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Human Mutation|March 6, 2018
ABCA3 missense mutations causing surfactant dysfunction disorders have distinct cellular phenotypesUlrike Schindlbeck, Thomas Wittmann, Stefanie Höppner, et al.
American Journal of Respiratory and Critical Care Medicine|April 20, 2019
Quantitative Lipidomics in Pulmonary Alveolar ProteinosisMatthias Griese, Francesco Bonella, Ulrich Costabel, et al.
Respirology (Carlton, Vic.)|June 2, 2017
Serum YKL-40 is a reliable biomarker for pulmonary alveolar proteinosisFrancesco Bonella, Xiaoping Long, Xuan He, et al.
Respiratory Research|November 9, 2005
Sequential analysis of surfactant, lung function and inflammation in cystic fibrosis patientsMatthias Griese, Robert Essl, Reinhold Schmidt, et al.
Biochimica Et Biophysica Acta|March 31, 2015
ABCA3 protects alveolar epithelial cells against free cholesterol induced cell deathRalf Zarbock, Eva Kaltenborn, Sabrina Frixel, et al.
Molecular Medicine (Cambridge, Mass.)|March 2, 2016
Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3Thomas Wittmann, Sabrina Frixel, Stefanie Höppner, et al.
Chest|May 15, 2026
Further genetic unravelling of persistent tachypnoea of infancy (PTI/NEHI)Christina K Rapp, Katharina Mauss-Schwarzer, Matthias Kappler, et al.
Plos One|April 1, 2016
Analysis of the Proteolytic Processing of ABCA3: Identification of Cleavage Site and Involved ProteasesNicole Hofmann, Dmitry Galetskiy, Daniela Rauch, et al.
American Journal of Respiratory and Critical Care Medicine|July 24, 2004
Pulmonary surfactant, lung function, and endobronchial inflammation in cystic fibrosisMatthias Griese, Robert Essl, Reinhold Schmidt, et al.
The European Respiratory Journal|May 2, 2015
CXCR4+ granulocytes reflect fungal cystic fibrosis lung diseaseMelanie Carevic, Anurag Singh, Nikolaus Rieber, et al.
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