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Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3.
Mol Med. 2016 Sep;22:183-191. doi: 10.2119/molmed.2015.00244. Epub 2016 Feb 26.
Mol Med. 2016.
PMID: 26928390
Free PMC article.
Tools to explore ABCA3 mutations causing interstitial lung disease.
Wittmann T, Schindlbeck U, Höppner S, Kinting S, Frixel S, Kröner C, Liebisch G, Hegermann J, Aslanidis C, Brasch F, Reu S, Lasch P, Zarbock R, Griese M.
Wittmann T, et al. Among authors: schindlbeck u.
Pediatr Pulmonol. 2016 Dec;51(12):1284-1294. doi: 10.1002/ppul.23471. Epub 2016 May 13.
Pediatr Pulmonol. 2016.
PMID: 27177387
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Quantification of volume and lipid filling of intracellular vesicles carrying the ABCA3 transporter.
Höppner S, Kinting S, Torrano AA, Schindlbeck U, Bräuchle C, Zarbock R, Wittmann T, Griese M.
Höppner S, et al. Among authors: schindlbeck u.
Biochim Biophys Acta Mol Cell Res. 2017 Dec;1864(12):2330-2335. doi: 10.1016/j.bbamcr.2017.08.013. Epub 2017 Sep 6.
Biochim Biophys Acta Mol Cell Res. 2017.
PMID: 28887056
Free article.
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Functional rescue of misfolding ABCA3 mutations by small molecular correctors.
Kinting S, Höppner S, Schindlbeck U, Forstner ME, Harfst J, Wittmann T, Griese M.
Kinting S, et al. Among authors: schindlbeck u.
Hum Mol Genet. 2018 Mar 15;27(6):943-953. doi: 10.1093/hmg/ddy011.
Hum Mol Genet. 2018.
PMID: 29325094
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ABCA3 missense mutations causing surfactant dysfunction disorders have distinct cellular phenotypes.
Schindlbeck U, Wittmann T, Höppner S, Kinting S, Liebisch G, Hegermann J, Griese M.
Schindlbeck U, et al.
Hum Mutat. 2018 Jun;39(6):841-850. doi: 10.1002/humu.23416. Epub 2018 Mar 25.
Hum Mutat. 2018.
PMID: 29505158
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Critical analysis of granulocyte function in 154 patients wtih different diseases.
Bültmann B, Wildfeuer A, Schindlbeck U, Kleihauer E, Heimpel H, Wigger HJ, Haferkamp O.
Bültmann B, et al. Among authors: schindlbeck u.
Klin Wochenschr. 1982 Oct 15;60(20):1289-95. doi: 10.1007/BF01727485.
Klin Wochenschr. 1982.
PMID: 7144064
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