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.: Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient. JIMD reports. 49, (2019).
PUB | DOI | PubMed | Europe PMC
 
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2934622
Walhorn, V., Moeller, A.-K., Bartz, C., Dierks, T., Anselmetti, D.: Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's Equality. BIOPHYSICAL JOURNAL. 116, p. 430A-431A. Cell Press (2019).
PUB | DOI | WoS
 
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934113
Krüger, T., Dierks, T., Sewald, N.: Formylglycine-generating enzymes for site-specific bioconjugation. BIOLOGICAL CHEMISTRY. 400, 289-297 (2019).
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.: Protein disulfide isomerase is a possible target for disease modification in multiple sulfatase deficiency. MOLECULAR GENETICS AND METABOLISM. MOLECULAR GENETICS AND METABOLISM. 126, p. S131-S132. ACADEMIC PRESS INC ELSEVIER SCIENCE, San Diego (2019).
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.: Attenuated multiple sulfatase deficiency: Description of two Brazilian patients showing interesting clinical and genetic findings. MOLECULAR GENETICS AND METABOLISM. MOLECULAR GENETICS AND METABOLISM. 126, p. S135-S136. ACADEMIC PRESS INC ELSEVIER SCIENCE, (2019).
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.: Recognition and ER Quality Control of Misfolded Formylglycine-Generating Enzyme by Protein Disulfide Isomerase. Cell Reports. 24, 27-37.e4 (2018).
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.: Two-fold Bioorthogonal Derivatization by Different Formylglycine-Generating Enzymes. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION. 57, 7245-7249 (2018).
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.: A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans. GENETICS IN MEDICINE. 20, 1004-1012 (2018).
PUB | DOI | WoS | PubMed | Europe PMC
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933928
Maynard, D., Gröger, H., Dierks, T., Dietz, K.-J.: The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development. JOURNAL OF EXPERIMENTAL BOTANY. 69, 5341-5354 (2018).
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.: Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice. FRONTIERS IN BEHAVIORAL NEUROSCIENCE. 12, : 15 (2018).
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.: Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement. MOLECULAR GENETICS AND METABOLISM. 123, 337-346 (2018).
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.: Genetically modified human type II collagen for N- and C-terminal covalent tagging. CANADIAN JOURNAL OF CHEMISTRY. 96, 204-211 (2018).
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.: Loss of HSulf-1: The Missing Link between Autophagy and Lipid Droplets in Ovarian Cancer. SCIENTIFIC REPORTS. 7, : 41977 (2017).
PUB | DOI | WoS | PubMed | Europe PMC
 
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909150
Pan, X., Wang, Y., Lübke, T., Hinek, A., Pshezhetsky, A.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, : e0172854 (2017).
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.: 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 (2017).
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.: Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase. ACS Chemical Biology. 12, 367-373 (2017).
PUB | DOI | WoS | PubMed | Europe PMC
 
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124
Kruszewski, K., Luellmann-Rauch, R., Dierks, T., Bartsch, U., Damme, M.: Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 57, 1120-1131 (2016).
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.: 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 (2016).
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.: 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 (2015).
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.: Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reaction. FEBS Journal. 282, 3262-3274 (2015).
PUB | DOI | WoS | PubMed | Europe PMC
 

Filter und Suchbegriffe

department=17967

Suche

Publikationen filtern

Darstellung / Sortierung

Zitationsstil: lncs

Export / Einbettung