PUB - Publikationen an der Universität Bielefeld

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• [14]
  

  2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124

  K. Kruszewski, et al., “Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice”, INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, vol. 57, 2016, pp. 1120-1131.

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

  2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616

  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.

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• [12]
  

  2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2709463

  B. Kowalewski, et al., “Ataxia is the major neuropathological finding in Arylsulfatase G deficient mice: Similarities and dissimilarities to Sanfilippo disease (Mucopolysaccharidosis type III)”, Human Molecular Genetics, vol. 24, 2015, pp. 1856-1868.

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• [11]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2658538

  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.

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• [10]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2484642

  M. Thelen, et al., “Disruption of the Autophagy-Lysosome Pathway is Involved in Neuropathology of the nclf Mouse Model of Neuronal Ceroid Lipofuscinosis”, PLOS ONE, vol. 7, 2012, : e35493.

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• [9]
  

  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.

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• [8]
  

  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.

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• [7]
  

  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.

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• [6]
  

  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.

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• [5]
  

  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.

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• [4]
  

  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
   
• [3]
  

  2009 | Dissertation | PUB-ID: 2352701

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

  PUB | Download (ext.)
   
• [2]
  

  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.

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• [1]
  

  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.

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