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Biochimica Et Biophysica Acta
|
October 21, 1991
Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation group
E A Wiemer, M Out, A Schelen, et al.
Biochimica Et Biophysica Acta
|
August 8, 1989
Properties of acid ceramidase from human spleen
B J Al, C W Tiffany, D S Gomes de Mesquita, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1986
Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease
A W Schram, A Strijland, T Hashimoto, et al.
Journal of the Neurological Sciences
|
August 1, 1990
Infantile phytanic acid storage disease, a disorder of peroxisome biogenesis: a case report
R J Wanders, E Boltshauser, B Steinmann, et al.
European Journal of Biochemistry
|
March 15, 1984
Isolation and characterization of a precursor form of lysosomal alpha-glucosidase from human urine
R P Oude Elferink, E M Brouwer-Kelder, I Surya, et al.
The Journal of Clinical Investigation
|
March 1, 1993
Role of pH in determining the cell-type-specific residual activity of glucocerebrosidase in type 1 Gaucher disease
S van Weely, M van den Berg, J A Barranger, et al.
Ultrastructural Pathology
|
September 1, 1988
An immunoelectron microscopic study of glucocerebrosidase in type 1 Gaucher's disease spleen
R Willemsen, J M van Dongen, J M Aerts, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment
R B Schutgens, R J Wanders, H S Heymans, et al.
Experimental Cell Research
|
August 1, 1988
Characterization of glucocerebrosidase in peripheral blood cells and cultured blastoid cells
J M Aerts, J Heikoop, S van Weely, et al.
Biochimica Et Biophysica Acta
|
December 1, 1986
Comparison of the properties of a soluble form of glucocerebrosidase from human urine with those of the membrane-associated tissue enzyme
J M Aerts, W E Donker-Koopman, M Koot, et al.
Page
of 18
Search research articles
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Showing results (111-120 of 177) with videos related to
Sort By:
Page
of 18
Biochimica Et Biophysica Acta
|
October 21, 1991
Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation group
E A Wiemer, M Out, A Schelen, et al.
Biochimica Et Biophysica Acta
|
August 8, 1989
Properties of acid ceramidase from human spleen
B J Al, C W Tiffany, D S Gomes de Mesquita, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1986
Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease
A W Schram, A Strijland, T Hashimoto, et al.
Journal of the Neurological Sciences
|
August 1, 1990
Infantile phytanic acid storage disease, a disorder of peroxisome biogenesis: a case report
R J Wanders, E Boltshauser, B Steinmann, et al.
European Journal of Biochemistry
|
March 15, 1984
Isolation and characterization of a precursor form of lysosomal alpha-glucosidase from human urine
R P Oude Elferink, E M Brouwer-Kelder, I Surya, et al.
The Journal of Clinical Investigation
|
March 1, 1993
Role of pH in determining the cell-type-specific residual activity of glucocerebrosidase in type 1 Gaucher disease
S van Weely, M van den Berg, J A Barranger, et al.
Ultrastructural Pathology
|
September 1, 1988
An immunoelectron microscopic study of glucocerebrosidase in type 1 Gaucher's disease spleen
R Willemsen, J M van Dongen, J M Aerts, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment
R B Schutgens, R J Wanders, H S Heymans, et al.
Experimental Cell Research
|
August 1, 1988
Characterization of glucocerebrosidase in peripheral blood cells and cultured blastoid cells
J M Aerts, J Heikoop, S van Weely, et al.
Biochimica Et Biophysica Acta
|
December 1, 1986
Comparison of the properties of a soluble form of glucocerebrosidase from human urine with those of the membrane-associated tissue enzyme
J M Aerts, W E Donker-Koopman, M Koot, et al.
Page
of 18