Enzyme replacement and gene therapy for Gaucher's disease
Author:
Publisher
Wiley
Subject
Cell Biology,Organic Chemistry,Biochemistry
Reference19 articles.
1. Brady, R.O., Kanfer, J.N., and Shapiro, D. (1965) Metabolism of Glucocerebrosides. II. Evidence of an Enzymatic Deficiency in Gaucher's Disease,Biochem. Biophys. Res. Comm. 18, 221–225.
2. Kattlove, H.E., Williams, J.C., Gaynor, E., Spivack, M., Bradley, R.M., and Brady, R.O. (1969) Gaucher Cells in Chronic Myelocytic Leukemia: An Acquired Abnormality,Blood 33, 379–390.
3. Brady, R.O. (1966) The Sphingolipidoses,N. Engl. J. Med. 275, 312–318.
4. Pentchev, P.G., Brady, R.O., Hibbert, S.R., Gal, A.E., and Shapiro, D. (1973) Isolation and Characterization of Glucocerebrosidase from Human Placental Tissue,J. Biol. Chem. 248, 5256–5261.
5. Brady, R.O., Pentchev, P.G., Gal, A.E., Hibbert, S.R., and Dekaban, A.S. (1974) Replacement Therapy for Inherited Enzyme Deficiency: Use of Purified Glucocerebrosidase in Gaucher's Disease,N. Engl. J. Med. 291, 989–993.
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