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The American Journal of Pathology
|
November 1, 1982
Canine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I
R M Shull, R J Munger, E Spellacy, et al.
The American Journal of Pathology
|
March 1, 1984
Morphologic and biochemical studies of canine mucopolysaccharidosis I
R M Shull, R G Helman, E Spellacy, et al.
Methods in Enzymology
|
January 1, 1983
Studies of lysosomal enzyme biosynthesis in cultured cells
R Myerowitz, A R Robbins, R L Proia, 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 syndrome
R M Shull, E D Kakkis, M F McEntee, et al.
Pediatrics
|
January 1, 1976
The iduronidase-deficient mucopolysaccharidoses: clinical and roentgenorgraphic features
R E Stevenson, R R Howell, V A McKusick, et al.
American Journal of Human Genetics
|
April 1, 1986
Two abnormalities of hexosaminidase A in clinically normal individuals
E E Grebner, D A Mansfield, S S Raghavan, et al.
The Journal of Biological Chemistry
|
April 5, 1992
Cloning and characterization of cDNA encoding canine alpha-L-iduronidase. mRNA deficiency in mucopolysaccharidosis I dog
L J Stoltzfus, B Sosa-Pineda, S M Moskowitz, 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 I
E D Kakkis, M F McEntee, A Schmidtchen, et al.
The New England Journal of Medicine
|
February 15, 2001
Enzyme-replacement therapy in mucopolysaccharidosis I
E D Kakkis, J Muenzer, G E Tiller, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 10, 1999
Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding alpha-N-acetylglucosaminidase
H H Li, W H Yu, N Rozengurt, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 104) with videos related to
Sort By:
Page
of 11
The American Journal of Pathology
|
November 1, 1982
Canine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I
R M Shull, R J Munger, E Spellacy, et al.
The American Journal of Pathology
|
March 1, 1984
Morphologic and biochemical studies of canine mucopolysaccharidosis I
R M Shull, R G Helman, E Spellacy, et al.
Methods in Enzymology
|
January 1, 1983
Studies of lysosomal enzyme biosynthesis in cultured cells
R Myerowitz, A R Robbins, R L Proia, 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 syndrome
R M Shull, E D Kakkis, M F McEntee, et al.
Pediatrics
|
January 1, 1976
The iduronidase-deficient mucopolysaccharidoses: clinical and roentgenorgraphic features
R E Stevenson, R R Howell, V A McKusick, et al.
American Journal of Human Genetics
|
April 1, 1986
Two abnormalities of hexosaminidase A in clinically normal individuals
E E Grebner, D A Mansfield, S S Raghavan, et al.
The Journal of Biological Chemistry
|
April 5, 1992
Cloning and characterization of cDNA encoding canine alpha-L-iduronidase. mRNA deficiency in mucopolysaccharidosis I dog
L J Stoltzfus, B Sosa-Pineda, S M Moskowitz, 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 I
E D Kakkis, M F McEntee, A Schmidtchen, et al.
The New England Journal of Medicine
|
February 15, 2001
Enzyme-replacement therapy in mucopolysaccharidosis I
E D Kakkis, J Muenzer, G E Tiller, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 10, 1999
Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding alpha-N-acetylglucosaminidase
H H Li, W H Yu, N Rozengurt, et al.
Page
of 11