Measurement of lysosomal glucocerebrosidase activity in mouse liver using a fluorescence-activated cell sorter assay
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
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4. Replacement therapy for inherited enzyme deficiency: macrophage targeted glucocerebrosidase for Gaucher’s disease;Barton;N. Engl. J. Med.,1991
5. Binding, internalization, and degradation of mannose-terminated glucocerebrosidase by macrophages;Sato;J. Clin. Invest.,1993
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2. Delineating pathological pathways in a chemically induced mouse model of Gaucher disease;The Journal of Pathology;2016-07-05
3. Identification and Characterization of Pharmacological Chaperones to Correct Enzyme Deficiencies in Lysosomal Storage Disorders;ASSAY and Drug Development Technologies;2011-06
4. The pharmacological chaperone isofagomine increases the activity of the Gaucher disease L444P mutant form of β-glucosidase;FEBS Journal;2010-02-10
5. A sensitive and reproducible fluorescent-based HPLC assay to measure the activity of acid as well as neutral β-glucocerebrosidases;Analytical Biochemistry;2008-12
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