On the public citation graph

The extracellular matrix – the under‐recognized element in lung disease?

https://doi.org/10.1002/path.4808
0 signed · 378 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1001/archinte.1922.00110120002001openalex-snapshot
THE PATHOLOGY OF BRONCHIAL ASTHMA
inferredcites →https://doi.org/10.1002/jcp.1041470319openalex-snapshot
Proliferation of cultured fibroblasts is inhibited by L ‐Iduronate—containing glycosaminoglycans
inferredcites →https://doi.org/10.1002/jcp.20836openalex-snapshot
Opposite effect of corticosteroids and long‐acting β 2 ‐agonists on serum‐ and TGF‐β 1 ‐induced extracellular matrix deposition by primary human lung fibroblasts
inferredcites →https://doi.org/10.1002/path.1818openalex-snapshot
Airway proteoglycans are differentially altered in fatal asthma
inferredcites →https://doi.org/10.1006/excr.1993.1124openalex-snapshot
L-Iduronate-Rich Glycosaminoglycans Inhibit Growth of Normal Fibroblasts Independently of Serum or Added Growth Factors
inferredcites →https://doi.org/10.1016/0003-9861(77)90012-1openalex-snapshot
Turnover of proteoglycans in guinea pig costal cartilage
inferredcites →https://doi.org/10.1016/0016-5085(95)90630-4openalex-snapshot
Corticosteroids increase procollagen gene expression, synthesis, and secretion by human intestinal smooth muscle cells
inferredcites →https://doi.org/10.1016/0046-8177(89)90152-4openalex-snapshot
Morphogenesis of abnormal elastic fibers in lungs of patients with panacinar and centriacinar emphysema
inferredcites →https://doi.org/10.1016/j.biocel.2004.01.009openalex-snapshot
Lung fibroblast clones from normal and fibrotic subjects differ in hyaluronan and decorin production and rate of proliferation
inferredcites →https://doi.org/10.1016/j.biocel.2008.02.012openalex-snapshot
Fibrocytes are a potential source of lung fibroblasts in idiopathic pulmonary fibrosis
inferredcites →https://doi.org/10.1016/j.biocel.2009.02.020openalex-snapshot
Fibrocyte CXCR4 regulation as a therapeutic target in pulmonary fibrosis
inferredcites →https://doi.org/10.1016/j.ceb.2013.06.003openalex-snapshot
Guiding cell migration by tugging
inferredcites →https://doi.org/10.1016/j.healun.2011.04.006openalex-snapshot
Fibroblast phenotypes and their activity are changed in the wound healing process after lung transplantation
inferredcites →https://doi.org/10.1016/j.jaci.2003.12.312openalex-snapshot
Extracellular matrix proteins modulate asthmatic airway smooth muscle cell proliferation via an autocrine mechanism
inferredcites →https://doi.org/10.1016/j.jaci.2006.05.019openalex-snapshot
A phosphodiesterase 4 inhibitor inhibits matrix protein deposition in airways in vitro
inferredcites →https://doi.org/10.1016/j.jaci.2007.06.031openalex-snapshot
Asthma therapy and airway remodeling
inferredcites →https://doi.org/10.1016/j.jaci.2009.02.032openalex-snapshot
The outer wall of small airways is a major site of remodeling in fatal asthma
inferredcites →https://doi.org/10.1016/j.jsb.2010.04.006openalex-snapshot
Extracellular matrix remodeling of lung alveolar walls in three dimensional space identified using second harmonic generation and multiphoton excitation fluorescence
inferredcites →https://doi.org/10.1016/j.matbio.2015.02.002openalex-snapshot
Matrix metalloproteinases in destructive lung disease
inferredcites →https://doi.org/10.1016/j.rmed.2013.08.008openalex-snapshot
Amount of elastic fibers predicts prognosis of idiopathic pulmonary fibrosis
inferredcites →https://doi.org/10.1016/j.stem.2014.11.004openalex-snapshot
Perivascular Gli1+ Progenitors Are Key Contributors to Injury-Induced Organ Fibrosis
inferredcites →https://doi.org/10.1016/j.tips.2014.09.006openalex-snapshot
Integrins: therapeutic targets in airway hyperresponsiveness and remodelling?
inferredcites →https://doi.org/10.1016/j.yexcr.2014.09.007openalex-snapshot
Beta 1 integrin binding plays a role in the constant traction force generation in response to varying stiffness for cells grown on mature cardiac extracellular matrix
inferredcites →https://doi.org/10.1016/s0014-5793(02)03439-7openalex-snapshot
Tumour necrosis factor‐α interacts with biglycan and decorin
inferredcites →https://doi.org/10.1016/s0140-6736(12)61144-1openalex-snapshot
New cellular and molecular mechanisms of lung injury and fibrosis in idiopathic pulmonary fibrosis
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/s1569-9048(02)00111-8openalex-snapshot
In vitro wounding of airway smooth muscle cell monolayers increases expression of TGF-β receptors
inferredcites →https://doi.org/10.1038/nature10152openalex-snapshot
Latent TGF-β structure and activation
inferredcites →https://doi.org/10.1038/nm.2208openalex-snapshot
Allosteric inhibition of lysyl oxidase–like-2 impedes the development of a pathologic microenvironment
inferredcites →https://doi.org/10.1038/nm.2848openalex-snapshot
Lineage tracing and genetic ablation of ADAM12+ perivascular cells identify a major source of profibrotic cells during acute tissue injury
inferredcites →https://doi.org/10.1038/nrm3897openalex-snapshot
Physical influences of the extracellular environment on cell migration
inferredcites →https://doi.org/10.1038/nrm3902openalex-snapshot
Extracellular matrix assembly: a multiscale deconstruction
inferredcites →https://doi.org/10.1056/nejmoa1402582openalex-snapshot
A Phase 3 Trial of Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis
inferredcites →https://doi.org/10.1056/nejmoa1402584openalex-snapshot
Efficacy and Safety of Nintedanib in Idiopathic Pulmonary Fibrosis
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/copd-200050678openalex-snapshot
Different Modulation of Decorin Production by Lung Fibroblasts from Patients with Mild and Severe Emphysema
inferredcites →https://doi.org/10.1083/jcb.200704042openalex-snapshot
Myofibroblast contraction activates latent TGF-β1 from the extracellular matrix
inferredcites →https://doi.org/10.1083/jcb.201004082openalex-snapshot
Feedback amplification of fibrosis through matrix stiffening and COX-2 suppression
inferredcites →https://doi.org/10.1084/jem.20070956openalex-snapshot
Bronchial smooth muscle remodeling involves calcium-dependent enhanced mitochondrial biogenesis in asthma
inferredcites →https://doi.org/10.1089/adt.2012.474openalex-snapshot
Extracellular Matrix Remodeling: The Common Denominator in Connective Tissue Diseases Possibilities for Evaluation and Current Understanding of the Matrix as More Than a Passive Architecture, but a Key Player in Tissue Failure
inferredcites →https://doi.org/10.1093/glycob/8.12.1149openalex-snapshot
Heparan sulfate upregulates platelet-derived growth factor receptors on human lung fibroblasts
inferredcites →https://doi.org/10.1097/mcp.0b013e3283566721openalex-snapshot
EMT and interstitial lung disease
inferredcites →https://doi.org/10.1111/j.1365-2222.2005.02334.xopenalex-snapshot
Bronchial matrix and inflammation respond to inhaled steroids despite ongoing allergen exposure in asthma
inferredcites →https://doi.org/10.1111/j.1398-9995.2004.00516.xopenalex-snapshot
In vitro effects of flunisolide on MMP‐9, TIMP‐1, fibronectin, TGF‐β1 release and apoptosis in sputum cells freshly isolated from mild to moderate asthmatics
inferredcites →https://doi.org/10.1111/j.1398-9995.2011.02773.xopenalex-snapshot
Extracellular matrix in airway smooth muscle is associated with dynamics of airway function in asthma
inferredcites →https://doi.org/10.1111/j.1582-4934.2008.00401.xopenalex-snapshot
Surface morphology and mechanical properties of fibroblasts from scleroderma patients
inferredcites →https://doi.org/10.1111/j.1752-699x.2010.00190.xopenalex-snapshot
Pathological airway remodelling in inflammation
inferredcites →https://doi.org/10.1117/1.jbo.19.3.036005openalex-snapshot
Quantification of collagen I in airway tissues using second harmonic generation
inferredcites →https://doi.org/10.1126/science.1092053openalex-snapshot
Cell Migration: Integrating Signals from Front to Back
inferredcites →https://doi.org/10.1126/science.1189345openalex-snapshot
Tissue-Engineered Lungs for in Vivo Implantation
inferredcites →https://doi.org/10.1136/bmjresp-2014-000027openalex-snapshot
Primary mesenchymal stem cells in human transplanted lungs are CD90/CD105 perivascularly located tissue-resident cells
inferredcites →https://doi.org/10.1136/thoraxjnl-2014-205091openalex-snapshot
A large lung gene expression study identifying fibulin-5 as a novel player in tissue repair in COPD
inferredcites →https://doi.org/10.1146/annurev-pathol-020712-163930openalex-snapshot
Host Responses in Tissue Repair and Fibrosis
inferredcites →https://doi.org/10.1152/ajpcell.1987.252.1.c1openalex-snapshot
Dynamic state of collagen: pathways of collagen degradation in vivo and their possible role in regulation of collagen mass
inferredcites →https://doi.org/10.1152/ajplung.00059.2011openalex-snapshot
Dendritic cell functional properties in a three-dimensional tissue model of human lung mucosa
inferredcites →https://doi.org/10.1152/ajplung.00300.2014openalex-snapshot
Mechanosignaling through YAP and TAZ drives fibroblast activation and fibrosis
inferredcites →https://doi.org/10.1152/ajplung.1998.274.4.l499openalex-snapshot
Dexamethasone activates expression of the PDGF-α receptor and induces lung fibroblast proliferation
inferredcites →https://doi.org/10.1159/000213148openalex-snapshot
Connective Tissue in Aging Lung
inferredcites →https://doi.org/10.1159/000447017openalex-snapshot
Molecular Mechanisms of Stress-Responsive Changes in Collagen and Elastin Networks in Skin
inferredcites →https://doi.org/10.1164/ajrccm.149.4.8143066openalex-snapshot
Effect of Glucocorticoids on Collagen Accumulation in Pulmonary Vascular Remodeling in the Rat
inferredcites →https://doi.org/10.1164/ajrccm.154.6.8970376openalex-snapshot
Proteoglycan Deposition in Pulmonary Fibrosis
inferredcites →https://doi.org/10.1164/ajrccm.160.6.9706031openalex-snapshot
Cellular and Connective Tissue Changes in Alveolar Septal Walls in Emphysema
inferredcites →https://doi.org/10.1164/ajrccm.162.6.9909111openalex-snapshot
The Production of Extracellular Matrix Proteins by Human Passively Sensitized Airway Smooth-Muscle Cells in Culture
inferredcites →https://doi.org/10.1164/ajrccm.164.3.2010109openalex-snapshot
Airway Smooth Muscle Cell Proliferation is Increased in Asthma
inferredcites →https://doi.org/10.1164/ajrccm.186.6.568openalex-snapshot
Airway Smooth Muscle Hypertrophy and Hyperplasia in Asthma
inferredcites →https://doi.org/10.1164/ajrccm/140.2.410openalex-snapshot
Age-related Changes in Lung Collagen Metabolism: A Role for Degradation in Regulating Lung Collagen Production
inferredcites →https://doi.org/10.1164/ajrccm/140.6.1693openalex-snapshot
An Immunohistochemical Study of Architectural Remodeling and Connective Tissue Synthesis in Pulmonary Fibrosis
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/arrd.1975.111.2.184openalex-snapshot
The effects of proteolytic enzymes on the tensile strength of human lung.
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.200209-1030ocopenalex-snapshot
Airway Structural Alterations Selectively Associated with Severe Asthma
inferredcites →https://doi.org/10.1164/rccm.200403-305ocopenalex-snapshot
Abnormal Alveolar Attachments with Decreased Elastic Fiber Content in Distal Lung in Fatal Asthma
inferredcites →https://doi.org/10.1164/rccm.200404-507ocopenalex-snapshot
Presence of Activated Mobile Fibroblasts in Bronchoalveolar Lavage from Patients with Mild Asthma
inferredcites →https://doi.org/10.1164/rccm.200508-1218ocopenalex-snapshot
Regional Fibroblast Heterogeneity in the Lung
inferredcites →https://doi.org/10.1164/rccm.200509-1420ocopenalex-snapshot
Extracellular Matrix Regulates Enhanced Eotaxin Expression in Asthmatic Airway Smooth Muscle Cells
inferredcites →https://doi.org/10.1164/rccm.200812-1902ocopenalex-snapshot
Differential Expression of Tissue Repair Genes in the Pathogenesis of Chronic Obstructive Pulmonary Disease
inferredcites →https://doi.org/10.1164/rccm.201003-0494ocopenalex-snapshot
Persisting Remodeling and Less Airway Wall Eosinophil Activation in Complete Remission of Asthma
inferredcites →https://doi.org/10.1164/rccm.201110-1849ocopenalex-snapshot
Airway Smooth Muscle Hypertrophy and Hyperplasia in Asthma
inferredcites →https://doi.org/10.1164/rccm.201204-0754ocopenalex-snapshot
Acellular Normal and Fibrotic Human Lung Matrices as a Culture System for In Vitro Investigation
inferredcites →https://doi.org/10.1164/rccm.201403-0509ppopenalex-snapshot
New Therapeutic Targets in Idiopathic Pulmonary Fibrosis. Aiming to Rein in Runaway Wound-Healing Responses
inferredcites →https://doi.org/10.1164/rccm.201407-1374leopenalex-snapshot
Reduction of Airway Smooth Muscle Mass by Bronchial Thermoplasty in Patients with Severe Asthma
inferredcites →https://doi.org/10.1165/ajrcmb.23.3.3990openalex-snapshot
Differential Effects of Extracellular Matrix Proteins on Human Airway Smooth Muscle Cell Proliferation and Phenotype
inferredcites →https://doi.org/10.1165/ajrcmb.25.5.4605openalex-snapshot
Effects of Growth Factors and Extracellular Matrix on Survival of Human Airway Smooth Muscle Cells
inferredcites →https://doi.org/10.1165/rcmb.2012-0335ocopenalex-snapshot
Matrices of Physiologic Stiffness Potently Inactivate Idiopathic Pulmonary Fibrosis Fibroblasts
inferredcites →https://doi.org/10.1172/jci115204openalex-snapshot
Marked longevity of human lung parenchymal elastic fibers deduced from prevalence of D-aspartate and nuclear weapons-related radiocarbon.
inferredcites →https://doi.org/10.1172/jci36183openalex-snapshot
Biomarkers for epithelial-mesenchymal transitions
inferredcites →https://doi.org/10.1172/jci71386openalex-snapshot
Fibrotic extracellular matrix activates a profibrotic positive feedback loop
inferredcites →https://doi.org/10.1183/09031936.00016815openalex-snapshot
Bronchial thermoplasty in asthma: 2-year follow-up using optical coherence tomography
inferredcites →https://doi.org/10.1183/09031936.00017207openalex-snapshot
Changes in elastic fibres in the small airways and alveoli in COPD
inferredcites →https://doi.org/10.1183/09031936.00047905openalex-snapshot
Differences in proteoglycan deposition in the airways of moderate and severe asthmatics
inferredcites →https://doi.org/10.1183/09031936.00123008openalex-snapshot
Elastin expression in very severe human COPD
inferredcites →https://doi.org/10.1183/09031936.00135205openalex-snapshot
BALF-derived fibroblasts differ from biopsy-derived fibroblasts in systemic sclerosis
inferredcites →https://doi.org/10.1183/09031936.00147807openalex-snapshot
Extracellular matrix components and regulators in the airway smooth muscle in asthma
inferredcites →https://doi.org/10.1183/09031936.00192611openalex-snapshot
Extracellular matrix composition in COPD
inferredcites →https://doi.org/10.1183/09031936.06.00056405openalex-snapshot
Ultrastructure of the reticular basement membrane in asthmatic adults, children and infants
inferredcites →https://doi.org/10.1186/1465-9921-11-55openalex-snapshot
Altered fibroblast proteoglycan production in COPD
inferredcites →https://doi.org/10.1186/1465-9921-12-76openalex-snapshot
Fibrocytes and the tissue niche in lung repair
inferredcites →https://doi.org/10.1186/1465-9921-15-67openalex-snapshot
Controlled and uncontrolled asthma display distinct alveolar tissue matrix compositions
inferredcites →https://doi.org/10.1186/1465-9921-7-11openalex-snapshot
Functional and phenotypical comparison of myofibroblasts derived from biopsies and bronchoalveolar lavage in mild asthma and scleroderma
inferredcites →https://doi.org/10.1186/1465-9921-7-50openalex-snapshot
Tissue fibrocytes in patients with mild asthma: A possible link to thickness of reticular basement membrane?
inferredcites →https://doi.org/10.1186/1465-9921-9-41openalex-snapshot
Changes in elastin, elastin binding protein and versican in alveoli in chronic obstructive pulmonary disease
inferredcites →https://doi.org/10.1186/1471-2466-14-120openalex-snapshot
Lung fibrotic tenascin-C upregulation is associated with other extracellular matrix proteins and induced by TGFβ1
inferredcites →https://doi.org/10.1186/s12931-015-0225-3openalex-snapshot
Accelerated extracellular matrix turnover during exacerbations of COPD
inferredcites →https://doi.org/10.1189/jlb.3ta0513-303ropenalex-snapshot
Technical Advance: Live-imaging analysis of human dendritic cell migrating behavior under the influence of immune-stimulating reagents in an organotypic model of lung
inferredcites →https://doi.org/10.1242/jcs.00808openalex-snapshot
Biglycan and decorin induce morphological and cytoskeletal changes involving signalling by the small GTPases RhoA and Rac1 resulting in lung fibroblast migration
inferredcites →https://doi.org/10.1242/jcs.023820openalex-snapshot
The extracellular matrix at a glance
inferredcites →https://doi.org/10.1371/journal.pcbi.1001125openalex-snapshot
Linking Microscopic Spatial Patterns of Tissue Destruction in Emphysema to Macroscopic Decline in Stiffness Using a 3D Computational Model
inferredcites →https://doi.org/10.1371/journal.pone.0063430openalex-snapshot
Inhaled Steroids Modulate Extracellular Matrix Composition in Bronchial Biopsies of COPD Patients: A Randomized, Controlled Trial
inferredcites →https://doi.org/10.1378/chest.127.1.257openalex-snapshot
Anti-Tissue Remodeling Effects of Corticosteroids
inferredcites →https://doi.org/10.1513/annalsats.201406-240mgopenalex-snapshot
Lung Extracellular Matrix and Fibroblast Function
inferredcites →https://doi.org/10.1513/pats.200601-009awopenalex-snapshot
The Stumbling Block in Lung Repair of Emphysema: Elastic Fiber Assembly
inferredcites →https://doi.org/10.2174/138161212802430396openalex-snapshot
Cellular Players in Lung Fibrosis
inferredcites →https://doi.org/10.3892/mmr.2015.3231openalex-snapshot
Yes-associated protein regulates the growth of human non-small cell lung cancer in response to matrix stiffness

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.4656875openalex-extracted
inferred← citeshttps://doi.org/10.1002/adhm.202304254openalex-snapshot
Stiffness Mediated‐Mechanosensation of Airway Smooth Muscle Cells on Linear Stiffness Gradient Hydrogels
inferred← citeshttps://doi.org/10.1002/advs.77244openalex-snapshot
A Biofabricated Human Acinus‐on‐a‐Chip Unveils Mechanotransductive Drivers of Ventilator‐Induced Lung Injury via Decoupling Volutrauma and Barotrauma
inferred← citeshttps://doi.org/10.1002/ajmg.c.31953openalex-snapshot
Respiratory manifestations in the Ehlers–Danlos syndromes
inferred← citeshttps://doi.org/10.1002/anbr.202300110openalex-snapshot
Polymer Design of Microwell Hydrogels Influences Epithelial–Mesenchymal Interactions During Human Bronchosphere Formation
inferred← citeshttps://doi.org/10.1002/biof.2020openalex-snapshot
Investigating rutin as a potential transforming growth factor‐β type I receptor antagonist for the inhibition of bleomycin‐induced lung fibrosis
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.2040-4603.2023.tb00284.xopenalex-snapshot
Mechanosensitive Channels in Lung Health and Disease
inferred← citeshttps://doi.org/10.1002/lary.32227openalex-snapshot
Partial Decellularization Retains Cartilage Immune Privilege in Tissue Engineered Tracheal Grafts
inferred← citeshttps://doi.org/10.1002/ohn.1211openalex-snapshot
Assessing the Impact of Partial Decellularization on Tracheal Chondrocytes and Extracellular Matrix in Airway Reconstruction
inferred← citeshttps://doi.org/10.1002/path.4942openalex-snapshot
The peritoneum: healing, immunity, and diseases
inferred← citeshttps://doi.org/10.1002/path.5364openalex-snapshot
Recent advances in chronic obstructive pulmonary disease pathogenesis: from disease mechanisms to precision medicine
inferred← citeshttps://doi.org/10.1002/path.5632openalex-snapshot
Macrophage–stroma interactions in fibrosis: biochemical, biophysical, and cellular perspectives
inferred← citeshttps://doi.org/10.1002/pgr2.70022openalex-snapshot
Alveolar Glycocalyces During Health and Critical Illness
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/10.1007/978-1-0716-4985-5_11openalex-snapshot
Phenotypic Drug Screening for Novel Antifibrotic Therapeutics in Lung Health
inferred← citeshttps://doi.org/10.1007/978-3-030-29403-8_3openalex-snapshot
Comparison of the Regenerative Potential for Lung Tissue of Mesenchymal Stromal Cells from Different Sources/Locations Within the Body
inferred← citeshttps://doi.org/10.1007/978-3-030-29403-8_5openalex-snapshot
Preclinical Evidence for the Role of Stem/Stromal Cells in COPD
inferred← citeshttps://doi.org/10.1007/978-3-030-29403-8_6openalex-snapshot
Clinical Application of Stem/Stromal Cells in COPD
inferred← citeshttps://doi.org/10.1007/978-3-030-92090-6_5-1openalex-snapshot
Mechanical Properties of the Extracellular Matrix
inferred← citeshttps://doi.org/10.1007/978-3-031-26625-6_1openalex-snapshot
An Introduction to Engineering and Modeling the Lung
inferred← citeshttps://doi.org/10.1007/978-3-031-26625-6_10openalex-snapshot
Lung-on-a-Chip Models of the Lung Parenchyma
inferred← citeshttps://doi.org/10.1007/978-3-031-26625-6_5openalex-snapshot
Basic Science Perspective on Engineering and Modeling the Large Airways
inferred← citeshttps://doi.org/10.1007/978-3-031-56363-8_5openalex-snapshot
Mechanical Properties of the Extracellular Matrix
inferred← citeshttps://doi.org/10.1007/978-3-319-98143-7_9openalex-snapshot
Dynamic Reciprocity: The Role of the Extracellular Matrix Microenvironment in Amplifying and Sustaining Pathological Lung Fibrosis
inferred← citeshttps://doi.org/10.1007/978-981-33-6962-7_7openalex-snapshot
The Applications of the Recellularization Organs in Organ Replacement at the Stage of Animal Research
inferred← citeshttps://doi.org/10.1007/s00018-018-2899-4openalex-snapshot
Fibroblast-to-myofibroblast transition in bronchial asthma
inferred← citeshttps://doi.org/10.1007/s00018-025-05729-2openalex-snapshot
LncRNA SYISL promotes fibroblast myofibroblast transition via miR-23a-mediated TRIOBP regulation
inferred← citeshttps://doi.org/10.1007/s00018-026-06242-wopenalex-snapshot
SYISL promotes pulmonary epithelial-mesenchymal transition and fibrosis through DSP–Hippo/YAP pathway
inferred← citeshttps://doi.org/10.1007/s10237-020-01336-1openalex-snapshot
A viscoelastic two-dimensional network model of the lung extracellular matrix
inferred← citeshttps://doi.org/10.1007/s10439-019-02337-7openalex-snapshot
ECM in Differentiation: A Review of Matrix Structure, Composition and Mechanical Properties
inferred← citeshttps://doi.org/10.1007/s10517-024-06005-2openalex-snapshot
The Influence of Exosomes Derived from Mesenchymal Stem Cells on the Development of Fibrosis In Vitro
inferred← citeshttps://doi.org/10.1007/s10753-018-0744-4openalex-snapshot
The lncRNA H19 Mediates Pulmonary Fibrosis by Regulating the miR-196a/COL1A1 Axis
inferred← citeshttps://doi.org/10.1007/s12016-025-09045-2openalex-snapshot
Targeting IL-13 and IL-4 in Asthma: Therapeutic Implications on Airway Remodeling in Severe Asthma
inferred← citeshttps://doi.org/10.1007/s40134-018-0271-yopenalex-snapshot
Cystic Lung Disease from Protein Deposition: Pathogenesis and Associated Conditions
inferred← citeshttps://doi.org/10.1007/s40265-018-1001-8openalex-snapshot
Chronic Obstructive Pulmonary Disease and Lung Cancer: Underlying Pathophysiology and New Therapeutic Modalities
inferred← citeshttps://doi.org/10.1007/s40778-017-0082-8openalex-snapshot
Engineering Bioartificial Lungs for Transplantation
inferred← citeshttps://doi.org/10.1007/s43152-021-00031-2openalex-snapshot
The Multi-Faceted Extracellular Matrix: Unlocking Its Secrets for Understanding the Perpetuation of Lung Fibrosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-809880-6.00060-6openalex-snapshot
Regenerative Medicine of the Respiratory Tract
inferred← citeshttps://doi.org/10.1016/b978-0-12-820310-1.00010-0openalex-snapshot
Recent advances in imaging of cell elasticity
inferred← citeshttps://doi.org/10.1016/b978-0-323-54431-3.00003-2openalex-snapshot
Mechanisms of Fibrosis
inferred← citeshttps://doi.org/10.1016/b978-0-323-90871-9.00012-7openalex-snapshot
Three dimensional lung models - Three dimensional extracellular matrix models
inferred← citeshttps://doi.org/10.1016/bs.apha.2023.04.002openalex-snapshot
Anti-fibrotic strategies and pulmonary fibrosis
inferred← citeshttps://doi.org/10.1016/j.actbio.2022.05.031openalex-snapshot
An in vitro model of fibrosis using crosslinked native extracellular matrix-derived hydrogels to modulate biomechanics without changing composition
inferred← citeshttps://doi.org/10.1016/j.actbio.2024.02.008openalex-snapshot
Three dimensional fibrotic extracellular matrix directs microenvironment fiber remodeling by fibroblasts
inferred← citeshttps://doi.org/10.1016/j.actbio.2024.07.014openalex-snapshot
Binary fabrication of decellularized lung extracellular matrix hybridgels for in vitro chronic obstructive pulmonary disease modeling
inferred← citeshttps://doi.org/10.1016/j.addr.2017.07.010openalex-snapshot
Drug targeting to myofibroblasts: Implications for fibrosis and cancer
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2017.06.027openalex-snapshot
Fibrillin-2 and Tenascin-C bridge the age gap in lung epithelial regeneration
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2024.122546openalex-snapshot
A functional 3D full-thickness model for comprehending the interaction between airway epithelium and connective tissue in cystic fibrosis
inferred← citeshttps://doi.org/10.1016/j.bprint.2022.e00255openalex-snapshot
Biomaterial inks and bioinks for fabricating 3D biomimetic lung tissue: A delicate balancing act between biocompatibility and mechanical printability
inferred← citeshttps://doi.org/10.1016/j.cellimm.2016.12.003openalex-snapshot
Interplay of extracellular matrix and leukocytes in lung inflammation
inferred← citeshttps://doi.org/10.1016/j.clinbiomech.2018.01.002openalex-snapshot
Integrated lung tissue mechanics one piece at a time: Computational modeling across the scales of biology
inferred← citeshttps://doi.org/10.1016/j.cmet.2026.05.008openalex-snapshot
The senescence-stiffening loop: Extracellular matrix remodeling, hypoperfusion, and mitochondrial dysfunction drive tissue aging
inferred← citeshttps://doi.org/10.1016/j.cophys.2021.05.007openalex-snapshot
Imaging the pulmonary extracellular matrix
inferred← citeshttps://doi.org/10.1016/j.cpcardiol.2022.101539openalex-snapshot
Potential Mechanisms Between HF and COPD: New Insights From Bioinformatics
inferred← citeshttps://doi.org/10.1016/j.crphys.2025.100140openalex-snapshot
Microvascular endothelial cells display organ-specific responses to extracellular matrix stiffness
inferred← citeshttps://doi.org/10.1016/j.envres.2024.120395openalex-snapshot
Wildfire-relevant woodsmoke and extracellular vesicles (EVs): Alterations in EV proteomic signatures involved in extracellular matrix degradation and tissue injury in airway organotypic models
inferred← citeshttps://doi.org/10.1016/j.intimp.2021.107608openalex-snapshot
Inflammatory mediators in various molecular pathways involved in the development of pulmonary fibrosis
inferred← citeshttps://doi.org/10.1016/j.isci.2025.113993openalex-snapshot
Mechanobiology and the extracellular matrix in pulmonary fibrosis
inferred← citeshttps://doi.org/10.1016/j.jaci.2017.12.982openalex-snapshot
Airway pathological heterogeneity in asthma: Visualization of disease microclusters using topological data analysis
inferred← citeshttps://doi.org/10.1016/j.jaci.2021.03.035openalex-snapshot
Airway smooth muscle pathophysiology in asthma
inferred← citeshttps://doi.org/10.1016/j.jaci.2023.06.005openalex-snapshot
Eosinophils and tissue remodeling: Relevance to airway disease
inferred← citeshttps://doi.org/10.1016/j.jprot.2018.02.027openalex-snapshot
Quantitative proteomic characterization of the lung extracellular matrix in chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis
inferred← citeshttps://doi.org/10.1016/j.jtemb.2025.127766openalex-snapshot
Ferroptosis and iron homeostasis in chronic obstructive pulmonary disease: Therapeutic opportunities of iron chelators
inferred← citeshttps://doi.org/10.1016/j.jviromet.2021.114076openalex-snapshot
Assay of extracellular matrix degradation and transmigration of chicken peripheral blood mononuclear cells after infection with genotype VII Newcastle disease virus in vitro
inferred← citeshttps://doi.org/10.1016/j.matbio.2017.12.004openalex-snapshot
Matrix biomechanics and dynamics in pulmonary fibrosis
inferred← citeshttps://doi.org/10.1016/j.matbio.2018.01.019openalex-snapshot
The big five in fibrosis: Macrophages, myofibroblasts, matrix, mechanics, and miscommunication
inferred← citeshttps://doi.org/10.1016/j.matbio.2018.02.013openalex-snapshot
The multifaceted roles of perlecan in fibrosis
inferred← citeshttps://doi.org/10.1016/j.matbio.2018.02.020openalex-snapshot
Therapeutic approaches to control tissue repair and fibrosis: Extracellular matrix as a game changer
inferred← citeshttps://doi.org/10.1016/j.matbio.2018.03.012openalex-snapshot
Matrix remodeling in chronic lung diseases
inferred← citeshttps://doi.org/10.1016/j.matbio.2018.06.006openalex-snapshot
Defective lung function following influenza virus is due to prolonged, reversible hyaluronan synthesis
inferred← citeshttps://doi.org/10.1016/j.matdes.2025.114617openalex-snapshot
Biomimetic elastin-collagen hybrid hydrogels crosslinked by energetic electrons: towards a tunable in vitro extracellular matrix model of the lung
inferred← citeshttps://doi.org/10.1016/j.mbplus.2021.100058openalex-snapshot
The critical role of collagen VI in lung development and chronic lung disease
inferred← citeshttps://doi.org/10.1016/j.mcpro.2025.100950openalex-snapshot
A Single-Step Protein Extraction for Lung Extracellular Matrix Proteomics Enabled by the Photocleavable Surfactant Azo and timsTOF Pro
inferred← citeshttps://doi.org/10.1016/j.mito.2021.03.005openalex-snapshot
Cellular and mitochondrial calcium communication in obstructive lung disorders
inferred← citeshttps://doi.org/10.1016/j.nantod.2025.102655openalex-snapshot
Evaluation of a bioprinted 3D airway tissue model for toxicity testing of nanomaterials; Pathway to integration into a tiered testing strategy for hazard assessment to support safety-by-design
inferred← citeshttps://doi.org/10.1016/j.pathol.2022.05.002openalex-snapshot
Usual interstitial pneumonia: a review of the pathogenesis and discussion of elastin fibres, type II pneumocytes and proposed roles in the pathogenesis
inferred← citeshttps://doi.org/10.1016/j.pharmr.2026.100124openalex-snapshot
Regenerative therapeutics for chronic obstructive pulmonary disease
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2021.107839openalex-snapshot
Therapeutic targets in lung tissue remodelling and fibrosis
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2021.107941openalex-snapshot
The role of osteoprotegerin (OPG) in fibrosis: its potential as a biomarker and/or biological target for the treatment of fibrotic diseases
inferred← citeshttps://doi.org/10.1016/j.rmed.2025.108268openalex-snapshot
Probiotics: An adjuvant treatment strategy for chronic respiratory diseases
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.163073openalex-snapshot
Long-term cadmium exposure induces chronic obstructive pulmonary disease-like lung lesions in a mouse model
inferred← citeshttps://doi.org/10.1016/j.taap.2025.117640openalex-snapshot
Ambrisentan ameliorates methotrexate-induced pulmonary injury in rats: involvement of ET-1/ETA, NF-κB, and MMP-9/TIMP-1 pathways
inferred← citeshttps://doi.org/10.1016/j.tice.2025.102863openalex-snapshot
Procyanidin B2 mitigate asthmatic airway remodeling by inhibiting TGF-β1-induced airway smooth muscle proliferation through ROS signaling
inferred← citeshttps://doi.org/10.1016/j.yexcr.2026.114953openalex-snapshot
Cadherin-26 contributes to an M2-like macrophage polarization and TGF-β1 expression via the CTNNB1-STAT3 axis in interstitial lung disease
inferred← citeshttps://doi.org/10.1016/j.yexmp.2021.104664openalex-snapshot
Critical roles of microRNA-196 in normal physiology and non-malignant diseases: Diagnostic and therapeutic implications
inferred← citeshttps://doi.org/10.1016/j.ymthe.2018.06.020openalex-snapshot
lncRNA PFAR Promotes Lung Fibroblast Activation and Fibrosis by Targeting miR-138 to Regulate the YAP1-Twist Axis
inferred← citeshttps://doi.org/10.1021/acs.jproteome.3c00532openalex-snapshot
High-Throughput Extracellular Matrix Proteomics of Human Lungs Enabled by Photocleavable Surfactant and diaPASEF
inferred← citeshttps://doi.org/10.1021/acsabm.2c00143openalex-snapshot
Biomechanical Dependence of SARS-CoV-2 Infections
inferred← citeshttps://doi.org/10.1021/acsabm.2c00275openalex-snapshot
Harnessing the Structural and Functional Diversity of Protein Filaments as Biomaterial Scaffolds
inferred← citeshttps://doi.org/10.1021/acsami.2c18330openalex-snapshot
Chemical Modification of Human Decellularized Extracellular Matrix for Incorporation into Phototunable Hybrid-Hydrogel Models of Tissue Fibrosis
inferred← citeshttps://doi.org/10.1021/acsbiomaterials.7b00384openalex-snapshot
Electrospun Decellularized Lung Matrix Scaffold for Airway Smooth Muscle Culture
inferred← citeshttps://doi.org/10.1038/pr.2018.36openalex-snapshot
Pulmonary and diaphragmatic pathology in collagen type I α1 mutant mice with osteogenesis imperfecta
inferred← citeshttps://doi.org/10.1038/s41419-020-02747-9openalex-snapshot
CircRNA TADA2A relieves idiopathic pulmonary fibrosis by inhibiting proliferation and activation of fibroblasts
inferred← citeshttps://doi.org/10.1038/s41584-019-0324-5openalex-snapshot
Evasion of apoptosis by myofibroblasts: a hallmark of fibrotic diseases
inferred← citeshttps://doi.org/10.1038/s41598-018-23702-xopenalex-snapshot
Quantifying extracellular matrix turnover in human lung scaffold cultures
inferred← citeshttps://doi.org/10.1038/s41598-018-25321-yopenalex-snapshot
Chronic features of allergic asthma are enhanced in the absence of resistin-like molecule-beta
inferred← citeshttps://doi.org/10.1038/s41598-018-31880-xopenalex-snapshot
Optimization of cell-laden bioinks for 3D bioprinting and efficient infection with influenza A virus
inferred← citeshttps://doi.org/10.1038/s41598-018-37958-wopenalex-snapshot
Expression, activity and localization of lysosomal sulfatases in Chronic Obstructive Pulmonary Disease
inferred← citeshttps://doi.org/10.1038/s41598-023-36863-1openalex-snapshot
Development of a novel air–liquid interface airway tissue equivalent model for in vitro respiratory modeling studies
inferred← citeshttps://doi.org/10.1038/s41598-023-44797-xopenalex-snapshot
Lung stiffness of C57BL/6 versus BALB/c mice
inferred← citeshttps://doi.org/10.1038/s41598-024-83187-9openalex-snapshot
SOCS domain targets ECM assembly in lung fibroblasts and experimental lung fibrosis
inferred← citeshttps://doi.org/10.1038/s41598-025-00438-zopenalex-snapshot
A next-generation system for smoke inhalation integrated with a breathing lung-on-chip to model human lung responses to cigarette exposure
inferred← citeshttps://doi.org/10.1038/s42003-021-01695-0openalex-snapshot
Second-generation lung-on-a-chip with an array of stretchable alveoli made with a biological membrane
inferred← citeshttps://doi.org/10.1038/s43856-026-01406-yopenalex-snapshot
Intraoperative biopsy imaging of lung cancer risk
inferred← citeshttps://doi.org/10.1039/c9lc00267gopenalex-snapshot
Magnetic microboats for floating, stiffness tunable, air–liquid interface epithelial cultures
inferred← citeshttps://doi.org/10.1039/d0tb00613kopenalex-snapshot
Clickable decellularized extracellular matrix as a new tool for building hybrid-hydrogels to model chronic fibrotic diseases in vitro
inferred← citeshttps://doi.org/10.1039/d2bm00827kopenalex-snapshot
Alveolar epithelial cells and microenvironmental stiffness synergistically drive fibroblast activation in three-dimensional hydrogel lung models
inferred← citeshttps://doi.org/10.1042/bst20190569openalex-snapshot
Three-dimensional models of the lung: past, present and future: a mini review
inferred← citeshttps://doi.org/10.1042/cs20190893openalex-snapshot
Regulation of cellular senescence by extracellular matrix during chronic fibrotic diseases
inferred← citeshttps://doi.org/10.1053/j.semperi.2019.07.009openalex-snapshot
Basic and translational science advances in congenital diaphragmatic hernia
inferred← citeshttps://doi.org/10.1063/5.0289275openalex-snapshot
Integration of single-cell and bulk transcriptomics uncovers CHST6 as a shared pathogenic driver in idiopathic pulmonary fibrosis and lung cancer
inferred← citeshttps://doi.org/10.1080/01913123.2020.1858214openalex-snapshot
Smoking effect on the ultrastructural properties of cultured lung myofibroblasts
inferred← citeshttps://doi.org/10.1080/08820139.2026.2644290openalex-snapshot
Propofol Exerted an Anti-Asthmatic Effect by Attenuating Extracellular Matrix Deposition and Viability of Airway Smooth Muscle Cells
inferred← citeshttps://doi.org/10.1080/15257770.2023.2300982openalex-snapshot
Integrative bioinformatics analysis reveals ECM and nicotine-related genes in both LUAD and LUSC, but different lung fibrosis-related genes are involved in LUAD and LUSC
inferred← citeshttps://doi.org/10.1080/17476348.2019.1623028openalex-snapshot
Pulmonary fibrosis: a disease of alveolar collapse and collagen deposition
inferred← citeshttps://doi.org/10.1088/1758-5090/ad91e2openalex-snapshot
Integration of bioprinting advances and biomechanical strategies for in vitro lung modelling
inferred← citeshttps://doi.org/10.1088/1758-5090/ae2e44openalex-snapshot
Microengineered alveolar array lung-on-chip with hydrogel membrane and simulated breathing mechanics for anti-fibrotic testing
inferred← citeshttps://doi.org/10.1089/gtmb.2019.0119openalex-snapshot
Association of the Collagen Type IV Alpha 1 Chain Gene rs3783107 GG Genotype with Hypertension, Asthma, and Eczema: The Tampere Adult Population Cardiovascular Risk Study
inferred← citeshttps://doi.org/10.1089/ten.tec.2017.0283openalex-snapshot
Generation of a Close-to-Native In Vitro System to Study Lung Cells–Extracellular Matrix Crosstalk
inferred← citeshttps://doi.org/10.1093/gerona/glac226openalex-snapshot
Periostin Plasma Levels and Changes on Physical and Cognitive Capacities in Community-Dwelling Older Adults
inferred← citeshttps://doi.org/10.1093/hmg/ddz069openalex-snapshot
Exploring the cross-phenotype network region of disease modules reveals concordant and discordant pathways between chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis
inferred← citeshttps://doi.org/10.1093/imammb/dqad004openalex-snapshot
A dynamical model of TGF- β activation in asthmatic airways
inferred← citeshttps://doi.org/10.1097/mot.0000000000000584openalex-snapshot
Lung bioengineering: advances and challenges in lung decellularization and recellularization
inferred← citeshttps://doi.org/10.1101/2021.03.10.434858openalex-snapshot
The NOTCH3 Downstream Target HEYL Regulates Human Airway Epithelial Club Cell Differentiation
inferred← citeshttps://doi.org/10.1101/2022.09.21.508886openalex-snapshot
Development of a Novel Air-Liquid Interface Airway Tissue Equivalent Model for In Vitro Respiratory Modeling Studies
inferred← citeshttps://doi.org/10.1101/2023.05.03.539323openalex-snapshot
Pulmonary Matrix Derived Hydrogels from Patients with Idiopathic Pulmonary Fibrosis Induce a Proinflammatory State in Lung Fibroblasts In Vitro
inferred← citeshttps://doi.org/10.1101/2023.08.09.552718openalex-snapshot
Epigenetic Regulation of Endothelial Extracellular Matrix Components is Critical for Murine Lung Development
inferred← citeshttps://doi.org/10.1101/2024.12.05.626371openalex-snapshot
Interaction of osteoprotegerin with fibulin-1 is essential for extracellular matrix deposition in fibrotic lung tissue
inferred← citeshttps://doi.org/10.1101/608919openalex-snapshot
Second-generation lung-on-a-chip array with a stretchable biological membrane
inferred← citeshttps://doi.org/10.1101/813907openalex-snapshot
Targeting Lysyl oxidase-like 2 in Idiopathic Pulmonary Fibrosis
inferred← citeshttps://doi.org/10.1101/855155openalex-snapshot
Persistence of a novel regeneration-associated transitional cell state in pulmonary fibrosis
inferred← citeshttps://doi.org/10.1109/tbme.2025.3553375openalex-snapshot
Quantification of Lung Stiffness Using Magnetic Resonance Elastography (MRE): Clinical Validation for Smokers
inferred← citeshttps://doi.org/10.1111/resp.13142openalex-snapshot
VEGF synthesis is induced by prostacyclin and TGF ‐β in distal lung fibroblasts from COPD patients and control subjects: I mplications for pulmonary vascular remodelling
inferred← citeshttps://doi.org/10.1115/1.4051118openalex-snapshot
Mechanobiology of Pulmonary Diseases: A Review of Engineering Tools to Understand Lung Mechanotransduction
inferred← citeshttps://doi.org/10.1126/sciadv.aef1694openalex-snapshot
Targeting LOXL4-driven matrix stiffening with acetyldigoxin restores CD8 + T cell function in lung cancer
inferred← citeshttps://doi.org/10.1136/thorax-2026-225369openalex-snapshot
Breathing immunity into in vitro lung models
inferred← citeshttps://doi.org/10.1152/ajpcell.00060.2023openalex-snapshot
Strategic outline of interventions targeting extracellular matrix for promoting healthy longevity
inferred← citeshttps://doi.org/10.1152/ajpcell.00162.2022openalex-snapshot
Defining the versican interactome in lung health and disease
inferred← citeshttps://doi.org/10.1152/ajpcell.01007.2024openalex-snapshot
Compositional changes of the lung extracellular matrix in acute respiratory distress syndrome
inferred← citeshttps://doi.org/10.1152/ajplung.00037.2018openalex-snapshot
Fibroblast senescence in the pathology of idiopathic pulmonary fibrosis
inferred← citeshttps://doi.org/10.1152/ajplung.00053.2017openalex-snapshot
TGF-β1-induced deposition of provisional extracellular matrix by tracheal basal cells promotes epithelial-to-mesenchymal transition in a c-Jun NH2-terminal kinase-1-dependent manner
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.00222.2019openalex-snapshot
Laminin α4 contributes to airway remodeling and inflammation in asthma
inferred← citeshttps://doi.org/10.1152/ajplung.00265.2025openalex-snapshot
Immunomodulation of the Innate Host Response by Mesenchymal-Derived Versican during Influenza A Virus Infection
inferred← citeshttps://doi.org/10.1152/ajplung.00325.2018openalex-snapshot
Small airway hyperresponsiveness in COPD: relationship between structure and function in lung slices
inferred← citeshttps://doi.org/10.1152/ajplung.00353.2018openalex-snapshot
Tissue-informed engineering strategies for modeling human pulmonary diseases
inferred← citeshttps://doi.org/10.1152/ajplung.00415.2017openalex-snapshot
Aging and anatomical variations in lung tissue stiffness
inferred← citeshttps://doi.org/10.1152/ajplung.00445.2022openalex-snapshot
Mucopolysaccharidosis (MPS IIIA) mice have increased lung compliance and airway resistance, decreased diaphragm strength, and no change in alveolar structure
inferred← citeshttps://doi.org/10.1152/ajplung.00451.2019openalex-snapshot
Human lung extracellular matrix hydrogels resemble the stiffness and viscoelasticity of native lung tissue
inferred← citeshttps://doi.org/10.1152/japplphysiol.00554.2020openalex-snapshot
Stiffening of the extracellular matrix is a sufficient condition for airway hyperreactivity
inferred← citeshttps://doi.org/10.1152/physiol.00039.2020openalex-snapshot
The Stress of Lung Aging: Endoplasmic Reticulum and Senescence Tête-à-Tête
inferred← citeshttps://doi.org/10.1155/2019/3638469openalex-snapshot
Transcriptomic Sequencing of Airway Epithelial Cell NCI-H292 Induced by Synthetic Cationic Polypeptides
inferred← citeshttps://doi.org/10.1155/2020/4260204openalex-snapshot
Exposure to Air Pollution Exacerbates Inflammation in Rats with Preexisting COPD
inferred← citeshttps://doi.org/10.1155/2021/8243378openalex-snapshot
Interplay between Extracellular Matrix and Neutrophils in Diseases
inferred← citeshttps://doi.org/10.11606/d.5.2018.tde-15082018-082634openalex-snapshot
O efeito do anti-IL-17 na inflama~ção, remodelamento e estresse oxidativo em modelo experimental de inflamação pulmonar alérgica crônica exacerbado por LPS
inferred← citeshttps://doi.org/10.11606/t.5.2018.tde-31102018-101055openalex-snapshot
Anti-IL17 na modulação da mecânica pulmonar, inflamação, estresse oxidativo e remodelamento da matriz extracelular em camundongos com inflamação pulmonar alérgica crônica exarcebada pelo LPS
inferred← citeshttps://doi.org/10.1161/atvbaha.124.320881openalex-snapshot
Endothelial Chromatin-Remodeling Enzymes Regulate the Production of Critical ECM Components During Murine Lung Development
inferred← citeshttps://doi.org/10.1164/rccm.201910-1958ocopenalex-snapshot
Genome-Wide Association Study: Functional Variant rs2076295 Regulates Desmoplakin Expression in Airway Epithelial Cells
inferred← citeshttps://doi.org/10.1164/rccm.201912-2338ocopenalex-snapshot
Lung Development Genes and Adult Lung Function
inferred← citeshttps://doi.org/10.1164/rccm.202310-1972ppopenalex-snapshot
Molecular Characterization of the Distal Lung: Novel Insights from Chronic Obstructive Pulmonary Disease Omics
inferred← citeshttps://doi.org/10.1165/rcmb.2017-0252ocopenalex-snapshot
Lysyl Oxidase–Like 1 Protein Deficiency Protects Mice from Adenoviral Transforming Growth Factor-β1–induced Pulmonary Fibrosis
inferred← citeshttps://doi.org/10.1165/rcmb.2023-0176psopenalex-snapshot
Extracellular Matrix as a Driver of Chronic Lung Diseases
inferred← citeshttps://doi.org/10.1172/jci.insight.131232openalex-snapshot
Interleukin-13 disrupts type 2 pneumocyte stem cell activity
inferred← citeshttps://doi.org/10.1172/jci.insight.153058openalex-snapshot
Increased expression and accumulation of GDF15 in IPF extracellular matrix contribute to fibrosis
inferred← citeshttps://doi.org/10.1172/jci170499openalex-snapshot
Pulmonary inflammation and fibroblast immunoregulation: from bench to bedside
inferred← citeshttps://doi.org/10.1177/02676591221128141openalex-snapshot
Relaxation and creep response of the alveolar lung to diagnosis and treatments for respiratory and lung disorders
inferred← citeshttps://doi.org/10.1177/2041731418810164openalex-snapshot
Equine lung decellularization: a potential approach for in vitro modeling the role of the extracellular matrix in asthma
inferred← citeshttps://doi.org/10.1183/13993003.01805-2016openalex-snapshot
The instructive extracellular matrix of the lung: basic composition and alterations in chronic lung disease
inferred← citeshttps://doi.org/10.1183/13993003.02665-2017openalex-snapshot
Multi-omic molecular profiling of lung cancer in COPD
inferred← citeshttps://doi.org/10.1183/16000617.0124-2019openalex-snapshot
Extracellular matrix remodelling in COPD
inferred← citeshttps://doi.org/10.1183/16000617.0155-2025openalex-snapshot
The importance of mechanical forces in chronic respiratory diseases
inferred← citeshttps://doi.org/10.1183/16000617.0202-2021openalex-snapshot
Chronic lung diseases: entangled in extracellular matrix
inferred← citeshttps://doi.org/10.1183/20734735.0147-2022openalex-snapshot
Idiopathic pulmonary fibrosis and lung cancer: future directions and challenges
inferred← citeshttps://doi.org/10.1183/20734735.0260-2025openalex-snapshot
The metabolic code of pulmonary disease: from mechanisms to therapeutic opportunities
inferred← citeshttps://doi.org/10.1186/s12014-019-9226-4openalex-snapshot
Quantitative proteomic characterization of lung tissue in idiopathic pulmonary fibrosis
inferred← citeshttps://doi.org/10.1186/s12885-018-4772-0openalex-snapshot
Diagnostic role of circulating extracellular matrix-related proteins in non-small cell lung cancer
inferred← citeshttps://doi.org/10.1186/s12890-023-02678-zopenalex-snapshot
Integrated bioinformatics analysis for the identification of idiopathic pulmonary fibrosis–related genes and potential therapeutic drugs
inferred← citeshttps://doi.org/10.1186/s12931-018-0768-1openalex-snapshot
FK506-binding protein 10 (FKBP10) regulates lung fibroblast migration via collagen VI synthesis
inferred← citeshttps://doi.org/10.1186/s12931-019-1192-xopenalex-snapshot
Protein phosphatase 2A (PP2A): a key phosphatase in the progression of chronic obstructive pulmonary disease (COPD) to lung cancer
inferred← citeshttps://doi.org/10.1186/s12931-023-02548-6openalex-snapshot
3D in vitro hydrogel models to study the human lung extracellular matrix and fibroblast function
inferred← citeshttps://doi.org/10.1186/s12931-024-02907-xopenalex-snapshot
Altered hypoxia-induced cellular responses and inflammatory profile in lung fibroblasts from COPD patients compared to control subjects
inferred← citeshttps://doi.org/10.1186/s12931-024-03007-6openalex-snapshot
MiR-1307-5p enhances fibroblast transdifferentiation to exacerbate chronic obstructive pulmonary disease through regulating FBXL16/HIF1α axis
inferred← citeshttps://doi.org/10.1186/s12943-023-01744-8openalex-snapshot
Extracellular matrix remodeling in tumor progression and immune escape: from mechanisms to treatments
inferred← citeshttps://doi.org/10.1186/s12964-022-01032-wopenalex-snapshot
Resistin-like molecules: a marker, mediator and therapeutic target for multiple diseases
inferred← citeshttps://doi.org/10.1186/s13054-024-04942-yopenalex-snapshot
Effects of mechanical ventilation on the interstitial extracellular matrix in healthy lungs and lungs affected by acute respiratory distress syndrome: a narrative review
inferred← citeshttps://doi.org/10.1186/s13287-022-02830-2openalex-snapshot
Reconstructing the pulmonary niche with stem cells: a lung story
inferred← citeshttps://doi.org/10.1186/s42490-019-0014-zopenalex-snapshot
A high content, phenotypic ‘scar-in-a-jar’ assay for rapid quantification of collagen fibrillogenesis using disease-derived pulmonary fibroblasts
inferred← citeshttps://doi.org/10.1186/s43556-026-00436-1openalex-snapshot
The extracellular matrix: structure, composition, biological functions, diseases, and therapeutic targets
inferred← citeshttps://doi.org/10.1242/dmm.030114openalex-snapshot
Lysyl oxidases regulate fibrillar collagen remodelling in idiopathic pulmonary fibrosis
inferred← citeshttps://doi.org/10.12677/acm.2025.1541258openalex-snapshot
Research Progress of Exosomes in Extracellular Matrix Related Diseases
inferred← citeshttps://doi.org/10.1371/journal.pone.0254710openalex-snapshot
Aging increases senescence, calcium signaling, and extracellular matrix deposition in human airway smooth muscle
inferred← citeshttps://doi.org/10.1371/journal.pone.0281640openalex-snapshot
Glycolytic reprogramming is involved in tissue remodeling on chronic rhinosinusitis
inferred← citeshttps://doi.org/10.14814/phy2.15275openalex-snapshot
Haploinsufficiency of Col5a1 causes intrinsic lung and respiratory changes in a mouse model of classical Ehlers‐Danlos syndrome
inferred← citeshttps://doi.org/10.17691/stm2018.10.4.25openalex-snapshot
Metabolism of the Extracellular Matrix in Bronchial Asthma (Review)
inferred← citeshttps://doi.org/10.18093/0869-0189-2020-30-1-17-22openalex-snapshot
The role of mutations in metalloproteinases and the epithelial growth factor receptor genes in the pathogenesis of children bronchial asthma
inferred← citeshttps://doi.org/10.18297/etd/3049openalex-snapshot
Perinatal nicotine with or without early life influenza infection leads to lung dysfunction with age.
inferred← citeshttps://doi.org/10.21037/jtd.2017.11.41openalex-snapshot
Best of Milan 2017—repair of the emphysematous lung: mesenchymal stromal cell and matrix
inferred← citeshttps://doi.org/10.2147/copd.s150401openalex-snapshot
Low back pain and gastroesophageal reflux in patients with COPD: the disease in the breath
showing the first 200 of 265 · page through all 265
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.