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Journal of Medical Systems|May 28, 2010
Prediction of clinical conditions after coronary bypass surgery using dynamic data analysisK Van Loon, F Guiza, G Meyfroidt, et al.
The Journal of Biological Chemistry|November 22, 2000
Identification of a novel acidic mammalian chitinase distinct from chitotriosidaseR G Boot, E F Blommaart, E Swart, et al.
European Journal of Biochemistry|March 1, 1997
Synthesis, sorting, and processing into distinct isoforms of human macrophage chitotriosidaseG H Renkema, R G Boot, A Strijland, et al.
Journal of Inherited Metabolic Disease|February 11, 2005
Plasma chitotriosidase and CCL18: early biochemical surrogate markers in type B Niemann-Pick diseaseJ Brinkman, F A Wijburg, C E Hollak, et al.
Clinical Genetics|September 1, 1990
Activity of glucocerebrosidase in extracts of different cell types from type 1 Gaucher disease patientsM C Sa Miranda, J M Aerts, R Pinto, et al.
Biochemical and Biophysical Research Communications|December 15, 1986
Efficient routing of glucocerebrosidase to lysosomes requires complex oligosaccharide chain formationJ M Aerts, S Brul, W E Donker-Koopman, et al.
Virchows Archiv : an International Journal of Pathology|November 1, 1996
A case of type I Gaucher disease with cardiopulmonary amyloidosis and chitotriosidase deficiencyM Hrebícek, J Zeman, J Musilová, et al.
Journal of Molecular Endocrinology|September 20, 2013
Functional characteristics of neonatal rat β cells with distinct markersG A Martens, E Motté, G Kramer, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 12, 1999
Strong induction of members of the chitinase family of proteins in atherosclerosis: chitotriosidase and human cartilage gp-39 expressed in lesion macrophagesR G Boot, T A van Achterberg, B E van Aken, et al.
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