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Fibulin-1 Is Increased in Asthma – A Novel Mediator of Airway Remodeling?
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Wound repair in the context of extracellular matrix
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GON-1 and Fibulin Have Antagonistic Roles in Control of Organ Shape
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Characterization and functional analysis of osteoblast-derived fibulins in the human hematopoietic stem cell niche
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Extracellular matrix proteins modulate asthmatic airway smooth muscle cell proliferation via an autocrine mechanism
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Airway smooth muscle remodeling is a dynamic process in severe long-standing asthma
inferredcites →https://doi.org/10.1016/s0091-6749(00)90066-6openalex-snapshot
Epithelial-mesenchymal interactions in the pathogenesis of asthma
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Correlation between airway responsiveness and proteoglycan production by bronchial fibroblasts from normal and asthmatic subjects
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Suppression of anchorage-independent growth and matrigel invasion and delayed tumor formation by elevated expression of fibulin-1D in human fibrosarcoma-derived cell lines
inferredcites →https://doi.org/10.1038/sj.onc.1205171openalex-snapshot
Estrogen induction and overexpression of fibulin-1C mRNA in ovarian cancer cells
inferredcites →https://doi.org/10.1038/sj.onc.1207323openalex-snapshot
Immunological and pathobiological roles of fibulin-1 in breast cancer
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Annual Scientific Meeting of ASCEPT, 1999 Role Of Human Airway Smooth Muscle In Altered Extracellular Matrix Production In Asthma
inferredcites →https://doi.org/10.1074/jbc.272.36.22600openalex-snapshot
The Self-association and Fibronectin-binding Sites of Fibulin-1 Map to Calcium-binding Epidermal Growth Factor-like Domains
inferredcites →https://doi.org/10.1080/02713680701411269openalex-snapshot
Expression of Extracellular Matrix Proteins Fibulin-1 and Fibulin-2 by Human Corneal Fibroblasts
inferredcites →https://doi.org/10.1083/jcb.109.2.863openalex-snapshot
Analysis of fibronectin receptor function with monoclonal antibodies: roles in cell adhesion, migration, matrix assembly, and cytoskeletal organization.
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/10.1093/oxfordjournals.bmb.a072537openalex-snapshot
Pathology of asthma
inferredcites →https://doi.org/10.1128/mcb.21.20.7025-7034.2001openalex-snapshot
Perinatal Lethality and Endothelial Cell Abnormalities in Several Vessel Compartments of Fibulin-1-Deficient Mice
inferredcites →https://doi.org/10.1136/thorax.58.9.772openalex-snapshot
TGF- 1 causes airway fibrosis and increased collagen I and III mRNA in mice
inferredcites →https://doi.org/10.1159/000236981openalex-snapshot
Inhaled Corticosteroid Treatment and Extracellular Matrix in the Airways in Asthma
inferredcites →https://doi.org/10.1164/ajrccm.156.2.9605065openalex-snapshot
Transforming Growth Factor- β 1 in Asthma
inferredcites →https://doi.org/10.1164/ajrccm.156.2.9609066openalex-snapshot
Transforming Growth Factor- β Expression in Mucosal Biopsies in Asthma and Chronic Bronchitis
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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/148.3.720openalex-snapshot
Cellular Hypertrophy and Hyperplasia of Airway Smooth Muscles Underlying Bronchial Asthma: A 3-D Morphometric Study
inferredcites →https://doi.org/10.1164/rccm.200205-416ocopenalex-snapshot
Expression of Connective Tissue Growth Factor in Asthmatic Airway Smooth Muscle Cells
inferredcites →https://doi.org/10.1164/rccm.200311-1529ocopenalex-snapshot
Hyperplasia of Smooth Muscle in Mild to Moderate Asthma without Changes in Cell Size or Gene Expression
inferredcites →https://doi.org/10.1164/rccm.200406-703ocopenalex-snapshot
Connective Tissue Growth Factor Induces Extracellular Matrix in Asthmatic Airway Smooth Muscle
inferredcites →https://doi.org/10.1164/rccm.200607-1005ocopenalex-snapshot
Neonatal Chlamydial Infection Induces Mixed T-Cell Responses That Drive Allergic Airway Disease
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/7.2.149openalex-snapshot
Modulation of Fibronectin Production of Bovine Bronchial Epithelial Cells by Transforming Growth Factor-β
inferredcites →https://doi.org/10.1165/ajrcmb/7.6.574openalex-snapshot
Quantifying Proliferation of Cultured Human and Rabbit Airway Smooth Muscle Cells in Response to Serum and Platelet-derived Growth Factor
inferredcites →https://doi.org/10.1172/jci17912openalex-snapshot
Dissection of experimental asthma with DNA microarray analysis identifies arginase in asthma pathogenesis
inferredcites →https://doi.org/10.1177/43.4.7534784openalex-snapshot
The association of human fibulin-1 with elastic fibers: an immunohistological, ultrastructural, and RNA study.
inferredcites →https://doi.org/10.1183/09031936.04.00113103openalex-snapshot
Extracellular matrix regulates human airway smooth muscle cell migration
inferredcites →https://doi.org/10.1186/1465-9921-6-9openalex-snapshot
The effect of IL-13 and IL-13R130Q, a naturally occurring IL-13 polymorphism, on the gene expression of human airway smooth muscle cells
inferredcites →https://doi.org/10.1186/1471-2164-5-21openalex-snapshot
Functional classes of bronchial mucosa genes that are differentially expressed in asthma
inferredcites →https://doi.org/10.1242/jcs.114.24.4587openalex-snapshot
Fibulin-1 suppression of fibronectin-regulated cell adhesion and motility
inferredcites →https://doi.org/10.15036/arerugi.45.792openalex-snapshot
GLOBAL STRATEGY FOR ASTHMA MANAGEMENT AND PREVENTION
inferredcites →https://doi.org/10.2174/1874-470210902010110openalex-snapshot
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Macrophage–stroma interactions in fibrosis: biochemical, biophysical, and cellular perspectives
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Smooth Muscle Cells
inferred← citeshttps://doi.org/10.1016/b978-0-323-08593-9.00021-8openalex-snapshot
Noncontractile Functions of Airway Smooth Muscle
inferred← citeshttps://doi.org/10.1016/b978-0-323-08593-9.00047-4openalex-snapshot
Airway Smooth Muscle Function in Asthma
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/j.aller.2011.11.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ccm.2012.05.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.chest.2025.10.047openalex-snapshot
Impact of Mepolizumab on Airway Remodeling and Inflammation in Severe Eosinophilic Asthma
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Fibulin-1 regulates the pathogenesis of tissue remodeling in respiratory diseases
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Airway Remodeling and Pulmonary Fibrosis in Asthma
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