Human recombinant lysosomal enzymes produced in microorganisms

Author:

Espejo-Mojica Ángela J.,Alméciga-Díaz Carlos J.,Rodríguez Alexander,Mosquera Ángela,Díaz Dennis,Beltrán Laura,Díaz Sergio,Pimentel Natalia,Moreno Jefferson,Sánchez Jhonnathan,Sánchez Oscar F.,Córdoba Henry,Poutou-Piñales Raúl A.,Barrera Luis A.

Funder

Administrative Department of Science, Technology and Innovation (COLCIENCIAS), Colombia

Pontificia Universidad Javeriana

Young Researcher scholarship from COLCIENCIAS

COLCIENCIAS

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference126 articles.

1. Treating lysosomal storage disorders: current practice and future prospects;Platt;Biochim. Biophys. Acta,2009

2. Lysosomal storage disorders: old diseases, present and future challenges;Klein;Pediatr. Endocrinol. Rev.,2013

3. Recent patents in diagnosis and treatment for inborn errors of metabolism;Espejo;Recent Pat. Endocr. Metab. Immune Drug Discov.,2010

4. Enzyme replacement therapy for lysosomal diseases: lessons from 20years of experience and remaining challenges;Desnick;Annu. Rev. Genomics Hum. Genet.,2012

5. Efficacy and safety of enzyme replacement therapy with BMN 110 (elosulfase alfa) for Morquio A syndrome (mucopolysaccharidosis IVA): a phase 3 randomised placebo-controlled study;Hendriksz;J. Inherit. Metab. Dis.,2014

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