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Journal of Lipid Research
|
November 30, 1998
Sensitive analysis of serum 3alpha, 7alpha, 12alpha,24-tetrahydroxy- 5beta-cholestan-26-oic acid diastereomers using gas chromatography-mass spectrometry and its application in peroxisomal D-bifunctional protein deficiency
P Vreken, A van Rooij, S Denis, et al.
Biochimica Et Biophysica Acta
|
December 5, 1986
Acyl-CoA:dihydroxyacetone phosphate acyltransferase in human skin fibroblasts: study of its properties using a new assay method
R B Schutgens, G J Romeyn, R Ofman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 15, 1985
Deficiency of acyl-CoA:dihydroxyacetone phosphate acyltransferase in thrombocytes of Zellweger patients: a simple postnatal diagnostic test
R J Wanders, G van Weringh, G Schrakamp, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Respiratory chain function in Leber's hereditary optic neuropathy: lack of correlation with clinical disease
J C Cornelissen, R J Wanders, P A Bolhuis, et al.
Biochemical and Biophysical Research Communications
|
April 16, 1984
Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome
R B Schutgens, G J Romeyn, R J Wanders, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
First prenatal diagnosis of acyl-CoA oxidase deficiency
R J Wanders, A Schelen, N Feller, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype
L Ijlst, S Uskikubo, T Kamijo, et al.
Journal of Lipid Research
|
March 1, 1988
Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursors
G Schrakamp, C G Schalkwijk, R B Schutgens, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Prenatal and perinatal diagnosis of peroxisomal disorders
R B Schutgens, G Schrakamp, R J Wanders, et al.
Archives of Biochemistry and Biophysics
|
August 15, 1987
On the origin of the limited control of mitochondrial respiration by the adenine nucleotide translocator
H V Westerhoff, P J Plomp, A K Groen, et al.
Page
of 50
Search research articles
Search
Showing results (251-260 of 497) with videos related to
Sort By:
Page
of 50
Journal of Lipid Research
|
November 30, 1998
Sensitive analysis of serum 3alpha, 7alpha, 12alpha,24-tetrahydroxy- 5beta-cholestan-26-oic acid diastereomers using gas chromatography-mass spectrometry and its application in peroxisomal D-bifunctional protein deficiency
P Vreken, A van Rooij, S Denis, et al.
Biochimica Et Biophysica Acta
|
December 5, 1986
Acyl-CoA:dihydroxyacetone phosphate acyltransferase in human skin fibroblasts: study of its properties using a new assay method
R B Schutgens, G J Romeyn, R Ofman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 15, 1985
Deficiency of acyl-CoA:dihydroxyacetone phosphate acyltransferase in thrombocytes of Zellweger patients: a simple postnatal diagnostic test
R J Wanders, G van Weringh, G Schrakamp, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Respiratory chain function in Leber's hereditary optic neuropathy: lack of correlation with clinical disease
J C Cornelissen, R J Wanders, P A Bolhuis, et al.
Biochemical and Biophysical Research Communications
|
April 16, 1984
Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome
R B Schutgens, G J Romeyn, R J Wanders, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
First prenatal diagnosis of acyl-CoA oxidase deficiency
R J Wanders, A Schelen, N Feller, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype
L Ijlst, S Uskikubo, T Kamijo, et al.
Journal of Lipid Research
|
March 1, 1988
Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursors
G Schrakamp, C G Schalkwijk, R B Schutgens, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Prenatal and perinatal diagnosis of peroxisomal disorders
R B Schutgens, G Schrakamp, R J Wanders, et al.
Archives of Biochemistry and Biophysics
|
August 15, 1987
On the origin of the limited control of mitochondrial respiration by the adenine nucleotide translocator
H V Westerhoff, P J Plomp, A K Groen, et al.
Page
of 50