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J P Ruiter

Showing results (11-20 of 17) with videos related to

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Biochemical and Biophysical Research Communications|February 13, 2001
Functional analysis of mutant human carnitine acylcarnitine translocases in yeastL IJlst, C W van Roermund, V Iacobazzi, et al.
Biochimica Et Biophysica Acta|March 24, 1993
Differentiation and proliferation of respiration-deficient human myoblastsN H Herzberg, R Zwart, R A Wolterman, et al.
Human Genetics|June 21, 2001
Molecular and functional characterisation of mild MCAD deficiencyJ Zschocke, A Schulze, M Lindner, et al.
Analytical Biochemistry|February 22, 2001
Synthesis and intramitochondrial levels of valproyl-coenzyme A metabolitesM F Silva, J P Ruiter, L IJlst, et al.
Pediatric Research|January 7, 2000
Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancyA M Innes, L E Seargeant, K Balachandra, et al.
European Journal of Pediatrics|December 10, 1997
Succinyl-CoA:acetoacetate transferase deficiency: identification of a new patient with a neonatal onset and review of the literatureK E Niezen-Koning, R J Wanders, J P Ruiter, et al.
American Journal of Human Genetics|October 3, 2000
Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolismB S Andresen, E Christensen, T J Corydon, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Biochemical and Biophysical Research Communications|February 13, 2001
Functional analysis of mutant human carnitine acylcarnitine translocases in yeastL IJlst, C W van Roermund, V Iacobazzi, et al.
Biochimica Et Biophysica Acta|March 24, 1993
Differentiation and proliferation of respiration-deficient human myoblastsN H Herzberg, R Zwart, R A Wolterman, et al.
Human Genetics|June 21, 2001
Molecular and functional characterisation of mild MCAD deficiencyJ Zschocke, A Schulze, M Lindner, et al.
Analytical Biochemistry|February 22, 2001
Synthesis and intramitochondrial levels of valproyl-coenzyme A metabolitesM F Silva, J P Ruiter, L IJlst, et al.
Pediatric Research|January 7, 2000
Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancyA M Innes, L E Seargeant, K Balachandra, et al.
European Journal of Pediatrics|December 10, 1997
Succinyl-CoA:acetoacetate transferase deficiency: identification of a new patient with a neonatal onset and review of the literatureK E Niezen-Koning, R J Wanders, J P Ruiter, et al.
American Journal of Human Genetics|October 3, 2000
Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolismB S Andresen, E Christensen, T J Corydon, et al.
Pageof 2