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E F Neufeld

Showing results (41-50 of 104) with videos related to

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Biochemical and Biophysical Research Communications|June 5, 1970
Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresisM Cantz, A Chrambach, E F Neufeld
Advances in Experimental Medicine and Biology|January 1, 1976
Iduronate sulfatase determination for the diagnosis of the Hunter syndrome and the detection of the carrier stateE F Neufeld, I Liebaers, T W Lim
Human Mutation|January 1, 1994
A mutant stop codon (TAG) in the IDUA gene is used as an acceptor splice site in a patient with Hurler syndrome (MPS IH)P T Tieu, K Menon, E F Neufeld
The Journal of Biological Chemistry|March 10, 1984
Association of alpha- and beta-subunits during the biosynthesis of beta-hexosaminidase in cultured human fibroblastsR L Proia, A d'Azzo, E F Neufeld
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1979
Direct demonstration of binding of a lysosomal enzyme, alpha-L-iduronidase, to receptors on cultured fibroblastsL H Rome, B Weissmann, E F Neufeld
The Journal of Pediatrics|March 1, 1977
Iduronate sulfatase in amniotic fluid: an aid in the prenatal diagnosis of the hunter syndromeI Liebaers, P Di Natale, E F Neufeld
Biochemical and Biophysical Research Communications|March 15, 1974
A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblastsS Hickman, L J Shapiro, E F Neufeld
Archives of Biochemistry and Biophysics|March 1, 1973
A -glucuronidase deficiency mucopolysaccharidosis: studies in cultured fibroblastsC W Hall, M Cantz, E F Neufeld
Human Mutation|January 1, 1993
Mutation in Scheie syndrome (MPS IS): a G-->A transition creates new splice site in intron 5 of one IDUA alleleS M Moskowitz, P T Tieu, E F Neufeld
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1989
Molecular basis of adult-onset and chronic GM2 gangliosidoses in patients of Ashkenazi Jewish origin: substitution of serine for glycine at position 269 of the alpha-subunit of beta-hexosaminidaseB H Paw, M M Kaback, E F Neufeld
Pageof 11

Showing results (41-50 of 104) with videos related to

Sort By:
Pageof 11
Biochemical and Biophysical Research Communications|June 5, 1970
Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresisM Cantz, A Chrambach, E F Neufeld
Advances in Experimental Medicine and Biology|January 1, 1976
Iduronate sulfatase determination for the diagnosis of the Hunter syndrome and the detection of the carrier stateE F Neufeld, I Liebaers, T W Lim
Human Mutation|January 1, 1994
A mutant stop codon (TAG) in the IDUA gene is used as an acceptor splice site in a patient with Hurler syndrome (MPS IH)P T Tieu, K Menon, E F Neufeld
The Journal of Biological Chemistry|March 10, 1984
Association of alpha- and beta-subunits during the biosynthesis of beta-hexosaminidase in cultured human fibroblastsR L Proia, A d'Azzo, E F Neufeld
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1979
Direct demonstration of binding of a lysosomal enzyme, alpha-L-iduronidase, to receptors on cultured fibroblastsL H Rome, B Weissmann, E F Neufeld
The Journal of Pediatrics|March 1, 1977
Iduronate sulfatase in amniotic fluid: an aid in the prenatal diagnosis of the hunter syndromeI Liebaers, P Di Natale, E F Neufeld
Biochemical and Biophysical Research Communications|March 15, 1974
A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblastsS Hickman, L J Shapiro, E F Neufeld
Archives of Biochemistry and Biophysics|March 1, 1973
A -glucuronidase deficiency mucopolysaccharidosis: studies in cultured fibroblastsC W Hall, M Cantz, E F Neufeld
Human Mutation|January 1, 1993
Mutation in Scheie syndrome (MPS IS): a G-->A transition creates new splice site in intron 5 of one IDUA alleleS M Moskowitz, P T Tieu, E F Neufeld
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1989
Molecular basis of adult-onset and chronic GM2 gangliosidoses in patients of Ashkenazi Jewish origin: substitution of serine for glycine at position 269 of the alpha-subunit of beta-hexosaminidaseB H Paw, M M Kaback, E F Neufeld
Pageof 11