Please note that PUB no longer supports Internet Explorer versions 8 or 9 (or earlier).

We recommend upgrading to the latest Internet Explorer, Google Chrome, or Firefox.

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)
PUB | DOI | PubMed | Europe PMC
 
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. In: BIOPHYSICAL JOURNAL. Cell Press. (116). S. 430A-431A.
PUB | DOI | WoS
 
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.
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.; Radhakrishnan, K. (2019): Protein disulfide isomerase is a possible target for disease modification in multiple sulfatase deficiency. In: MOLECULAR GENETICS AND METABOLISM. San Diego: ACADEMIC PRESS INC ELSEVIER SCIENCE. (MOLECULAR GENETICS AND METABOLISM, 126). S. 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.; Schwartz, I. V. D. (2019): Attenuated multiple sulfatase deficiency: Description of two Brazilian patients showing interesting clinical and genetic findings. In: MOLECULAR GENETICS AND METABOLISM. ACADEMIC PRESS INC ELSEVIER SCIENCE,. (MOLECULAR GENETICS AND METABOLISM, 126). S. 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.; Radhakrishnan, K. (2018): Recognition and ER Quality Control of Misfolded Formylglycine-Generating Enzyme by Protein Disulfide Isomerase Cell Reports,24:(1): 27-37.e4.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920942
Krüger, T.; Weiland, S.; Falck, G.; Gerlach, M.; Boschanski, M.; Alam, S.; Müller, K.; Dierks, T.; Sewald, N. (2018): Two-fold Bioorthogonal Derivatization by Different Formylglycine-Generating Enzymes ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,57:(24): 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.; Banin, E.; Rivolta, C.; Sharon, D. (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.
PUB | DOI | WoS | PubMed | Europe PMC
 
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.
PUB | DOI | WoS | PubMed | Europe PMC
 
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
PUB | DOI | WoS | PubMed | Europe PMC
 
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.; Kirmse, B.; Klepper, J.; Lee, M.; Olsen, A.; Parenti, G.; Vossough, A.; Vanderver, A.; Adang, L. A. (2018): Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement MOLECULAR GENETICS AND METABOLISM,123:(3): 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.; 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.
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.; Shridhar, V. (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.; 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
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.; 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:(3): 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.; Esko, J. D. (2017): Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase ACS Chemical Biology,12:(2): 367-373.
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.
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.; 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:(9): 1015-1028.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
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.; 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:(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.; Schmidt, B. (2015): Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reaction FEBS Journal,282:(17): 3262-3274.
PUB | DOI | WoS | PubMed | Europe PMC
 

Filter und Suchbegriffe

department=17967

Suche

Publikationen filtern

Darstellung / Sortierung

Zitationsstil: wels

Export / Einbettung