Expression of lysosomal protective protein/cathepsin A in a stably transformed human neuroblastoma cell line during bi-directional differentiation into neuronal and Schwannian cells

Author:

Itoh Kohji,Satoh Yurie,Kadota Yoshito,Oheda Yukako,Kuwahara Jun,Shimmoto Michie,Sakuraba Hitoshi

Publisher

Elsevier BV

Subject

Cell Biology,Cellular and Molecular Neuroscience

Reference40 articles.

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2. d’Azzo, A., Andria, G., Strisciuglio, P., Galjaard, H., 2000. Galactosialidosis. In: Scriver, C.R., Beaudet, A.L., Sly, W.S., Valle, D. (Eds.), The Metabolic and Molecular Bases of Inherited Disease, eighth ed. McGraw-Hill, New York, pp. 3811–3826.

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

4. Safety and efficacy of recombinant human α-galactosidase A replacement therapy in Fabry’s disease;Eng;N. Engl. J. Med.,2001

5. Expression of cDNA encoding the human ‘protective protein’ associated with lysosomal β-galactosidase and neuraminidase: homology to yeast proteases;Galjart;Cell,1988

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