The glycosylation design space for recombinant lysosomal replacement enzymes produced in CHO cells
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry
Link
http://www.nature.com/articles/s41467-019-09809-3.pdf
Reference70 articles.
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3. Parenti, G., Pignata, C., Vajro, P. & Salerno, M. New strategies for the treatment of lysosomal storage diseases (review). Int. J. Mol. Med 31, 11–20 (2013).
4. Desnick, R. J. & Schuchman, E. H. Enzyme replacement therapy for lysosomal diseases: lessons from 20 years of experience and remaining challenges. Annu. Rev. Genom. Hum. Genet. 13, 307–335 (2012).
5. Grubb, J. H., Vogler, C. & Sly, W. S. New strategies for enzyme replacement therapy for lysosomal storage diseases. Rejuvenation Res. 13, 229–236 (2010).
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