Search research articles
Contact Us
Filters
Showing results (1-10 of 51) with videos related to
Page
of 6
Sort By:
Annals of Medicine
|
April 30, 1998
Animal model for fragile X syndrome
B A Oostra, A T Hoogeveen
Journal of Inherited Metabolic Disease
|
June 1, 1997
The fragile X syndrome
A T Hoogeveen, B A Oostra
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 Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
September 1, 1985
A fluorescence staining method for the demonstration and measurement of lysosomal enzyme activities in single cells
G P Luyten, A T Hoogeveen, H Galjaard
Biochemical and Biophysical Research Communications
|
March 16, 1990
Lysosomal tartrate sensitive acid phosphatase deficiency in cells which contain lysosomal "high uptake forms"
P Hu, G Parenti, J Keulemans, et al.
The Journal of Biological Chemistry
|
May 5, 1986
GM1-gangliosidosis. Defective recognition site on beta-galactosidase precursor
A T Hoogeveen, A J Reuser, M Kroos, et al.
Nature
|
June 12, 1980
Genetic heterogeneity in human neuraminidase deficiency
A T Hoogeveen, F W Verheijen, A d'Azzo, et al.
The Journal of Biological Chemistry
|
February 10, 1984
Processing of human beta-galactosidase in GM1-gangliosidosis and Morquio B syndrome
A T Hoogeveen, H Graham-Kawashima, 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.
Page
of 6
Search research articles
Search
Showing results (1-10 of 51) with videos related to
Sort By:
Page
of 6
Annals of Medicine
|
April 30, 1998
Animal model for fragile X syndrome
B A Oostra, A T Hoogeveen
Journal of Inherited Metabolic Disease
|
June 1, 1997
The fragile X syndrome
A T Hoogeveen, B A Oostra
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 Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
September 1, 1985
A fluorescence staining method for the demonstration and measurement of lysosomal enzyme activities in single cells
G P Luyten, A T Hoogeveen, H Galjaard
Biochemical and Biophysical Research Communications
|
March 16, 1990
Lysosomal tartrate sensitive acid phosphatase deficiency in cells which contain lysosomal "high uptake forms"
P Hu, G Parenti, J Keulemans, et al.
The Journal of Biological Chemistry
|
May 5, 1986
GM1-gangliosidosis. Defective recognition site on beta-galactosidase precursor
A T Hoogeveen, A J Reuser, M Kroos, et al.
Nature
|
June 12, 1980
Genetic heterogeneity in human neuraminidase deficiency
A T Hoogeveen, F W Verheijen, A d'Azzo, et al.
The Journal of Biological Chemistry
|
February 10, 1984
Processing of human beta-galactosidase in GM1-gangliosidosis and Morquio B syndrome
A T Hoogeveen, H Graham-Kawashima, 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.
Page
of 6