14 Publikationen

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  • [14]
    2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124
    Kruszewski, K., Luellmann-Rauch, R., Dierks, T., Bartsch, U., and Damme, M. (2016). Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 57, 1120-1131.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [13]
    2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616 OA
    Wolf, H., Damme, M., Stroobants, S., D'Hooge, R., Beck, H. C., Hermans-Borgmeyer, I., Lüllmann-Rauch, R., Dierks, T., and Lübke, T. (2016). A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease. Disease Models & Mechanisms 9, 1015-1028.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [12]
    2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2709463
    Kowalewski, B., Heimann, P., Ortkras, T., Lüllmann-Rauch, R., Sawada, T., Walkley, S. U., Dierks, T., and Damme, M. (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, 1856-1868.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [11]
    2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2658538 OA
    Kong, X. Y., Nesset, C. K., Damme, M., Loeberg, E. - M., Lübke, T., Maehlen, J., Andersson, K. B., Roos, N., Thoresen, G. H., Rustan, A. C., 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, 351-362.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [10]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2484642
    Thelen, M., Damme, M., Schweizer, M., Hagel, C., Wong, A., Cooper, J. D., Braulke, T., and Galliciotti, G. (2012). Disruption of the Autophagy-Lysosome Pathway is Involved in Neuropathology of the nclf Mouse Model of Neuronal Ceroid Lipofuscinosis. PLOS ONE 7:e35493.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [9]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2471754
    Makrypidi, G., Damme, M., Müller-Loennies, S., Trusch, M., Schmidt, B., Schlüter, H., Heeren, J., Lübke, T., Saftig, P., and Braulke, T. (2012). Mannose 6 dephosphorylation of lysosomal proteins mediated by Acid phosphatases acp2 and acp5. Molecular and cellular biology 32, 774-782.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [8]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2529586
    Kollmann, K., Damme, M., Markmann, S., Morelle, W., Schweizer, M., Hermans-Borgmeyer, I., Rochert, A. K., Pohl, S., Lübke, T., Michalski, J. - C., et al. (2012). Lysosomal dysfunction causes neurodegeneration in mucolipidosis II 'knock-in' mice. Brain 135, 2661-2675.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [7]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2494022
    Kowalewski, B., Lamanna, W. C., Lawrence, R., Damme, M., Padva, M., Stroobants, S., Kalus, I., Frese, M. - A., Lübke, T., Lüllmann-Rauch, R., 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, 10310-10315.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [6]
    2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940515
    Damme, M., Stroobants, S., Walkley, S. U., Lüllmann-Rauch, R., D'Hooge, R., Fogh, J., Saftig, P., Lübke, T., and Blanz, J. (2011). Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in alpha-mannosidosis. Journal of Neuropathology & Experimental Neurology 70, 83-94.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [5]
    2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2352585
    Savalas, L. R., Gasnier, B., Damme, M., Lübke, T., Wrocklage, C., Debacker, C., Jezeqou, A., Reinheckel, T., Hasilik, A., Saftig, P., 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, 113-121.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [4]
    2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902203
    Damme, M., Morelle, W., Schmidt, B., Andersson, C., Fogh, J., Michalski, J. - C., and Lübke, T. (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, 273-283.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [3]
    2009 | Dissertation | PUB-ID: 2352701
    Damme, M. (2009). Zellbiologische Untersuchung α-Mannosidase-defizienter und Enzym-behandelter Mäuse.
    PUB | Download (ext.)
     
  • [2]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902143
    Schieweck, O., Damme, M., Schröder, B., Hasilik, A., Schmidt, B., and Lübke, T. (2009). NCU-G1 is a highly glycosylated integral membrane protein of the lysosome. Biochemical Journal 422, 83-90.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [1]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940533
    Kollmann, K., Damme, M., Deuschl, F., Kahle, J., D'Hooge, R., Lüllmann-Rauch, R., and Lübke, T. (2009). Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1. Febs Journal 276, 1356-1369.
    PUB | DOI | WoS | PubMed | Europe PMC
     

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