Search research articles
Contact Us
Filters
Showing results (151-160 of 177) with videos related to
Page
of 18
Sort By:
The Journal of Clinical Investigation
|
June 1, 1988
Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis
S Brul, A Westerveld, A Strijland, et al.
Prenatal Diagnosis
|
September 1, 1985
The cerebro-hepato-renal (Zellweger) syndrome: prenatal detection based on impaired biosynthesis of plasmalogens
R B Schutgens, G Schrakamp, R J Wanders, et al.
Journal of the Neurological Sciences
|
April 1, 1988
Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's disease
R J Wanders, H S Heymans, R B Schutgens, et al.
Biochimica Et Biophysica Acta
|
July 26, 1985
The effect of detergents on immunoprecipitability of lysosomal sphingomyelinase
M Driessen, G Weitz, E M Brouwer-Kelder, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1987
Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disorders
R J Wanders, M J van Wijland, C W van Roermund, et al.
The Journal of Clinical Investigation
|
December 1, 1987
Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders
R J Wanders, C W van Roermund, M J van Wijland, et al.
European Journal of Biochemistry
|
April 1, 1987
Biosynthesis and maturation of glucocerebrosidase in Gaucher fibroblasts
L M Jonsson, G J Murray, S H Sorrell, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 30, 1986
Peroxisomal beta-oxidation of palmitoyl-CoA in human liver homogenates and its deficiency in the cerebro-hepato-renal (Zellweger) syndrome
R J Wanders, C W van Roermund, C T de Vries, et al.
European Journal of Biochemistry
|
August 17, 1990
Function of oligosaccharide modification in glucocerebrosidase, a membrane-associated lysosomal hydrolase
S Van Weely, J M Aerts, M B Van Leeuwen, et al.
Biochemical and Biophysical Research Communications
|
February 15, 1985
Peroxisomal beta-oxidation enzyme proteins in the Zellweger syndrome
J M Tager, W A Van der Beek, R J Wanders, et al.
Page
of 18
Search research articles
Search
Showing results (151-160 of 177) with videos related to
Sort By:
Page
of 18
The Journal of Clinical Investigation
|
June 1, 1988
Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis
S Brul, A Westerveld, A Strijland, et al.
Prenatal Diagnosis
|
September 1, 1985
The cerebro-hepato-renal (Zellweger) syndrome: prenatal detection based on impaired biosynthesis of plasmalogens
R B Schutgens, G Schrakamp, R J Wanders, et al.
Journal of the Neurological Sciences
|
April 1, 1988
Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's disease
R J Wanders, H S Heymans, R B Schutgens, et al.
Biochimica Et Biophysica Acta
|
July 26, 1985
The effect of detergents on immunoprecipitability of lysosomal sphingomyelinase
M Driessen, G Weitz, E M Brouwer-Kelder, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1987
Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disorders
R J Wanders, M J van Wijland, C W van Roermund, et al.
The Journal of Clinical Investigation
|
December 1, 1987
Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders
R J Wanders, C W van Roermund, M J van Wijland, et al.
European Journal of Biochemistry
|
April 1, 1987
Biosynthesis and maturation of glucocerebrosidase in Gaucher fibroblasts
L M Jonsson, G J Murray, S H Sorrell, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 30, 1986
Peroxisomal beta-oxidation of palmitoyl-CoA in human liver homogenates and its deficiency in the cerebro-hepato-renal (Zellweger) syndrome
R J Wanders, C W van Roermund, C T de Vries, et al.
European Journal of Biochemistry
|
August 17, 1990
Function of oligosaccharide modification in glucocerebrosidase, a membrane-associated lysosomal hydrolase
S Van Weely, J M Aerts, M B Van Leeuwen, et al.
Biochemical and Biophysical Research Communications
|
February 15, 1985
Peroxisomal beta-oxidation enzyme proteins in the Zellweger syndrome
J M Tager, W A Van der Beek, R J Wanders, et al.
Page
of 18