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389 Publikationen

2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2934622
Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's Equality
Walhorn V, Moeller A-K, Bartz C, Dierks T, Anselmetti D (2019)
In: BIOPHYSICAL JOURNAL., 116(3). Cell Press: 430A-431A.
PUB | DOI | WoS
 
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934113
Formylglycine-generating enzymes for site-specific bioconjugation
Krüger T, Dierks T, Sewald N (2019)
BIOLOGICAL CHEMISTRY 400(3): 289-297.
PUB | DOI | WoS | PubMed | Europe PMC
 
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933913
Protein disulfide isomerase is a possible target for disease modification in multiple sulfatase deficiency
Schlotawa L, Wachs M, Bernhard O, Mayer FJ, Dierks T, Schmidt B, Radhakrishnan K (2019)
In: MOLECULAR GENETICS AND METABOLISM. MOLECULAR GENETICS AND METABOLISM, 126(2). San Diego: ACADEMIC PRESS INC ELSEVIER SCIENCE: S131-S132.
PUB | DOI | WoS
 
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933914
Attenuated multiple sulfatase deficiency: Description of two Brazilian patients showing interesting clinical and genetic findings
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)
In: MOLECULAR GENETICS AND METABOLISM. MOLECULAR GENETICS AND METABOLISM, 126(2). ACADEMIC PRESS INC ELSEVIER SCIENCE,: S135-S136.
PUB | DOI | WoS
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2921018
Recognition and ER Quality Control of Misfolded Formylglycine-Generating Enzyme by Protein Disulfide Isomerase
Schlotawa L, Wachs M, Bernhard O, Mayer FJ, Dierks T, Schmidt B, Radhakrishnan K (2018)
Cell Reports 24(1): 27-37.e4.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933928
The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development
Maynard D, Gröger H, Dierks T, Dietz K-J (2018)
JOURNAL OF EXPERIMENTAL BOTANY 69(22): 5341-5354.
PUB | DOI | WoS | PubMed | Europe PMC
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271
Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice
Stroobants S, Wolf H, Callaerts-Vegh Z, Dierks T, Lübke T, D'Hooge R (2018)
FRONTIERS IN BEHAVIORAL NEUROSCIENCE 12: 15.
PUB | DOI | WoS | PubMed | Europe PMC
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931507
A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans
Khateb S, Kowalewski B, Bedoni N, Damme M, Pollack N, Saada A, Obolensky A, Ben-Yosef T, Gross M, Dierks T, Banin E, et al. (2018)
GENETICS IN MEDICINE 20(9): 1004-1012.
PUB | DOI | WoS
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920942
Two-fold Bioorthogonal Derivatization by Different Formylglycine-Generating Enzymes
Krüger T, Weiland S, Falck G, Gerlach M, Boschanski M, Alam S, Müller K, Dierks T, Sewald N (2018)
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 57(24): 7245-7249.
PUB | DOI | WoS | PubMed | Europe PMC
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2919061
Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement
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, et al. (2018)
MOLECULAR GENETICS AND METABOLISM 123(3): 337-346.
PUB | DOI | WoS | PubMed | Europe PMC
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2918283
Genetically modified human type II collagen for N- and C-terminal covalent tagging
Wieczorek A, Chan CK, Kovacic S, Li C, Dierks T, Forde NR (2018)
CANADIAN JOURNAL OF CHEMISTRY 96(2): 204-211.
PUB | DOI | WoS
 
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909071
Loss of HSulf-1: The Missing Link between Autophagy and Lipid Droplets in Ovarian Cancer
Roy D, Mondal S, Khurana A, Jung D-B, Hoffmann R, He X, Kalogera E, Dierks T, Hammond E, Dredge K, Shridhar V (2017)
SCIENTIFIC REPORTS 7: 41977.
PUB | DOI | WoS | PubMed | Europe PMC
 
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909150 PUB | DOI | WoS | PubMed | Europe PMC
 
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916520
Expanding the genetic cause of multiple sulfatase deficiency: A novel SUMF1 variant in a patient displaying a severe late infantile form of the disease
Jaszczuk I, Schlotawa L, Dierks T, Ohlenbusch A, Koppenhoefer D, Babicz M, Lejman M, Radhakrishnan K, Lugowska A (2017)
MOLECULAR GENETICS AND METABOLISM 121(3): 252-258.
PUB | DOI | WoS | PubMed | Europe PMC
 
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778
Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase
Dhamale OP, Lawrence R, Wiegmann E, Shah BA, Al-Mafraji K, Lamanna WC, Lübke T, Dierks T, Boons G-J, Esko JD (2017)
ACS Chemical Biology 12(2): 367-373.
PUB | DOI | WoS | PubMed | Europe PMC
 
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124
Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice
Kruszewski K, Luellmann-Rauch R, Dierks T, Bartsch U, Damme M (2016)
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 57(3): 1120-1131.
PUB | DOI | WoS | PubMed | Europe PMC
 
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616
A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease
Wolf H, Damme M, Stroobants S, D'Hooge R, Beck HC, Hermans-Borgmeyer I, Lüllmann-Rauch R, Dierks T, Lübke T (2016)
Disease Models & Mechanisms 9(9): 1015-1028.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2784664
Sulf1 and Sulf2 Differentially Modulate Heparan Sulfate Proteoglycan Sulfation during Postnatal Cerebellum Development: Evidence for Neuroprotective and Neurite Outgrowth Promoting Functions
Kalus I, Rohn S, Puvirajesinghe TM, Guimond SE, Eyckerman-Kölln P, ten Dam G, van Kuppevelt TH, Turnbull JE, Dierks T (2015)
PLoS ONE 10(10): e0139853.
PUB | DOI | WoS | PubMed | Europe PMC
 
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2780450
Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reaction
Peng J, Alam S, Radhakrishnan K, Mariappan M, Rudolph MG, May C, Dierks T, von Figura K, Schmidt B (2015)
FEBS Journal 282(17): 3262-3274.
PUB | DOI | WoS | PubMed | Europe PMC
 
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2709463
Ataxia is the major neuropathological finding in Arylsulfatase G deficient mice: Similarities and dissimilarities to Sanfilippo disease (Mucopolysaccharidosis type III)
Kowalewski B, Heimann P, Ortkras T, Lüllmann-Rauch R, Sawada T, Walkley SU, Dierks T, Damme M (2015)
Human Molecular Genetics 24(7): 1856-1868.
PUB | DOI | WoS | PubMed | Europe PMC
 

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