Loss of structural integrity and function of surfactant protein D (SP-D) by cystic fibrosis- related proteases Source: Eur Respir J 2001; 18: Suppl. 33, 537s Year: 2001
Characterization of the activity of the different oligomeric forms of pulmonary human surfactant protein SP-D Source: International Congress 2019 – Host-microbe interactions in lung disease and exacerbations Year: 2019
Global gene expression analyses highlight the role of plasma membrane remodeling as a molecular functions of airway epithelium in response to interleukin-13 treatment Source: International Congress 2015 – Promising novel findings in translational pulmonary research Year: 2015
Old and novel surfactant protein C (SP-C) mutations in children Source: Annual Congress 2011 - Rare diffuse lung diseases Year: 2011
SFTA3, a novel protein of the lung: three-dimensional structure, characterisation and immune activation Source: Eur Respir J 2014; 44: 447-456 Year: 2014
Effects of Cys85 on biochemical properties and biological function of human SP-A variants Source: Annual Congress 2007 - Bronchiolitis - genetics and immunity Year: 2007
Increased expression of Lysosomal-associated membrane protein 1 (LAMP-1) found in small airway epithelium of COPD may have functional consequence and role in autophagy. Source: International Congress 2017 – Towards personalised medicine in COPD: biological and clinical phenotypes Year: 2017
Understanding the regulation of surfactant gene expression Source: Eur Respir J 2003; 22: 6-7 Year: 2003
Visualization of apoptosis-related proteins in lung treated with recombinant human active protein C in sepsis model Source: Eur Respir J 2005; 26: Suppl. 49, 221s Year: 2005
A mycobacterial encoded hypothetical protein is localized in mitochondria and regulates oxidative phosphorylation of infected macrophage. Source: International Congress 2019 – Tuberculosis: from diagnosis to complications Year: 2019
The possible molecular mechanism of immune injury in the mice treated with SARS-CoV spike protein Source: Eur Respir J 2007; 30: Suppl. 51, 406s Year: 2007
Identification of a novel water-soluble activator of wild-type and F508del CFTR: GPact-11a Source: Eur Respir J 2010; 36: 311 Year: 2010
A novel non-BRICHOS surfactant protein C mutation causing infantile interstitial lung disease is associated with reduced mature SP-C level Source: International Congress 2018 – Orphan diseases in children Year: 2018
MAV(S)erick mitochondria: an unconventional role for mitochondrial antiviral signalling protein in pulmonary fibrosis Source: Eur Respir J, 57 (4) 2004500; 10.1183/13993003.04500-2020 Year: 2021
FK506-binding protein 11, a novel plasma cell specific antibody folding catalyst, is increased in idiopathic pulmonary fibrosis Source: Virtual Congress 2020 – Novel immunopathological mechanisms of lung disease: knowledge from translational studies Year: 2020
Expression and function of a novel membrane-spanning protein, MS4A8B, in the human airways Source: International Congress 2015 – Translational studies in airway cell biology Year: 2015
Characterizations and potential functions of protein arginine methyltransferase 1 in primary lung structural cells Source: International Congress 2015 – Systemic and airway biomarkers Year: 2015
Role of ABCA3 in paediatric interstitial lung disease associated with surfactant protein C gene mutations Source: Annual Congress 2009 - Genetics of lung diseases Year: 2009
Cellular and biochimical evidence of pathobiology in hypersensitiviy Source: Research Sem. 13 Year: 2013