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Progress in Clinical and Biological Research
|
January 1, 1992
Activation and oxidation of pristanic acid in rat liver: identification of a distinct, clofibrate non-inducible pristanoyl-CoA oxidase
R J Wanders, S Denis, C Jakobs, et al.
Biochimica Et Biophysica Acta
|
November 14, 1991
Peroxisomal enzyme activities in the human hepatoblastoma cell line HepG2 as compared to human liver
R J Wanders, C W van Roermund, M Griffioen, et al.
Archives of Disease in Childhood
|
November 26, 1997
Increased plasma malondialdehyde associated with cerebellar structural defects
V T Ramaekers, B Bosman, G A Jansen, et al.
Journal of Inherited Metabolic Disease
|
October 13, 1999
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: neonatal manifestation at the first day of life presenting with tachypnoea
C Thiel, S Baudach, U Schnackenberg, et al.
Biochimica Et Biophysica Acta
|
October 1, 1991
Oxidation of very-long-chain fatty acids in rat brain: cerotic acid is beta-oxidized exclusively in rat brain peroxisomes
W Lageweg, J E Sykes, M Lopes-Cardozo, et al.
Molecular and Cellular Endocrinology
|
February 13, 2001
Molecular basis of D-bifunctional protein deficiency
G Möller, E G van Grunsven, R J Wanders, et al.
Biochimica Et Biophysica Acta
|
December 8, 1994
Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein
L IJlst, R J Wanders, S Ushikubo, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Histochemistry of peroxisomal enzyme activities: a tool in the diagnosis of Zellweger syndrome
W M Frederiks, K S Bosch, M Ankum, et al.
Biochimica Et Biophysica Acta
|
December 14, 1995
Localization of peroxisomal 3-oxoacyl-CoA thiolase in particles of varied density in rat liver: implications for peroxisome biogenesis
C W van Roermund, M van den Berg, R J Wanders
Prenatal Diagnosis
|
November 1, 1988
Measurement of 3-hydroxy-3-methylglutaryl-CoA lyase activity in amniotic cells and in chorionic villi
V Barash, O Elpeleg, R Sheffer, et al.
Page
of 50
Search research articles
Search
Showing results (71-80 of 497) with videos related to
Sort By:
Page
of 50
Progress in Clinical and Biological Research
|
January 1, 1992
Activation and oxidation of pristanic acid in rat liver: identification of a distinct, clofibrate non-inducible pristanoyl-CoA oxidase
R J Wanders, S Denis, C Jakobs, et al.
Biochimica Et Biophysica Acta
|
November 14, 1991
Peroxisomal enzyme activities in the human hepatoblastoma cell line HepG2 as compared to human liver
R J Wanders, C W van Roermund, M Griffioen, et al.
Archives of Disease in Childhood
|
November 26, 1997
Increased plasma malondialdehyde associated with cerebellar structural defects
V T Ramaekers, B Bosman, G A Jansen, et al.
Journal of Inherited Metabolic Disease
|
October 13, 1999
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: neonatal manifestation at the first day of life presenting with tachypnoea
C Thiel, S Baudach, U Schnackenberg, et al.
Biochimica Et Biophysica Acta
|
October 1, 1991
Oxidation of very-long-chain fatty acids in rat brain: cerotic acid is beta-oxidized exclusively in rat brain peroxisomes
W Lageweg, J E Sykes, M Lopes-Cardozo, et al.
Molecular and Cellular Endocrinology
|
February 13, 2001
Molecular basis of D-bifunctional protein deficiency
G Möller, E G van Grunsven, R J Wanders, et al.
Biochimica Et Biophysica Acta
|
December 8, 1994
Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein
L IJlst, R J Wanders, S Ushikubo, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Histochemistry of peroxisomal enzyme activities: a tool in the diagnosis of Zellweger syndrome
W M Frederiks, K S Bosch, M Ankum, et al.
Biochimica Et Biophysica Acta
|
December 14, 1995
Localization of peroxisomal 3-oxoacyl-CoA thiolase in particles of varied density in rat liver: implications for peroxisome biogenesis
C W van Roermund, M van den Berg, R J Wanders
Prenatal Diagnosis
|
November 1, 1988
Measurement of 3-hydroxy-3-methylglutaryl-CoA lyase activity in amniotic cells and in chorionic villi
V Barash, O Elpeleg, R Sheffer, et al.
Page
of 50