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Group by: Item Type | Date
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 [PDF, 1MB]

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

This list was generated on Sun Sep 17 04:00:52 2023 CEST.