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Number of items: 5.
Journal article
Schindlbeck, Ulrike; Wittnnann, Thomas; Hoeppner, Stefanie; Kinting, Susanna; Liebisch, Gerhard; Hegermann, Jan and Griese, Matthias
(2018):
ABCA3 missense mutations causing surfactant dysfunction disorders have distinct cellular phenotypes.
In: Human Mutation, Vol. 39, No. 6: pp. 841-850
Kinting, Susanna; Hoeppner, Stefanie; Schindlbeck, Ulrike; Forstner, Maria E.; Harfst, Jacqueline; Wittmann, Thomas and Griese, Matthias
(2018):
Functional rescue of misfolding ABCA3 mutations by small molecular correctors.
In: Human Molecular Genetics, Vol. 27, No. 6: pp. 943-953
Höppner, Stefanie; Kinting, Susanna; Torrano, Adriano A.; Schindlbeck, Ulrike; Bräuchle, Christoph; Zarbock, Ralf; Wittmann, Thomas and Griese, Matthias
(2017):
Quantification of volume and lipid filling of intracellular vesicles carrying the ABCA3 transporter.
In: Biochimica et Biophysica Acta-Molecular Cell Research, Vol. 1864, No. 12: pp. 2330-2335
Wittmann, Thomas; Frixel, Sabrina; Höppner, Stefanie; Schindlbeck, Ulrike; Schams, Andrea; Kappler, Matthias; Hegermann, Jan; Wrede, Christoph; Liebisch, Gerhard; Vierzig, Anne; Zacharasiewicz, Angela; Kopp, Matthias Volkmar; Poets, Christian F.; Baden, Winfried; Hartl, Dominik; Kaam, Anton H. van; Lohse, Peter; Aslanidis, Charalampos; Zarbock, Ralf and Griese, Matthias
(2016):
Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3.
In: Molecular Medicine, Vol. 22
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Wittmann, Thomas; Schindlbeck, Ulrike; Höppner, Stefanie; Kinting, Susanna; Frixel, Sabrina; Kröner, Carolin; Liebisch, Gerhard; Hegermann, Jan; Aslanidis, Charalampos; Brasch, Frank; Reu, Simone; Lasch, Peter; Zarbock, Ralf and Griese, Matthias
(2016):
Tools to explore ABCA3 mutations causing interstitial lung disease.
In: Pediatric Pulmonology, Vol. 51, No. 12: pp. 1284-1294