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390 Publikationen

2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937586
L. Schlotawa, T. Dierks, S. Christoph, E. Cloppenburg, A. Ohlenbusch, G. C. Korenke, and J. Gartner, “Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient.”, JIMD reports, 2019, 49.
PUB | DOI | PubMed | Europe PMC
 
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2934622
V. Walhorn, A. - K. Moeller, C. Bartz, T. Dierks, and D. Anselmetti, in BIOPHYSICAL JOURNAL, Cell Press, 2019, p. 430A-431A.
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2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934113
T. Krüger, T. Dierks, and N. Sewald, “Formylglycine-generating enzymes for site-specific bioconjugation”, BIOLOGICAL CHEMISTRY, 2019, 400, 289-297.
PUB | DOI | WoS | PubMed | Europe PMC
 
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933913
L. Schlotawa, M. Wachs, O. Bernhard, F. J. Mayer, T. Dierks, B. Schmidt, and K. Radhakrishnan, in MOLECULAR GENETICS AND METABOLISM, Academic Press Inc Elsevier Science, San Diego, 2019, p. S131-S132.
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2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933914
T. O. Silva, C. F. M. Souza, J. W. B. Rocha, A. C. Brusius-Facchin, K. Michellin-Tirelli, M. G. Burin, R. Giugliani, K. Radhakrishnan, L. Schlotawa, T. Dierks, et al., in MOLECULAR GENETICS AND METABOLISM, Academic Press Inc Elsevier Science,, 2019, p. S135-S136.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2921018 OA
L. Schlotawa, M. Wachs, O. Bernhard, F. J. Mayer, T. Dierks, B. Schmidt, and K. Radhakrishnan, “Recognition and ER Quality Control of Misfolded Formylglycine-Generating Enzyme by Protein Disulfide Isomerase”, Cell Reports, 2018, 24, 27-37.e4.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920942
T. Krüger, S. Weiland, G. Falck, M. Gerlach, M. Boschanski, S. Alam, K. Müller, T. Dierks, and N. Sewald, “Two-fold Bioorthogonal Derivatization by Different Formylglycine-Generating Enzymes”, ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57, 7245-7249.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931507
S. Khateb, B. Kowalewski, N. Bedoni, M. Damme, N. Pollack, A. Saada, A. Obolensky, T. Ben-Yosef, M. Gross, T. Dierks, et al., “A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans”, GENETICS IN MEDICINE, 2018, 20, 1004-1012.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933928
D. Maynard, H. Gröger, T. Dierks, and K. - J. Dietz, “The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development”, JOURNAL OF EXPERIMENTAL BOTANY, 2018, 69, 5341-5354.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271
S. Stroobants, H. Wolf, Z. Callaerts-Vegh, T. Dierks, T. Lübke, and R. D'Hooge, “Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice”, FRONTIERS IN BEHAVIORAL NEUROSCIENCE, 2018, 12, : 15.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2919061
R. Ahrens-Nicklas, L. Schlotawa, A. Ballabio, N. Brunetti-Pierri, M. De Castro, T. Dierks, F. Eichler, C. Ficicioglu, A. Finglas, J. Gaertner, et al., “Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement”, MOLECULAR GENETICS AND METABOLISM, 2018, 123, 337-346.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2918283
A. Wieczorek, C. K. Chan, S. Kovacic, C. Li, T. Dierks, and N. R. Forde, “Genetically modified human type II collagen for N- and C-terminal covalent tagging”, CANADIAN JOURNAL OF CHEMISTRY, 2018, 96, 204-211.
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909071
D. Roy, S. Mondal, A. Khurana, D. - B. Jung, R. Hoffmann, X. He, E. Kalogera, T. Dierks, E. Hammond, K. Dredge, et al., “Loss of HSulf-1: The Missing Link between Autophagy and Lipid Droplets in Ovarian Cancer”, SCIENTIFIC REPORTS, 2017, 7, : 41977.
PUB | DOI | WoS | PubMed | Europe PMC
 
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909150
X. Pan, Y. Wang, T. Lübke, A. Hinek, and A. V. Pshezhetsky, “Mice, double deficient in lysosomal serine carboxypeptidases Scpep1 and Cathepsin A develop the hyperproliferative vesicular corneal dystrophy and hypertrophic skin thickenings”, PLoS One, 2017, 12, : e0172854.
PUB | DOI | WoS | PubMed | Europe PMC
 
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916520
I. Jaszczuk, L. Schlotawa, T. Dierks, A. Ohlenbusch, D. Koppenhoefer, M. Babicz, M. Lejman, K. Radhakrishnan, and A. Lugowska, “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, 2017, 121, 252-258.
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778
O. P. Dhamale, R. Lawrence, E. Wiegmann, B. A. Shah, K. Al-Mafraji, W. C. Lamanna, T. Lübke, T. Dierks, G. - J. Boons, and J. D. Esko, “Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase”, ACS Chemical Biology, 2017, 12, 367-373.
PUB | DOI | WoS | PubMed | Europe PMC
 
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124
K. Kruszewski, R. Luellmann-Rauch, T. Dierks, U. Bartsch, and M. Damme, “Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice”, INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2016, 57, 1120-1131.
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2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616 OA
H. Wolf, M. Damme, S. Stroobants, R. D'Hooge, H. C. Beck, I. Hermans-Borgmeyer, R. Lüllmann-Rauch, T. Dierks, and T. Lübke, “A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease”, Disease Models & Mechanisms, 2016, 9, 1015-1028.
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2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2784664
I. Kalus, S. Rohn, T. M. Puvirajesinghe, S. E. Guimond, P. Eyckerman-Kölln, G. ten Dam, T. H. van Kuppevelt, J. E. Turnbull, and T. Dierks, “Sulf1 and Sulf2 Differentially Modulate Heparan Sulfate Proteoglycan Sulfation during Postnatal Cerebellum Development: Evidence for Neuroprotective and Neurite Outgrowth Promoting Functions”, PLoS ONE, 2015, 10, : e0139853.
PUB | DOI | WoS | PubMed | Europe PMC
 
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2780450
J. Peng, S. Alam, K. Radhakrishnan, M. Mariappan, M. G. Rudolph, C. May, T. Dierks, K. von Figura, and B. Schmidt, “Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reaction”, FEBS Journal, 2015, 282, 3262-3274.
PUB | DOI | WoS | PubMed | Europe PMC
 

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