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American Journal of Respiratory Cell and Molecular Biology|October 9, 2012
Expression and regulation of interferon-related development regulator-1 in cystic fibrosis neutrophilsAndreas Hector, Michael Kormann, Julia Kammermeier, et al.
Plos One|September 28, 2011
The chitinase-like protein YKL-40 modulates cystic fibrosis lung diseaseAndreas Hector, Michael S D Kormann, Ines Mack, et al.
BMC Pulmonary Medicine|August 13, 2015
GATA2 deficiency in children and adults with severe pulmonary alveolar proteinosis and hematologic disordersMatthias Griese, Ralf Zarbock, Ulrich Costabel, 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.
International Journal of Molecular Sciences|September 27, 2019
Causes and Consequences of A Glutamine Induced Normoxic HIF1 Activity for the Tumor MetabolismMatthias Kappler, Ulrike Pabst, Claus Weinholdt, et al.
Thorax|August 13, 2016
Lung disease caused by ABCA3 mutationsCarolin Kröner, Thomas Wittmann, Simone Reu, et al.
American Journal of Respiratory and Critical Care Medicine|May 2, 2013
Inhalation treatment with glutathione in patients with cystic fibrosis. A randomized clinical trialMatthias Griese, Matthias Kappler, Claudia Eismann, et al.
American Journal of Human Genetics|February 3, 2009
Mutations in SPINT2 cause a syndromic form of congenital sodium diarrheaPeter Heinz-Erian, Thomas Müller, Birgit Krabichler, et al.
Ebiomedicine|June 15, 2020
DRH1 - a novel blood-based HPV tumour markerThomas Weiland, Alexander Eckert, Peter Valentin Tomazic, et al.
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