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American Journal of Respiratory Cell and Molecular Biology|June 9, 2009
TLR-4-mediated innate immunity is reduced in cystic fibrosis airway cellsGerrit John, Ali O Yildirim, Bruce K Rubin, et al.Chest|January 21, 2006
Mucus properties in children with primary ciliary dyskinesia: comparison with cystic fibrosisAndrew Bush, Donald Payne, Sarah Pike, et al.Respiratory Medicine Case Reports|February 26, 2025
Reduced tracheal stenosing effect of nintedanib in a patient with scarred posttraumatic tracheal stenosis and airflow limitation - a case reportStefanie Klampfleitner, Andreas Fertl, Ositha Prinz, et al.American Journal of Respiratory Cell and Molecular Biology|February 28, 2004
MUC5AC and MUC5B Mucins Are Decreased in Cystic Fibrosis Airway SecretionsMarkus O Henke, Armin Renner, Rudolf M Huber, et al.Experimental Lung Research|November 9, 2006
Up-regulation of S100A8 and S100A9 protein in bronchial epithelial cells by lipopolysaccharideMarkus O Henke, Armin Renner, Bruce K Rubin, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 4, 2015
A small molecule neutrophil elastase inhibitor, KRP-109, inhibits cystic fibrosis mucin degradationShashi Chillappagari, Christian Müller, Poornima Mahavadi, et al.Pediatric Pulmonology|January 24, 2012
Clarithromycin therapy for patients with cystic fibrosis: a randomized controlled trialP Robinson, Michael S Schechter, Peter D Sly, et al.Respiratory Research|July 15, 2015
Altered protease and antiprotease balance during a COPD exacerbation contributes to mucus obstructionShashi Chillappagari, Jenni Preuss, Sebastian Licht, et al.American Journal of Physiology. Lung Cellular and Molecular Physiology|September 21, 2014
Impaired TLR4 and HIF expression in cystic fibrosis bronchial epithelial cells downregulates hemeoxygenase-1 and alters iron homeostasis in vitroShashi Chillappagari, Shalini Venkatesan, Virajith Garapati, et al.Pageof 2