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E F Neufeld

Showing results (61-70 of 104) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 1, 1973
The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfataseG Bach, F Eisenberg, M Cantz, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1983
A canine model of human alpha-L-iduronidase deficiencyE Spellacy, R M Shull, G Constantopoulos, et al.
The Journal of Biological Chemistry|October 15, 1990
Two mutations produce intron insertion in mRNA and elongated beta-subunit of human beta-hexosaminidaseB Dlott, A d'Azzo, D V Quon, et al.
Journal of Neurochemistry|October 1, 1985
Neurochemical characterization of canine alpha-L-iduronidase deficiency disease (model of human mucopolysaccharidosis I)G Constantopoulos, R M Shull, N Hastings, et al.
Birth Defects Original Article Series|January 1, 1975
Biochemical studies in mucolipidoses II and IIIL J Shapiro, S Hickman, C W Hall, et al.
Methods in Enzymology|January 1, 1978
Enzymic diagnosis of the genetic mucopolysaccharide storage disordersC W Hall, I Liebaers, P Di Natale, et al.
Carbohydrate Research|October 1, 1974
An assay for iduronate sulfatase (Hunter corrective factor)T W Lim, I G Leder, G Bach, et al.
American Journal of Human Genetics|June 1, 1987
A shortened beta-hexosaminidase alpha-chain in an Italian patient with infantile Tay-Sachs diseaseG Zokaeem, J Bayleran, P Kaplan, et al.
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.
Human Mutation|January 1, 1995
Four novel mutations underlying mild or intermediate forms of alpha-L-iduronidase deficiency (MPS IS and MPS IH/S)P T Tieu, G Bach, A Matynia, et al.
Pageof 11

Showing results (61-70 of 104) with videos related to

Sort By:
Pageof 11
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1973
The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfataseG Bach, F Eisenberg, M Cantz, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1983
A canine model of human alpha-L-iduronidase deficiencyE Spellacy, R M Shull, G Constantopoulos, et al.
The Journal of Biological Chemistry|October 15, 1990
Two mutations produce intron insertion in mRNA and elongated beta-subunit of human beta-hexosaminidaseB Dlott, A d'Azzo, D V Quon, et al.
Journal of Neurochemistry|October 1, 1985
Neurochemical characterization of canine alpha-L-iduronidase deficiency disease (model of human mucopolysaccharidosis I)G Constantopoulos, R M Shull, N Hastings, et al.
Birth Defects Original Article Series|January 1, 1975
Biochemical studies in mucolipidoses II and IIIL J Shapiro, S Hickman, C W Hall, et al.
Methods in Enzymology|January 1, 1978
Enzymic diagnosis of the genetic mucopolysaccharide storage disordersC W Hall, I Liebaers, P Di Natale, et al.
Carbohydrate Research|October 1, 1974
An assay for iduronate sulfatase (Hunter corrective factor)T W Lim, I G Leder, G Bach, et al.
American Journal of Human Genetics|June 1, 1987
A shortened beta-hexosaminidase alpha-chain in an Italian patient with infantile Tay-Sachs diseaseG Zokaeem, J Bayleran, P Kaplan, et al.
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.
Human Mutation|January 1, 1995
Four novel mutations underlying mild or intermediate forms of alpha-L-iduronidase deficiency (MPS IS and MPS IH/S)P T Tieu, G Bach, A Matynia, et al.
Pageof 11