48 Publikationen

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  • [48]
    2024 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2987979
    M. Sun, et al., “A novel homozygous missense variant in ARSK causes MPS X, a new subtype of mucopolysaccharidosis”, Genes & Diseases, vol. 11, 2024, : 101025.
    PUB | DOI
     
  • [47]
    2023 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2981846
    M. Sun, et al., “A novel homozygous missense variant in ARSK causes MPS X, a new subtype of mucopolysaccharidosis”, Genes & Diseases, 2023.
    PUB | DOI | PubMed | Europe PMC
     
  • [46]
    2022 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2962857 OA
    A. Linhorst and T. Lübke, “The Human Ntn-Hydrolase Superfamily: Structure, Functions and Perspectives”, Cells, vol. 11, 2022, : 1592.
    PUB | PDF | DOI | Download (ext.) | WoS | PubMed | Europe PMC
     
  • [45]
    2022 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2967253
    K. Smith, et al., “Establishment of Blood Glycosidase Activities and their Excursions in Sepsis”, Glycobiology , vol. 32, 2022, pp. 1034-1035.
    PUB | WoS
     
  • [44]
    2022 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2965167
    B.S. Haslund-Gourley, et al., “Establishment of blood glycosidase activities and their excursions in sepsis”, PNAS Nexus, vol. 1, 2022, : pgac113.
    PUB | DOI | PubMed | Europe PMC
     
  • [43]
    2021 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2961637
    P.V. Aziz, et al., “Excursions of blood glycosidase activities in the pathogenesis and prognosis of Sepsis”, Glycobiology , vol. 31, 2021, pp. 1700.
    PUB | DOI | WoS
     
  • [42]
    2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2960244 OA
    S. Verheyen, et al., “Novel subtype of mucopolysaccharidosis caused by arylsulfatase K (ARSK) deficiency”, Journal of Medical Genetics, 2021, : jmedgenet-2021-108061.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [41]
    2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2956816
    B. Kowalewski, et al., “Decoding the consecutive lysosomal degradation of 3-O-sulfate containing heparan sulfate by Arylsulfatase G (ARSG)”, Biochemical Journal, 2021.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [40]
    2020 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2946513
    P. Aziz, et al., “Altered glycosidase Activities at Physiological pH in the Pathogenesis of Sepsis”, FASEB JOURNAL, vol. 34, Hoboken: Wiley, 2020.
    PUB | DOI | WoS
     
  • [39]
    2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2948390
    T. Lübke and M. Damme, “Lysosomal sulfatases: a growing family*”, Biochemical Journal, vol. 477, 2020, pp. 3963-3983.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [38]
    2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2945876
    C. Trabszo, et al., “Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfate”, Biochemical Journal, 2020.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [37]
    2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937243
    M. Korf-Klingebiel, et al., “Heparan Sulfate-Editing Extracellular Sulfatases Enhance Vascular Endothelial Growth Factor Bioavailability for Ischemic Heart Repair”, Circulation research, vol. 125, 2019, pp. 787-801.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [36]
    2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271
    S. Stroobants, et al., “Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice”, FRONTIERS IN BEHAVIORAL NEUROSCIENCE, vol. 12, 2018, : 15.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [35]
    2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909150
    X. Pan, et al., “Mice, double deficient in lysosomal serine carboxypeptidases Scpep1 and Cathepsin A develop the hyperproliferative vesicular corneal dystrophy and hypertrophic skin thickenings”, PLoS One, vol. 12, 2017, : e0172854.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [34]
    2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778
    O.P. Dhamale, et al., “Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase”, ACS Chemical Biology, vol. 12, 2017, pp. 367-373.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [33]
    2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616 OA
    H. Wolf, et al., “A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease”, Disease Models & Mechanisms, vol. 9, 2016, pp. 1015-1028.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [32]
    2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2658538 OA
    X.Y. Kong, et al., “Loss of lysosomal membrane protein NCU-G1 in mice results in spontaneous liver fibrosis with accumulation of lipofuscin and iron in Kupffer cells”, Disease Models & Mechanisms, vol. 7, 2014, pp. 351-362.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [31]
    2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2672894 OA
    X. Pan, et al., “Serine carboxypeptidase SCPEP1 and Cathepsin A play complementary roles in regulation of vasoconstriction via inactivation of endothelin-1”, PLoS genetics, vol. 10, 2014, : e1004146.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [30]
    2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2699273
    B. Kowalewski, et al., “Molecular Characterization of Arylsulfatase G: EXPRESSION, PROCESSING, GLYCOSYLATION, TRANSPORT, AND ACTIVITY”, The Journal of biological chemistry, vol. 289, 2014, pp. 27992-28005.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [29]
    2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623550
    E. Wiegmann, et al., “Arylsulfatase K, a Novel Lysosomal Sulfatase”, Journal of Biological Chemistry, vol. 288, 2013, pp. 30019-30028.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [28]
    2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623533
    F. Milz, et al., “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, vol. 1830, 2013, pp. 5287-5298.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [27]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2471754
    G. Makrypidi, et al., “Mannose 6 dephosphorylation of lysosomal proteins mediated by Acid phosphatases acp2 and acp5”, Molecular and cellular biology, vol. 32, 2012, pp. 774-782.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [26]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2529586
    K. Kollmann, et al., “Lysosomal dysfunction causes neurodegeneration in mucolipidosis II 'knock-in' mice”, Brain, vol. 135, 2012, pp. 2661-2675.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [25]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2494022
    B. Kowalewski, et al., “Arylsulfatase G Inactivation Causes Loss of Heparan Sulfate 3-O-Sulfatase Activity and Mucopolysaccharidosis in Mice”, Proc. Natl. Acad. Sci. USA, vol. 109, 2012, pp. 10310-10315.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [24]
    2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940515
    M. Damme, et al., “Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in alpha-mannosidosis”, Journal of Neuropathology & Experimental Neurology, vol. 70, 2011, pp. 83-94.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [23]
    2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2352585
    L.R. Savalas, et al., “Disrupted in renal carcinoma 2 (DIRC2), a novel transporter of the lysosomal membrane, is proteolytically processed by cathepsin L.”, Biochemical Journal, vol. 436, 2011, pp. 113-121.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [22]
    2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939855
    C. Rosner, et al., “Erratum to: Rhesus macaque MHC class I molecules show differential subcellular localizations”, Immunogenetics, vol. 62, 2010, pp. 409-418.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [21]
    2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2776186
    C. Rosner, et al., “Rhesus macaque MHC class I molecules show differential subcellular localizations”, Immunogenetics, vol. 62, 2010, pp. 149-158.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [20]
    2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939885
    K. Kollmann, et al., “Mannose phosphorylation in health and disease”, European Journal of Cell Biology, vol. 89, 2010, pp. 117-123.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [19]
    2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902203
    M. Damme, et al., “Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosis.”, Molecular and Cellular Biology, vol. 30, 2010, pp. 273-283.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [18]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939923
    K. Lakomek, et al., “Initial insight into the function of the lysosomal 66.3 kDa protein from mouse by means of X-ray crystallography”, BMC Structural Biology, vol. 9, 2009, pp. 56-72.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [17]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902143
    O. Schieweck, et al., “NCU-G1 is a highly glycosylated integral membrane protein of the lysosome.”, Biochemical Journal, vol. 422, 2009, pp. 83-90.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [16]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939981
    T. Lübke, P. Lobel, and D.E. Sleat, “Proteomics of the lysosome”, Biochimica et Biophysica Acta, vol. 1793, 2009, pp. 625-635.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [15]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940533
    K. Kollmann, et al., “Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1”, Febs Journal, vol. 276, 2009, pp. 1356-1369.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [14]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939939
    K. Lakomek, et al., “De novo sulfur SAD phasing of the lysosomal 66.3 kDa protein from mouse”, Acta Crystallographica Section D, vol. 65, 2009, pp. 220-228.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [13]
    2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939993
    A.O. Fedele, et al., “Mutational analysis of the HGSNAT gene in Italian patients with mucopolysaccharidosis IIIC (Sanfilippo C syndrome)”, Human Mutation, vol. 28, 2007, pp. 523.
    PUB | DOI
     
  • [12]
    2007 | Zeitschriftenaufsatz | PUB-ID: 1940006
    C. Hellbusch, et al., “Golgi GDP-fucose transporter-deficient mice mimic congenital disorder of glycosylation IIc/leukocyte adhesion deficiency II”, Journal of Biological Chemistry, vol. 282, 2007, pp. 10762-10772.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [11]
    2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940030
    F. Deuschl, et al., “Molecular characterization of the hypothetical 66.3-kDa protein in mouse: lysosomal targeting, glycosylation, processing and tissue distribution”, Febs Letters, vol. 580, 2006, pp. 5747-5752.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [10]
    2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940045
    C. Thiel, et al., “Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality”, Molecular and Cellular Biology, vol. 26, 2006, pp. 5615-5620.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [9]
    2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940057
    S. Tiede, et al., “Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferase”, Nature Medicine, vol. 11, 2006, pp. 1109-1112.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [8]
    2005 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 1940182
    T. Lübke and J. Landgrebe, “Lysosomal Proteome and Transcriptome”, Lysosomes, P. Saftig, ed., Georgetown, Texas, USA: Landes Bioscience, 2005, pp.130-143.
    PUB | DOI
     
  • [7]
    2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940072
    K. Kollmann, et al., “Identification of novel lysosomal matrix proteins by proteome analysis”, Proteomics, vol. 5, 2005, pp. 3966-3978.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [6]
    2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940085
    D. Hartmann, et al., “The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblasts”, Human Molecular Genetics, vol. 11, 2002, pp. 2615-2624.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [5]
    2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940103
    B. Hansske, et al., “Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId”, Journal of Clinical Investigation, vol. 109, 2002, pp. 725-733.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [4]
    2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940119
    T. Lübke, et al., “Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency”, Nature Genetics, vol. 28, 2001, pp. 73-76.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [3]
    2001 | Dissertation | PUB-ID: 1940291
    T. Lübke, Congenital Disorder of Glycosylation (CDG)-IIc: Eine retrovirale Expressionsklonierung identifiziert das CDG-IIc Syndrom (Leukozyten Adhäsionsdefekt II) als eine GDP-Fukose Transporter Defizienz, Göttingen, Deutschland: Elektronische Dissertation der Georg-August-Universität Göttingen, 2001.
    PUB
     
  • [2]
    2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940146
    L.A. Andersson, et al., “ModE-dependent molybdate regulation of the molybdenum cofactor operon moa in Escherichia coli”, Journal of Bacteriology, vol. 182, 2000, pp. 7035-7043.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [1]
    1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940173
    T. Lübke, et al., “A new type of carbohydrate-deficient glycoprotein syndrome due to a decreased import of GDP-fucose into the golgi”, Journal of Biological Chemistry, vol. 274, 1999, pp. 25986-25989.
    PUB | DOI | WoS | PubMed | Europe PMC
     

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