PUB - Publikationen an der Universität Bielefeld

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• [48]
  

  2023 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2981846

  Sun, Miao, Kaminsky, Cornelia K., Deppe, Philip, Ilse, Mai-Britt, Vaz, Frédéric M., Plecko, Barbara, Lübke, Torben, and Randolph, Linda M. “A novel homozygous missense variant in ARSK causes MPS X, a new subtype of mucopolysaccharidosis”. Genes & Diseases 11.3 (2023): 101025.

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• [47]
  

  2023 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2988232

  Smith, Kathryn, Haslund-Gourley, Benjamin S., Aziz, Peter V., Heithoff, Douglas M., Restagno, Damien, Fried, Jeffrey C., Ilse, Mai-Britt, Bäumges, Hannah, Mahan, Michael J., Lübke, Torben, and Marth, Jamey D. “Establishment of Blood Glycosidase Activities and their Excursions in Sepsis”. Glycobiology 33.11 (2023): 1016.

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• [46]
  

  2022 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2962857

  Linhorst, Arne, and Lübke, Torben. “The Human Ntn-Hydrolase Superfamily: Structure, Functions and Perspectives”. Cells 11.10 (2022): 1592.

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• [45]
  

  2022 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2967253

  Smith, Kathryn, Haslund-Gourley, Benjamin S., Aziz, Peter V., Heithoff, Douglas M., Restagno, Damien, Fried, Jeffrey C., Ilse, Mai-Britt, Bäumges, Hannah, Mahan, Michael J., Lübke, Torben, and Marth, Jamey D. “Establishment of Blood Glycosidase Activities and their Excursions in Sepsis”. Glycobiology 32.11 (2022): 1034-1035.

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• [44]
  

  2022 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2965167

  Haslund-Gourley, Benjamin S, Aziz, Peter V, Heithoff, Douglas M, Restagno, Damien, Fried, Jeffrey C, Ilse, Mai-Britt, Bäumges, Hannah, Mahan, Michael J, Lübke, Torben, and Marth, Jamey D. “Establishment of blood glycosidase activities and their excursions in sepsis”. PNAS Nexus 1.3 (2022): pgac113.

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• [43]
  

  2021 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2961637

  Aziz, Peter V., Lewis, Benjamin J., Haslund-Gourley, Benjamin S., Heithoff, Douglas M., Westman, Julia S., Restagno, Damien, Fried, Jeffrey C., Ilse, Mai-Britt, Lübke, Torben, and Marth, Jamey D. “Excursions of blood glycosidase activities in the pathogenesis and prognosis of Sepsis”. Glycobiology 31.12 (2021): 1700.

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• [42]
  

  2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2960244

  Verheyen, Sarah, Blatterer, Jasmin, Speicher, Michael R, Bhavani, Gandham SriLakshmi, Boons, Geert-Jan, Ilse, Mai-Britt, Andrae, Dominik, Sproß, Jens, Vaz, Frédéric Maxime, Kircher, Susanne G, Posch-Pertl, Laura, Baumgartner, Daniela, Lübke, Torben, Shah, Hitesh, Al Kaissi, Ali, Girisha, Katta M, and Plecko, Barbara. “Novel subtype of mucopolysaccharidosis caused by arylsulfatase K (ARSK) deficiency”. Journal of Medical Genetics (2021): jmedgenet-2021-108061.

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• [41]
  

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

  Kowalewski, Björn, Lange, Heike, Galle, Sabrina, Dierks, Thomas, Lübke, Torben, and Damme, Markus. “Decoding the consecutive lysosomal degradation of 3-O-sulfate containing heparan sulfate by Arylsulfatase G (ARSG)”. Biochemical Journal (2021).

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• [40]
  

  2020 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2946513

  Aziz, Peter, Haslund-Gourley, Benjamin, Heithoff, Douglas, Westman, Julia, Restagno, Damien, Lewis, Benjamin, Fried, Jeffrey, Ilse, Mai-Britt, Lübke, Torben, and Marth, Jamey. “Altered glycosidase Activities at Physiological pH in the Pathogenesis of Sepsis”. FASEB JOURNAL. Hoboken: Wiley, 2020.Vol. 34.

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• [39]
  

  2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2948390

  Lübke, Torben, and Damme, Markus. “Lysosomal sulfatases: a growing family*”. Biochemical Journal 477.20 (2020): 3963-3983.

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• [38]
  

  2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2945876

  Trabszo, Christof, Ramms, Bastian, Chopra, Pradeep, Lüllmann-Rauch, Renate, Stroobants, Stijn, Sproß, Jens, Jeschke, Anke, Schinke, Thorsten, Boons, Geert-Jan, Esko, Jeffrey, Lübke, Torben, and Dierks, Thomas. “Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfate”. Biochemical Journal (2020).

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• [37]
  

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

  Korf-Klingebiel, Mortimer, Reboll, Marc R, Grote, Karsten, Schleiner, Hauke, Wang, Yong, Wu, Xuekun, Klede, Stefanie, Mikhed, Yuliya, Bauersachs, Johann, Klintschar, Michael, Rudat, Carsten, Kispert, Andreas, Niessen, Hans Wm, Lübke, Torben, Dierks, Thomas, and Wollert, Kai C. “Heparan Sulfate-Editing Extracellular Sulfatases Enhance Vascular Endothelial Growth Factor Bioavailability for Ischemic Heart Repair”. Circulation research 125.9 (2019): 787-801.

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• [36]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271

  Stroobants, Stijn, Wolf, Heike, Callaerts-Vegh, Zsuzsanna, Dierks, Thomas, Lübke, Torben, and D'Hooge, Rudi. “Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice”. FRONTIERS IN BEHAVIORAL NEUROSCIENCE 12 (2018): 15.

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• [35]
  

  2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909150

  Pan, Xuefang, Wang, Yanting, Lübke, Torben, Hinek, Aleksander, and Pshezhetsky, Alexey V. “Mice, double deficient in lysosomal serine carboxypeptidases Scpep1 and Cathepsin A develop the hyperproliferative vesicular corneal dystrophy and hypertrophic skin thickenings”. PLoS One 12.2 (2017): e0172854.

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• [34]
  

  2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778

  Dhamale, Omkar P., Lawrence, Roger, Wiegmann, Elena, Shah, Bhawal A., Al-Mafraji, Kanar, Lamanna, William C., Lübke, Torben, Dierks, Thomas, Boons, Geert-Jan, and Esko, Jeffrey D. “Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase”. ACS Chemical Biology 12.2 (2017): 367-373.

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• [33]
  

  2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616

  Wolf, Heike, Damme, Markus, Stroobants, Stijn, D'Hooge, Rudi, Beck, Hans Christian, Hermans-Borgmeyer, Irm, Lüllmann-Rauch, Renate, Dierks, Thomas, and Lübke, Torben. “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): 1015-1028.

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• [32]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2658538

  Kong, Xiang Yi, Nesset, Cecilie K., Damme, Markus, Loeberg, Else-Marit, Lübke, Torben, Maehlen, Jan, Andersson, Kristin B., Roos, Norbert, Thoresen, G. Hege, Rustan, Arild C., Kase, Eili T., and Eskild, Winnie. “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 7.3 (2014): 351-362.

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• [31]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2672894

  Pan, Xuefang, Grigoryeva, Lubov, Seyrantepe, Volkan, Peng, Junzheng, Kollmann, Katrin, Tremblay, Johanne, Lavoie, Julie L., Hinek, Aleksander, Lübke, Torben, and Pshezhetsky, Alexey V. “Serine carboxypeptidase SCPEP1 and Cathepsin A play complementary roles in regulation of vasoconstriction via inactivation of endothelin-1”. PLoS genetics 10.2 (2014): e1004146.

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• [30]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2699273

  Kowalewski, Björn, Lübke, Torben, Kollmann, Katrin, Braulke, Thomas, Reinheckel, Thomas, Dierks, Thomas, and Damme, Markus. “Molecular Characterization of Arylsulfatase G: EXPRESSION, PROCESSING, GLYCOSYLATION, TRANSPORT, AND ACTIVITY”. The Journal of biological chemistry 289.40 (2014): 27992-28005.

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• [29]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623550

  Wiegmann, Elena, Westendorf, Eva, Kalus, Ina, Pringle, Thomas H., Lübke, Torben, and Dierks, Thomas. “Arylsulfatase K, a Novel Lysosomal Sulfatase”. Journal of Biological Chemistry 288.42 (2013): 30019-30028.

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• [28]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623533

  Milz, Fabian, Harder, Alexander, Neuhaus, Phillipp, Breitkreuz-Korff, Olga, Walhorn, Volker, Lübke, Torben, Anselmetti, Dario, and Dierks, Thomas. “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): 5287-5298.

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• [27]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2471754

  Makrypidi, Georgia, Damme, Markus, Müller-Loennies, Sven, Trusch, Maria, Schmidt, Bernhard, Schlüter, Hartmut, Heeren, Joerg, Lübke, Torben, Saftig, Paul, and Braulke, Thomas. “Mannose 6 dephosphorylation of lysosomal proteins mediated by Acid phosphatases acp2 and acp5”. Molecular and cellular biology 32.4 (2012): 774-782.

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• [26]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2529586

  Kollmann, K, Damme, Markus, Markmann, S, Morelle, W, Schweizer, M, Hermans-Borgmeyer, I, Rochert, A K, Pohl, S, Lübke, Torben, Michalski, J-C, Kakela, R, Walkley, S U, and Braulke, T. “Lysosomal dysfunction causes neurodegeneration in mucolipidosis II 'knock-in' mice”. Brain 135.9 (2012): 2661-2675.

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• [25]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2494022

  Kowalewski, Björn, Lamanna, William Christopher, Lawrence, Roger, Damme, Markus, Padva, Michael, Stroobants, Stijn, Kalus, Ina, Frese, Marc-André, Lübke, Torben, Lüllmann-Rauch, Renate, D'Hooge, Rudi, Esko, Jeffrey D, and Dierks, Thomas. “Arylsulfatase G Inactivation Causes Loss of Heparan Sulfate 3-O-Sulfatase Activity and Mucopolysaccharidosis in Mice”. Proc. Natl. Acad. Sci. USA 109.26 (2012): 10310-10315.

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• [24]
  

  2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940515

  Damme, Markus, Stroobants, Stijn, Walkley, Steven U., Lüllmann-Rauch, Renate, D'Hooge, Rudi, Fogh, Jens, Saftig, Paul, Lübke, Torben, and Blanz, Judith. “Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in alpha-mannosidosis”. Journal of Neuropathology & Experimental Neurology 70.1 (2011): 83-94.

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• [23]
  

  2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2352585

  Savalas, LR, Gasnier, B, Damme, Markus, Lübke, Torben, Wrocklage, C, Debacker, C, Jezeqou, A, Reinheckel, T, Hasilik, A, Saftig, P, and Schröder, Bernd. “Disrupted in renal carcinoma 2 (DIRC2), a novel transporter of the lysosomal membrane, is proteolytically processed by cathepsin L.”. Biochemical Journal 436.1 (2011): 113-121.

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• [22]
  

  2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939855

  Rosner, Cornelia, Kruse, Philip H., Lübke, Torben, and Walter, Lutz. “Erratum to: Rhesus macaque MHC class I molecules show differential subcellular localizations”. Immunogenetics 62.6 (2010): 409-418.

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• [21]
  

  2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2776186

  Rosner, Cornelia, Kruse, Philip H., Lübke, Torben, and Walter, Lutz. “Rhesus macaque MHC class I molecules show differential subcellular localizations”. Immunogenetics 62.3 (2010): 149-158.

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• [20]
  

  2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939885

  Kollmann, Katrin, Pohl, Sandra, Marschner, Katrin, Encarnacao, Marisa, Sakwa, Imme, Tiede, Stephan, Poorthuis, Ben J., Lübke, Torben, Müller-Loennies, Sven, Storch, Stephan, and Braulke, Thomas. “Mannose phosphorylation in health and disease”. European Journal of Cell Biology 89.1 (2010): 117-123.

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• [19]
  

  2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902203

  Damme, Markus, Morelle, Willy, Schmidt, Bernhard, Andersson, Claes, Fogh, Jens, Michalski, Jean-Claude, and Lübke, Torben. “Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosis.”. Molecular and Cellular Biology 30.1 (2010): 273-283.

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• [18]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939923

  Lakomek, Kristina, Dickmanns, Achim, Kettwig, Matthias, Urlaub, Henning, Ficner, Ralf, and Lübke, Torben. “Initial insight into the function of the lysosomal 66.3 kDa protein from mouse by means of X-ray crystallography”. BMC Structural Biology 9.1 (2009): 56-72.

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• [17]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902143

  Schieweck, Oliver, Damme, Markus, Schröder, Bernd, Hasilik, Andrey, Schmidt, Bernhard, and Lübke, Torben. “NCU-G1 is a highly glycosylated integral membrane protein of the lysosome.”. Biochemical Journal 422.1 (2009): 83-90.

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• [16]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939981

  Lübke, Torben, Lobel, Peter, and Sleat, David E. “Proteomics of the lysosome”. Biochimica et Biophysica Acta 1793.4 (2009): 625-635.

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• [15]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940533

  Kollmann, Katrin, Damme, Markus, Deuschl, Florian, Kahle, Jörg, D'Hooge, Rudi, Lüllmann-Rauch, Renate, and Lübke, Torben. “Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1”. Febs Journal 276.5 (2009): 1356-1369.

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• [14]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939939

  Lakomek, Kristina, Dickmanns, Achim, Mueller, Uwe, Kollmann, Katrin, Deuschl, Florian, Berndt, Annette, Lübke, Torben, and Ficner, Ralf. “De novo sulfur SAD phasing of the lysosomal 66.3 kDa protein from mouse”. Acta Crystallographica Section D 65.3 (2009): 220-228.

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• [13]
  

  2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939993

  Fedele, Anthony O., Filocamo, Mirella, Di Rocco, Maja, Sersale, Giovanna, Lübke, Torben, di Natale, Paola, Cosma, Maria Pia, and Ballabio, Andrea. “Mutational analysis of the HGSNAT gene in Italian patients with mucopolysaccharidosis IIIC (Sanfilippo C syndrome)”. Human Mutation 28.5 (2007): 523.

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• [12]
  

  2007 | Zeitschriftenaufsatz | PUB-ID: 1940006

  Hellbusch, Christina, Sperandio, Markus, Frommhold, David, Yakubenia, Sviatlana, Wild, Martin K., Popovici, Diana, Vestweber, Dietmar, Gröne, Hermann-Josef, von Figura, Kurt, Lübke, Torben, and Körner, Christian. “Golgi GDP-fucose transporter-deficient mice mimic congenital disorder of glycosylation IIc/leukocyte adhesion deficiency II”. Journal of Biological Chemistry 282.14 (2007): 10762-10772.

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• [11]
  

  2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940030

  Deuschl, Florian, Kollmann, Katrin, von Figura, Kurt, and Lübke, Torben. “Molecular characterization of the hypothetical 66.3-kDa protein in mouse: lysosomal targeting, glycosylation, processing and tissue distribution”. Febs Letters 580.24 (2006): 5747-5752.

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• [10]
  

  2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940045

  Thiel, Christian, Lübke, Torben, Matthijs, Gert, von Figura, Kurt, and Körner, Christian. “Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality”. Molecular and Cellular Biology 26.15 (2006): 5615-5620.

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• [9]
  

  2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940057

  Tiede, Stephan, Storch, Stephan, Lübke, Torben, Henrissat, Bernhard, Bargal, Ruth, Raas-Rothschild, Annick, and Braulke, Thomas. “Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferase”. Nature Medicine 11.10 (2006): 1109-1112.

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• [8]
  

  2005 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 1940182

  Lübke, Torben, and Landgrebe, Jobst. “Lysosomal Proteome and Transcriptome”. Lysosomes. Ed. Paul Saftig. Georgetown, Texas, USA: Landes Bioscience, 2005. 130-143.

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• [7]
  

  2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940072

  Kollmann, Katrin, Mutenda, Kudzai E., Balleininger, Martina, Eckermann, Ellen, von Figura, Kurt, Schmidt, Bernhard, and Lübke, Torben. “Identification of novel lysosomal matrix proteins by proteome analysis”. Proteomics 5.15 (2005): 3966-3978.

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• [6]
  

  2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940085

  Hartmann, Dieter, de Strooper, Bart, Serneels, Lutgarde, Craessaerts, Katleen, Herreman, An, Annaert, Wim, Umans, Lieve, Lübke, Torben, Illert, Anna Lena, von Figura, Kurt, and Saftig, Paul. “The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblasts”. Human Molecular Genetics 11.21 (2002): 2615-2624.

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• [5]
  

  2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940103

  Hansske, Bengt, Thiel, Christian, Lübke, Torben, Hasilik, Martin, Höning, Stefan, Peters, Verena, Heidemann, Peter H., Hoffmann, Georg F., Berger, Eric G., von Figura, Kurt, and Körner, Christian. “Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId”. Journal of Clinical Investigation 109.6 (2002): 725-733.

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• [4]
  

  2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940119

  Lübke, Torben, Marquardt, Thorsten, Etzioni, Amos, Hartmann, Enno, von Figura, Kurt, and Körner, Christian. “Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency”. Nature Genetics 28.1 (2001): 73-76.

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• [3]
  

  2001 | Dissertation | PUB-ID: 1940291

  Lübke, Torben. 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.

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• [2]
  

  2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940146

  Andersson, Lisa A., McNairn, Elizabeth, Lübke, Torben, Pau, Richard N., and Boxer, David H. “ModE-dependent molybdate regulation of the molybdenum cofactor operon moa in Escherichia coli”. Journal of Bacteriology 182.24 (2000): 7035-7043.

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• [1]
  

  1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940173

  Lübke, Torben, Marquardt, Thorsten, von Figura, Kurt, and Körner, Christian. “A new type of carbohydrate-deficient glycoprotein syndrome due to a decreased import of GDP-fucose into the golgi”. Journal of Biological Chemistry 274.37 (1999): 25986-25989.

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