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The Biochemical Journal|June 4, 2009
NCU-G1 is a highly glycosylated integral membrane protein of the lysosomeOliver Schieweck, Markus Damme, Bernd Schröder, et al.
Disease Models & Mechanisms|November 7, 2025
Recovery of α-L-fucosidase in fucosidosis nonsense variants by readthrough stimulation and release factor degradationHannah Bäumges, Dennis Lebeda, Philip Deppe, et al.
Frontiers in Behavioral Neuroscience|May 1, 2018
Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis MiceStijn Stroobants, Heike Wolf, Zsuzsanna Callaerts-Vegh, et al.
The Journal of Biological Chemistry|August 30, 2013
Arylsulfatase K, a novel lysosomal sulfataseElena Marie Wiegmann, Eva Westendorf, Ina Kalus, et al.
The Journal of Biological Chemistry|August 20, 2014
Molecular characterization of arylsulfatase G: expression, processing, glycosylation, transport, and activityBjörn Kowalewski, Torben Lübke, Katrin Kollmann, et al.
Molecular and Cellular Biology|November 4, 2009
Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosisMarkus Damme, Willy Morelle, Bernhard Schmidt, et al.
Nature Medicine|October 4, 2005
Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferaseStephan Tiede, Stephan Storch, Torben Lübke, et al.
The FEBS Journal|February 4, 2009
Molecular characterization and gene disruption of mouse lysosomal putative serine carboxypeptidase 1Katrin Kollmann, Markus Damme, Florian Deuschl, et al.
Acta Crystallographica. Section D, Biological Crystallography|February 25, 2009
De novo sulfur SAD phasing of the lysosomal 66.3 kDa protein from mouseKristina Lakomek, Achim Dickmanns, Uwe Mueller, et al.
Proteomics|September 8, 2005
Identification of novel lysosomal matrix proteins by proteome analysisKatrin Kollmann, Kudzai E Mutenda, Martina Balleininger, et al.
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