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Biochimica Et Biophysica Acta
|
October 13, 1992
A new, simple assay for long-chain acyl-CoA dehydrogenase in cultured skin fibroblasts using stable isotopes and GC-MS
K E Niezen-Koning, R J Wanders, G T Nagel, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis
R J Wanders, C W van Roermund, S Brul, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome
C W van Roermund, S Brul, J M Tager, et al.
Biochimica Et Biophysica Acta
|
July 20, 1990
Properties of the ATPase activity associated with peroxisome-enriched fractions from rat liver: comparison with mitochondrial F1F0-ATPase
E J Wolvetang, R J Wanders, R B Schutgens, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Prenatal diagnosis of systemic disorders of the respiratory chain in cultured chorionic villus fibroblasts by study of ATP-synthesis in digitonin-permeabilized cells
R J Wanders, J P Ruiter, F A Wijburg, et al.
European Journal of Pediatrics
|
April 1, 1993
Isolated defect of peroxisomal beta-oxidation in a 16-year-old patient
R Santer, A Claviez, H D Oldigs, et al.
Biochemical and Biophysical Research Communications
|
August 8, 1997
Resolution of the phytanic acid alpha-oxidation pathway: identification of pristanal as product of the decarboxylation of 2-hydroxyphytanoyl-CoA
N M Verhoeven, D S Schor, H J ten Brink, et al.
European Journal of Pediatrics
|
April 1, 1986
A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cells
R J Wanders, G Schrakamp, H van den Bosch, et al.
Neurology
|
January 5, 2002
Late onset white matter disease in peroxisome biogenesis disorder
P G Barth, J Gootjes, H Bode, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Rhizomelic chondrodysplasia punctata--a new clinical variant
R G Gray, A Green, S Chapman, et al.
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Search research articles
Search
Showing results (181-190 of 497) with videos related to
Sort By:
Page
of 50
Biochimica Et Biophysica Acta
|
October 13, 1992
A new, simple assay for long-chain acyl-CoA dehydrogenase in cultured skin fibroblasts using stable isotopes and GC-MS
K E Niezen-Koning, R J Wanders, G T Nagel, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis
R J Wanders, C W van Roermund, S Brul, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome
C W van Roermund, S Brul, J M Tager, et al.
Biochimica Et Biophysica Acta
|
July 20, 1990
Properties of the ATPase activity associated with peroxisome-enriched fractions from rat liver: comparison with mitochondrial F1F0-ATPase
E J Wolvetang, R J Wanders, R B Schutgens, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Prenatal diagnosis of systemic disorders of the respiratory chain in cultured chorionic villus fibroblasts by study of ATP-synthesis in digitonin-permeabilized cells
R J Wanders, J P Ruiter, F A Wijburg, et al.
European Journal of Pediatrics
|
April 1, 1993
Isolated defect of peroxisomal beta-oxidation in a 16-year-old patient
R Santer, A Claviez, H D Oldigs, et al.
Biochemical and Biophysical Research Communications
|
August 8, 1997
Resolution of the phytanic acid alpha-oxidation pathway: identification of pristanal as product of the decarboxylation of 2-hydroxyphytanoyl-CoA
N M Verhoeven, D S Schor, H J ten Brink, et al.
European Journal of Pediatrics
|
April 1, 1986
A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cells
R J Wanders, G Schrakamp, H van den Bosch, et al.
Neurology
|
January 5, 2002
Late onset white matter disease in peroxisome biogenesis disorder
P G Barth, J Gootjes, H Bode, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Rhizomelic chondrodysplasia punctata--a new clinical variant
R G Gray, A Green, S Chapman, et al.
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of 50