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FEBS Letters|May 23, 1998
Natural ceramide is unable to escape the lysosome, in contrast to a fluorescent analogueM Chatelut, M Leruth, K Harzer, et al.The Journal of Pathology|August 10, 1999
Intracellular transport of acid beta-glucosidase and lysosome-associated membrane proteins is affected in Gaucher's disease (G202R mutation)K P Zimmer, P le Coutre, H M Aerts, et al.American Journal of Human Genetics|March 1, 1980
Morquio syndrome (mucopolysaccharidosis IV B) associated with beta-galactosidase deficiency. Report of two casesH Groebe, M Krins, H Schmidberger, et al.Developmental Neuroscience|January 1, 1991
Type C Niemann-Pick disease: biochemical aspects and phenotypic heterogeneityM T Vanier, C Rodriguez-Lafrasse, R Rousson, et al.The Journal of Peptide Research : Official Journal of the American Peptide Society|March 25, 2005
Immunostimulants and Toll-like receptor ligands obtained by screening combinatorial lipopeptide collectionsF Reutter, G Jung, W Baier, et al.The American Journal of Physiology|August 1, 1992
Insulin-like growth factors decrease oxygen-regulated erythropoietin production by human hepatoma cells (Hep G2)H Scholz, W Baier, P Ratcliffe, et al.Anesthesia and Analgesia|June 21, 2017
A Shared Opportunity for Improving Electronic Medical Record DataAmanda W Baier, Daniel J Snyder, Izabela C Leahy, et al.Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1990
Cardiocyte storage and hypertrophy as a sole manifestation of Fabry's disease. Report on a case simulating hypertrophic non-obstructive cardiomyopathyM Elleder, V Bradová, F Smíd, et al.Forensic Science International|November 12, 2018
Micro-CT for saw mark analysis on human boneD G Norman, W Baier, D G Watson, et al.The Journal of Biological Chemistry|February 15, 1992
Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common geneD Schnabel, M Schröder, W Fürst, et al.Pageof 14