PUB - Publikationen an der Universität Bielefeld

Alle markieren

• [14]
  

  2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124

  Kruszewski, Katharina, Luellmann-Rauch, Renate, Dierks, Thomas, Bartsch, Udo, and Damme, Markus. 2016. “Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice”. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 57 (3): 1120-1131.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [13]
  

  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. 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): 1015-1028.

  PUB | PDF | DOI | WoS | PubMed | Europe PMC
   
• [12]
  

  2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2709463

  Kowalewski, Björn, Heimann, Peter, Ortkras, Theresa, Lüllmann-Rauch, Renate, Sawada, Tomo, Walkley, Steven U, Dierks, Thomas, and Damme, Markus. 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): 1856-1868.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [11]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2658538

  Kong, Xiang Yi, Nesset, Cecilie K., Damme, Markus, Loeberg, Else-Marit, Lübke, Torben, Maehlen, Jan, Andersson, Kristin B., et al. 2014. “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): 351-362.

  PUB | PDF | DOI | WoS | PubMed | Europe PMC
   
• [10]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2484642

  Thelen, Melanie, Damme, Markus, Schweizer, Michaela, Hagel, Christian, Wong, Andrew, Cooper, Jonathan D., Braulke, Thomas, and Galliciotti, Giovanna. 2012. “Disruption of the Autophagy-Lysosome Pathway is Involved in Neuropathology of the nclf Mouse Model of Neuronal Ceroid Lipofuscinosis”. PLOS ONE 7 (4): e35493.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [9]
  

  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. 2012. “Mannose 6 dephosphorylation of lysosomal proteins mediated by Acid phosphatases acp2 and acp5”. Molecular and cellular biology 32 (4): 774-782.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [8]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2529586

  Kollmann, K, Damme, Markus, Markmann, S, Morelle, W, Schweizer, M, Hermans-Borgmeyer, I, Rochert, A K, et al. 2012. “Lysosomal dysfunction causes neurodegeneration in mucolipidosis II 'knock-in' mice”. Brain 135 (9): 2661-2675.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [7]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2494022

  Kowalewski, Björn, Lamanna, William Christopher, Lawrence, Roger, Damme, Markus, Padva, Michael, Stroobants, Stijn, Kalus, Ina, 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): 10310-10315.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [6]
  

  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. 2011. “Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in alpha-mannosidosis”. Journal of Neuropathology & Experimental Neurology 70 (1): 83-94.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [5]
  

  2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2352585

  Savalas, LR, Gasnier, B, Damme, Markus, Lübke, Torben, Wrocklage, C, Debacker, C, Jezeqou, A, et al. 2011. “Disrupted in renal carcinoma 2 (DIRC2), a novel transporter of the lysosomal membrane, is proteolytically processed by cathepsin L.”. Biochemical Journal 436 (1): 113-121.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [4]
  

  2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902203

  Damme, Markus, Morelle, Willy, Schmidt, Bernhard, Andersson, Claes, Fogh, Jens, Michalski, Jean-Claude, and Lübke, Torben. 2010. “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): 273-283.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [3]
  

  2009 | Dissertation | PUB-ID: 2352701

  Damme, Markus. 2009. Zellbiologische Untersuchung α-Mannosidase-defizienter und Enzym-behandelter Mäuse.

  PUB | Download (ext.)
   
• [2]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902143

  Schieweck, Oliver, Damme, Markus, Schröder, Bernd, Hasilik, Andrey, Schmidt, Bernhard, and Lübke, Torben. 2009. “NCU-G1 is a highly glycosylated integral membrane protein of the lysosome.”. Biochemical Journal 422 (1): 83-90.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [1]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940533

  Kollmann, Katrin, Damme, Markus, Deuschl, Florian, Kahle, Jörg, D'Hooge, Rudi, Lüllmann-Rauch, Renate, and Lübke, Torben. 2009. “Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1”. Febs Journal 276 (5): 1356-1369.

  PUB | DOI | WoS | PubMed | Europe PMC