Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency
Körner, Christian, Lübke, Torben, Marquardt, Thorsten, Etzioni, Amos, Hartmann, Enno, von Figura, Kurt
Published in Nature genetics (01.05.2001)
Published in Nature genetics (01.05.2001)
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A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease
Wolf, Heike, Damme, Markus, Stroobants, Stijn, D'Hooge, Rudi, Beck, Hans Christian, Hermans-Borgmeyer, Irm, Lüllmann-Rauch, Renate, Dierks, Thomas, Lübke, Torben
Published in Disease models & mechanisms (01.09.2016)
Published in Disease models & mechanisms (01.09.2016)
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Establishment of blood glycosidase activities and their excursions in sepsis
Haslund-Gourley, Benjamin S, Aziz, Peter V, Heithoff, Douglas M, Restagno, Damien, Fried, Jeffrey C, Ilse, Mai-Britt, Bäumges, Hannah, Mahan, Michael J, Lübke, Torben, Marth, Jamey D
Published in PNAS nexus (01.07.2022)
Published in PNAS nexus (01.07.2022)
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Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfate
Trabszo, Christof, Ramms, Bastian, Chopra, Pradeep, Lüllmann-Rauch, Renate, Stroobants, Stijn, Sproß, Jens, Jeschke, Anke, Schinke, Thorsten, Boons, Geert-Jan, Esko, Jeffrey D, Lübke, Torben, Dierks, Thomas
Published in Biochemical journal (18.09.2020)
Published in Biochemical journal (18.09.2020)
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Heparan Sulfate–Editing Extracellular Sulfatases Enhance VEGF Bioavailability for Ischemic Heart Repair
Korf-Klingebiel, Mortimer, Reboll, Marc R, Grote, Karsten, Schleiner, Hauke, Wang, Yong, Wu, Xuekun, Klede, Stefanie, Mikhed, Yuliya, Bauersachs, Johann, Klintschar, Michael, Rudat, Carsten, Kispert, Andreas, Niessen, Hans W, Lübke, Torben, Dierks, Thomas, Wollert, Kai C
Published in Circulation research (11.10.2019)
Published in Circulation research (11.10.2019)
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Arylsulfatase G inactivation causes loss of heparan sulfate 3-O-sulfatase activity and mucopolysaccharidosis in mice
Kowalewski, Björn, Lamanna, William C, Lawrence, Roger, Damme, Markus, Stroobants, Stijn, Padva, Michael, Kalus, Ina, Frese, Marc-André, Lübke, Torben, Lüllmann-Rauch, Renate, D’Hooge, Rudi, Esko, Jeffrey D, Dierks, Thomas
Published in Proceedings of the National Academy of Sciences - PNAS (26.06.2012)
Published in Proceedings of the National Academy of Sciences - PNAS (26.06.2012)
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The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for α-secretase activity in fibroblasts
Hartmann, Dieter, de Strooper, Bart, Serneels, Lutgarde, Craessaerts, Katleen, Herreman, An, Annaert, Wim, Umans, Lieve, Lübke, Torben, Lena Illert, Anna, von Figura, Kurt, Saftig, Paul
Published in Human molecular genetics (01.10.2002)
Published in Human molecular genetics (01.10.2002)
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A novel homozygous missense variant in ARSK causes MPS X, a new subtype of mucopolysaccharidosis
Sun, Miao, Kaminsky, Cornelia K., Deppe, Philip, Ilse, Mai-Britt, Vaz, Frédéric M., Plecko, Barbara, Lübke, Torben, Randolph, Linda M.
Published in Genes & diseases (01.05.2024)
Published in Genes & diseases (01.05.2024)
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Serine carboxypeptidase SCPEP1 and Cathepsin A play complementary roles in regulation of vasoconstriction via inactivation of endothelin-1
Pan, Xuefang, Grigoryeva, Lubov, Seyrantepe, Volkan, Peng, Junzheng, Kollmann, Katrin, Tremblay, Johanne, Lavoie, Julie L, Hinek, Aleksander, Lübke, Torben, Pshezhetsky, Alexey V
Published in PLoS genetics (01.02.2014)
Published in PLoS genetics (01.02.2014)
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Mice, double deficient in lysosomal serine carboxypeptidases Scpep1 and Cathepsin A develop the hyperproliferative vesicular corneal dystrophy and hypertrophic skin thickenings
Pan, Xuefang, Wang, Yanting, Lübke, Torben, Hinek, Aleksander, Pshezhetsky, Alexey V
Published in PloS one (24.02.2017)
Published in PloS one (24.02.2017)
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Mannose 6 Dephosphorylation of Lysosomal Proteins Mediated by Acid Phosphatases Acp2 and Acp5
Georgia Makrypidi, Markus Damme, Sven Müller-Loennies, Maria Trusch, Bernhard Schmidt, Hartmut Schlüter, Joerg Heeren, Torben Lübke, Paul Saftig, Thomas Braulke
Published in Molecular and Cellular Biology (01.02.2012)
Published in Molecular and Cellular Biology (01.02.2012)
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Arylsulfatase K is the Lysosomal 2‑Sulfoglucuronate Sulfatase
Dhamale, Omkar P, Lawrence, Roger, Wiegmann, Elena M, Shah, Bhahwal A, Al-Mafraji, Kanar, Lamanna, William C, Lübke, Torben, Dierks, Thomas, Boons, Geert-Jan, Esko, Jeffrey D
Published in ACS chemical biology (17.02.2017)
Published in ACS chemical biology (17.02.2017)
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Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice
Stroobants, Stijn, Wolf, Heike, Callaerts-Vegh, Zsuzsanna, Dierks, Thomas, Lübke, Torben, D'Hooge, Rudi
Published in Frontiers in behavioral neuroscience (12.04.2018)
Published in Frontiers in behavioral neuroscience (12.04.2018)
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Impaired Lysosomal Trimming of N-Linked Oligosaccharides Leads to Hyperglycosylation of Native Lysosomal Proteins in Mice with α-Mannosidosis
Damme, Markus, Morelle, Willy, Schmidt, Bernhard, Andersson, Claes, Fogh, Jens, Michalski, Jean-Claude, Lübke, Torben
Published in Molecular and Cellular Biology (01.01.2010)
Published in Molecular and Cellular Biology (01.01.2010)
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Disrupted in renal carcinoma 2 (DIRC2), a novel transporter of the lysosomal membrane, is proteolytically processed by cathepsin L
Savalas, Lalu Rudyat Telly, Gasnier, Bruno, Damme, Markus, Lübke, Torben, Wrocklage, Christian, Debacker, Cécile, Jézégou, Adrien, Reinheckel, Thomas, Hasilik, Andrej, Saftig, Paul, Schröder, Bernd
Published in Biochemical journal (01.10.2011)
Published in Biochemical journal (01.10.2011)
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NCU-G1 is a highly glycosylated integral membrane protein of the lysosome
Schieweck, Oliver, Damme, Markus, Schröder, Bernd, Hasilik, Andrej, Schmidt, Bernhard, Lübke, Torben
Published in Biochemical journal (29.07.2009)
Published in Biochemical journal (29.07.2009)
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