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23 Publikationen

2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2565333
Ennemann, E., Radhakrishnan, K., Mariappan, M., Wachs, M., Pringle, T. H., Schmidt, B., & Dierks, T. (2013). Proprotein Convertases Process and Thereby Inactivate Formylglycine-generating Enzyme. Journal of Biological Chemistry, 288(8), 5828-5839. doi:10.1074/jbc.M112.405159
PUB | DOI | WoS | PubMed | Europe PMC
 
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351519
Lenger, J., Schröder, M., Ennemann, E., Müller, B., Wong, C. - H., Noll, T., Dierks, T., et al. (2012). Evaluation of sulfatase-directed quinone methide traps for proteomics. Bioorganic & Medical Chemistry, 20(2), 622-627. doi:10.1016/j.bmc.2011.04.044
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2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2474206
Hayano, S., Kurosaka, H., Yanagita, T., Kalus, I., Milz, F., Ishihara, Y., Nururu, M. N., et al. (2012). Roles of heparan sulfate sulfation in dentinogenesis. J. Biol. Chem., 287(15), 12217-12229. doi:10.1074/jbc.M111.332924
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2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2517966
Kowalewski, B., Poppe, J., Demmer, U., Warkentin, E., Dierks, T., Ermler, U., & Schneider, K. (2012). Nature's Polyoxometalate Chemistry: X-ray Structure of the Mo Storage Protein Loaded with Discrete Polynuclear Mo-O Clusters. Journal of the American Chemical Society, 134(23), 9768-9774. doi:10.1021/ja303084n
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2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2494022
Kowalewski, B., Lamanna, W. C., Lawrence, R., Damme, M., Padva, M., Stroobants, S., Kalus, I., et al. (2012). Arylsulfatase G Inactivation Causes Loss of Heparan Sulfate 3-O-Sulfatase Activity and Mucopolysaccharidosis in Mice. Proc. Natl. Acad. Sci. USA, 109(26), 10310-10315. doi:10.1073/pnas.1202071109
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2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2003211
Schlotawa, L., Ennemann, E., Radhakrishnan, K., Schmidt, B., Chakrapani, A., Christen, H. - J., Moser, H., et al. (2011). SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiency. European Journal of Human Genetics, 19(3), 253-261. doi:10.1038/ejhg.2010.219
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2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1968383
Harder, A., Walhorn, V., Dierks, T., Fernandez-Busquets, X., & Anselmetti, D. (2010). Single-Molecule Force Spectroscopy of Cartilage Aggrecan Self-Adhesion. Biophysical Journal, 99(10), 3498-3504. doi:10.1016/j.bpj.2010.09.002
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2009 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2352302
von Figura, K., Dierks, T., & Schmidt, B. (2009). Multiple Sulfatase Deficiency. In F. Lang (Ed.), Encyclopedia of Molecular Mechanisms of Disease (pp. 1374-1375). Berlin Heidelberg: Springer.
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2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1634198
Dierks, T., Schlotawa, L., Frese, M. - A., Radhakrishnan, K., von Figura, K., & Schmidt, B. (2009). Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann-Pick C1 disease - Lysosomal storage disorders caused by defects of non-lysosomal proteins. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1793(4), 710-725. doi:10.1016/j.bbamcr.2008.11.015
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2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1796606
Kalus, I., Salmen, B., Viebahn, C., von Figura, K., Schmitz, D., D'Hooge, R., & Dierks, T. (2009). Differential involvement of the extracellular 6-O-endosulfatases Sulf1 and Sulf2 in brain development and neuronal and behavioural plasticity. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 13(11-12), 4505-4521. doi:10.1111/j.1582-4934.2008.00558.x
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