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Enzyme
|
January 1, 1987
alpha-Glucosidase deficiency (Pompe's disease)
J M Tager, R P Oude Elferink, A Reuser, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 15, 1990
Human liver L-alanine-glyoxylate aminotransferase: characteristics and activity in controls and hyperoxaluria type I patients using a simple spectrophotometric method
R J Wanders, J Ruiter, C W van Roermund, et al.
The Journal of Biological Chemistry
|
February 25, 1991
Characterization of human glucocerebrosidase from different mutant alleles
T Ohashi, C M Hong, S Weiler, et al.
Journal of the Neurological Sciences
|
December 1, 1988
Peroxisomal disorders in neurology
R J Wanders, H S Heymans, R B Schutgens, et al.
Analytical Biochemistry
|
May 1, 1986
A procedure for the rapid purification in high yield of human glucocerebrosidase using immunoaffinity chromatography with monoclonal antibodies
J M Aerts, W E Donker-Koopman, G J Murray, et al.
Acta Biologica Et Medica Germanica
|
January 1, 1981
Control mechanisms of energy-dependent metabolic pathways in hepatocytes
J M Tager, R J Wanders, A K Groen, et al.
FEBS Letters
|
December 13, 1982
Biosynthesis of acid alpha-glucosidase in late-onset forms of glycogenosis type II (Pompe's disease)
F Steckel, V Gieselmann, A Waheed, et al.
Biochemical and Biophysical Research Communications
|
October 30, 1990
Identification of pristanoyl-CoA oxidase activity in human liver and its deficiency in the Zellweger syndrome
R J Wanders, H J ten Brink, C W van Roermund, et al.
Biochimica Et Biophysica Acta
|
October 18, 1990
Conditions affecting the activity of glucocerebrosidase purified from spleens of control subjects and patients with type 1 Gaucher disease
J M Aerts, M C Sa Miranda, E M Brouwer-Kelder, et al.
Biochemical and Biophysical Research Communications
|
July 15, 1988
Identification of L-pipecolate oxidase in human liver and its deficiency in the Zellweger syndrome
R J Wanders, G J Romeyn, C W van Roermund, et al.
Page
of 18
Search research articles
Search
Showing results (101-110 of 177) with videos related to
Sort By:
Page
of 18
Enzyme
|
January 1, 1987
alpha-Glucosidase deficiency (Pompe's disease)
J M Tager, R P Oude Elferink, A Reuser, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 15, 1990
Human liver L-alanine-glyoxylate aminotransferase: characteristics and activity in controls and hyperoxaluria type I patients using a simple spectrophotometric method
R J Wanders, J Ruiter, C W van Roermund, et al.
The Journal of Biological Chemistry
|
February 25, 1991
Characterization of human glucocerebrosidase from different mutant alleles
T Ohashi, C M Hong, S Weiler, et al.
Journal of the Neurological Sciences
|
December 1, 1988
Peroxisomal disorders in neurology
R J Wanders, H S Heymans, R B Schutgens, et al.
Analytical Biochemistry
|
May 1, 1986
A procedure for the rapid purification in high yield of human glucocerebrosidase using immunoaffinity chromatography with monoclonal antibodies
J M Aerts, W E Donker-Koopman, G J Murray, et al.
Acta Biologica Et Medica Germanica
|
January 1, 1981
Control mechanisms of energy-dependent metabolic pathways in hepatocytes
J M Tager, R J Wanders, A K Groen, et al.
FEBS Letters
|
December 13, 1982
Biosynthesis of acid alpha-glucosidase in late-onset forms of glycogenosis type II (Pompe's disease)
F Steckel, V Gieselmann, A Waheed, et al.
Biochemical and Biophysical Research Communications
|
October 30, 1990
Identification of pristanoyl-CoA oxidase activity in human liver and its deficiency in the Zellweger syndrome
R J Wanders, H J ten Brink, C W van Roermund, et al.
Biochimica Et Biophysica Acta
|
October 18, 1990
Conditions affecting the activity of glucocerebrosidase purified from spleens of control subjects and patients with type 1 Gaucher disease
J M Aerts, M C Sa Miranda, E M Brouwer-Kelder, et al.
Biochemical and Biophysical Research Communications
|
July 15, 1988
Identification of L-pipecolate oxidase in human liver and its deficiency in the Zellweger syndrome
R J Wanders, G J Romeyn, C W van Roermund, et al.
Page
of 18