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Human Molecular Genetics|October 2, 2002
The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblastsDieter Hartmann, Bart de Strooper, Lutgarde Serneels, et al.
The Journal of Biological Chemistry|February 6, 2007
Golgi GDP-fucose transporter-deficient mice mimic congenital disorder of glycosylation IIc/leukocyte adhesion deficiency IIChristina C Hellbusch, Markus Sperandio, David Frommhold, et al.
The Journal of Clinical Investigation|March 20, 2002
Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IIdBengt Hansske, Christian Thiel, Torben Lübke, et al.
The Biochemical Journal|August 29, 2020
Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfateChristof Trabszo, Bastian Ramms, Pradeep Chopra, et al.
ACS Chemical Biology|January 6, 2017
Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate SulfataseOmkar P Dhamale, Roger Lawrence, Elena M Wiegmann, et al.
PNAS Nexus|August 15, 2022
Establishment of blood glycosidase activities and their excursions in sepsisBenjamin S Haslund-Gourley, Peter V Aziz, Douglas M Heithoff, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 13, 2012
Arylsulfatase G inactivation causes loss of heparan sulfate 3-O-sulfatase activity and mucopolysaccharidosis in miceBjörn Kowalewski, William C Lamanna, Roger Lawrence, et al.
Disease Models & Mechanisms|February 4, 2014
Loss of lysosomal membrane protein NCU-G1 in mice results in spontaneous liver fibrosis with accumulation of lipofuscin and iron in Kupffer cellsXiang Y Kong, Cecilie Kasi Nesset, Markus Damme, et al.
Circulation Research|August 23, 2019
Heparan Sulfate-Editing Extracellular Sulfatases Enhance VEGF Bioavailability for Ischemic Heart RepairMortimer Korf-Klingebiel, Marc R Reboll, Karsten Grote, et al.
Journal of Medical Genetics|December 17, 2021
Novel subtype of mucopolysaccharidosis caused by arylsulfatase K (ARSK) deficiencySarah Verheyen, Jasmin Blatterer, Michael R Speicher, et al.
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