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402 Publikationen

2020 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2946513
Altered glycosidase Activities at Physiological pH in the Pathogenesis of Sepsis
Aziz P, Haslund-Gourley B, Heithoff D, Westman J, Restagno D, Lewis B, Fried J, Ilse M-B, Lübke T, Marth J (2020)
In: FASEB JOURNAL., 34(S1). Hoboken: Wiley.
PUB | DOI | WoS
 
2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2941491 OA
A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiency.
Staretz-Chacham O, Schlotawa L, Wormser O, Golan-Tripto I, Birk OS, Ferreira CR, Dierks T, Radhakrishnan K (2020)
Molecular genetics & genomic medicine 8(9): e1167.
PUB | PDF | DOI | WoS | PubMed | Europe PMC
 
2020 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2945204
Natural history of multiple sulfatase deficiency: retrospective phenotyping and functional variant analysis to characterize an ultra-rare disease.
Adang LA, Schlotawa L, Groeschel S, Kehrer C, Harzer K, Staretz-Chacham O, Oliveira Silva T, Schwartz IVD, Gartner J, De Castro M, Costin C, et al. (2020)
Journal of inherited metabolic disease.
PUB | DOI | WoS | PubMed | Europe PMC
 
2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2943713
Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification.
Schlotawa L, Adang LA, Radhakrishnan K, Ahrens-Nicklas RC (2020)
International journal of molecular sciences 21(10): 3448.
PUB | DOI | WoS | PubMed | Europe PMC
 
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937243
Heparan Sulfate-Editing Extracellular Sulfatases Enhance Vascular Endothelial Growth Factor Bioavailability for Ischemic Heart Repair
Korf-Klingebiel M, Reboll MR, Grote K, Schleiner H, Wang Y, Wu X, Klede S, Mikhed Y, Bauersachs J, Klintschar M, Rudat C, et al. (2019)
Circulation research 125(9): 787-801.
PUB | DOI | WoS | PubMed | Europe PMC
 
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2936936
Conversion of Serine-Type Aldehyde Tags by the Radical SAM Protein AtsB from Methanosarcina mazei
Krüger T, Weiland S, Boschanski M, Sinha PK, Falck G, Müller K, Dierks T, Sewald N (2019)
ChemBioChem 20(16: Special Issue: 10th IPS): 2074-2078.
PUB | DOI | WoS | PubMed | Europe PMC
 
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2933342
Expression, characterization, and site-specific covalent immobilization of an L-amino acid oxidase from the fungus Hebeloma cylindrosporum
Bloess S, Beuel T, Krüger T, Sewald N, Dierks T, Fischer von Mollard G (2019)
Applied microbiology and biotechnology 103(5): 2229-2241.
PUB | DOI | WoS | PubMed | Europe PMC
 
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2943600
The lysosomal transporter MFSD1 is essential for liver homeostasis and critically depends on its accessory subunit GLMP
Lopez DM, Thelen M, Stahl F, Thiel C, Linhorst A, Sylvester M, Hermanns-Borgmeyer I, Luellmann-Rauch R, Eskild W, Saftig P, Damme M (2019)
ELIFE 8: e50025.
PUB | DOI | WoS | PubMed | Europe PMC
 
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 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937586
Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient.
Schlotawa L, Dierks T, Christoph S, Cloppenburg E, Ohlenbusch A, Korenke GC, Gartner J (2019)
JIMD reports 49(1): 48-52.
PUB | DOI | PubMed | Europe PMC
 
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 | 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: 2932772
Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's Equality
Walhorn V, Möller A-K, Bartz C, Dierks T, Anselmetti D (2018)
Scientific Reports 8(1): 16849.
PUB | DOI | WoS | PubMed | Europe PMC
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2944898
Zweifach-bioorthogonale Derivatisierung durch verschiedene Formylglycin-generierende Enzyme
Krüger T, Weiland S, Falck G, Gerlach M, Boschanski M, Alam S, Müller K, Dierks T, Sewald N (2018)
Angewandte Chemie 130(24): 7365-7369.
PUB | DOI
 
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2921018 OA
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: 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: 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: 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 | 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
 

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