Miglustat (NB-DNJ) works as a chaperone for mutated acid β-glucosidase in cells transfected with several Gaucher disease mutations-Reference-Cited by-同舟云学术

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Miglustat (NB-DNJ) works as a chaperone for mutated acid β-glucosidase in cells transfected with several Gaucher disease mutations

Published:2005-09 Issue:2 Volume:35 Page:268-276
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Alfonso Pilar,Pampín Sandra,Estrada Jorge,Rodríguez-Rey José Carlos,Giraldo Pilar,Sancho Javier,Pocoví Miguel

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference39 articles.

1. The cell biology of lysosomal storage disorders;Futerman;Nat. Rev., Mol. Cell Biol.,2004

2. Replacement therapy for inherited enzyme deficiency-macrophage-targeted glucocerebrosidase for Gaucher's disease;Barton;N. Engl. J. Med.,1991

3. Prospective study of neurological responses to treatment with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher's disease;Schiffmann;Ann. Neurol.,1997

4. Novel oral treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis;Cox;Lancet,2000

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