Stefanie Höppner

Functional rescue of misfolding ABCA3 mutations by small molecular correctors

Susanna Kinting, Stefanie Höppner, Ulrike Schindlbeck et al. · Human Molecular Genetics · 2018 · 56 citations · Full text

Functional Rescue, Inflammatory Lung Disease, Structural Bioinformatics +18

ABCA3 missense mutations causing surfactant dysfunction disorders have distinct cellular phenotypes

Ulrike Schindlbeck, Thomas Wittmann, Stefanie Höppner et al. · Human Mutation · 2018 · 38 citations

Abca3 Missense Mutations, Molecular Biology, Pathology +16

Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3

Thomas Wittmann, Sabrina Frixel, Stefanie Höppner et al. · Molecular Medicine · 2016 · 26 citations · Full text

Tools to explore ABCA3 mutations causing interstitial lung disease

Thomas Wittmann, Ulrike Schindlbeck, Stefanie Höppner et al. · Pediatric Pulmonology · 2016 · 24 citations

Quantification of volume and lipid filling of intracellular vesicles carrying the ABCA3 transporter

Stefanie Höppner, Susanna Kinting, Adriano A. Torrano et al. · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · 2017 · 18 citations

Membrane Transport, Physiology, Lipid Filling +12