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Protein Expression and Purification|June 1, 1994
Overexpression of the human lysosomal enzyme alpha-L-iduronidase in Chinese hamster ovary cellsE D Kakkis, A Matynia, A J Jonas, et al.American Journal of Medical Genetics|September 15, 1993
DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): a new patient and delineation of neurologic variability among recessive casesH J Lin, E D Kakkis, D J Eteson, et al.The Journal of Biological Chemistry|September 5, 1997
Carbohydrate structures of recombinant human alpha-L-iduronidase secreted by Chinese hamster ovary cellsK W Zhao, K F Faull, E D Kakkis, et al.Molecular Genetics and Metabolism|July 12, 2005
Penetration, diffusion, and uptake of recombinant human alpha-L-iduronidase after intraventricular injection into the rat brainP V Belichenko, P I Dickson, M Passage, et al.Proceedings of the National Academy of Sciences of the United States of America|December 20, 1994
Enzyme replacement in a canine model of Hurler syndromeR M Shull, E D Kakkis, M F McEntee, et al.Journal of Inherited Metabolic Disease|June 30, 2009
Continuous infusion of enzyme replacement therapy is inferior to weekly infusions in MPS I dogsM B Passage, A W Krieger, M C Peinovich, et al.Human Mutation|August 10, 2004
Identification and molecular characterization of alpha-L-iduronidase mutations present in mucopolysaccharidosis type I patients undergoing enzyme replacement therapyG Yogalingam, X-H Guo, V J Muller, et al.Biochemical and Molecular Medicine|August 1, 1996
Long-term and high-dose trials of enzyme replacement therapy in the canine model of mucopolysaccharidosis IE D Kakkis, M F McEntee, A Schmidtchen, et al.The New England Journal of Medicine|February 15, 2001
Enzyme-replacement therapy in mucopolysaccharidosis IE D Kakkis, J Muenzer, G E Tiller, et al.Molecular Genetics and Metabolism|March 13, 2001
Enzyme replacement therapy in feline mucopolysaccharidosis IE D Kakkis, E Schuchman, X He, et al.Pageof 1