Results 101 to 110 of about 209,966 (285)

Target inhibition of galectin-3 by inhaled TD139 in patients with idiopathic pulmonary fibrosis

open access: yesEuropean Respiratory Journal, 2020
Galectin (Gal)-3 is a profibrotic β-galactoside-binding lectin that plays a key role in the pathogenesis of idiopathic pulmonary fibrosis (IPF) and IPF exacerbations. TD139 is a novel and potent small-molecule inhibitor of Gal-3.
N. Hirani   +24 more
semanticscholar   +1 more source

Epidemiology of idiopathic pulmonary fibrosis

open access: yesClinical Epidemiology, 2013
Brett Ley, Harold R Collard Department of Medicine, Division of Pulmonary and Critical Care Medicine, University of California San Francisco, San Francisco, California, USA Abstract: Idiopathic pulmonary fibrosis is a chronic fibrotic lung disease of ...
Ley B, Collard HR
doaj  

Diffuse pulmonary ossification associated with fibrosing interstitial lung disease

open access: yesRespiratory Medicine Case Reports, 2019
Diffuse pulmonary ossification (DPO) is a rare condition that presents with metaplastic mature bone formation in the pulmonary parenchyma. DPO is usually associated with cardiovascular or respiratory disease.
Badreeddine Alami   +6 more
doaj   +1 more source

Genetic partitioning of interleukin-6 signalling in mice dissociates Stat3 from Smad3-mediated lung fibrosis [PDF]

open access: yes, 2012
Idiopathic pulmonary fibrosis (IPF) is a fatal disease that is unresponsive to current therapies and characterized by excessive collagen deposition and subsequent fibrosis.
Anderson, G.P.   +19 more
core   +2 more sources

Diagnostic test interpretation and referral delay in patients with interstitial lung disease. [PDF]

open access: yes, 2019
BACKGROUND:Diagnostic delays are common in patients with interstitial lung disease (ILD). A substantial percentage of patients experience a diagnostic delay in the primary care setting, but the factors underpinning this observation remain unclear.
Adegunsoye, Ayodeji   +11 more
core   +1 more source

Growth factors in idiopathic pulmonary fibrosis: relative roles [PDF]

open access: yes, 2001
Treatment of idiopathic pulmonary fibrosis patients has evolved very slowly; the fundamental approach of corticosteroids alone or in combination with other immunosuppressive agents has had little impact on long-term survival.
Allen, JT, Spiteri, MA
core   +3 more sources

DROSHA-Dependent AIM2 Inflammasome Activation Contributes to Lung Inflammation during Idiopathic Pulmonary Fibrosis

open access: yesCells, 2019
Idiopathic pulmonary fibrosis (IPF) has been linked to chronic lung inflammation. Drosha ribonuclease III (DROSHA), a class 2 ribonuclease III enzyme, plays a key role in microRNA (miRNA) biogenesis.
Soo Jung Cho   +6 more
doaj   +1 more source

Periostin as a biomarker of airway inflammation [PDF]

open access: yes, 2016
No abstract ...
Johnstone, Steven, McSharry, Charles
core   +1 more source

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