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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., and Gartner, J. (2019). Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient. JIMD reports 49.
PUB | DOI | PubMed | Europe PMC
 
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2934622
Walhorn, V., Moeller, A. - K., Bartz, C., Dierks, T., and Anselmetti, D. (2019). “Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's Equality” in BIOPHYSICAL JOURNAL, vol. 116, (Cell Press), 430A-431A.
PUB | DOI | WoS
 
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934113
Krüger, T., Dierks, T., and Sewald, N. (2019). Formylglycine-generating enzymes for site-specific bioconjugation. BIOLOGICAL CHEMISTRY 400, 289-297.
PUB | DOI | WoS | PubMed | Europe PMC
 
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933913
Schlotawa, L., Wachs, M., Bernhard, O., Mayer, F. J., Dierks, T., Schmidt, B., and Radhakrishnan, K. (2019). “Protein disulfide isomerase is a possible target for disease modification in multiple sulfatase deficiency” in MOLECULAR GENETICS AND METABOLISM MOLECULAR GENETICS AND METABOLISM, vol. 126, (San Diego: ACADEMIC PRESS INC ELSEVIER SCIENCE), S131-S132.
PUB | DOI | WoS
 
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., Radhakrishnan, K., Schlotawa, L., Dierks, T., et al. (2019). “Attenuated multiple sulfatase deficiency: Description of two Brazilian patients showing interesting clinical and genetic findings” in MOLECULAR GENETICS AND METABOLISM MOLECULAR GENETICS AND METABOLISM, vol. 126, (ACADEMIC PRESS INC ELSEVIER SCIENCE,), S135-S136.
PUB | DOI | WoS
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2921018 OA
Schlotawa, L., Wachs, M., Bernhard, O., Mayer, F. J., Dierks, T., Schmidt, B., and Radhakrishnan, K. (2018). Recognition and ER Quality Control of Misfolded Formylglycine-Generating Enzyme by Protein Disulfide Isomerase. Cell Reports 24, 27-37.e4.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920942
Krüger, T., Weiland, S., Falck, G., Gerlach, M., Boschanski, M., Alam, S., Müller, K., Dierks, T., and Sewald, N. (2018). Two-fold Bioorthogonal Derivatization by Different Formylglycine-Generating Enzymes. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 57, 7245-7249.
PUB | DOI | WoS | PubMed | Europe PMC
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931507
Khateb, S., Kowalewski, B., Bedoni, N., Damme, M., Pollack, N., Saada, A., Obolensky, A., Ben-Yosef, T., Gross, M., Dierks, T., 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, 1004-1012.
PUB | DOI | WoS | PubMed | Europe PMC
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933928
Maynard, D., Gröger, H., Dierks, T., and Dietz, K. - J. (2018). The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development. JOURNAL OF EXPERIMENTAL BOTANY 69, 5341-5354.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271
Stroobants, S., Wolf, H., Callaerts-Vegh, Z., Dierks, T., Lübke, T., and D'Hooge, R. (2018). Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice. FRONTIERS IN BEHAVIORAL NEUROSCIENCE 12:15.
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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., Ficicioglu, C., Finglas, A., Gaertner, J., et al. (2018). Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement. MOLECULAR GENETICS AND METABOLISM 123, 337-346.
PUB | DOI | WoS | PubMed | Europe PMC
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2918283
Wieczorek, A., Chan, C. K., Kovacic, S., Li, C., Dierks, T., and Forde, N. R. (2018). Genetically modified human type II collagen for N- and C-terminal covalent tagging. CANADIAN JOURNAL OF CHEMISTRY 96, 204-211.
PUB | DOI | WoS
 
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909071
Roy, D., Mondal, S., Khurana, A., Jung, D. - B., Hoffmann, R., He, X., Kalogera, E., Dierks, T., Hammond, E., Dredge, K., et al. (2017). Loss of HSulf-1: The Missing Link between Autophagy and Lipid Droplets in Ovarian Cancer. SCIENTIFIC REPORTS 7:41977.
PUB | DOI | WoS | PubMed | Europe PMC
 
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909150
Pan, X., Wang, Y., Lübke, T., Hinek, A., and 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:e0172854.
PUB | DOI | WoS | PubMed | Europe PMC
 
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916520
Jaszczuk, I., Schlotawa, L., Dierks, T., Ohlenbusch, A., Koppenhoefer, D., Babicz, M., Lejman, M., Radhakrishnan, K., and Lugowska, A. (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, 252-258.
PUB | DOI | WoS | PubMed | Europe PMC
 
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778
Dhamale, O. P., Lawrence, R., Wiegmann, E., Shah, B. A., Al-Mafraji, K., Lamanna, W. C., Lübke, T., Dierks, T., Boons, G. - J., and Esko, J. D. (2017). Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase. ACS Chemical Biology 12, 367-373.
PUB | DOI | WoS | PubMed | Europe PMC
 
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124
Kruszewski, K., Luellmann-Rauch, R., Dierks, T., Bartsch, U., and Damme, M. (2016). Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 57, 1120-1131.
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., Dierks, T., and Lübke, T. (2016). A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease. Disease Models & Mechanisms 9, 1015-1028.
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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., Turnbull, J. E., and Dierks, T. (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:e0139853.
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., von Figura, K., and Schmidt, B. (2015). Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reaction. FEBS Journal 282, 3262-3274.
PUB | DOI | WoS | PubMed | Europe PMC
 

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