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Biochimica Et Biophysica Acta|July 30, 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 sulfateFabian Milz, Alexander Harder, Phillipp Neuhaus, et al.
Analytical Chemistry|February 17, 2026
Unlocking Rare 3-O-Sulfation Patterns in Heparan Sulfate via ARSG-Directed Regioselective Desulfation and HILIC-MSSalomé Poyer, Agnès Denys, Nesrine El Omrani, et al.
Cells|September 13, 2025
Deciphering α-L-Fucosidase Activity Contribution in Human and Mouse: Tissue α-L-Fucosidase FUCA1 Meets Plasma α-L-Fucosidase FUCA2Hannah Bäumges, Svenja Jelinek, Heike Lange, et al.
Human Mutation|April 3, 2007
Mutational analysis of the HGSNAT gene in Italian patients with mucopolysaccharidosis IIIC (Sanfilippo C syndrome). Mutation in brief #959. OnlineAnthony Olind Fedele, Mirella Filocamo, Maja Di Rocco, et al.
Journal of Neuropathology and Experimental Neurology|December 16, 2010
Cerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in α-mannosidosisMarkus Damme, Stijn Stroobants, Steven U Walkley, et al.
Disease Models & Mechanisms|August 5, 2016
A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human diseaseHeike Wolf, Markus Damme, Stijn Stroobants, et al.
Molecular and Cellular Biology|December 14, 2011
Mannose 6 dephosphorylation of lysosomal proteins mediated by acid phosphatases Acp2 and Acp5Georgia Makrypidi, Markus Damme, Sven Müller-Loennies, et al.
Plos Genetics|March 4, 2014
Serine carboxypeptidase SCPEP1 and Cathepsin A play complementary roles in regulation of vasoconstriction via inactivation of endothelin-1Xuefang Pan, Lubov Grigoryeva, Volkan Seyrantepe, et al.
European Journal of Cell Biology|December 1, 2009
Mannose phosphorylation in health and diseaseKatrin Kollmann, Sandra Pohl, Katrin Marschner, et al.
The Biochemical Journal|June 23, 2011
Disrupted in renal carcinoma 2 (DIRC2), a novel transporter of the lysosomal membrane, is proteolytically processed by cathepsin LLalu Rudyat Telly Savalas, Bruno Gasnier, Markus Damme, et al.
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