Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

R J Wanders

Showing results (71-80 of 497) with videos related to

Pageof 50
Sort By:
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 oxidaseR 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 liverR 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 defectsV 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 tachypnoeaC 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 peroxisomesW Lageweg, J E Sykes, M Lopes-Cardozo, et al.
Molecular and Cellular Endocrinology|February 13, 2001
Molecular basis of D-bifunctional protein deficiencyG 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 proteinL 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 syndromeW 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 biogenesisC 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 villiV Barash, O Elpeleg, R Sheffer, et al.
Pageof 50

Showing results (71-80 of 497) with videos related to

Sort By:
Pageof 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 oxidaseR 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 liverR 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 defectsV 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 tachypnoeaC 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 peroxisomesW Lageweg, J E Sykes, M Lopes-Cardozo, et al.
Molecular and Cellular Endocrinology|February 13, 2001
Molecular basis of D-bifunctional protein deficiencyG 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 proteinL 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 syndromeW 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 biogenesisC 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 villiV Barash, O Elpeleg, R Sheffer, et al.
Pageof 50