PUB - Publikationen an der Universität Bielefeld

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• [122]
  

  2023 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2969064

  Schlotawa, L., et al., 2023. Drug screening identifies tazarotene and bexarotene as therapeutic agents in multiple sulfatase deficiency. EMBO Molecular Medicine, : e14837.

  PUB | PDF | DOI | WoS | PubMed | Europe PMC
   
• [121]
  

  2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2955530

  Boschanski, M., et al., 2021. Site-Specific Conjugation Strategy for Dual Antibody-Drug Conjugates Using Aerobic Formylglycine-Generating Enzymes. Bioconjugate chemistry.

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• [120]
  

  2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2956816

  Kowalewski, B., et al., 2021. Decoding the consecutive lysosomal degradation of 3-O-sulfate containing heparan sulfate by Arylsulfatase G (ARSG). Biochemical Journal.

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• [119]
  

  2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2945531

  Janson, N., et al., 2020. Bifunctional Reagents for Formylglycine Conjugation: Pitfalls and Breakthroughs. ChemBioChem, 21(24), p 3580-3593.

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• [118]
  

  2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2945876

  Trabszo, C., et al., 2020. Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfate. Biochemical Journal.

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• [117]
  

  2020 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2945204

  Adang, L.A., et al., 2020. Natural history of multiple sulfatase deficiency: retrospective phenotyping and functional variant analysis to characterize an ultra-rare disease. Journal of inherited metabolic disease.

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• [116]
  

  2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2941491

  Staretz-Chacham, O., et al., 2020. A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiency. Molecular genetics & genomic medicine, 8(9): e1167.

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• [115]
  

  2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934113

  Krüger, T., Dierks, T., & Sewald, N., 2019. Formylglycine-generating enzymes for site-specific bioconjugation. BIOLOGICAL CHEMISTRY, 400(3), p 289-297.

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• [114]
  

  2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2936936

  Krüger, T., et al., 2019. Conversion of Serine-Type Aldehyde Tags by the Radical SAM Protein AtsB from Methanosarcina mazei. ChemBioChem, 20(16: Special Issue: 10th IPS), p 2074-2078.

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• [113]
  

  2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937586

  Schlotawa, L., et al., 2019. Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient. JIMD reports, 49(1), p 48-52.

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• [112]
  

  2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937243

  Korf-Klingebiel, M., et al., 2019. Heparan Sulfate-Editing Extracellular Sulfatases Enhance Vascular Endothelial Growth Factor Bioavailability for Ischemic Heart Repair. Circulation research, 125(9), p 787-801.

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• [111]
  

  2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2933342

  Bloess, S., et al., 2019. Expression, characterization, and site-specific covalent immobilization of an L-amino acid oxidase from the fungus Hebeloma cylindrosporum. Applied microbiology and biotechnology, 103(5), p 2229-2241.

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• [110]
  

  2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2934622

  Walhorn, V., et al., 2019. Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's Equality. In BIOPHYSICAL JOURNAL. no.116 Cell Press, pp. 430A-431A.

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• [109]
  

  2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933913

  Schlotawa, L., et al., 2019. Protein disulfide isomerase is a possible target for disease modification in multiple sulfatase deficiency. In MOLECULAR GENETICS AND METABOLISM. MOLECULAR GENETICS AND METABOLISM. no.126 San Diego: ACADEMIC PRESS INC ELSEVIER SCIENCE, pp. S131-S132.

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• [108]
  

  2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933914

  Silva, T.O., et al., 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. no.126 ACADEMIC PRESS INC ELSEVIER SCIENCE,, pp. S135-S136.

  PUB | DOI | WoS
   
• [107]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2944898

  Krüger, T., et al., 2018. Zweifach-bioorthogonale Derivatisierung durch verschiedene Formylglycin-generierende Enzyme. Angewandte Chemie, 130(24), p 7365-7369.

  PUB | DOI
   
• [106]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920942

  Krüger, T., et al., 2018. Two-fold Bioorthogonal Derivatization by Different Formylglycine-Generating Enzymes. Angewandte Chemie International Edition, 57(24), p 7245-7249.

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• [105]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933928

  Maynard, D., et al., 2018. The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development. Journal of Experimental Botany , 69(22), p 5341-5354.

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• [104]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2932772

  Walhorn, V., et al., 2018. Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's Equality. Scientific Reports, 8(1): 16849.

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• [103]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271

  Stroobants, S., et al., 2018. Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice. FRONTIERS IN BEHAVIORAL NEUROSCIENCE, 12: 15.

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• [102]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2921018

  Schlotawa, L., et al., 2018. Recognition and ER Quality Control of Misfolded Formylglycine-Generating Enzyme by Protein Disulfide Isomerase. Cell Reports, 24(1), p 27-37.e4.

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• [101]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931507

  Khateb, S., et al., 2018. A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans. GENETICS IN MEDICINE, 20(9), p 1004-1012.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [100]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2919061

  Ahrens-Nicklas, R., et al., 2018. Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement. MOLECULAR GENETICS AND METABOLISM, 123(3), p 337-346.

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• [99]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2918283

  Wieczorek, A., et al., 2018. Genetically modified human type II collagen for N- and C-terminal covalent tagging. CANADIAN JOURNAL OF CHEMISTRY, 96(2), p 204-211.

  PUB | DOI | WoS
   
• [98]
  

  2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909071

  Roy, D., et al., 2017. Loss of HSulf-1: The Missing Link between Autophagy and Lipid Droplets in Ovarian Cancer. SCIENTIFIC REPORTS, 7(1): 41977.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [97]
  

  2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916520

  Jaszczuk, I., et al., 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), p 252-258.

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• [96]
  

  2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778

  Dhamale, O.P., et al., 2017. Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase. ACS Chemical Biology, 12(2), p 367-373.

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• [95]
  

  2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124

  Kruszewski, K., et al., 2016. Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 57(3), p 1120-1131.

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• [94]
  

  2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616

  Wolf, H., et al., 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), p 1015-1028.

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• [93]
  

  2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2784664

  Kalus, I., et al., 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.

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• [92]
  

  2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2788799

  Mondal, S., et al., 2015. HSulf-1 deficiency dictates a metabolic reprograming of glycolysis and TCA cycle in ovarian cancer. ONCOTARGET, 6(32), p 33705-33719.

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• [91]
  

  2015 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2908650

  Walhorn, V., et al., 2015. Single-Molecule Mechanics and Force Spectroscopy. In J. Dhont, et al., eds. Functional Soft Matter. Schlüsseltechnologien - Key Technologies. no.94 Jülich: Forschungszentrum Jülich Publisher, pp. C4.1-C4.17.

  PUB
   
• [90]
  

  2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2780450

  Peng, J., et al., 2015. Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reaction. FEBS Journal, 282(17), p 3262-3274.

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• [89]
  

  2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2709463

  Kowalewski, B., et al., 2015. Ataxia is the major neuropathological finding in Arylsulfatase G deficient mice: Similarities and dissimilarities to Sanfilippo disease (Mucopolysaccharidosis type III). Human Molecular Genetics, 24(7), p 1856-1868.

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• [88]
  

  2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2732684

  Harder, A., et al., 2015. Catch Bond Interaction between Cell-Surface Sulfatase Sulf1 and Glycosaminoglycans. Biophysical journal, 108(7), p 1709-1717.

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• [87]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2690696

  Poppe, J., et al., 2014. Structural diversity of polyoxomolybdate clusters along the three-fold axis of the molybdenum storage protein. Journal of Inorganic Biochemistry, 138, p 122-128.

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• [86]
  

  2014 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2685914

  Harder, A., et al., 2014. Catch Bond Interaction Between Glycosaminoglycans and Cell Surface Sulfatase Sulf1. Biophysical Journal, 106(2), p 450A-450A.

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• [85]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2699273

  Kowalewski, B., et al., 2014. Molecular Characterization of Arylsulfatase G: EXPRESSION, PROCESSING, GLYCOSYLATION, TRANSPORT, AND ACTIVITY. The Journal of biological chemistry, 289(40), p 27992-28005.

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• [84]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2607389

  Yoo, M., et al., 2013. Arylsulfatase B Improves Locomotor Function after Mouse Spinal Cord Injury. Plos One, 8(3): e57415.

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• [83]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2625696

  Schlotawa, L., et al., 2013. Rapid degradation of an active formylglycine generating enzyme variant leads to a late infantile severe form of multiple sulfatase deficiency. European Journal Of Human Genetics, 21(9), p 1020-1023.

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• [82]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623550

  Wiegmann, E., et al., 2013. Arylsulfatase K, a Novel Lysosomal Sulfatase. Journal of Biological Chemistry, 288(42), p 30019-30028.

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• [81]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623281

  Maltseva, I., et al., 2013. The SULFs, Extracellular Sulfatases for Heparan Sulfate, Promote the Migration of Corneal Epithelial Cells during Wound Repair. PloS one, 8(8): e69642.

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• [80]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2565333

  Ennemann, E., et al., 2013. Proprotein Convertases Process and Thereby Inactivate Formylglycine-generating Enzyme. Journal of Biological Chemistry, 288(8), p 5828-5839.

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• [79]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623253

  Kim, J.H., et al., 2013. Endosulfatases SULF1 and SULF2 limit Chlamydia muridarum infection. Cellular Microbiology, 15(9), p 1560-1571.

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• [78]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623533

  Milz, F., et al., 2013. Cooperation of binding sites at the hydrophilic domain of cell-surface sulfatase Sulf1 allows for dynamic interaction of the enzyme with its substrate heparan sulfate. Biochim Biophys Acta, 1830(11), p 5287-5298.

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• [77]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2612942

  Seffouh, A., et al., 2013. HSulf sulfatases catalyze processive and oriented 6-O-desulfation of heparan sulfate that differentially regulates fibroblast growth factor activity. The Faseb Journal, 27(6), p 2431-2439.

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• [76]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351519

  Lenger, J., et al., 2012. Evaluation of sulfatase-directed quinone methide traps for proteomics. Bioorganic & Medicinal Chemistry, 20(2), p 622-627.

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• [75]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2474206

  Hayano, S., et al., 2012. Roles of heparan sulfate sulfation in dentinogenesis. J. Biol. Chem., 287(15), p 12217-12229.

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• [74]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2517966

  Kowalewski, B., et al., 2012. Nature's Polyoxometalate Chemistry: X-ray Structure of the Mo Storage Protein Loaded with Discrete Polynuclear Mo-O Clusters. Journal of the American Chemical Society, 134(23), p 9768-9774.

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• [73]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2494022

  Kowalewski, B., et al., 2012. Arylsulfatase G Inactivation Causes Loss of Heparan Sulfate 3-O-Sulfatase Activity and Mucopolysaccharidosis in Mice. Proc. Natl. Acad. Sci. USA, 109(26), p 10310-10315.

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• [72]
  

  2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2003211

  Schlotawa, L., et al., 2011. SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiency. European Journal of Human Genetics, 19(3), p 253-261.

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• [71]
  

  2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1968383

  Harder, A., et al., 2010. Single-Molecule Force Spectroscopy of Cartilage Aggrecan Self-Adhesion. Biophysical Journal, 99(10), p 3498-3504.

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• [70]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1590897

  Guimond, S.E., et al., 2009. Rapid Purification and High Sensitivity Analysis of Heparan Sulfate from Cells and Tissues TOWARD GLYCOMICS PROFILING. JOURNAL OF BIOLOGICAL CHEMISTRY, 284(38), p 25714-25722.

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• [69]
  

  2009 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2352302

  von Figura, K., Dierks, T., & Schmidt, B., 2009. Multiple Sulfatase Deficiency. In F. Lang, ed. Encyclopedia of Molecular Mechanisms of Disease. Berlin Heidelberg: Springer, pp. 1374-1375.

  PUB
   
• [68]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1634198

  Dierks, T., et al., 2009. Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann-Pick C1 disease - Lysosomal storage disorders caused by defects of non-lysosomal proteins. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1793(4), p 710-725.

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• [67]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1796606

  Kalus, I., et al., 2009. Differential involvement of the extracellular 6-O-endosulfatases Sulf1 and Sulf2 in brain development and neuronal and behavioural plasticity. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 13(11-12), p 4505-4521.

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• [66]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1590564

  Frese, M.-A., et al., 2009. Characterization of the Human Sulfatase Sulf1 and Its High Affinity Heparin/Heparan Sulfate Interaction Domain. JOURNAL OF BIOLOGICAL CHEMISTRY, 284(41), p 28033-28044.

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• [65]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1635473

  Frese, M.-A., & Dierks, T., 2009. Formylglycine Aldehyde Tag-Protein Engineering through a Novel Post-translational Modification. CHEMBIOCHEM, 10(3), p 425-427.

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• [64]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1633371

  Busche, A., et al., 2009. Neonatal manifestation of multiple sulfatase deficiency. EUROPEAN JOURNAL OF PEDIATRICS, 168(8), p 969-973.

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• [63]
  

  2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351244

  Schlotawa, L., et al., 2008. Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency. Human Mutation, 29(1), p 205.

  PUB | DOI
   
• [62]
  

  2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1592682

  Ratzka, A., et al., 2008. Redundant function of the heparan sulfate 6-O-endosulfatases Sulf1 and Sulf2 during skeletal development. DEVELOPMENTAL DYNAMICS, 237(2), p 339-353.

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• [61]
  

  2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1592488

  Gande, S.L., et al., 2008. Paralog of the formylglycine-generating enzyme - retention in the endoplasmic reticulum by canonical and noncanonical signals. FEBS JOURNAL, 275(6), p 1118-1130.

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• [60]
  

  2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1592481

  Mariappan, M., et al., 2008. ERp44 mediates a thiol-independent retention of formylglycine-generating enzyme in the endoplasmic reticulum. JOURNAL OF BIOLOGICAL CHEMISTRY, 283(10), p 6375-6383.

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• [59]
  

  2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1588435

  Frese, M.-A., Schulz, S., & Dierks, T., 2008. Arylsulfatase G, a novel lysosomal sulfatase. JOURNAL OF BIOLOGICAL CHEMISTRY, 283(17), p 11388-11395.

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• [58]
  

  2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1588440

  Mariappan, M., et al., 2008. The non-catalytic N-terminal extension of formylglycine-generating enzyme is required for its biological activity and retention in the endoplasmic reticulum. JOURNAL OF BIOLOGICAL CHEMISTRY, 283(17), p 11556-11564.

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• [57]
  

  2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1586139

  Lamanna, W.C., et al., 2008. Sulf loss influences N-, 2-O-, and 6-O-sulfation of multiple heparan sulfate proteoglycans and modulates fibroblast growth factor signaling. JOURNAL OF BIOLOGICAL CHEMISTRY, 283(41), p 27724-27735.

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• [56]
  

  2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1593622

  Zito, E., et al., 2007. Sulfatase modifying factor 1 trafficking through the cells: from endoplasmic reticulum to the endoplasmic reticulum. EMBO JOURNAL, 26(10), p 2443-2453.

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• [55]
  

  2007 | Konferenzbeitrag | Veröffentlicht | PUB-ID: 1594028

  Lamanna, W.C., et al., 2007. The heparanome - The enigma of encoding and decoding heparan sulfate sulfation. In Journal of Biotechnology. JOURNAL OF BIOTECHNOLOGY. no.129 ELSEVIER SCIENCE BV, pp. 290-307.

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• [54]
  

  2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1597019

  Lamanna, W.C., et al., 2006. Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity. BIOCHEMICAL JOURNAL, 400(1), p 63-73.

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• [53]
  

  2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1600859

  Roeser, D., et al., 2006. A general binding mechanism for all human sulfatases by the formylglycine-generating enzyme. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 103(1), p 81-86.

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• [52]
  

  2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350692

  Dierks, T., et al., 2005. Molecular basis for multiple sulfatase deficiency and mechanism for formylglycine generation of the human formylglycine-generating enzyme. CELL, 121(4), p 541-552.

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  2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350712

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  2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350723

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  2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1603995

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  2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350732

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  2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350737

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  2004 | Patent | Veröffentlicht | PUB-ID: 2375304

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  2004 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2352318

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  2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350768

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  2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350753

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  2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350747

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  2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350759

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  2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350776

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  2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350782

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  2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350811

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  2001 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372494

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  2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350792

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  2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350800

  Boltes, I., et al., 2001. 1.3 angstrom structure of arylsulfatase from Pseudomonas aeruginosa establishes the catalytic mechanism of sulfate ester cleavage in the sulfatase family. STRUCTURE, 9(6), p 483-491.

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  2001 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372492

  Dierks, T., 2001. Cysteine-modifying enzyme. In T. E. Creighton, ed. Encyclopedia of Molecular Medicine. New York: J. Wiley, pp. 974-976.

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  2001 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372496

  Dierks, T., & Schmidt, B., 2001. Arylsulfatases. In T. E. Creighton, ed. Encyclopedia of Molecular Medicine. New York: J. Wiley, pp. 266-268.

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  1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350826

  Waldow, A., et al., 1999. Amino acid residues forming the active site of arylsulfatase A - Role in catalytic activity and substrate binding. JOURNAL OF BIOLOGICAL CHEMISTRY, 274(18), p 12284-12288.

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  1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350833

  Dierks, T., et al., 1999. Sequence determinants directing conversion of cysteine to formylglycine in eukaryotic sulfatases. EMBO JOURNAL, 18(8), p 2084-2091.

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  1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350818

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  1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350840

  Knaust, A., et al., 1998. Residues critical for formylglycine formation and/or catalytic activity of arylsulfatase A. BIOCHEMISTRY, 37(40), p 13941-13946.

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  1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350871

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  1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350847

  Dierks, T., et al., 1998. Posttranslational formation of formylglycine in prokaryotic sulfatases by modification of either cysteine or serine. JOURNAL OF BIOLOGICAL CHEMISTRY, 273(40), p 25560-25564.

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  1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350855

  Reiss, J., et al., 1998. Mutations in a polycistronic nuclear gene associated with molybdenum cofactor deficiency. NATURE GENETICS, 20(1), p 51-53.

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  1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350865

  Figura von, K., et al., 1998. A novel protein modification generating an aldehyde group in sulfatases: its role in catalysis and disease. BIOESSAYS, 20(6), p 505-510.

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  1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350877

  Miech, C., et al., 1998. Arylsulfatase from Klebsiella pneumoniae carries a formylglycine generated from a serine. JOURNAL OF BIOLOGICAL CHEMISTRY, 273(9), p 4835-4837.

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  1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350884

  Dierks, T., et al., 1998. Conversion of cysteine to formylglycine in eukaryotic sulfatases occurs by a common mechanism in the endoplasmic reticulum. FEBS LETTERS, 423(1), p 61-65.

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  1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350890

  Dierks, T., Schmidt, B., & VonFigura, K., 1997. Conversion of cysteine to formylglycine: A protein modification in the endoplasmic reticulum. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 94(22), p 11963-11968.

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  1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350895

  Dierks, T., et al., 1996. A microsomal ATP-binding protein involved in efficient protein transport into the mammalian endoplasmic reticulum. EMBO JOURNAL, 15(24), p 6931-6942.

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  1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350906

  Brunke, M., et al., 1996. Luciferase assembly after transport into mammalian microsomes involves molecular chaperones and peptidyl-prolyl cis/trans-isomerases. JOURNAL OF BIOLOGICAL CHEMISTRY, 271(38), p 23487-23494.

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  1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350925

  Klappa, P., Dierks, T., & Zimmermann, R., 1996. Cyclosporin A inhibits the degradation of signal sequences after processing of presecretory proteins by signal peptidase. EUROPEAN JOURNAL OF BIOCHEMISTRY, 239(2), p 509-518.

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  1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350916

  Tyedmers, J., et al., 1996. Efficient folding of firefly luciferase after transport into mammalian microsomes in the absence of luminal chaperones and folding catalysts. JOURNAL OF BIOLOGICAL CHEMISTRY, 271(32), p 19509-19513.

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  1994 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372523

  Dierks, T., Stappen, R., & Krämer, R., 1994. Channel properties of mitochondrial carriers. In M. Forte & M. Colombini, eds. Molecular Biology of Mitochondrial Transport Systems. Nato ASI Series. no.H83 Berlin: Springer, pp. 117-129.

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  1993 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350937

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  1993 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350944

  Dierks, T., et al., 1993. THE ROLE OF MOLECULAR CHAPERONES IN PROTEIN-TRANSPORT INTO THE ENDOPLASMIC-RETICULUM. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 339(1289), p 335-341.

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  1993 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372500

  Klappa, P., et al., 1993. Components and mechanisms involved in transport of proteins into the endoplasmic reticulum. In N. Borgese & J. R. Harris, eds. Endoplasmic reticulum. Subcellular Biochemistry. no.21 Berlin: Springer, pp. 17-40.

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  1993 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372529

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  1993 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350930

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  1992 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350950

  INDIVERI, C., et al., 1992. THE MITOCHONDRIAL CARNITINE CARRIER - CHARACTERIZATION OF SH-GROUPS RELEVANT FOR ITS TRANSPORT FUNCTION. BIOCHIMICA ET BIOPHYSICA ACTA, 1140(1), p 53-58.

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  1992 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350957

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  1992 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350963

  Dierks, T., et al., 1992. PROBING THE ACTIVE-SITE OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM BOVINE HEART-MITOCHONDRIA - CARBODIIMIDE-CATALYZED ACYLATION OF A FUNCTIONAL LYSINE RESIDUE. BIOCHIMICA ET BIOPHYSICA ACTA, 1103(1), p 13-24.

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  1991 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350977

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  1991 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350969

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  1990 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350989

  Dierks, T., SALENTIN, A., & KRAMER, R., 1990. PORE-LIKE AND CARRIER-LIKE PROPERTIES OF THE MITOCHONDRIAL ASPARTATE GLUTAMATE CARRIER AFTER MODIFICATION BY SH-REAGENTS - EVIDENCE FOR A PREFORMED CHANNEL AS A STRUCTURAL REQUIREMENT OF CARRIER-MEDIATED TRANSPORT. BIOCHIMICA ET BIOPHYSICA ACTA, 1028(3), p 281-288.

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  1990 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350983

  Dierks, T., et al., 1990. THE MITOCHONDRIAL ASPARTATE GLUTAMATE AND ADP/ATP CARRIER SWITCH FROM OBLIGATE COUNTEREXCHANGE TO UNIDIRECTIONAL TRANSPORT AFTER MODIFICATION BY SH-REAGENTS. BIOCHIMICA ET BIOPHYSICA ACTA, 1028(3), p 268-280.

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  1989 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350994

  INDIVERI, C., et al., 1989. KINETIC DISCRIMINATION OF 2 SUBSTRATE BINDING-SITES OF THE RECONSTITUTED DICARBOXYLATE CARRIER FROM RAT-LIVER MITOCHONDRIA. BIOCHIMICA ET BIOPHYSICA ACTA, 977(2), p 194-199.

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  1989 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372511

  Dierks, T., & Krämer, R., 1989. Reaction mechanism of the reconstituted aspartate / glutamate carrier from mitochondria. Reversible switching to uniport function. In A. Azzi, et al., eds. Anion Carriers of Mitochondrial Membranes. Berlin: Springer, pp. 99-110.

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  1988 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351000

  Dierks, T., RIEMER, E., & KRAMER, R., 1988. REACTION-MECHANISM OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM BOVINE HEART-MITOCHONDRIA. BIOCHIMICA ET BIOPHYSICA ACTA, 943(2), p 231-244.

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  1988 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351005

  Dierks, T., & KRAMER, R., 1988. ASYMMETRIC ORIENTATION OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM MITOCHONDRIA. BIOCHIMICA ET BIOPHYSICA ACTA, 937(1), p 112-126.

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