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Characterisation of TbSmee1 suggests endocytosis allows surface-bound cargo to enter the trypanosome flagellar pocket. Schichler D, Konle A, Spath EM, Riegler S, Klein A, Seleznev A, Jung S, Wuppermann T, Wetterich N, Borges A, Meyer-Natus E, Havlicek K, Pérez Cabrera S, Niedermüller K, Sajko S, Dohn M, Malzer X, Riemer E, Tumurbaatar T, Djinovic-Carugo K, Dong G, Janzen CJ, Morriswood B. J Cell Sci. 2023 Oct 15;136(20):jcs261548. doi: 10.1242/jcs.261548. Epub 2023 Oct 26.
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Genetic variants of unknown significance in alpha-galactosidase A: Cellular delineation from Fabry disease. Klein A, Klug K, Breyer M, Grüner J, Medala VK, Nordbeck P, Wanner C, Klopocki E, Üçeyler N. J Inherit Metab Dis. 2024 Jul;47(4):805-817. doi: 10.1002/jimd.12743. Epub 2024 Apr 15.
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In vitro characterization of cells derived from a patient with the GLA variant c.376A>G (p.S126G) highlights a non-pathogenic role in Fabry disease. Breyer M, Grüner J, Klein A, Finke L, Klug K, Sauer M, Üçeyler N. Mol Genet Metab Rep. 2023 Nov 25;38:101029. doi: 10.1016/j.ymgmr.2023.101029. eCollection 2024 Mar.
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Endothelial Cell Dysfunction and Hypoxia as Potential Mediators of Pain in Fabry Disease: A Human-Murine Translational Approach. Klug K, Spitzel M, Hans C, Klein A, Schottmann NM, Erbacher C, Üçeyler N. Int J Mol Sci. 2023 Oct 21;24(20):15422. doi: 10.3390/ijms242015422.
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| Last update Publications 30.06.2025 |
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