Reversibility of cellular and organ pathology in enzyme replacement trials in animal models of lysosomal storage diseases

Author:

Gieselmann Volkmar

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology, and Child Health

Reference26 articles.

1. Desnick, RJ and Schuchman, EH. (2002) Enzyme replacement and enhancement therapies: lessons from lysosomal disorders Nat Rev Genet, 3, pp. 954 - 66.

2. Yaghootfam, A and Schestag, F and Dierks, T and Gieselmann, V. (2003) Recognition of arylsulfatase A and B by the UDP-N-acetylglucosamine:lysosomal enzyme N-acetylglucosamine-phosphotransferase J Biol Chem, 278, pp. 32653 - 61.

3. Kornfeld, S and Mellman, I. (1989) The biogenesis of lysosomes Annu Rev Cell Biol, 5, pp. 483 - 525.

4. Pontow, SE and Kery, V and Stahl, PD. (1992) Mannose receptor Int Rev Cytol, 137B, pp. 221 - 44.

5. Ashwell, G and Harford, J. (1982) Carbohydrate-specific receptors of the liver Annu Rev Biochem, 51, pp. 531 - 54.

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