Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial lung disease of unknown origin
that usually results in death from secondary respiratory failure within 2–5 years of diagnosis …

Idiopathic pulmonary fibrosis (IPF) is a fatal lung disease manifested by overtly scarred
peripheral and basilar regions and more normal-appearing central lung areas. Lung tissues …

Interstitial lung diseases (ILDs) are a heterogeneous group of> 100 pulmonary disorders.
ILDs are characterized by an irreversible architectural distortion and impaired gas …

Airway hyperresponsiveness (AHR) often defines asthma. Murine allergic airway disease
(AAD), like human eosinophilic asthma, is characterized by AHR, eosinophilia, goblet cell …

Background Thickening of the lamina reticularis, a feature of remodeling in the asthmatic
airways, is now known to be present in young children who wheeze. Human rhinovirus …

AIM To test whether homocysteine (Hcy) can influence the transcriptional profile, we
hypothesized that Hcy can lead to the induction of proinflammatory molecules in the retinal …

CXC chemokine receptor 3 (CXCR3) A and its IFN-inducible ligands CXCL9 and CXCL10
regulate vascular remodeling and fibroblast motility. IL-13 is a profibrotic cytokine implicated …

Idiopathic pulmonary fibrosis (IPF) is a specific form of chronic, progressive fibrosing
interstitial pneumonia with poor diagnosis and a median survival of 2–3 years from initial …

Despite significant advances have been achieved in the genetic characterization of sporadic
colorectal cancer (sCRC), the precise genetic events leading to the development of distant …

IL-13 is a pro-fibrotic cytokine that can bind to two receptors, IL-13Rα1 and IL-13Rα2. IL-
13Rα2 used to be regarded as a decoy receptor. However, recent studies indicated that it …