PUB - Publikationen an der Universität Bielefeld

Alle markieren

• [49]
  

  2024 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2987979

  Sun, M., et al., 2024. A novel homozygous missense variant in ARSK causes MPS X, a new subtype of mucopolysaccharidosis. Genes & Diseases, 11(3): 101025.

  PUB | DOI
   
• [48]
  

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

  Smith, K., et al., 2023. Establishment of Blood Glycosidase Activities and their Excursions in Sepsis. Glycobiology, 33(11), p 1016.

  PUB | WoS
   
• [47]
  

  2023 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2981846

  Sun, M., et al., 2023. A novel homozygous missense variant in ARSK causes MPS X, a new subtype of mucopolysaccharidosis. Genes & Diseases.

  PUB | DOI | PubMed | Europe PMC
   
• [46]
  

  2022 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2962857

  Linhorst, A., & Lübke, T., 2022. The Human Ntn-Hydrolase Superfamily: Structure, Functions and Perspectives. Cells, 11(10): 1592.

  PUB | PDF | DOI | Download (ext.) | WoS | PubMed | Europe PMC
   
• [45]
  

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

  Smith, K., et al., 2022. Establishment of Blood Glycosidase Activities and their Excursions in Sepsis. Glycobiology , 32(11), p 1034-1035.

  PUB | WoS
   
• [44]
  

  2022 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2965167

  Haslund-Gourley, B.S., et al., 2022. Establishment of blood glycosidase activities and their excursions in sepsis. PNAS Nexus, 1(3): pgac113.

  PUB | DOI | PubMed | Europe PMC
   
• [43]
  

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

  Aziz, P.V., et al., 2021. Excursions of blood glycosidase activities in the pathogenesis and prognosis of Sepsis. Glycobiology , 31(12), p 1700.

  PUB | DOI | WoS
   
• [42]
  

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

  Verheyen, S., et al., 2021. Novel subtype of mucopolysaccharidosis caused by arylsulfatase K (ARSK) deficiency. Journal of Medical Genetics, : jmedgenet-2021-108061.

  PUB | PDF | DOI | WoS | PubMed | Europe PMC
   
• [41]
  

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

  Kowalewski, B., et al., 2021. Decoding the consecutive lysosomal degradation of 3-O-sulfate containing heparan sulfate by Arylsulfatase G (ARSG). Biochemical Journal.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [40]
  

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

  Aziz, P., et al., 2020. Altered glycosidase Activities at Physiological pH in the Pathogenesis of Sepsis. In FASEB JOURNAL. no.34 Hoboken: Wiley.

  PUB | DOI | WoS
   
• [39]
  

  2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2948390

  Lübke, T., & Damme, M., 2020. Lysosomal sulfatases: a growing family*. Biochemical Journal, 477(20), p 3963-3983.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [38]
  

  2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2945876

  Trabszo, C., et al., 2020. Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfate. Biochemical Journal.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [37]
  

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

  Korf-Klingebiel, M., et al., 2019. Heparan Sulfate-Editing Extracellular Sulfatases Enhance Vascular Endothelial Growth Factor Bioavailability for Ischemic Heart Repair. Circulation research, 125(9), p 787-801.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [36]
  

  2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271

  Stroobants, S., et al., 2018. Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice. FRONTIERS IN BEHAVIORAL NEUROSCIENCE, 12: 15.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [35]
  

  2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909150

  Pan, X., et al., 2017. 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): e0172854.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [34]
  

  2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778

  Dhamale, O.P., et al., 2017. Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase. ACS Chemical Biology, 12(2), p 367-373.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [33]
  

  2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616

  Wolf, H., et al., 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), p 1015-1028.

  PUB | PDF | DOI | WoS | PubMed | Europe PMC
   
• [32]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2658538

  Kong, X.Y., 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), p 351-362.

  PUB | PDF | DOI | WoS | PubMed | Europe PMC
   
• [31]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2672894

  Pan, X., et al., 2014. Serine carboxypeptidase SCPEP1 and Cathepsin A play complementary roles in regulation of vasoconstriction via inactivation of endothelin-1. PLoS genetics, 10(2): e1004146.

  PUB | PDF | DOI | WoS | PubMed | Europe PMC
   
• [30]
  

  2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2699273

  Kowalewski, B., et al., 2014. Molecular Characterization of Arylsulfatase G: EXPRESSION, PROCESSING, GLYCOSYLATION, TRANSPORT, AND ACTIVITY. The Journal of biological chemistry, 289(40), p 27992-28005.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [29]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623550

  Wiegmann, E., et al., 2013. Arylsulfatase K, a Novel Lysosomal Sulfatase. Journal of Biological Chemistry, 288(42), p 30019-30028.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [28]
  

  2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623533

  Milz, F., et al., 2013. 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), p 5287-5298.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [27]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2471754

  Makrypidi, G., et al., 2012. Mannose 6 dephosphorylation of lysosomal proteins mediated by Acid phosphatases acp2 and acp5. Molecular and cellular biology, 32(4), p 774-782.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [26]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2529586

  Kollmann, K., et al., 2012. Lysosomal dysfunction causes neurodegeneration in mucolipidosis II 'knock-in' mice. Brain, 135(9), p 2661-2675.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [25]
  

  2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2494022

  Kowalewski, B., 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), p 10310-10315.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [24]
  

  2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940515

  Damme, M., et al., 2011. Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in alpha-mannosidosis. Journal of Neuropathology & Experimental Neurology, 70(1), p 83-94.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [23]
  

  2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2352585

  Savalas, L.R., 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), p 113-121.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [22]
  

  2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939855

  Rosner, C., et al., 2010. Erratum to: Rhesus macaque MHC class I molecules show differential subcellular localizations. Immunogenetics, 62(6), p 409-418.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [21]
  

  2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2776186

  Rosner, C., et al., 2010. Rhesus macaque MHC class I molecules show differential subcellular localizations. Immunogenetics, 62(3), p 149-158.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [20]
  

  2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939885

  Kollmann, K., et al., 2010. Mannose phosphorylation in health and disease. European Journal of Cell Biology, 89(1), p 117-123.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [19]
  

  2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902203

  Damme, M., et al., 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), p 273-283.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [18]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939923

  Lakomek, K., et al., 2009. 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), p 56-72.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [17]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902143

  Schieweck, O., et al., 2009. NCU-G1 is a highly glycosylated integral membrane protein of the lysosome. Biochemical Journal, 422(1), p 83-90.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [16]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939981

  Lübke, T., Lobel, P., & Sleat, D.E., 2009. Proteomics of the lysosome. Biochimica et Biophysica Acta, 1793(4), p 625-635.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [15]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940533

  Kollmann, K., et al., 2009. Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1. Febs Journal, 276(5), p 1356-1369.

  PUB | DOI | WoS | PubMed | Europe PMC
   
• [14]
  

  2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939939

  Lakomek, K., et al., 2009. De novo sulfur SAD phasing of the lysosomal 66.3 kDa protein from mouse. Acta Crystallographica Section D, 65(3), p 220-228.

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

  2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939993

  Fedele, A.O., et al., 2007. Mutational analysis of the HGSNAT gene in Italian patients with mucopolysaccharidosis IIIC (Sanfilippo C syndrome). Human Mutation, 28(5), p 523.

  PUB | DOI
   
• [12]
  

  2007 | Zeitschriftenaufsatz | PUB-ID: 1940006

  Hellbusch, C., et al., 2007. Golgi GDP-fucose transporter-deficient mice mimic congenital disorder of glycosylation IIc/leukocyte adhesion deficiency II. Journal of Biological Chemistry, 282(14), p 10762-10772.

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

  2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940030

  Deuschl, F., et al., 2006. Molecular characterization of the hypothetical 66.3-kDa protein in mouse: lysosomal targeting, glycosylation, processing and tissue distribution. Febs Letters, 580(24), p 5747-5752.

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

  2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940045

  Thiel, C., et al., 2006. Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality. Molecular and Cellular Biology, 26(15), p 5615-5620.

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

  2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940057

  Tiede, S., et al., 2006. Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferase. Nature Medicine, 11(10), p 1109-1112.

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

  2005 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 1940182

  Lübke, T., & Landgrebe, J., 2005. Lysosomal Proteome and Transcriptome. In P. Saftig, ed. Lysosomes. Georgetown, Texas, USA: Landes Bioscience, pp. 130-143.

  PUB | DOI
   
• [7]
  

  2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940072

  Kollmann, K., et al., 2005. Identification of novel lysosomal matrix proteins by proteome analysis. Proteomics, 5(15), p 3966-3978.

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

  2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940085

  Hartmann, D., et al., 2002. The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblasts. Human Molecular Genetics, 11(21), p 2615-2624.

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

  2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940103

  Hansske, B., et al., 2002. 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), p 725-733.

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

  2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940119

  Lübke, T., et al., 2001. Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency. Nature Genetics, 28(1), p 73-76.

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

  2001 | Dissertation | PUB-ID: 1940291

  Lübke, T., 2001. 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.

  PUB
   
• [2]
  

  2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940146

  Andersson, L.A., et al., 2000. ModE-dependent molybdate regulation of the molybdenum cofactor operon moa in Escherichia coli. Journal of Bacteriology, 182(24), p 7035-7043.

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

  1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940173

  Lübke, T., et al., 1999. 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), p 25986-25989.

  PUB | DOI | WoS | PubMed | Europe PMC