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390 Publikationen

2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937586
Schlotawa, Lars, Dierks, Thomas, Christoph, Sophie, Cloppenburg, Eva, Ohlenbusch, Andreas, Korenke, G Christoph, and Gartner, Jutta. “Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient.”. JIMD reports 49.1 (2019).
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2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2934622
Walhorn, Volker, Moeller, Ann-Kristin, Bartz, Christian, Dierks, Thomas, and Anselmetti, Dario. “Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's Equality”. BIOPHYSICAL JOURNAL. Cell Press, 2019.Vol. 116. 430A-431A.
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2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934113
Krüger, Tobias, Dierks, Thomas, and Sewald, Norbert. “Formylglycine-generating enzymes for site-specific bioconjugation”. BIOLOGICAL CHEMISTRY 400.3 (2019): 289-297.
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2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933913
Schlotawa, Lars, Wachs, Michaela, Bernhard, Olaf, Mayer, Franz J., Dierks, Thomas, Schmidt, Bernhard, and Radhakrishnan, Karthikeyan. “Protein disulfide isomerase is a possible target for disease modification in multiple sulfatase deficiency”. MOLECULAR GENETICS AND METABOLISM. San Diego: ACADEMIC PRESS INC ELSEVIER SCIENCE, 2019.Vol. 126. MOLECULAR GENETICS AND METABOLISM. S131-S132.
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2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933914
Silva, Thiag O., Souza, Carolina F. M., Rocha, Joshua W. B., Brusius-Facchin, Ana C., Michellin-Tirelli, Kristiane, Burin, Maira G., Giugliani, Roberto, Radhakrishnan, Karthikeyan, Schlotawa, Lars, Dierks, Thomas, and Schwartz, Ida V. D. “Attenuated multiple sulfatase deficiency: Description of two Brazilian patients showing interesting clinical and genetic findings”. MOLECULAR GENETICS AND METABOLISM. ACADEMIC PRESS INC ELSEVIER SCIENCE,, 2019.Vol. 126. MOLECULAR GENETICS AND METABOLISM. S135-S136.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2921018 OA
Schlotawa, Lars, Wachs, Michaela, Bernhard, Olaf, Mayer, Franz J., Dierks, Thomas, Schmidt, Bernhard, and Radhakrishnan, Karthikeyan. “Recognition and ER Quality Control of Misfolded Formylglycine-Generating Enzyme by Protein Disulfide Isomerase”. Cell Reports 24.1 (2018): 27-37.e4.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920942
Krüger, Tobias, Weiland, Stefanie, Falck, Georg, Gerlach, Marcus, Boschanski, Mareile, Alam, Sarfaraz, Müller, Kristian, Dierks, Thomas, and Sewald, Norbert. “Two-fold Bioorthogonal Derivatization by Different Formylglycine-Generating Enzymes”. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 57.24 (2018): 7245-7249.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931507
Khateb, Samer, Kowalewski, Björn, Bedoni, Nicola, Damme, Markus, Pollack, Netta, Saada, Ann, Obolensky, Alexey, Ben-Yosef, Tamar, Gross, Menachem, Dierks, Thomas, Banin, Eyal, Rivolta, Carlo, and Sharon, Dror. “A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans”. GENETICS IN MEDICINE 20.9 (2018): 1004-1012.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933928
Maynard, Daniel, Gröger, Harald, Dierks, Thomas, and Dietz, Karl-Josef. “The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development”. JOURNAL OF EXPERIMENTAL BOTANY 69.22 (2018): 5341-5354.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271
Stroobants, Stijn, Wolf, Heike, Callaerts-Vegh, Zsuzsanna, Dierks, Thomas, Lübke, Torben, and D'Hooge, Rudi. “Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice”. FRONTIERS IN BEHAVIORAL NEUROSCIENCE 12 (2018): 15.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2919061
Ahrens-Nicklas, Rebecca, Schlotawa, Lars, Ballabio, Andrea, Brunetti-Pierri, Nicola, De Castro, Mauricio, Dierks, Thomas, Eichler, Florian, Ficicioglu, Can, Finglas, Alan, Gaertner, Jutta, Kirmse, Brian, Klepper, Joerg, Lee, Marcus, Olsen, Amber, Parenti, Giancarlo, Vossough, Arastoo, Vanderver, Adeline, and Adang, Laura A. “Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement”. MOLECULAR GENETICS AND METABOLISM 123.3 (2018): 337-346.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2918283
Wieczorek, Andrew, Chan, Clara K., Kovacic, Suzana, Li, Cindy, Dierks, Thomas, and Forde, Nancy R. “Genetically modified human type II collagen for N- and C-terminal covalent tagging”. CANADIAN JOURNAL OF CHEMISTRY 96.2 (2018): 204-211.
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909071
Roy, Debarshi, Mondal, Susmita, Khurana, Ashwani, Jung, Deok-Beom, Hoffmann, Robert, He, Xiaoping, Kalogera, Eleftheria, Dierks, Thomas, Hammond, Edward, Dredge, Keith, and Shridhar, Viji. “Loss of HSulf-1: The Missing Link between Autophagy and Lipid Droplets in Ovarian Cancer”. SCIENTIFIC REPORTS 7 (2017): 41977.
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909150
Pan, Xuefang, Wang, Yanting, Lübke, Torben, Hinek, Aleksander, and Pshezhetsky, Alexey V. “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 (2017): e0172854.
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916520
Jaszczuk, Ilona, Schlotawa, Lars, Dierks, Thomas, Ohlenbusch, Andreas, Koppenhoefer, Dominique, Babicz, Mariusz, Lejman, Monika, Radhakrishnan, Karthikeyan, and Lugowska, Agnieszka. “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 (2017): 252-258.
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778
Dhamale, Omkar P., Lawrence, Roger, Wiegmann, Elena, Shah, Bhawal A., Al-Mafraji, Kanar, Lamanna, William C., Lübke, Torben, Dierks, Thomas, Boons, Geert-Jan, and Esko, Jeffrey D. “Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase”. ACS Chemical Biology 12.2 (2017): 367-373.
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2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124
Kruszewski, Katharina, Luellmann-Rauch, Renate, Dierks, Thomas, Bartsch, Udo, and Damme, Markus. “Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice”. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 57.3 (2016): 1120-1131.
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2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616 OA
Wolf, Heike, Damme, Markus, Stroobants, Stijn, D'Hooge, Rudi, Beck, Hans Christian, Hermans-Borgmeyer, Irm, Lüllmann-Rauch, Renate, Dierks, Thomas, and Lübke, Torben. “A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease”. Disease Models & Mechanisms 9.9 (2016): 1015-1028.
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2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2784664
Kalus, Ina, Rohn, Susanne, Puvirajesinghe, Tania M., Guimond, Scott E., Eyckerman-Kölln, Pieter, ten Dam, Gerdy, van Kuppevelt, Toin H., Turnbull, Jeremy E., and Dierks, Thomas. “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 (2015): e0139853.
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2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2780450
Peng, Jianhe, Alam, Sarfaraz, Radhakrishnan, Karthikeyan, Mariappan, Malaiyalam, Rudolph, Markus Georg, May, Caroline, Dierks, Thomas, von Figura, Kurt, and Schmidt, Bernhard. “Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reaction”. FEBS Journal 282.17 (2015): 3262-3274.
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