling in asthma: from mouse to man

inferred← citeshttps://doi.org/10.1111/cea.12670openalex-snapshot

Effect of roflumilast on airway remodelling in a murine model of chronic asthma

inferred← citeshttps://doi.org/10.1111/cea.12859openalex-snapshot

Neutrophil autophagy and extracellular DNA traps contribute to airway inflammation in severe asthma

inferred← citeshttps://doi.org/10.1111/cea.12881openalex-snapshot

The current and future role of biomarkers in type 2 cytokine‐mediated asthma management

inferred← citeshttps://doi.org/10.1111/cea.13049openalex-snapshot

Developments in the field of allergy in 2016 through the eyes of Clinical and Experimental Allergy

inferred← citeshttps://doi.org/10.1111/cea.13318openalex-snapshot

Developments in the field of allergy in 2017 through the eyes of Clinical and Experimental Allergy

inferred← citeshttps://doi.org/10.1111/cea.13367openalex-snapshot

Endothelin‐1 mediates Aspergillus fumigatus‐induced airway inflammation and remodelling

inferred← citeshttps://doi.org/10.1111/cea.14489openalex-snapshot

Role of IL ‐5 in asthma and airway remodelling

inferred← citeshttps://doi.org/10.1111/crj.12135openalex-snapshot

Inflammation and infections in asthma

inferred← citeshttps://doi.org/10.1111/evj.13514openalex-snapshot

Airway smooth muscle remodelling in mild and moderate equine asthma

inferred← citeshttps://doi.org/10.1111/imr.70020openalex-snapshot

Emerging Concepts in Cytokine Regulation of Airway Remodeling in Asthma

inferred← citeshttps://doi.org/10.1111/pai.12119openalex-snapshot

Structural changes in the bronchial mucosa of young children at risk of developing asthma

inferred← citeshttps://doi.org/10.1111/resp.12546openalex-snapshot

Characteristics of IL ‐25 and allergen‐induced airway fibrosis in a murine model of asthma

inferred← citeshttps://doi.org/10.1111/resp.12727openalex-snapshot

Airway remodelling in asthma: It's not going away

inferred← citeshttps://doi.org/10.1111/resp.12771openalex-snapshot

Year in review 2015: Asthma and chronic obstructive pulmonary disease

inferred← citeshttps://doi.org/10.1117/1.jbo.21.1.015009openalex-snapshot

Assessment of asthmatic inflammation using hybrid fluorescence molecular tomography–x-ray computed tomography

inferred← citeshttps://doi.org/10.1126/sciadv.adr2282openalex-snapshot

The oxygen level in air directs airway epithelial cell differentiation by controlling mitochondrial citrate export

inferred← citeshttps://doi.org/10.1128/iai.00548-21openalex-snapshot

CC16 Deficiency in the Context of Early-Life Mycoplasma pneumoniae Infection Results in Augmented Airway Responses in Adult Mice

inferred← citeshttps://doi.org/10.1136/bmjopen-2019-031740openalex-snapshot

Observational cohort study to investigate the unmet need and time waiting for referral for specialist opinion in adult asthma in England (UNTWIST asthma)

inferred← citeshttps://doi.org/10.1139/bcb-2022-0185openalex-snapshot

2-Undecanone alleviates asthma by inhibiting NF-κB pathway

inferred← citeshttps://doi.org/10.1152/ajplung.00050.2015openalex-snapshot

Contribution of SRF, Elk-1, and myocardin to airway smooth muscle remodeling in heaves, an asthma-like disease of horses

inferred← citeshttps://doi.org/10.1152/ajplung.00090.2019openalex-snapshot

Characterization of cystic fibrosis airway smooth muscle cell proliferative and contractile activities

inferred← citeshttps://doi.org/10.1152/ajplung.00103.2021openalex-snapshot

Human microphysiological models of airway and alveolar epithelia

inferred← citeshttps://doi.org/10.1152/ajplung.00121.2021openalex-snapshot

Pathogenesis, clinical features of asthma COPD overlap, and therapeutic modalities

inferred← citeshttps://doi.org/10.1152/ajplung.00137.2022openalex-snapshot

Differential airway remodeling changes were observed in patients with asthma COPD overlap compared to patients with asthma and COPD alone

inferred← citeshttps://doi.org/10.1152/ajplung.00145.2024openalex-snapshot

Aging, brain-derived neurotrophic factor, and allergen-induced pulmonary responses in mice

inferred← citeshttps://doi.org/10.1152/ajplung.00146.2022openalex-snapshot

Cellular senescence is increased in airway smooth muscle cells of elderly persons with asthma

inferred← citeshttps://doi.org/10.1152/ajplung.00237.2019openalex-snapshot

Airway epithelial-targeted nanoparticles for asthma therapy

inferred← citeshttps://doi.org/10.1152/ajplung.00244.2021openalex-snapshot

Corticosteroid insensitivity persists in the absence of STAT1 signaling in severe allergic airway inflammation

inferred← citeshttps://doi.org/10.1152/ajplung.00286.2014openalex-snapshot

Pericytes contribute to airway remodeling in a mouse model of chronic allergic asthma

inferred← citeshttps://doi.org/10.1152/ajplung.00438.2017openalex-snapshot

Dietary omega-6, but not omega-3, polyunsaturated or saturated fatty acids increase inflammation in primary lung mesenchymal cells

inferred← citeshttps://doi.org/10.1155/2015/458720openalex-snapshot

Hydrogen Sulfide: A Therapeutic Candidate for Fibrotic Disease?

inferred← citeshttps://doi.org/10.1155/2015/835204openalex-snapshot

Statins in Asthma: Potential Beneficial Effects and Limitations

inferred← citeshttps://doi.org/10.1155/2018/9274817openalex-snapshot

The Plant Proteinase InhibitorCrataBLPlays a Role in Controlling Asthma Response in Mice

inferred← citeshttps://doi.org/10.1155/2021/6862073openalex-snapshot

Andrographolide Inhibition of Th17-Regulated Cytokines and JAK1/STAT3 Signaling in OVA-Stimulated Asthma in Mice

inferred← citeshttps://doi.org/10.1155/2023/3695469openalex-snapshot

Dexmedetomidine Protects against Airway Inflammation and Airway Remodeling in a Murine Model of Chronic Asthma through TLR4/NF-κB Signaling Pathway

inferred← citeshttps://doi.org/10.1155/2023/4144138openalex-snapshot

Baicalin Inhibits Airway Smooth Muscle Cells Proliferation through the RAS Signaling Pathway in Murine Asthmatic Airway Remodeling Model

inferred← citeshttps://doi.org/10.11575/prism/37812openalex-snapshot

Modulation of TGFβ1-induced Fibroblast-to-Myofibroblast Transition in response to Prostaglandin E2 Production by Human Rhinovirus-Infected Airway Epithelial Cells

inferred← citeshttps://doi.org/10.1159/000434679openalex-snapshot

Parabromophenacyl Bromide Inhibits Subepithelial Fibrosis by Reducing TGF-β1 in a Chronic Mouse Model of Allergic Asthma

inferred← citeshttps://doi.org/10.1159/000515005openalex-snapshot

Distinct Patterns of Tissue Remodeling and Their Prognostic Role in Chronic Rhinosinusitis

inferred← citeshttps://doi.org/10.11606/t.5.2018.tde-13062018-094113openalex-snapshot

Efeitos do inibidor específico para serinoprotease rBmTI-A em modelo experimental de inflamação pulmonar alérgica crônica em camundongos Balb/c

inferred← citeshttps://doi.org/10.1164/rccm.201703-0532ocopenalex-snapshot

Activated Leukocyte Cell Adhesion Molecule Stimulates the T-Cell Response in Allergic Asthma

inferred← citeshttps://doi.org/10.1177/1753465817717134openalex-snapshot

Reslizumab in the treatment of inadequately controlled asthma in adults and adolescents with elevated blood eosinophils: clinical trial evidence and future prospects

inferred← citeshttps://doi.org/10.1183/13993003.01619-2023openalex-snapshot

Airway remodelling in asthma and the epithelium: on the edge of a new era

inferred← citeshttps://doi.org/10.1183/16000617.0159-2025openalex-snapshot

Neuroplasticity and neuroimmune interactions with type 2 inflammation in asthma

inferred← citeshttps://doi.org/10.1183/16000617.0183-2021openalex-snapshot

Holy Grail: the journey towards disease modification in asthma

inferred← citeshttps://doi.org/10.1183/16000617.0221-2024openalex-snapshot

The epithelial era of asthma research: knowledge gaps and future direction for patient care

inferred← citeshttps://doi.org/10.1183/23120541.00469-2024openalex-snapshot

Childhood lung function is associated with adolescent-onset and persistent asthma

inferred← citeshttps://doi.org/10.1183/23120541.01826-2025openalex-snapshot

Mapping airway smooth muscle remodelling in vivo using polarisation-sensitive optical coherence tomography

inferred← citeshttps://doi.org/10.1185/03007995.2013.821057openalex-snapshot

Could FEV1decline have a role in daily clinical practice for asthma monitoring?

inferred← citeshttps://doi.org/10.1186/s10020-021-00336-wopenalex-snapshot

Hypoxia-induced preadipocyte factor 1 expression in human lung fibroblasts through ERK/PEA3/c-Jun pathway

inferred← citeshttps://doi.org/10.1186/s12014-022-09351-3openalex-snapshot

Airway fibrin formation cascade in allergic asthma exacerbation: implications for inflammation and remodeling

inferred← citeshttps://doi.org/10.1186/s12890-026-04232-zopenalex-snapshot

Quantitative CT assessment of structural and functional response to omalizumab in severe allergic asthma: a prospective real-world study

inferred← citeshttps://doi.org/10.1186/s12906-017-1891-0openalex-snapshot

Effects of the combined extracts of Herba Epimedii and Fructus Ligustrilucidi on airway remodeling in the asthmatic rats with the treatment of budesonide

inferred← citeshttps://doi.org/10.1186/s12906-019-2743-xopenalex-snapshot

Inhibition of airway remodeling and inflammatory response by Icariin in asthma

inferred← citeshttps://doi.org/10.1186/s12929-016-0263-2openalex-snapshot

Dynamics of airway response in lung microsections: a tool for studying airway-extra cellular matrix interactions

inferred← citeshttps://doi.org/10.1186/s12931-015-0197-3openalex-snapshot

IL-25 induces airways angiogenesis and expression of multiple angiogenic factors in a murine asthma model

inferred← citeshttps://doi.org/10.1186/s12931-018-0851-7openalex-snapshot

Influenza A virus infection dysregulates the expression of microRNA-22 and its targets; CD147 and HDAC4, in epithelium of asthmatics

inferred← citeshttps://doi.org/10.1186/s12931-020-01513-xopenalex-snapshot

CASCADE: a phase 2, randomized, double-blind, placebo-controlled, parallel-group trial to evaluate the effect of tezepelumab on airway inflammation in patients with uncontrolled asthma

inferred← citeshttps://doi.org/10.1186/s12931-021-01910-wopenalex-snapshot

Role of Secretoglobin+ (club cell) NFκB/RelA-TGFβ signaling in aero-allergen-induced epithelial plasticity and subepithelial myofibroblast transdifferentiation

inferred← citeshttps://doi.org/10.1186/s12931-022-01968-0openalex-snapshot

Plasma proteome changes linked to late phase response after inhaled allergen challenge in asthmatics

inferred← citeshttps://doi.org/10.1186/s12931-023-02529-9openalex-snapshot

Rhinovirus induces airway remodeling: what are the physiological consequences?

inferred← citeshttps://doi.org/10.1186/s12931-024-03017-4openalex-snapshot

Kiss1 receptor knockout exacerbates airway hyperresponsiveness and remodeling in a mouse model of allergic asthma

inferred← citeshttps://doi.org/10.1186/s12967-015-0565-2openalex-snapshot

Complement mediators: key regulators of airway tissue remodeling in asthma

inferred← citeshttps://doi.org/10.1186/s12967-020-02632-1openalex-snapshot

Regulatory T cells mediated immunomodulation during asthma: a therapeutic standpoint

inferred← citeshttps://doi.org/10.1186/s12989-017-0228-yopenalex-snapshot

Mechanistic insight into the impact of nanomaterials on asthma and allergic airway disease

inferred← citeshttps://doi.org/10.1186/s12989-018-0261-5openalex-snapshot

Cerium dioxide nanoparticles exacerbate house dust mite induced type II airway inflammation

inferred← citeshttps://doi.org/10.1186/s40659-015-0017-8openalex-snapshot

Relaxant effects of a hydroalcoholic extract of Ruta graveolens on isolated rat tracheal rings

inferred← citeshttps://doi.org/10.1186/s40733-022-00084-6openalex-snapshot

A serological biomarker of type I collagen degradation is related to a more severe, high neutrophilic, obese asthma subtype

inferred← citeshttps://doi.org/10.1201/9781315152356-12openalex-snapshot

The Biology and Clinical Treatment of Asthma

inferred← citeshttps://doi.org/10.1201/9781315152356-13openalex-snapshot

Nanotherapeutics for Asthma

inferred← citeshttps://doi.org/10.12688/f1000research.14581.1openalex-snapshot

New targets for resolution of airway remodeling in obstructive lung diseases

inferred← citeshttps://doi.org/10.1371/journal.pone.0057442openalex-snapshot

Aldose Reductase Inhibition Prevents Allergic Airway Remodeling through PI3K/AKT/GSK3β Pathway in Mice

inferred← citeshttps://doi.org/10.1371/journal.pone.0143976openalex-snapshot

Allergic Non-Asthmatic Adults Have Regional Pulmonary Responses to Segmental Allergen Challenge

inferred← citeshttps://doi.org/10.1371/journal.pone.0149180openalex-snapshot

Vitamin D Supplementation Reduces Induction of Epithelial-Mesenchymal Transition in Allergen Sensitized and Challenged Mice

inferred← citeshttps://doi.org/10.1371/journal.pone.0242695openalex-snapshot

Enhanced mitophagy in bronchial fibroblasts from severe asthmatic patients

showing the first 200 of 297

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.