Source: Annual Congress 2010 - Pathogenesis of diffuse parenchymal lung disease
Disease area: Interstitial lung diseases



Rating:

Share or cite this content

Citations should be made in the following way:
D. Waisberg, E. Parra, R. Kairalla, C. Carvalho, J. Barbas, V. Capelozzi (Brazil). Early remodeling of collapsed areas in usual interstitial pneumonia is characterized by high expression of fibrogenic activity makers. Eur Respir J 2010; 36: Suppl. 54, 4173

Member's Comments

No comment yet.

Related content which might interest you: High expression of telomerase/endothelin-1 increase replication and activation of vascular myofibroblasts in usual interstitial pneumonia/idiopathic pulmonary fibrosis Source: Annual Congress 2010 - Pathogenesis of diffuse parenchymal lung disease Year: 2010 Vascular remodeling process in usual interstitial pneumonia Source: Eur Respir J 2004; 24: Suppl. 48, 320s Year: 2004 High mobility group box protein 1 (HMGB1) production in highly vascularized alveolar lesions causes acute exacerbation in idiopathic pulmonary fibrosis Source: Annual Congress 2005 - Progresses in lung fibrosis Year: 2005 Markers of fibrosis and tissue destruction in usual interstitial pneumonia associated with pulmonary emphysema Source: Eur Respir J 2007; 30: Suppl. 51, 489s Year: 2007 The markers of inflammatory process activity and fybrogenesis activity in patients with idiopathic pulmonary fibrosis Source: Annual Congress 2012 - Diffuse parenchymal lung disease I Year: 2012 SP-C deficiency causes early alveolar de-recruitment resulting in a combination of air spaces over-distension and spontaneous fibrotic remodeling in aging lungs Source: International Congress 2019 – New mechanistic insights into pulmonary fibrosis Year: 2019 Simultaneous existence of diffuse alveolar damage and subpleural limited usual interstitial pneumonia lesion ( focal-UIP ) in clinical acute interstitial pneumonia Source: Eur Respir J 2003; 22: Suppl. 45, 43s Year: 2003 Procoagulant and antifibrynolitic activities strongly correlate with fibrosis and tissue turn-over markers in patients with active idiopathic pulmonary fibrosis and hypersensitivity pneumonitis Source: Annual Congress 2008 - Clinical aspects of interstitial lung disease Year: 2008 Architectural remodelling in usual interstitial pneumonia: from alveolar collapse and mural organizing fibrosis to honeycombing Source: Eur Respir J 2004; 24: Suppl. 48, 557s Year: 2004 RhoA signalling influences cyclin D1 expression and associated fibroblast turnover: implications for idiopathic pulmonary fibrosis (IPF) Source: Annual Congress 2006 - Lung vascular and parenchymal remodeling Year: 2006 Treg alterations lead to systemic and local immune deregulation in idiopathic pulmonary fibrosis and collagen vascular disease-associated interstitial pneumonia Source: Annual Congress 2007 - Cell biology of asthma and COPD Year: 2007 Histology and pathogenesis of usual interstitial pneumonia (UIP) versus nonspecific interstitial pneumonia (NSIP): progressive remodeling or resolution and healing? Source: Annual Congress 2006 - Usual interstitial pneumonia (UIP) and nonspecific interstitial pneumonia (NSIP), idiopathic or not: new concepts in diagnosis and treatment Year: 2006 Lymphatic fluctuation in parenchymal remodelling stage of organising pneumonia, nonspecific interstitial pneumonia and idiopathic pulmonary fibrosis Source: Annual Congress 2009 - Various backgrounds in diffuse parenchymal lung disease Year: 2009 Experimental model resembling the histological pattern of usual interstitial pneumonia and reinforcing the epithelial injury as pathway Source: Annual Congress 2011 - Experimental models and research in diffuse parenchymal lung diseases Year: 2011 The progressive fibrotic phenotype in fibrotic ILDs: the critical importance of observed disease behaviour Source: International Congress 2019 – Lumping and splitting of fibrotic interstitial lung diseases Year: 2019 The activity of the inflammatory process and markers of an extracellular matrix destruction in pulmonary tuberculoma Source: Virtual Congress 2020 – Mechanistic insight into lung injury and repair Year: 2020 Clinical course and lung function change of idiopathic nonspecific interstitial pneumonia Source: Eur Respir J 2009; 33: 68-76 Year: 2009 Accumulation of mast cell subtypes in areas of remodeling in COPD and cystic fibrosis Source: Annual Congress 2008 - Basic science in asthma and COPD Year: 2008 The expression of antioxidants in small airways in COPD is increased, heterogeneous and correlates with local histopathological alterations Source: Annual Congress 2009 - COPD: basic science and clinical studies Year: 2009 Differences in expression of apoptosis regulatory proteins in idiopathic pulmonary fibrosis and cryptogenic organizing pneumonia Source: Eur Respir J 2006; 28: Suppl. 50, 306s Year: 2006