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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 GC, 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. 116. Cell Press: 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 FJ, 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. MOLECULAR GENETICS AND METABOLISM, 126. San Diego: ACADEMIC PRESS INC ELSEVIER SCIENCE: S131-S132.
PUB | DOI | WoS
 
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933914
Silva TO, Souza CFM, Rocha JWB, Brusius-Facchin AC, Michellin-Tirelli K, Burin MG, Giugliani R, Radhakrishnan K, Schlotawa L, Dierks T, Schwartz IVD (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, 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 FJ, 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 LA (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 CK, Kovacic S, Li C, Dierks T, Forde NR (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 AV (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 OP, Lawrence R, Wiegmann E, Shah BA, Al-Mafraji K, Lamanna WC, Lübke T, Dierks T, Boons G-J, Esko JD (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 HC, 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 TM, Guimond SE, Eyckerman-Kölln P, ten Dam G, van Kuppevelt TH, Turnbull JE, 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 MG, 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
 

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