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European Journal of Biochemistry
|
March 16, 1987
Relationship between the two immunologically distinguishable forms of glucocerebrosidase in tissue extracts
J M Aerts, W E Donker-Koopman, C van Laar, et al.
Experimental Cell Research
|
May 1, 1987
Peroxisomes and peroxisomal functions in muscle. Studies with muscle cells from controls and a patient with the cerebro-hepato-renal (Zellweger) syndrome
R J Wanders, P G Barth, C W van Roermund, et al.
European Journal of Pediatrics
|
August 1, 1986
Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal beta-oxidation enzyme proteins
R J Wanders, R B Schutgens, G Schrakamp, et al.
Biochemical and Biophysical Research Communications
|
May 16, 1988
Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disorders
S Brul, E A Wiemer, A Westerveld, et al.
European Journal of Biochemistry
|
August 15, 1983
Monoclonal antibodies against human beta-glucocerebrosidase
R A Barneveld, F P Tegelaers, E I Ginns, et al.
Biochemical and Biophysical Research Communications
|
September 28, 1984
Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome
R J Wanders, M Kos, B Roest, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1987
Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome
R J Wanders, C W van Roermund, R Westra, et al.
Neurology
|
October 1, 1981
A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studies
M C Loonen, H F Busch, J F Koster, et al.
Clinical Genetics
|
January 1, 1981
Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency)
M C Loonen, A W Schram, J F Koster, et al.
Biochimica Et Biophysica Acta
|
March 17, 1988
Glucocerebrosidase, a lysosomal enzyme that does not undergo oligosaccharide phosphorylation
J M Aerts, A W Schram, A Strijland, et al.
Page
of 18
Search research articles
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Showing results (161-170 of 177) with videos related to
Sort By:
Page
of 18
European Journal of Biochemistry
|
March 16, 1987
Relationship between the two immunologically distinguishable forms of glucocerebrosidase in tissue extracts
J M Aerts, W E Donker-Koopman, C van Laar, et al.
Experimental Cell Research
|
May 1, 1987
Peroxisomes and peroxisomal functions in muscle. Studies with muscle cells from controls and a patient with the cerebro-hepato-renal (Zellweger) syndrome
R J Wanders, P G Barth, C W van Roermund, et al.
European Journal of Pediatrics
|
August 1, 1986
Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal beta-oxidation enzyme proteins
R J Wanders, R B Schutgens, G Schrakamp, et al.
Biochemical and Biophysical Research Communications
|
May 16, 1988
Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disorders
S Brul, E A Wiemer, A Westerveld, et al.
European Journal of Biochemistry
|
August 15, 1983
Monoclonal antibodies against human beta-glucocerebrosidase
R A Barneveld, F P Tegelaers, E I Ginns, et al.
Biochemical and Biophysical Research Communications
|
September 28, 1984
Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome
R J Wanders, M Kos, B Roest, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1987
Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome
R J Wanders, C W van Roermund, R Westra, et al.
Neurology
|
October 1, 1981
A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studies
M C Loonen, H F Busch, J F Koster, et al.
Clinical Genetics
|
January 1, 1981
Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency)
M C Loonen, A W Schram, J F Koster, et al.
Biochimica Et Biophysica Acta
|
March 17, 1988
Glucocerebrosidase, a lysosomal enzyme that does not undergo oligosaccharide phosphorylation
J M Aerts, A W Schram, A Strijland, et al.
Page
of 18