122 Publikationen
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2023 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2969064Drug screening identifies tazarotene and bexarotene as therapeutic agents in multiple sulfatase deficiencyPUB | PDF | DOI | WoS | PubMed | Europe PMC
Schlotawa, Lars, Drug screening identifies tazarotene and bexarotene as therapeutic agents in multiple sulfatase deficiency. EMBO Molecular Medicine (). , 2023 -
2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2955530Site-Specific Conjugation Strategy for Dual Antibody-Drug Conjugates Using Aerobic Formylglycine-Generating EnzymesPUB | DOI | WoS | PubMed | Europe PMC
Boschanski, Mareile, Site-Specific Conjugation Strategy for Dual Antibody-Drug Conjugates Using Aerobic Formylglycine-Generating Enzymes. Bioconjugate chemistry (). , 2021 -
2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2956816Decoding the consecutive lysosomal degradation of 3-O-sulfate containing heparan sulfate by Arylsulfatase G (ARSG)PUB | DOI | WoS | PubMed | Europe PMC
Kowalewski, Björn, Decoding the consecutive lysosomal degradation of 3-O-sulfate containing heparan sulfate by Arylsulfatase G (ARSG). Biochemical Journal (). , 2021 -
2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2945531Bifunctional Reagents for Formylglycine Conjugation: Pitfalls and BreakthroughsPUB | PDF | DOI | WoS | PubMed | Europe PMC
Janson, Nils, Bifunctional Reagents for Formylglycine Conjugation: Pitfalls and Breakthroughs. ChemBioChem 21 (24). , 2020 -
2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2945876Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfatePUB | DOI | WoS | PubMed | Europe PMC
Trabszo, Christof, Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfate. Biochemical Journal (). , 2020 -
2020 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2945204Natural history of multiple sulfatase deficiency: retrospective phenotyping and functional variant analysis to characterize an ultra-rare disease.PUB | DOI | WoS | PubMed | Europe PMC
Adang, Laura A., Natural history of multiple sulfatase deficiency: retrospective phenotyping and functional variant analysis to characterize an ultra-rare disease.. Journal of inherited metabolic disease (). , 2020 -
2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2941491A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiency.PUB | PDF | DOI | WoS | PubMed | Europe PMC
Staretz-Chacham, Orna, 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). , 2020 -
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934113Formylglycine-generating enzymes for site-specific bioconjugationPUB | DOI | WoS | PubMed | Europe PMC
Krüger, Tobias, Formylglycine-generating enzymes for site-specific bioconjugation. BIOLOGICAL CHEMISTRY 400 (3). , 2019 -
2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2936936Conversion of Serine-Type Aldehyde Tags by the Radical SAM Protein AtsB from Methanosarcina mazeiPUB | DOI | WoS | PubMed | Europe PMC
Krüger, Tobias, Conversion of Serine-Type Aldehyde Tags by the Radical SAM Protein AtsB from Methanosarcina mazei. ChemBioChem 20 (16: Special Issue: 10th IPS). , 2019 -
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937586Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patientPUB | PDF | DOI | PubMed | Europe PMC
Schlotawa, Lars, Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient. JIMD reports 49 (1). , 2019 -
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937243Heparan Sulfate-Editing Extracellular Sulfatases Enhance Vascular Endothelial Growth Factor Bioavailability for Ischemic Heart RepairPUB | DOI | WoS | PubMed | Europe PMC
Korf-Klingebiel, Mortimer, Heparan Sulfate-Editing Extracellular Sulfatases Enhance Vascular Endothelial Growth Factor Bioavailability for Ischemic Heart Repair. Circulation research 125 (9). , 2019 -
2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2933342Expression, characterization, and site-specific covalent immobilization of an L-amino acid oxidase from the fungus Hebeloma cylindrosporumPUB | DOI | WoS | PubMed | Europe PMC
Bloess, Svenja, Expression, characterization, and site-specific covalent immobilization of an L-amino acid oxidase from the fungus Hebeloma cylindrosporum. Applied microbiology and biotechnology 103 (5). , 2019 -
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2934622Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's EqualityPUB | DOI | WoS
Walhorn, Volker, Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's Equality. BIOPHYSICAL JOURNAL 116 (3). , 2019 -
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933913Protein disulfide isomerase is a possible target for disease modification in multiple sulfatase deficiencyPUB | DOI | WoS
Schlotawa, Lars, Protein disulfide isomerase is a possible target for disease modification in multiple sulfatase deficiency. MOLECULAR GENETICS AND METABOLISM 126 (2). San Diego, 2019 -
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933914Attenuated multiple sulfatase deficiency: Description of two Brazilian patients showing interesting clinical and genetic findingsPUB | DOI | WoS
Silva, Thiag O., Attenuated multiple sulfatase deficiency: Description of two Brazilian patients showing interesting clinical and genetic findings. MOLECULAR GENETICS AND METABOLISM 126 (2). , 2019 -
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2944898Zweifach-bioorthogonale Derivatisierung durch verschiedene Formylglycin-generierende EnzymePUB | DOI
Krüger, Tobias, Zweifach-bioorthogonale Derivatisierung durch verschiedene Formylglycin-generierende Enzyme. Angewandte Chemie 130 (24). , 2018 -
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920942Two-fold Bioorthogonal Derivatization by Different Formylglycine-Generating EnzymesPUB | DOI | WoS | PubMed | Europe PMC
Krüger, Tobias, Two-fold Bioorthogonal Derivatization by Different Formylglycine-Generating Enzymes. Angewandte Chemie International Edition 57 (24). , 2018 -
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933928The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and developmentPUB | DOI | WoS | PubMed | Europe PMC
Maynard, Daniel, The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development. Journal of Experimental Botany 69 (22). , 2018 -
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2932772Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's EqualityPUB | DOI | WoS | PubMed | Europe PMC
Walhorn, Volker, Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's Equality. Scientific Reports 8 (1). , 2018 -
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis MicePUB | DOI | WoS | PubMed | Europe PMC
Stroobants, Stijn, Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice. FRONTIERS IN BEHAVIORAL NEUROSCIENCE 12 (). , 2018 -
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2921018Recognition and ER Quality Control of Misfolded Formylglycine-Generating Enzyme by Protein Disulfide IsomerasePUB | PDF | DOI | WoS | PubMed | Europe PMC
Schlotawa, Lars, Recognition and ER Quality Control of Misfolded Formylglycine-Generating Enzyme by Protein Disulfide Isomerase. Cell Reports 24 (1). , 2018 -
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931507A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humansPUB | DOI | WoS | PubMed | Europe PMC
Khateb, Samer, A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans. GENETICS IN MEDICINE 20 (9). , 2018 -
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2919061Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statementPUB | DOI | WoS | PubMed | Europe PMC
Ahrens-Nicklas, Rebecca, Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement. MOLECULAR GENETICS AND METABOLISM 123 (3). , 2018 -
2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2918283Genetically modified human type II collagen for N- and C-terminal covalent taggingPUB | DOI | WoS
Wieczorek, Andrew, Genetically modified human type II collagen for N- and C-terminal covalent tagging. CANADIAN JOURNAL OF CHEMISTRY 96 (2). , 2018 -
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909071Loss of HSulf-1: The Missing Link between Autophagy and Lipid Droplets in Ovarian CancerPUB | DOI | WoS | PubMed | Europe PMC
Roy, Debarshi, Loss of HSulf-1: The Missing Link between Autophagy and Lipid Droplets in Ovarian Cancer. SCIENTIFIC REPORTS 7 (1). , 2017 -
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916520Expanding the genetic cause of multiple sulfatase deficiency: A novel SUMF1 variant in a patient displaying a severe late infantile form of the diseasePUB | DOI | WoS | PubMed | Europe PMC
Jaszczuk, Ilona, 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). , 2017 -
2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate SulfatasePUB | DOI | WoS | PubMed | Europe PMC
Dhamale, Omkar P., Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase. ACS Chemical Biology 12 (2). , 2017 -
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient MicePUB | DOI | WoS | PubMed | Europe PMC
Kruszewski, Katharina, Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 57 (3). , 2016 -
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human diseasePUB | PDF | DOI | WoS | PubMed | Europe PMC
Wolf, Heike, A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease. Disease Models & Mechanisms 9 (9). , 2016 -
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2784664Sulf1 and Sulf2 Differentially Modulate Heparan Sulfate Proteoglycan Sulfation during Postnatal Cerebellum Development: Evidence for Neuroprotective and Neurite Outgrowth Promoting FunctionsPUB | DOI | WoS | PubMed | Europe PMC
Kalus, Ina, 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). , 2015 -
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2788799HSulf-1 deficiency dictates a metabolic reprograming of glycolysis and TCA cycle in ovarian cancerPUB | DOI | WoS | PubMed | Europe PMC
Mondal, Susmita, HSulf-1 deficiency dictates a metabolic reprograming of glycolysis and TCA cycle in ovarian cancer. ONCOTARGET 6 (32). , 2015 -
2015 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2908650Single-Molecule Mechanics and Force SpectroscopyPUB
Walhorn, Volker, Single-Molecule Mechanics and Force Spectroscopy. Functional Soft Matter 94 (). Jülich, 2015 -
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2780450Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reactionPUB | DOI | WoS | PubMed | Europe PMC
Peng, Jianhe, Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reaction. FEBS Journal 282 (17). , 2015 -
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2709463Ataxia is the major neuropathological finding in Arylsulfatase G deficient mice: Similarities and dissimilarities to Sanfilippo disease (Mucopolysaccharidosis type III)PUB | DOI | WoS | PubMed | Europe PMC
Kowalewski, Björn, 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). , 2015 -
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2732684Catch Bond Interaction between Cell-Surface Sulfatase Sulf1 and GlycosaminoglycansPUB | DOI | WoS | PubMed | Europe PMC
Harder, Alexander, Catch Bond Interaction between Cell-Surface Sulfatase Sulf1 and Glycosaminoglycans. Biophysical journal 108 (7). , 2015 -
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2690696Structural diversity of polyoxomolybdate clusters along the three-fold axis of the molybdenum storage proteinPUB | DOI | WoS | PubMed | Europe PMC
Poppe, Juliane, Structural diversity of polyoxomolybdate clusters along the three-fold axis of the molybdenum storage protein. Journal of Inorganic Biochemistry 138 (). , 2014 -
2014 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2685914Catch Bond Interaction Between Glycosaminoglycans and Cell Surface Sulfatase Sulf1PUB | DOI | WoS
Harder, Alexander, Catch Bond Interaction Between Glycosaminoglycans and Cell Surface Sulfatase Sulf1. 106 (2). Cambridge, 2014 -
2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2699273Molecular Characterization of Arylsulfatase G: EXPRESSION, PROCESSING, GLYCOSYLATION, TRANSPORT, AND ACTIVITYPUB | DOI | WoS | PubMed | Europe PMC
Kowalewski, Björn, Molecular Characterization of Arylsulfatase G: EXPRESSION, PROCESSING, GLYCOSYLATION, TRANSPORT, AND ACTIVITY. The Journal of biological chemistry 289 (40). , 2014 -
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2607389Arylsulfatase B Improves Locomotor Function after Mouse Spinal Cord InjuryPUB | DOI | WoS | PubMed | Europe PMC
Yoo, Myungsik, Arylsulfatase B Improves Locomotor Function after Mouse Spinal Cord Injury. Plos One 8 (3). , 2013 -
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2625696Rapid degradation of an active formylglycine generating enzyme variant leads to a late infantile severe form of multiple sulfatase deficiencyPUB | DOI | WoS | PubMed | Europe PMC
Schlotawa, Lars, 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). , 2013 -
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623550Arylsulfatase K, a Novel Lysosomal SulfatasePUB | DOI | WoS | PubMed | Europe PMC
Wiegmann, Elena, Arylsulfatase K, a Novel Lysosomal Sulfatase. Journal of Biological Chemistry 288 (42). , 2013 -
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623281The SULFs, Extracellular Sulfatases for Heparan Sulfate, Promote the Migration of Corneal Epithelial Cells during Wound RepairPUB | DOI | WoS | PubMed | Europe PMC
Maltseva, Inna, The SULFs, Extracellular Sulfatases for Heparan Sulfate, Promote the Migration of Corneal Epithelial Cells during Wound Repair. PloS one 8 (8). , 2013 -
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2565333Proprotein Convertases Process and Thereby Inactivate Formylglycine-generating EnzymePUB | DOI | WoS | PubMed | Europe PMC
Ennemann, Eva, Proprotein Convertases Process and Thereby Inactivate Formylglycine-generating Enzyme. Journal of Biological Chemistry 288 (8). , 2013 -
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623253Endosulfatases SULF1 and SULF2 limit Chlamydia muridarum infectionPUB | DOI | WoS | PubMed | Europe PMC
Kim, J H, Endosulfatases SULF1 and SULF2 limit Chlamydia muridarum infection. Cellular Microbiology 15 (9). , 2013 -
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623533Cooperation of binding sites at the hydrophilic domain of cell-surface sulfatase Sulf1 allows for dynamic interaction of the enzyme with its substrate heparan sulfatePUB | DOI | WoS | PubMed | Europe PMC
Milz, Fabian, 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). , 2013 -
2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2612942HSulf sulfatases catalyze processive and oriented 6-O-desulfation of heparan sulfate that differentially regulates fibroblast growth factor activityPUB | DOI | WoS | PubMed | Europe PMC
Seffouh, Amal, HSulf sulfatases catalyze processive and oriented 6-O-desulfation of heparan sulfate that differentially regulates fibroblast growth factor activity. The Faseb Journal 27 (6). , 2013 -
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351519Evaluation of sulfatase-directed quinone methide traps for proteomicsPUB | DOI | WoS | PubMed | Europe PMC
Lenger, Janina, Evaluation of sulfatase-directed quinone methide traps for proteomics. Bioorganic & Medicinal Chemistry 20 (2). , 2012 -
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2474206Roles of heparan sulfate sulfation in dentinogenesisPUB | DOI | WoS | PubMed | Europe PMC
Hayano, S., Roles of heparan sulfate sulfation in dentinogenesis. J. Biol. Chem. 287 (15). , 2012 -
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2517966Nature's Polyoxometalate Chemistry: X-ray Structure of the Mo Storage Protein Loaded with Discrete Polynuclear Mo-O ClustersPUB | DOI | WoS | PubMed | Europe PMC
Kowalewski, Björn, 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). , 2012 -
2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2494022Arylsulfatase G Inactivation Causes Loss of Heparan Sulfate 3-O-Sulfatase Activity and Mucopolysaccharidosis in MicePUB | DOI | WoS | PubMed | Europe PMC
Kowalewski, Björn, Arylsulfatase G Inactivation Causes Loss of Heparan Sulfate 3-O-Sulfatase Activity and Mucopolysaccharidosis in Mice. Proc. Natl. Acad. Sci. USA 109 (26). , 2012 -
2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2003211SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiencyPUB | DOI | WoS | PubMed | Europe PMC
Schlotawa, Lars, SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiency. European Journal of Human Genetics 19 (3). , 2011 -
2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1968383Single-Molecule Force Spectroscopy of Cartilage Aggrecan Self-AdhesionPUB | DOI | WoS | PubMed | Europe PMC
Harder, Alexander, Single-Molecule Force Spectroscopy of Cartilage Aggrecan Self-Adhesion. Biophysical Journal 99 (10). , 2010 -
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1590897Rapid Purification and High Sensitivity Analysis of Heparan Sulfate from Cells and Tissues TOWARD GLYCOMICS PROFILINGPUB | DOI | WoS | PubMed | Europe PMC
Guimond, Scott E., Rapid Purification and High Sensitivity Analysis of Heparan Sulfate from Cells and Tissues TOWARD GLYCOMICS PROFILING. JOURNAL OF BIOLOGICAL CHEMISTRY 284 (38). , 2009 -
2009 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2352302Multiple Sulfatase DeficiencyPUB
von Figura, Kurt, Multiple Sulfatase Deficiency. Encyclopedia of Molecular Mechanisms of Disease (). Berlin Heidelberg, 2009 -
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1634198Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann-Pick C1 disease - Lysosomal storage disorders caused by defects of non-lysosomal proteinsPUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, 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). , 2009 -
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1796606Differential involvement of the extracellular 6-O-endosulfatases Sulf1 and Sulf2 in brain development and neuronal and behavioural plasticityPUB | DOI | WoS | PubMed | Europe PMC
Kalus, Ina, 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). , 2009 -
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1590564Characterization of the Human Sulfatase Sulf1 and Its High Affinity Heparin/Heparan Sulfate Interaction DomainPUB | DOI | WoS | PubMed | Europe PMC
Frese, Marc-Andre, Characterization of the Human Sulfatase Sulf1 and Its High Affinity Heparin/Heparan Sulfate Interaction Domain. JOURNAL OF BIOLOGICAL CHEMISTRY 284 (41). , 2009 -
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1635473Formylglycine Aldehyde Tag-Protein Engineering through a Novel Post-translational ModificationPUB | DOI | WoS | PubMed | Europe PMC
Frese, Marc-Andre, Formylglycine Aldehyde Tag-Protein Engineering through a Novel Post-translational Modification. CHEMBIOCHEM 10 (3). , 2009 -
2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1633371Neonatal manifestation of multiple sulfatase deficiencyPUB | DOI | WoS | PubMed | Europe PMC
Busche, Andreas, Neonatal manifestation of multiple sulfatase deficiency. EUROPEAN JOURNAL OF PEDIATRICS 168 (8). , 2009 -
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351244Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiencyPUB | DOI
Schlotawa, Lars, 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). , 2008 -
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1592682Redundant function of the heparan sulfate 6-O-endosulfatases Sulf1 and Sulf2 during skeletal developmentPUB | DOI | WoS | PubMed | Europe PMC
Ratzka, Andreas, Redundant function of the heparan sulfate 6-O-endosulfatases Sulf1 and Sulf2 during skeletal development. DEVELOPMENTAL DYNAMICS 237 (2). , 2008 -
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1592488Paralog of the formylglycine-generating enzyme - retention in the endoplasmic reticulum by canonical and noncanonical signalsPUB | DOI | WoS | PubMed | Europe PMC
Gande, Santosh Lakshmi, Paralog of the formylglycine-generating enzyme - retention in the endoplasmic reticulum by canonical and noncanonical signals. FEBS JOURNAL 275 (6). , 2008 -
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1592481ERp44 mediates a thiol-independent retention of formylglycine-generating enzyme in the endoplasmic reticulumPUB | DOI | WoS | PubMed | Europe PMC
Mariappan, Malaiyalam, ERp44 mediates a thiol-independent retention of formylglycine-generating enzyme in the endoplasmic reticulum. JOURNAL OF BIOLOGICAL CHEMISTRY 283 (10). , 2008 -
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1588435Arylsulfatase G, a novel lysosomal sulfatasePUB | DOI | WoS | PubMed | Europe PMC
Frese, Marc-Andre, Arylsulfatase G, a novel lysosomal sulfatase. JOURNAL OF BIOLOGICAL CHEMISTRY 283 (17). , 2008 -
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1588440The non-catalytic N-terminal extension of formylglycine-generating enzyme is required for its biological activity and retention in the endoplasmic reticulumPUB | DOI | WoS | PubMed | Europe PMC
Mariappan, Malaiyalam, 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). , 2008 -
2008 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1586139Sulf loss influences N-, 2-O-, and 6-O-sulfation of multiple heparan sulfate proteoglycans and modulates fibroblast growth factor signalingPUB | DOI | WoS | PubMed | Europe PMC
Lamanna, William C., 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). , 2008 -
2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1593622Sulfatase modifying factor 1 trafficking through the cells: from endoplasmic reticulum to the endoplasmic reticulumPUB | DOI | WoS | PubMed | Europe PMC
Zito, Ester, Sulfatase modifying factor 1 trafficking through the cells: from endoplasmic reticulum to the endoplasmic reticulum. EMBO JOURNAL 26 (10). , 2007 -
2007 | Konferenzbeitrag | Veröffentlicht | PUB-ID: 1594028The heparanome - The enigma of encoding and decoding heparan sulfate sulfationPUB | DOI | WoS | PubMed | Europe PMC
Lamanna, William C., The heparanome - The enigma of encoding and decoding heparan sulfate sulfation. Journal of Biotechnology 129 (2). , 2007 -
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1597019Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativityPUB | DOI | WoS | PubMed | Europe PMC
Lamanna, William C., Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity. BIOCHEMICAL JOURNAL 400 (1). , 2006 -
2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1600859A general binding mechanism for all human sulfatases by the formylglycine-generating enzymePUB | DOI | WoS | PubMed | Europe PMC
Roeser, D, 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). , 2006 -
2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350692Molecular basis for multiple sulfatase deficiency and mechanism for formylglycine generation of the human formylglycine-generating enzymePUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, Molecular basis for multiple sulfatase deficiency and mechanism for formylglycine generation of the human formylglycine-generating enzyme. CELL 121 (4). , 2005 -
2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350712Expression, localization, structural, and functional characterization of pFGE, the paralog of the C alpha-formylglycine-generating enzymePUB | DOI | WoS | PubMed | Europe PMC
Mariappan, M, Expression, localization, structural, and functional characterization of pFGE, the paralog of the C alpha-formylglycine-generating enzyme. JOURNAL OF BIOLOGICAL CHEMISTRY 280 (15). , 2005 -
2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350723Crystal structure of human pFGE, the paralog of the C alpha-formylglycine-generating enzymePUB | DOI | WoS | PubMed | Europe PMC
Dickmanns, A, Crystal structure of human pFGE, the paralog of the C alpha-formylglycine-generating enzyme. JOURNAL OF BIOLOGICAL CHEMISTRY 280 (15). , 2005 -
2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1603995Molecular characterization of the human C alpha-formylglycine-generating enzymePUB | DOI | WoS | PubMed | Europe PMC
Preusser-Kunze, A, Molecular characterization of the human C alpha-formylglycine-generating enzyme. JOURNAL OF BIOLOGICAL CHEMISTRY 280 (15). , 2005 -
2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350732Post-translational formylglycine modification of bacterial sulfatases by the radical S-adenosylmethionine protein AtsBPUB | DOI | WoS | PubMed | Europe PMC
Fang, QH, Post-translational formylglycine modification of bacterial sulfatases by the radical S-adenosylmethionine protein AtsB. JOURNAL OF BIOLOGICAL CHEMISTRY 279 (15). , 2004 -
2004 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350737Crystal structure of the alkylsulfatase AtsK: Insights into the catalytic mechanism of the Fe(II) alpha-ketoglutarate-dependent dioxygenase superfamilyPUB | DOI | WoS | PubMed | Europe PMC
Muller, I, Crystal structure of the alkylsulfatase AtsK: Insights into the catalytic mechanism of the Fe(II) alpha-ketoglutarate-dependent dioxygenase superfamily. BIOCHEMISTRY 43 (11). , 2004 -
2004 | Patent | Veröffentlicht | PUB-ID: 2375304Diagnosis and treatment of multiple sulfatase deficiency and other sulfatase deficienciesPUB
von Figura, Kurt, Diagnosis and treatment of multiple sulfatase deficiency and other sulfatase deficiencies. (). , 2004 -
2004 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2352318Defects in lysosomal enzyme modification for catalytic activityPUB | DOI
von Figura, Kurt, Defects in lysosomal enzyme modification for catalytic activity. Lysosomal Disorders of the Brain (). Oxford, 2004 -
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350768Posttranslational modification of serine to formylglycine in bacterial sulfatases - Recognition of the modification motif by the iron-sulfur protein AtsBPUB | DOI | WoS | PubMed | Europe PMC
Marquordt, C, Posttranslational modification of serine to formylglycine in bacterial sulfatases - Recognition of the modification motif by the iron-sulfur protein AtsB. JOURNAL OF BIOLOGICAL CHEMISTRY 278 (4). , 2003 -
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350753Recognition of arylsulfatase A and B by the UDP-N-acetylglucosamine : lysosomal enzyme N-acetylglucosamine-phosphotransferasePUB | DOI | WoS | PubMed | Europe PMC
Yaghootfam, A, Recognition of arylsulfatase A and B by the UDP-N-acetylglucosamine : lysosomal enzyme N-acetylglucosamine-phosphotransferase. JOURNAL OF BIOLOGICAL CHEMISTRY 278 (35). , 2003 -
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350747The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotesPUB | DOI | WoS | PubMed | Europe PMC
Landgrebe, J, The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotes. GENE 316 (). , 2003 -
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350759Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C-alpha-formylglycine generating enzymePUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C-alpha-formylglycine generating enzyme. CELL 113 (4). , 2003 -
2003 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350776Identification of formylglycine in sulfatases by matrix-assisted laser desorption/ionization time-of-flight mass spectrometryPUB | DOI | WoS | PubMed | Europe PMC
Peng, JH, Identification of formylglycine in sulfatases by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. JOURNAL OF MASS SPECTROMETRY 38 (1). , 2003 -
2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350782Defective oligomerization of arylsulfatase A as a cause of its instability in lysosomes and metachromatic leukodystrophyPUB | DOI | WoS | PubMed | Europe PMC
Bulow von, R, Defective oligomerization of arylsulfatase A as a cause of its instability in lysosomes and metachromatic leukodystrophy. JOURNAL OF BIOLOGICAL CHEMISTRY 277 (11). , 2002 -
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350811Crystal structure of an enzyme-substrate complex provides insight into the interaction between human arylsulfatase A and its substrates during catalysisPUB | DOI | WoS | PubMed | Europe PMC
Bulow von, R, Crystal structure of an enzyme-substrate complex provides insight into the interaction between human arylsulfatase A and its substrates during catalysis. JOURNAL OF MOLECULAR BIOLOGY 305 (2). , 2001 -
2001 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372494SulfatasesPUB
Dierks, Thomas, Sulfatases. Encyclopedia of Molecular Medicine (). New York, 2001 -
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350792Characterization of posttranslational formylglycine formation by luminal components of the endoplasmic reticulumPUB | DOI | WoS | PubMed | Europe PMC
Fey, J, Characterization of posttranslational formylglycine formation by luminal components of the endoplasmic reticulum. JOURNAL OF BIOLOGICAL CHEMISTRY 276 (50). , 2001 -
2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 23508001.3 angstrom structure of arylsulfatase from Pseudomonas aeruginosa establishes the catalytic mechanism of sulfate ester cleavage in the sulfatase familyPUB | DOI | WoS | PubMed | Europe PMC
Boltes, I, 1.3 angstrom structure of arylsulfatase from Pseudomonas aeruginosa establishes the catalytic mechanism of sulfate ester cleavage in the sulfatase family. STRUCTURE 9 (6). , 2001 -
2001 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372492Cysteine-modifying enzymePUB
Dierks, Thomas, Cysteine-modifying enzyme. Encyclopedia of Molecular Medicine (). New York, 2001 -
2001 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372496ArylsulfatasesPUB
Dierks, Thomas, Arylsulfatases. Encyclopedia of Molecular Medicine (). New York, 2001 -
1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350826Amino acid residues forming the active site of arylsulfatase A - Role in catalytic activity and substrate bindingPUB | DOI | WoS | PubMed | Europe PMC
Waldow, A, Amino acid residues forming the active site of arylsulfatase A - Role in catalytic activity and substrate binding. JOURNAL OF BIOLOGICAL CHEMISTRY 274 (18). , 1999 -
1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350833Sequence determinants directing conversion of cysteine to formylglycine in eukaryotic sulfatasesPUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, Sequence determinants directing conversion of cysteine to formylglycine in eukaryotic sulfatases. EMBO JOURNAL 18 (8). , 1999 -
1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350818The iron sulfur protein AtsB is required for posttranslational formation of formylglycine in the Klebsiella sulfatasePUB | DOI | WoS | PubMed | Europe PMC
Szameit, C, The iron sulfur protein AtsB is required for posttranslational formation of formylglycine in the Klebsiella sulfatase. JOURNAL OF BIOLOGICAL CHEMISTRY 274 (22). , 1999 -
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350840Residues critical for formylglycine formation and/or catalytic activity of arylsulfatase APUB | DOI | WoS | PubMed | Europe PMC
Knaust, A, Residues critical for formylglycine formation and/or catalytic activity of arylsulfatase A. BIOCHEMISTRY 37 (40). , 1998 -
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350871Sulfatases, trapping of the sulfated enzyme intermediate by substituting the active site formylglycinePUB
Recksiek, R, Sulfatases, trapping of the sulfated enzyme intermediate by substituting the active site formylglycine. JOURNAL OF BIOLOGICAL CHEMISTRY 273 (11). , 1998 -
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350847Posttranslational formation of formylglycine in prokaryotic sulfatases by modification of either cysteine or serinePUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, Posttranslational formation of formylglycine in prokaryotic sulfatases by modification of either cysteine or serine. JOURNAL OF BIOLOGICAL CHEMISTRY 273 (40). , 1998 -
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350855Mutations in a polycistronic nuclear gene associated with molybdenum cofactor deficiencyPUB | DOI | WoS | PubMed | Europe PMC
Reiss, J, Mutations in a polycistronic nuclear gene associated with molybdenum cofactor deficiency. NATURE GENETICS 20 (1). , 1998 -
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350865A novel protein modification generating an aldehyde group in sulfatases: its role in catalysis and diseasePUB | DOI | WoS | PubMed | Europe PMC
Figura von, K, A novel protein modification generating an aldehyde group in sulfatases: its role in catalysis and disease. BIOESSAYS 20 (6). , 1998 -
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350877Arylsulfatase from Klebsiella pneumoniae carries a formylglycine generated from a serinePUB | DOI | WoS | PubMed | Europe PMC
Miech, C, Arylsulfatase from Klebsiella pneumoniae carries a formylglycine generated from a serine. JOURNAL OF BIOLOGICAL CHEMISTRY 273 (9). , 1998 -
1998 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350884Conversion of cysteine to formylglycine in eukaryotic sulfatases occurs by a common mechanism in the endoplasmic reticulumPUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, Conversion of cysteine to formylglycine in eukaryotic sulfatases occurs by a common mechanism in the endoplasmic reticulum. FEBS LETTERS 423 (1). , 1998 -
1997 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350890Conversion of cysteine to formylglycine: A protein modification in the endoplasmic reticulumPUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, 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). , 1997 -
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350895A microsomal ATP-binding protein involved in efficient protein transport into the mammalian endoplasmic reticulumPUB
Dierks, Thomas, A microsomal ATP-binding protein involved in efficient protein transport into the mammalian endoplasmic reticulum. EMBO JOURNAL 15 (24). , 1996 -
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350906Luciferase assembly after transport into mammalian microsomes involves molecular chaperones and peptidyl-prolyl cis/trans-isomerasesPUB
Brunke, M, Luciferase assembly after transport into mammalian microsomes involves molecular chaperones and peptidyl-prolyl cis/trans-isomerases. JOURNAL OF BIOLOGICAL CHEMISTRY 271 (38). , 1996 -
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350925Cyclosporin A inhibits the degradation of signal sequences after processing of presecretory proteins by signal peptidasePUB | DOI | WoS | PubMed | Europe PMC
Klappa, P, Cyclosporin A inhibits the degradation of signal sequences after processing of presecretory proteins by signal peptidase. EUROPEAN JOURNAL OF BIOCHEMISTRY 239 (2). , 1996 -
1996 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350916Efficient folding of firefly luciferase after transport into mammalian microsomes in the absence of luminal chaperones and folding catalystsPUB
Tyedmers, J, 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). , 1996 -
1994 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372523Channel properties of mitochondrial carriersPUB
Dierks, Thomas, Channel properties of mitochondrial carriers. Molecular Biology of Mitochondrial Transport Systems H83 (). Berlin, 1994 -
1993 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350937REACTION-MECHANISM OF THE RECONSTITUTED TRICARBOXYLATE CARRIER FROM RAT-LIVER MITOCHONDRIAPUB | DOI | WoS | PubMed | Europe PMC
BISACCIA, F, REACTION-MECHANISM OF THE RECONSTITUTED TRICARBOXYLATE CARRIER FROM RAT-LIVER MITOCHONDRIA. BIOCHIMICA ET BIOPHYSICA ACTA 1142 (1-2). , 1993 -
1993 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350944THE ROLE OF MOLECULAR CHAPERONES IN PROTEIN-TRANSPORT INTO THE ENDOPLASMIC-RETICULUMPUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, 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). , 1993 -
1993 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372500Components and mechanisms involved in transport of proteins into the endoplasmic reticulumPUB
Klappa, Peter, Components and mechanisms involved in transport of proteins into the endoplasmic reticulum. Endoplasmic reticulum 21 (). Berlin, 1993 -
1993 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372529The role of molecular chaperones in protein transport into the endoplasmic reticulumPUB
Dierks, Thomas, The role of molecular chaperones in protein transport into the endoplasmic reticulum. Molecular Chaperones (). London, 1993 -
1993 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350930KINETIC CHARACTERIZATION OF THE RECONSTITUTED DICARBOXYLATE CARRIER FROM MITOCHONDRIA - A 4-BINDING-SITE SEQUENTIAL TRANSPORT-SYSTEMPUB | DOI | WoS | PubMed | Europe PMC
INDIVERI, C, KINETIC CHARACTERIZATION OF THE RECONSTITUTED DICARBOXYLATE CARRIER FROM MITOCHONDRIA - A 4-BINDING-SITE SEQUENTIAL TRANSPORT-SYSTEM. BIOCHIMICA ET BIOPHYSICA ACTA 1143 (3). , 1993 -
1992 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350950THE MITOCHONDRIAL CARNITINE CARRIER - CHARACTERIZATION OF SH-GROUPS RELEVANT FOR ITS TRANSPORT FUNCTIONPUB | DOI | WoS | PubMed | Europe PMC
INDIVERI, C, THE MITOCHONDRIAL CARNITINE CARRIER - CHARACTERIZATION OF SH-GROUPS RELEVANT FOR ITS TRANSPORT FUNCTION. BIOCHIMICA ET BIOPHYSICA ACTA 1140 (1). , 1992 -
1992 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350957PROBING THE ACTIVE-SITE OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM MITOCHONDRIA - STRUCTURE-FUNCTION RELATIONSHIP INVOLVING ONE LYSINE AND 2 CYSTEINE RESIDUESPUB | DOI | WoS | PubMed | Europe PMC
STAPPEN, R, PROBING THE ACTIVE-SITE OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM MITOCHONDRIA - STRUCTURE-FUNCTION RELATIONSHIP INVOLVING ONE LYSINE AND 2 CYSTEINE RESIDUES. EUROPEAN JOURNAL OF BIOCHEMISTRY 210 (1). , 1992 -
1992 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350963PROBING THE ACTIVE-SITE OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM BOVINE HEART-MITOCHONDRIA - CARBODIIMIDE-CATALYZED ACYLATION OF A FUNCTIONAL LYSINE RESIDUEPUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, 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). , 1992 -
1991 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350977REACTION-MECHANISM OF THE RECONSTITUTED OXOGLUTARATE CARRIER FROM BOVINE HEART-MITOCHONDRIAPUB | DOI | WoS | PubMed | Europe PMC
INDIVERI, C, REACTION-MECHANISM OF THE RECONSTITUTED OXOGLUTARATE CARRIER FROM BOVINE HEART-MITOCHONDRIA. EUROPEAN JOURNAL OF BIOCHEMISTRY 198 (2). , 1991 -
1991 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350969KINETIC-STUDY OF THE ASPARTATE GLUTAMATE CARRIER IN INTACT RAT-HEART MITOCHONDRIA AND COMPARISON WITH A RECONSTITUTED SYSTEMPUB | DOI | WoS | PubMed | Europe PMC
SLUSE, FE, KINETIC-STUDY OF THE ASPARTATE GLUTAMATE CARRIER IN INTACT RAT-HEART MITOCHONDRIA AND COMPARISON WITH A RECONSTITUTED SYSTEM. BIOCHIMICA ET BIOPHYSICA ACTA 1058 (3). , 1991 -
1990 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350989PORE-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 TRANSPORTPUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, 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). , 1990 -
1990 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350983THE MITOCHONDRIAL ASPARTATE GLUTAMATE AND ADP/ATP CARRIER SWITCH FROM OBLIGATE COUNTEREXCHANGE TO UNIDIRECTIONAL TRANSPORT AFTER MODIFICATION BY SH-REAGENTSPUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, 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). , 1990 -
1989 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2350994KINETIC DISCRIMINATION OF 2 SUBSTRATE BINDING-SITES OF THE RECONSTITUTED DICARBOXYLATE CARRIER FROM RAT-LIVER MITOCHONDRIAPUB | DOI | WoS | PubMed | Europe PMC
INDIVERI, C, KINETIC DISCRIMINATION OF 2 SUBSTRATE BINDING-SITES OF THE RECONSTITUTED DICARBOXYLATE CARRIER FROM RAT-LIVER MITOCHONDRIA. BIOCHIMICA ET BIOPHYSICA ACTA 977 (2). , 1989 -
1989 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 2372511Reaction mechanism of the reconstituted aspartate / glutamate carrier from mitochondria. Reversible switching to uniport functionPUB
Dierks, Thomas, Reaction mechanism of the reconstituted aspartate / glutamate carrier from mitochondria. Reversible switching to uniport function. Anion Carriers of Mitochondrial Membranes (). Berlin, 1989 -
1988 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351000REACTION-MECHANISM OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM BOVINE HEART-MITOCHONDRIAPUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, REACTION-MECHANISM OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM BOVINE HEART-MITOCHONDRIA. BIOCHIMICA ET BIOPHYSICA ACTA 943 (2). , 1988 -
1988 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2351005ASYMMETRIC ORIENTATION OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM MITOCHONDRIAPUB | DOI | WoS | PubMed | Europe PMC
Dierks, Thomas, ASYMMETRIC ORIENTATION OF THE RECONSTITUTED ASPARTATE GLUTAMATE CARRIER FROM MITOCHONDRIA. BIOCHIMICA ET BIOPHYSICA ACTA 937 (1). , 1988