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R J Wanders

Showing results (381-390 of 497) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1996
Organic acid profiles resembling a beta-oxidation defect in two patients with coeliac diseaseC G Costa, N M Verhoeven, C M Kneepkens, et al.
Lancet (London, England)|July 1, 1989
Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenaseR J Wanders, M Duran, L Ijlst, et al.
Molecular and Cellular Biology|June 25, 1998
PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12pK Okumoto, N Shimozawa, A Kawai, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidationR J Wanders, L IJlst, A H van Gennip, et al.
Journal of Medical Genetics|October 21, 1999
Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disordersN Shimozawa, A Imamura, Z Zhang, et al.
FEBS Letters|January 10, 1983
Control of mitochondrial respirationJ M Tager, R J Wanders, A K Groen, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
The inborn errors of peroxisomal beta-oxidation: a reviewR J Wanders, C W van Roermund, R B Schutgens, et al.
Human Molecular Genetics|March 11, 1999
Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiencyN L Tang, V Ganapathy, X Wu, et al.
The Journal of Pediatrics|October 1, 1994
A new type of peroxisomal disorder with variable expression in liver and fibroblastsH Mandel, M Espeel, F Roels, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Di- and trihydroxycholestanaemia in twin sistersR J Wanders, C W van Roermund, A Schelen, et al.
Pageof 50

Showing results (381-390 of 497) with videos related to

Sort By:
Pageof 50
Journal of Inherited Metabolic Disease|January 1, 1996
Organic acid profiles resembling a beta-oxidation defect in two patients with coeliac diseaseC G Costa, N M Verhoeven, C M Kneepkens, et al.
Lancet (London, England)|July 1, 1989
Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenaseR J Wanders, M Duran, L Ijlst, et al.
Molecular and Cellular Biology|June 25, 1998
PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12pK Okumoto, N Shimozawa, A Kawai, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidationR J Wanders, L IJlst, A H van Gennip, et al.
Journal of Medical Genetics|October 21, 1999
Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disordersN Shimozawa, A Imamura, Z Zhang, et al.
FEBS Letters|January 10, 1983
Control of mitochondrial respirationJ M Tager, R J Wanders, A K Groen, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
The inborn errors of peroxisomal beta-oxidation: a reviewR J Wanders, C W van Roermund, R B Schutgens, et al.
Human Molecular Genetics|March 11, 1999
Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiencyN L Tang, V Ganapathy, X Wu, et al.
The Journal of Pediatrics|October 1, 1994
A new type of peroxisomal disorder with variable expression in liver and fibroblastsH Mandel, M Espeel, F Roels, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Di- and trihydroxycholestanaemia in twin sistersR J Wanders, C W van Roermund, A Schelen, et al.
Pageof 50