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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.Journal of Inherited Metabolic Disease|January 1, 1992
Animal models for lysosomal storage diseases: a new case of feline mucopolysaccharidosis VIP Di Natale, T Annella, A Daniele, et al.Clinical Genetics|April 19, 2003
Analysis of Sanfilippo A gene mutations in a large pedigreeP Di Natale, G R D Villani, C Di Domenico, et al.Human Gene Therapy|October 19, 2006
Limited transgene immune response and long-term expression of human alpha-L-iduronidase in young adult mice with mucopolysaccharidosis type I by liver-directed gene therapyC Di Domenico, D Di Napoli, E Gonzalez Y Reyero, et al.Molecular Genetics and Metabolism|January 4, 2001
Short-term enzyme replacement in the murine model of Sanfilippo syndrome type BW H Yu, K W Zhao, S Ryazantsev, et al.American Journal of Human Genetics|August 1, 1993
Molecular analysis of Hurler syndrome in Druze and Muslim Arab patients in Israel: multiple allelic mutations of the IDUA gene in a small geographic areaG Bach, S M Moskowitz, P T Tieu, et al.Proceedings of the National Academy of Sciences of the United States of America|June 11, 1996
The molecular basis of Sanfilippo syndrome type BH G Zhao, H H Li, G Bach, et al.Biochimie|April 2, 1998
Echistatin inhibits pp72syk and pp125FAK phosphorylation in fibrinogen-adherent plateletsN Staiano, R Della Morte, C Di Domenico, et al.Journal of Inherited Metabolic Disease|January 1, 1993
Biochemical diagnosis of mucopolysaccharidoses: experience of 297 diagnoses in a 15-year period (1977-1991)P Di Natale, T Annella, A Daniele, et al.American Journal of Human Genetics|September 1, 1977
X-linked Hunter syndrome: the heterozygous phenotype in cell cultureB R Migeon, J A Sprenkle, I Liebaers, et al.Pageof 12