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European Journal of Biochemistry
|
January 2, 1987
Purification and partial characterization of lysosomal neuraminidase from human placenta
F W Verheijen, S Palmeri, H Galjaard
Human Genetics
|
July 1, 1986
Free N-acetylneuraminic acid (NANA) storage disorders: evidence for defective NANA transport across the lysosomal membrane
G M Mancini, F W Verheijen, H Galjaard
The Journal of Biological Chemistry
|
October 25, 1983
The relation between human lysosomal beta-galactosidase and its protective protein
A T Hoogeveen, F W Verheijen, H Galjaard
The Journal of Biological Chemistry
|
July 25, 1990
Glucose transport in lysosomal membrane vesicles. Kinetic demonstration of a carrier for neutral hexoses
G M Mancini, C E Beerens, F W Verheijen
Journal of Inherited Metabolic Disease
|
June 23, 2000
Lysosomal transport disorders
G M Mancini, A C Havelaar, F W Verheijen
Nature
|
June 12, 1980
Genetic heterogeneity in human neuraminidase deficiency
A T Hoogeveen, F W Verheijen, A d'Azzo, et al.
American Journal of Human Genetics
|
February 1, 1986
Galactosialidosis: molecular heterogeneity among distinct clinical phenotypes
S Palmeri, A T Hoogeveen, F W Verheijen, et al.
European Journal of Biochemistry
|
June 3, 1985
Human placental neuraminidase. Activation, stabilization and association with beta-galactosidase and its protective protein
F W Verheijen, S Palmeri, A T Hoogeveen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 15, 1992
Functional reconstitution of the lysosomal sialic acid carrier into proteoliposomes
G M Mancini, C E Beerens, H Galjaard, et al.
Annals of Human Genetics
|
May 1, 1981
Complementation analysis of human sialidase deficiency using natural substrates
D M Swallow, A T Hoogeveen, F W Verheijen, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 36) with videos related to
Sort By:
Page
of 4
European Journal of Biochemistry
|
January 2, 1987
Purification and partial characterization of lysosomal neuraminidase from human placenta
F W Verheijen, S Palmeri, H Galjaard
Human Genetics
|
July 1, 1986
Free N-acetylneuraminic acid (NANA) storage disorders: evidence for defective NANA transport across the lysosomal membrane
G M Mancini, F W Verheijen, H Galjaard
The Journal of Biological Chemistry
|
October 25, 1983
The relation between human lysosomal beta-galactosidase and its protective protein
A T Hoogeveen, F W Verheijen, H Galjaard
The Journal of Biological Chemistry
|
July 25, 1990
Glucose transport in lysosomal membrane vesicles. Kinetic demonstration of a carrier for neutral hexoses
G M Mancini, C E Beerens, F W Verheijen
Journal of Inherited Metabolic Disease
|
June 23, 2000
Lysosomal transport disorders
G M Mancini, A C Havelaar, F W Verheijen
Nature
|
June 12, 1980
Genetic heterogeneity in human neuraminidase deficiency
A T Hoogeveen, F W Verheijen, A d'Azzo, et al.
American Journal of Human Genetics
|
February 1, 1986
Galactosialidosis: molecular heterogeneity among distinct clinical phenotypes
S Palmeri, A T Hoogeveen, F W Verheijen, et al.
European Journal of Biochemistry
|
June 3, 1985
Human placental neuraminidase. Activation, stabilization and association with beta-galactosidase and its protective protein
F W Verheijen, S Palmeri, A T Hoogeveen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 15, 1992
Functional reconstitution of the lysosomal sialic acid carrier into proteoliposomes
G M Mancini, C E Beerens, H Galjaard, et al.
Annals of Human Genetics
|
May 1, 1981
Complementation analysis of human sialidase deficiency using natural substrates
D M Swallow, A T Hoogeveen, F W Verheijen, et al.
Page
of 4