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390 Publikationen

2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937586
Schlotawa, L., Dierks, T., Christoph, S., Cloppenburg, E., Ohlenbusch, A., Korenke, G. C., & Gartner, J. (2019). Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient. JIMD reports, 49(1). doi:10.1002/jmd2.12074
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2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2934622
Walhorn, V., Moeller, A. - K., Bartz, C., Dierks, T., & Anselmetti, D. (2019). Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's Equality. BIOPHYSICAL JOURNAL, 116, 430A-431A. Cell Press. doi:10.1016/j.bpj.2018.11.2316
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2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934113
Krüger, T., Dierks, T., & Sewald, N. (2019). Formylglycine-generating enzymes for site-specific bioconjugation. BIOLOGICAL CHEMISTRY, 400(3), 289-297. doi:10.1515/hsz-2018-0358
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2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933913
Schlotawa, L., Wachs, M., Bernhard, O., Mayer, F. J., Dierks, T., Schmidt, B., & Radhakrishnan, K. (2019). Protein disulfide isomerase is a possible target for disease modification in multiple sulfatase deficiency. MOLECULAR GENETICS AND METABOLISM, MOLECULAR GENETICS AND METABOLISM, 126, S131-S132. San Diego: ACADEMIC PRESS INC ELSEVIER SCIENCE. doi:10.1016/j.ymgme.2018.12.338
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2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933914
Silva, T. O., Souza, C. F. M., Rocha, J. W. B., Brusius-Facchin, A. C., Michellin-Tirelli, K., Burin, M. G., Giugliani, R., et al. (2019). Attenuated multiple sulfatase deficiency: Description of two Brazilian patients showing interesting clinical and genetic findings. MOLECULAR GENETICS AND METABOLISM, MOLECULAR GENETICS AND METABOLISM, 126, S135-S136. ACADEMIC PRESS INC ELSEVIER SCIENCE,. doi:10.1016/j.ymgme.2018.12.349
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2921018 OA
Schlotawa, L., Wachs, M., Bernhard, O., Mayer, F. J., Dierks, T., Schmidt, B., & Radhakrishnan, K. (2018). Recognition and ER Quality Control of Misfolded Formylglycine-Generating Enzyme by Protein Disulfide Isomerase. Cell Reports, 24(1), 27-37.e4. doi:10.1016/j.celrep.2018.06.016
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920942
Krüger, T., Weiland, S., Falck, G., Gerlach, M., Boschanski, M., Alam, S., Müller, K., et al. (2018). Two-fold Bioorthogonal Derivatization by Different Formylglycine-Generating Enzymes. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 57(24), 7245-7249. doi:10.1002/anie.201803183
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931507
Khateb, S., Kowalewski, B., Bedoni, N., Damme, M., Pollack, N., Saada, A., Obolensky, A., et al. (2018). A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans. GENETICS IN MEDICINE, 20(9), 1004-1012. doi:10.1038/gim.2017.227
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933928
Maynard, D., Gröger, H., Dierks, T., & Dietz, K. - J. (2018). The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development. JOURNAL OF EXPERIMENTAL BOTANY, 69(22), 5341-5354. doi:10.1093/jxb/ery316
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271
Stroobants, S., Wolf, H., Callaerts-Vegh, Z., Dierks, T., Lübke, T., & D'Hooge, R. (2018). Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice. FRONTIERS IN BEHAVIORAL NEUROSCIENCE, 12, 15. doi:10.3389/fnbeh.2018.00069
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2919061
Ahrens-Nicklas, R., Schlotawa, L., Ballabio, A., Brunetti-Pierri, N., De Castro, M., Dierks, T., Eichler, F., et al. (2018). Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement. MOLECULAR GENETICS AND METABOLISM, 123(3), 337-346. doi:10.1016/j.ymgme.2018.01.005
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2918283
Wieczorek, A., Chan, C. K., Kovacic, S., Li, C., Dierks, T., & Forde, N. R. (2018). Genetically modified human type II collagen for N- and C-terminal covalent tagging. CANADIAN JOURNAL OF CHEMISTRY, 96(2), 204-211. doi:10.1139/cjc-2017-0335
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909071
Roy, D., Mondal, S., Khurana, A., Jung, D. - B., Hoffmann, R., He, X., Kalogera, E., et al. (2017). Loss of HSulf-1: The Missing Link between Autophagy and Lipid Droplets in Ovarian Cancer. SCIENTIFIC REPORTS, 7, 41977. doi:10.1038/srep41977
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909150
Pan, X., Wang, Y., Lübke, T., Hinek, A., & Pshezhetsky, A. V. (2017). Mice, double deficient in lysosomal serine carboxypeptidases Scpep1 and Cathepsin A develop the hyperproliferative vesicular corneal dystrophy and hypertrophic skin thickenings. PLoS One, 12(2), e0172854. doi:10.1371/journal.pone.0172854
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916520
Jaszczuk, I., Schlotawa, L., Dierks, T., Ohlenbusch, A., Koppenhoefer, D., Babicz, M., Lejman, M., et al. (2017). Expanding the genetic cause of multiple sulfatase deficiency: A novel SUMF1 variant in a patient displaying a severe late infantile form of the disease. MOLECULAR GENETICS AND METABOLISM, 121(3), 252-258. doi:10.1016/j.ymgme.2017.05.013
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778
Dhamale, O. P., Lawrence, R., Wiegmann, E., Shah, B. A., Al-Mafraji, K., Lamanna, W. C., Lübke, T., et al. (2017). Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase. ACS Chemical Biology, 12(2), 367-373. doi:10.1021/acschembio.6b01033
PUB | DOI | WoS | PubMed | Europe PMC
 
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124
Kruszewski, K., Luellmann-Rauch, R., Dierks, T., Bartsch, U., & Damme, M. (2016). Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 57(3), 1120-1131. doi:10.1167/iovs.15-17645
PUB | DOI | WoS | PubMed | Europe PMC
 
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616 OA
Wolf, H., Damme, M., Stroobants, S., D'Hooge, R., Beck, H. C., Hermans-Borgmeyer, I., Lüllmann-Rauch, R., et al. (2016). A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease. Disease Models & Mechanisms, 9(9), 1015-1028. doi:10.1242/dmm.025122
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2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2784664
Kalus, I., Rohn, S., Puvirajesinghe, T. M., Guimond, S. E., Eyckerman-Kölln, P., ten Dam, G., van Kuppevelt, T. H., et al. (2015). Sulf1 and Sulf2 Differentially Modulate Heparan Sulfate Proteoglycan Sulfation during Postnatal Cerebellum Development: Evidence for Neuroprotective and Neurite Outgrowth Promoting Functions. PLoS ONE, 10(10), e0139853. doi:10.1371/journal.pone.0139853
PUB | DOI | WoS | PubMed | Europe PMC
 
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2780450
Peng, J., Alam, S., Radhakrishnan, K., Mariappan, M., Rudolph, M. G., May, C., Dierks, T., et al. (2015). Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reaction. FEBS Journal, 282(17), 3262-3274. doi:10.1111/febs.13347
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