48 Publikationen

Alle markieren

  • [48]
    2024 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2987979
    Sun, M., Kaminsky, C.K., Deppe, P., Ilse, M.-B., Vaz, F.M., Plecko, B., Lübke, T. & Randolph, L.M. (2024). A novel homozygous missense variant in ARSK causes MPS X, a new subtype of mucopolysaccharidosis. Genes & Diseases, 11(3): 101025. Elsevier BV. doi:10.1016/j.gendis.2023.06.003.
    PUB | DOI
     
  • [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. & Randolph, L.M. (2023). A novel homozygous missense variant in ARSK causes MPS X, a new subtype of mucopolysaccharidosis. Genes & Diseases. Elsevier . doi: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. MDPI AG. doi:10.3390/cells11101592.
    PUB | PDF | DOI | Download (ext.) | WoS | PubMed | Europe PMC
     
  • [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., Bäumges, H., Mahan, M.J., Lübke, T. & Marth, J.D. (2022). Establishment of Blood Glycosidase Activities and their Excursions in Sepsis (Glycobiology ), 32(11), 1034-1035. Gehalten auf der 2022 Annual Meeting of the Society for Glycobiology , Cary: Oxford University Press.
    PUB | WoS
     
  • [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., Mahan, M.J., Lübke, T. & Marth, J.D. (2022). Establishment of blood glycosidase activities and their excursions in sepsis. PNAS Nexus, 1(3): pgac113. Oxford University Press . doi: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., Ilse, M.-B., Lübke, T. & Marth, J.D. (2021). Excursions of blood glycosidase activities in the pathogenesis and prognosis of Sepsis (Glycobiology ), 31(12), 1700. Gehalten auf der Society for Glycobiology Annual Meeting 2021 , Cary: Oxford University Press . doi:10.1093/glycob/cwab121.
    PUB | DOI | WoS
     
  • [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., Sproß, J., Vaz, F.M., Kircher, S.G., Posch-Pertl, L., Baumgartner, D., Lübke, T., Shah, H., Al Kaissi, A., Girisha, K.M. & Plecko, B. (2021). Novel subtype of mucopolysaccharidosis caused by arylsulfatase K (ARSK) deficiency. Journal of Medical Genetics: jmedgenet-2021-108061. BMJ. doi:10.1136/jmedgenet-2021-108061.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [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. Portland Press Ltd. doi: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., Ilse, M.-B., Lübke, T. & Marth, J. (2020). Altered glycosidase Activities at Physiological pH in the Pathogenesis of Sepsis. FASEB JOURNAL. Gehalten auf der Annual Meeting on Experimental Biology, Hoboken: Wiley. doi: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. Portland Press Ltd. doi:10.1042/bcj20200586.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [38]
    2020 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2945876
    Trabszo, C., Ramms, B., Chopra, P., Lüllmann-Rauch, R., Stroobants, S., Sproß, J., Jeschke, A., Schinke, T., Boons, G.-J., Esko, J., Lübke, T. & Dierks, T. (2020). Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfate. Biochemical Journal. Portland Press . 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., Mikhed, Y., Bauersachs, J., Klintschar, M., Rudat, C., Kispert, A., Niessen, H.W., Lübke, T., Dierks, T. & Wollert, K.C. (2019). Heparan Sulfate-Editing Extracellular Sulfatases Enhance Vascular Endothelial Growth Factor Bioavailability for Ischemic Heart Repair. Circulation research, 125(9), 787-801. American Heart Association. 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. Frontiers Media SA. doi:10.3389/fnbeh.2018.00069.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. Public Library of Science (PLoS). doi:10.1371/journal.pone.0172854.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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., Dierks, T., Boons, G.-J. & Esko, J.D. (2017). Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase. ACS Chemical Biology, 12(2), 367-373. ACS. doi:10.1021/acschembio.6b01033.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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., Dierks, T. & 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(9), 1015-1028. The Company of Biologists. doi:10.1242/dmm.025122.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [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., Roos, N., Thoresen, G.H., Rustan, A.C., Kase, E.T. & Eskild, W. (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. The Company of Biologists. doi:10.1242/dmm.014050.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [31]
    2014 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2672894 OA
    Pan, X., Grigoryeva, L., Seyrantepe, V., Peng, J., Kollmann, K., Tremblay, J., Lavoie, J.L., Hinek, A., Lübke, T. & Pshezhetsky, A.V. (2014). Serine carboxypeptidase SCPEP1 and Cathepsin A play complementary roles in regulation of vasoconstriction via inactivation of endothelin-1. PLoS genetics, 10(2): e1004146. Public Library of Science (PLoS). doi:10.1371/journal.pgen.1004146.
    PUB | PDF | DOI | WoS | PubMed | Europe PMC
     
  • [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. American Society for Biochemistry & Molecular Biology (ASBMB). doi:10.1074/jbc.M114.584144.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. American Society for Biochemistry & Molecular Biology (ASBMB). doi:10.1074/jbc.M113.499541.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [28]
    2013 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2623533
    Milz, F., Harder, A., Neuhaus, P., Breitkreuz-Korff, O., Walhorn, V., Lübke, T., Anselmetti, D. & Dierks, T. (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. Elsevier BV. doi:10.1016/j.bbagen.2013.07.014.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [27]
    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. & Braulke, T. (2012). Mannose 6 dephosphorylation of lysosomal proteins mediated by Acid phosphatases acp2 and acp5. Molecular and cellular biology, 32(4), 774-782. American Society for Microbiology. doi:10.1128/MCB.06195-11.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [26]
    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., Kakela, R., Walkley, S.U. & Braulke, T. (2012). Lysosomal dysfunction causes neurodegeneration in mucolipidosis II 'knock-in' mice. Brain, 135(9), 2661-2675. Oxford University Press (OUP). doi:10.1093/brain/aws209.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [25]
    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., D'Hooge, R., Esko, J.D. & Dierks, T. (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. Proceedings of the National Academy of Sciences. doi:10.1073/pnas.1202071109.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [24]
    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. & 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(1), 83-94. Ovid Technologies (Wolters Kluwer Health). doi:10.1097/NEN.0b013e31820428fa.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [23]
    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. & Schröder, B. (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. Portland Press Ltd. doi:10.1042/BJ20101672.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. Springer. doi:10.1007/s00251-010-0447-y.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. Springer. doi:10.1007/s00251-010-0424-5.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [20]
    2010 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939885
    Kollmann, K., Pohl, S., Marschner, K., Encarnacao, M., Sakwa, I., Tiede, S., Poorthuis, B.J., Lübke, T., Müller-Loennies, S., Storch, S. & Braulke, T. (2010). Mannose phosphorylation in health and disease. European Journal of Cell Biology, 89(1), 117-123. Elsevier BV. doi:10.1016/j.ejcb.2009.10.008.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. American Society for Microbiology. doi:10.1128/MCB.01143-09.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. Springer Science + Business Media. doi:10.1186/1472-6807-9-56.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. Portland Press Ltd. doi:10.1042/BJ20090567.
    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), 625-635. Elsevier BV. doi: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. Wiley-Blackwell. doi:10.1111/j.1742-4658.2009.06877.x.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [14]
    2009 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1939939
    Lakomek, K., Dickmanns, A., Mueller, U., Kollmann, K., Deuschl, F., Berndt, A., Lübke, T. & Ficner, R. (2009). De novo sulfur SAD phasing of the lysosomal 66.3 kDa protein from mouse. Acta Crystallographica Section D, 65(3), 220-228. International Union of Crystallography (IUCr). doi:10.1107/s0907444908041814.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. & Ballabio, A. (2007). Mutational analysis of the HGSNAT gene in Italian patients with mucopolysaccharidosis IIIC (Sanfilippo C syndrome). Human Mutation, 28(5), 523. Wiley. doi: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., Gröne, H.-J., von Figura, K., Lübke, T. & Körner, C. (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. American Society for Biochemistry & Molecular Biology (ASBMB). doi:10.1074/jbc.M700314200.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. Wiley. doi:10.1016/j.febslet.2006.09.029.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. American Society for Microbiology. doi:10.1128/MCB.02391-05.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. Springer Science and Business Media LLC. doi:10.1038/nm1305.
    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 (Hrsg.), Lysosomes (S. 130-143). Georgetown, Texas, USA: Landes Bioscience. doi:10.1007/0-387-28957-7_11.
    PUB | DOI
     
  • [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. Wiley. doi:10.1002/pmic.200401247.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [6]
    2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940085
    Hartmann, D., de Strooper, B., Serneels, L., Craessaerts, K., Herreman, A., Annaert, W., Umans, L., Lübke, T., Illert, A.L., von Figura, K. & Saftig, P. (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. Oxford University Press (OUP). doi:10.1093/hmg/11.21.2615.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [5]
    2002 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1940103
    Hansske, B., Thiel, C., Lübke, T., Hasilik, M., Höning, S., Peters, V., Heidemann, P.H., Hoffmann, G.F., Berger, E.G., von Figura, K. & Körner, C. (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. doi:10.1172/JCI14010.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. Springer Nature. doi: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.
    PUB
     
  • [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. AMER SOC MICROBIOLOGY. doi:10.1128/JB.182.24.7035-7043.2000.
    PUB | DOI | WoS | PubMed | Europe PMC
     
  • [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. AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC. doi:10.1074/jbc.274.37.25986.
    PUB | DOI | WoS | PubMed | Europe PMC
     

Suche

Publikationen filtern

Darstellung / Sortierung

Export / Einbettung