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Biochimica Et Biophysica Acta|November 19, 2013
Gaucher disease and Fabry disease: new markers and insights in pathophysiology for two distinct glycosphingolipidosesMaria J Ferraz, Wouter W Kallemeijn, Mina Mirzaian, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|February 20, 2010
Inhibition of glycosphingolipid synthesis induces a profound reduction of plasma cholesterol and inhibits atherosclerosis development in APOE*3 Leiden and low-density lipoprotein receptor-/- miceFlorence Bietrix, Elisa Lombardo, Cindy P A A van Roomen, et al.Journal of Inherited Metabolic Disease|March 21, 1998
Oligosaccharide excretion in adult Gaucher diseaseJ G de Jong, J M Aerts, S van Weely, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|February 7, 2015
Lentiviral gene therapy using cellular promoters cures type 1 Gaucher disease in miceMaria Dahl, Alexander Doyle, Karin Olsson, et al.Biochimica Et Biophysica Acta|September 21, 2010
Reduction of elevated plasma globotriaosylsphingosine in patients with classic Fabry disease following enzyme replacement therapyMariëlle J van Breemen, Saskia M Rombach, Nick Dekker, et al.Hepatology (Baltimore, Md.)|December 17, 2008
Reduction of glycosphingolipid biosynthesis stimulates biliary lipid secretion in miceNora Bijl, Cindy P A A van Roomen, Vassilis Triantis, et al.Biochimica Et Biophysica Acta|May 15, 2007
Increased plasma macrophage inflammatory protein (MIP)-1alpha and MIP-1beta levels in type 1 Gaucher diseaseMariëlle J van Breemen, Maaike de Fost, Jane S A Voerman, et al.The Journal of Biological Chemistry|October 3, 1998
Generation of specific deoxynojirimycin-type inhibitors of the non-lysosomal glucosylceramidaseH S Overkleeft, G H Renkema, J Neele, et al.Cellular and Molecular Life Sciences : CMLS|May 27, 2008
Ydc1p ceramidase triggers organelle fragmentation, apoptosis and accelerated ageing in yeastA M Aerts, P Zabrocki, I E J A François, et al.Biochimica Et Biophysica Acta|March 17, 1988
Glucocerebrosidase, a lysosomal enzyme that does not undergo oligosaccharide phosphorylationJ M Aerts, A W Schram, A Strijland, et al.Pageof 25