48 Publikationen

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  • [48]
    2024 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2987979
    Sun, M., Kaminsky, C. K., Deppe, P., Ilse, M. - B., Vaz, F. M., Plecko, B., Lübke, T., et al. (2024). A novel homozygous missense variant in ARSK causes MPS X, a new subtype of mucopolysaccharidosis. Genes & Diseases, 11(3), 101025. https://doi.org/10.1016/j.gendis.2023.06.003
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  • [47]
    2023 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2981846
    Sun, M., Kaminsky, C. K., Deppe, P., Ilse, M. - B., Vaz, F. M., Plecko, B., Lübke, T., et al. (2023). A novel homozygous missense variant in ARSK causes MPS X, a new subtype of mucopolysaccharidosis. Genes & Diseases. https://doi.org/10.1016/j.gendis.2023.06.003
    PUB | DOI | PubMed | Europe PMC
     
  • [46]
    2022 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2962857 OA
    Linhorst, A., & Lübke, T. (2022). The Human Ntn-Hydrolase Superfamily: Structure, Functions and Perspectives. Cells, 11(10), 1592. https://doi.org/10.3390/cells11101592
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  • [45]
    2022 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2967253
    Smith, K., Haslund-Gourley, B. S., Aziz, P. V., Heithoff, D. M., Restagno, D., Fried, J. C., Ilse, M. - B., et al. (2022). Establishment of Blood Glycosidase Activities and their Excursions in Sepsis. Glycobiology , 32(11), 1034-1035.
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  • [44]
    2022 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2965167
    Haslund-Gourley, B. S., Aziz, P. V., Heithoff, D. M., Restagno, D., Fried, J. C., Ilse, M. - B., Bäumges, H., et al. (2022). Establishment of blood glycosidase activities and their excursions in sepsis. PNAS Nexus, 1(3), pgac113. https://doi.org/10.1093/pnasnexus/pgac113
    PUB | DOI | PubMed | Europe PMC
     
  • [43]
    2021 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2961637
    Aziz, P. V., Lewis, B. J., Haslund-Gourley, B. S., Heithoff, D. M., Westman, J. S., Restagno, D., Fried, J. C., et al. (2021). Excursions of blood glycosidase activities in the pathogenesis and prognosis of Sepsis. Glycobiology , 31(12), 1700. https://doi.org/10.1093/glycob/cwab121
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  • [42]
    2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2960244 OA
    Verheyen, S., Blatterer, J., Speicher, M. R., Bhavani, G. S. L., Boons, G. - J., Ilse, M. - B., Andrae, D., et al. (2021). Novel subtype of mucopolysaccharidosis caused by arylsulfatase K (ARSK) deficiency. Journal of Medical Genetics, jmedgenet-2021-108061. https://doi.org/10.1136/jmedgenet-2021-108061
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  • [41]
    2021 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2956816
    Kowalewski, B., Lange, H., Galle, S., Dierks, T., Lübke, T., & Damme, M. (2021). Decoding the consecutive lysosomal degradation of 3-O-sulfate containing heparan sulfate by Arylsulfatase G (ARSG). Biochemical Journal. https://doi.org/10.1042/BCJ20210415
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [40]
    2020 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2946513
    Aziz, P., Haslund-Gourley, B., Heithoff, D., Westman, J., Restagno, D., Lewis, B., Fried, J., et al. (2020). Altered glycosidase Activities at Physiological pH in the Pathogenesis of Sepsis. FASEB JOURNAL, 34 Hoboken: Wiley. https://doi.org/10.1096/fasebj.2020.34.s1.07166
    PUB | DOI | WoS
     
  • [39]
    2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2948390
    Lübke, T., & Damme, M. (2020). Lysosomal sulfatases: a growing family*. Biochemical Journal, 477(20), 3963-3983. doi:10.1042/bcj20200586
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  • [38]
    2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2945876
    Trabszo, C., Ramms, B., Chopra, P., Lüllmann-Rauch, R., Stroobants, S., Sproß, J., Jeschke, A., et al. (2020). Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfate. Biochemical Journal. doi:10.1042/bcj20200546
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [37]
    2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937243
    Korf-Klingebiel, M., Reboll, M. R., Grote, K., Schleiner, H., Wang, Y., Wu, X., Klede, S., et al. (2019). Heparan Sulfate-Editing Extracellular Sulfatases Enhance Vascular Endothelial Growth Factor Bioavailability for Ischemic Heart Repair. Circulation research, 125(9), 787-801. doi:10.1161/CIRCRESAHA.119.315023
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [36]
    2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271
    Stroobants, S., Wolf, H., Callaerts-Vegh, Z., Dierks, T., Lübke, T., & D'Hooge, R. (2018). Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice. FRONTIERS IN BEHAVIORAL NEUROSCIENCE, 12, 15. doi:10.3389/fnbeh.2018.00069
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  • [35]
    2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909150
    Pan, X., Wang, Y., Lübke, T., Hinek, A., & Pshezhetsky, A. V. (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. doi:10.1371/journal.pone.0172854
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  • [34]
    2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778
    Dhamale, O. P., Lawrence, R., Wiegmann, E., Shah, B. A., Al-Mafraji, K., Lamanna, W. C., Lübke, T., et al. (2017). Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase. ACS Chemical Biology, 12(2), 367-373. doi:10.1021/acschembio.6b01033
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  • [33]
    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., 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), 1015-1028. doi:10.1242/dmm.025122
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  • [32]
    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., 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. doi:10.1242/dmm.014050
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  • [31]
    2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2672894 OA
    Pan, X., Grigoryeva, L., Seyrantepe, V., Peng, J., Kollmann, K., Tremblay, J., Lavoie, J. L., 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. doi:10.1371/journal.pgen.1004146
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  • [30]
    2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2699273
    Kowalewski, B., Lübke, T., Kollmann, K., Braulke, T., Reinheckel, T., Dierks, T., & Damme, M. (2014). Molecular Characterization of Arylsulfatase G: EXPRESSION, PROCESSING, GLYCOSYLATION, TRANSPORT, AND ACTIVITY. The Journal of biological chemistry, 289(40), 27992-28005. doi:10.1074/jbc.M114.584144
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  • [29]
    2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623550
    Wiegmann, E., Westendorf, E., Kalus, I., Pringle, T. H., Lübke, T., & Dierks, T. (2013). Arylsulfatase K, a Novel Lysosomal Sulfatase. Journal of Biological Chemistry, 288(42), 30019-30028. doi:10.1074/jbc.M113.499541
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  • [28]
    2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623533
    Milz, F., Harder, A., Neuhaus, P., Breitkreuz-Korff, O., Walhorn, V., Lübke, T., Anselmetti, D., 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), 5287-5298. doi:10.1016/j.bbagen.2013.07.014
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  • [27]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2471754
    Makrypidi, G., Damme, M., Müller-Loennies, S., Trusch, M., Schmidt, B., Schlüter, H., Heeren, J., et al. (2012). Mannose 6 dephosphorylation of lysosomal proteins mediated by Acid phosphatases acp2 and acp5. Molecular and cellular biology, 32(4), 774-782. doi:10.1128/MCB.06195-11
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  • [26]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2529586
    Kollmann, K., Damme, M., 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. doi:10.1093/brain/aws209
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  • [25]
    2012 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2494022
    Kowalewski, B., Lamanna, W. C., Lawrence, R., Damme, M., Padva, M., Stroobants, S., Kalus, I., 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. doi:10.1073/pnas.1202071109
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  • [24]
    2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940515
    Damme, M., Stroobants, S., Walkley, S. U., Lüllmann-Rauch, R., D'Hooge, R., Fogh, J., Saftig, P., 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), 83-94. https://doi.org/10.1097/NEN.0b013e31820428fa
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  • [23]
    2011 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2352585
    Savalas, L. R., Gasnier, B., Damme, M., Lübke, T., 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. https://doi.org/10.1042/BJ20101672
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  • [22]
    2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939855
    Rosner, C., Kruse, P. H., Lübke, T., & Walter, L. (2010). Erratum to: Rhesus macaque MHC class I molecules show differential subcellular localizations. Immunogenetics, 62(6), 409-418. https://doi.org/10.1007/s00251-010-0447-y
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  • [21]
    2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2776186
    Rosner, C., Kruse, P. H., Lübke, T., & Walter, L. (2010). Rhesus macaque MHC class I molecules show differential subcellular localizations. Immunogenetics, 62(3), 149-158. https://doi.org/10.1007/s00251-010-0424-5
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  • [20]
    2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939885
    Kollmann, K., Pohl, S., Marschner, K., Encarnacao, M., Sakwa, I., Tiede, S., Poorthuis, B. J., et al. (2010). Mannose phosphorylation in health and disease. European Journal of Cell Biology, 89(1), 117-123. https://doi.org/10.1016/j.ejcb.2009.10.008
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  • [19]
    2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902203
    Damme, M., Morelle, W., Schmidt, B., Andersson, C., Fogh, J., Michalski, J. - C., & 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(1), 273-283. https://doi.org/10.1128/MCB.01143-09
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  • [18]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939923
    Lakomek, K., Dickmanns, A., Kettwig, M., Urlaub, H., Ficner, R., & Lübke, T. (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), 56-72. https://doi.org/10.1186/1472-6807-9-56
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  • [17]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1902143
    Schieweck, O., Damme, M., Schröder, B., Hasilik, A., Schmidt, B., & Lübke, T. (2009). NCU-G1 is a highly glycosylated integral membrane protein of the lysosome. Biochemical Journal, 422(1), 83-90. https://doi.org/10.1042/BJ20090567
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  • [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), 625-635. https://doi.org/10.1016/j.bbamcr.2008.09.018
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [15]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940533
    Kollmann, K., Damme, M., Deuschl, F., Kahle, J., D'Hooge, R., Lüllmann-Rauch, R., & Lübke, T. (2009). Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1. Febs Journal, 276(5), 1356-1369. https://doi.org/10.1111/j.1742-4658.2009.06877.x
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  • [14]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939939
    Lakomek, K., Dickmanns, A., Mueller, U., Kollmann, K., Deuschl, F., Berndt, A., Lübke, T., et al. (2009). De novo sulfur SAD phasing of the lysosomal 66.3 kDa protein from mouse. Acta Crystallographica Section D, 65(3), 220-228. https://doi.org/10.1107/s0907444908041814
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  • [13]
    2007 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939993
    Fedele, A. O., Filocamo, M., Di Rocco, M., Sersale, G., Lübke, T., di Natale, P., Cosma, M. P., et al. (2007). Mutational analysis of the HGSNAT gene in Italian patients with mucopolysaccharidosis IIIC (Sanfilippo C syndrome). Human Mutation, 28(5), 523. https://doi.org/10.1002/humu.9488
    PUB | DOI
     
  • [12]
    2007 | Zeitschriftenaufsatz | PUB-ID: 1940006
    Hellbusch, C., Sperandio, M., Frommhold, D., Yakubenia, S., Wild, M. K., Popovici, D., Vestweber, D., 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), 10762-10772. https://doi.org/10.1074/jbc.M700314200
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  • [11]
    2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940030
    Deuschl, F., Kollmann, K., von Figura, K., & Lübke, T. (2006). Molecular characterization of the hypothetical 66.3-kDa protein in mouse: lysosomal targeting, glycosylation, processing and tissue distribution. Febs Letters, 580(24), 5747-5752. https://doi.org/10.1016/j.febslet.2006.09.029
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  • [10]
    2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940045
    Thiel, C., Lübke, T., Matthijs, G., von Figura, K., & Körner, C. (2006). Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality. Molecular and Cellular Biology, 26(15), 5615-5620. https://doi.org/10.1128/MCB.02391-05
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  • [9]
    2006 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940057
    Tiede, S., Storch, S., Lübke, T., Henrissat, B., Bargal, R., Raas-Rothschild, A., & Braulke, T. (2006). Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferase. Nature Medicine, 11(10), 1109-1112. https://doi.org/10.1038/nm1305
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  • [8]
    2005 | Sammelwerksbeitrag | Veröffentlicht | PUB-ID: 1940182
    Lübke, T., & Landgrebe, J. (2005). Lysosomal Proteome and Transcriptome. In P. Saftig (Ed.), Lysosomes (pp. 130-143). Georgetown, Texas, USA: Landes Bioscience. https://doi.org/10.1007/0-387-28957-7_11
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  • [7]
    2005 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940072
    Kollmann, K., Mutenda, K. E., Balleininger, M., Eckermann, E., von Figura, K., Schmidt, B., & Lübke, T. (2005). Identification of novel lysosomal matrix proteins by proteome analysis. Proteomics, 5(15), 3966-3978. https://doi.org/10.1002/pmic.200401247
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  • [6]
    2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940085
    Hartmann, D., de Strooper, B., Serneels, L., Craessaerts, K., Herreman, A., Annaert, W., Umans, L., 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), 2615-2624. https://doi.org/10.1093/hmg/11.21.2615
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  • [5]
    2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940103
    Hansske, B., Thiel, C., Lübke, T., Hasilik, M., Höning, S., Peters, V., Heidemann, P. H., 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), 725-733. https://doi.org/10.1172/JCI14010
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  • [4]
    2001 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940119
    Lübke, T., Marquardt, T., Etzioni, A., Hartmann, E., von Figura, K., & Körner, C. (2001). Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency. Nature Genetics, 28(1), 73-76. https://doi.org/10.1038/ng0501-73
    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.
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  • [2]
    2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940146
    Andersson, L. A., McNairn, E., Lübke, T., Pau, R. N., & Boxer, D. H. (2000). ModE-dependent molybdate regulation of the molybdenum cofactor operon moa in Escherichia coli. Journal of Bacteriology, 182(24), 7035-7043. https://doi.org/10.1128/JB.182.24.7035-7043.2000
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  • [1]
    1999 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940173
    Lübke, T., Marquardt, T., von Figura, K., & Körner, C. (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), 25986-25989. https://doi.org/10.1074/jbc.274.37.25986
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