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Search Results to David A Schwartz

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

One or more keywords matched the following items that are connected to Schwartz, David

Item TypeName
Academic Article The effects of inhalation of grain dust extract and endotoxin on upper and lower airways.
Academic Article Subchronic endotoxin inhalation causes persistent airway disease.
Academic Article Ozone-induced acute pulmonary injury in inbred mouse strains.
Academic Article Altered surfactant protein A gene expression and protein metabolism associated with repeat exposure to inhaled endotoxin.
Academic Article Fibroproliferation in LPS-induced airway remodeling and bleomycin-induced fibrosis share common patterns of gene expression.
Academic Article TLR4 mutations are associated with endotoxin hyporesponsiveness in humans.
Academic Article The clinical and environmental determinants of airway transcriptional profiles in allergic asthma.
Academic Article Detrimental role of the airway mucin Muc5ac during ventilator-induced lung injury.
Academic Article The idiopathic pulmonary fibrosis honeycomb cyst contains a mucocilary pseudostratified epithelium.
Academic Article Compartmentalization of the inflammatory response to inhaled grain dust.
Academic Article The genetics of innate immunity.
Academic Article Leukocyte-derived IL-10 reduces subepithelial fibrosis associated with chronically inhaled endotoxin.
Concept Intestinal Mucosa
Concept Mucous Membrane
Concept Nasal Mucosa
Concept Respiratory Mucosa
Academic Article Muc5b is required for airway defence.
Academic Article Future directions in idiopathic pulmonary fibrosis research. An NHLBI workshop report.
Academic Article Idiopathic Pulmonary Fibrosis: A Genetic Disease That Involves Mucociliary Dysfunction of the Peripheral Airways.
Academic Article The nasal methylome and childhood atopic asthma.
Academic Article The Nasal Methylome: A Key to Understanding Allergic Asthma.
Academic Article Idiopathic Pulmonary Fibrosis Is a Genetic Disease Involving Mucus and the Peripheral Airways.
Academic Article Muc5b overexpression causes mucociliary dysfunction and enhances lung fibrosis in mice.
Academic Article Revealing the Secrets of Idiopathic Pulmonary Fibrosis.
Academic Article ILC2s mediate systemic innate protection by priming mucus production at distal mucosal sites.
Academic Article Genes, other than Muc5b, play a role in bleomycin-induced lung fibrosis.

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  • Mucous Membrane

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