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Biochemical and Biophysical Research Communications
|
June 5, 1970
Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresis
M 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 state
E 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 fibroblasts
R 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 fibroblasts
L 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 syndrome
I 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 fibroblasts
S Hickman, L J Shapiro, E F Neufeld
Archives of Biochemistry and Biophysics
|
March 1, 1973
A -glucuronidase deficiency mucopolysaccharidosis: studies in cultured fibroblasts
C 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 allele
S 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-hexosaminidase
B H Paw, M M Kaback, E F Neufeld
Page
of 11
Search research articles
Search
Showing results (41-50 of 104) with videos related to
Sort By:
Page
of 11
Biochemical and Biophysical Research Communications
|
June 5, 1970
Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresis
M 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 state
E 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 fibroblasts
R 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 fibroblasts
L 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 syndrome
I 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 fibroblasts
S Hickman, L J Shapiro, E F Neufeld
Archives of Biochemistry and Biophysics
|
March 1, 1973
A -glucuronidase deficiency mucopolysaccharidosis: studies in cultured fibroblasts
C 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 allele
S 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-hexosaminidase
B H Paw, M M Kaback, E F Neufeld
Page
of 11