Stephanie Hirtz

Lack of Neutrophil Elastase Reduces Inflammation, Mucus Hypersecretion, and Emphysema, but Not Mucus Obstruction, in Mice with Cystic Fibrosis–like Lung Disease

Stefanie Gehrig, Julia Duerr, Michael Weitnauer et al. · American Journal of Respiratory and Critical Care Medicine · 2014 · 154 citations · Full text

CFTR Cl− channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis

Stephanie Hirtz, Tanja Gonska, H. H. Seydewitz et al. · Gastroenterology · 2004 · 144 citations · Full text

Fibrosis, Molecular Physiology, Signal Transduction +6

Effects of Lumacaftor–Ivacaftor Therapy on Cystic Fibrosis Transmembrane Conductance Regulator Function in Phe508del Homozygous Patients with Cystic Fibrosis

Simon Y. Graeber, Christian Dopfer, Lutz Naehrlich et al. · American Journal of Respiratory and Critical Care Medicine · 2018 · 116 citations

Preventive but Not Late Amiloride Therapy Reduces Morbidity and Mortality of Lung Disease in βENaC-overexpressing Mice

Zhe Zhou, Diana Treis, Susanne Schubert‐Bast et al. · American Journal of Respiratory and Critical Care Medicine · 2008 · 111 citations

The ΔF508 mutation results in loss of CFTR function and mature protein in native human colon

Marcus Mall, Silvia M. Kreda, April Mengos et al. · Gastroenterology · 2003 · 106 citations

Molecular Physiology, Genetics, Pathology +6