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Showing results (271-280 of 417) with videos related to

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International Journal of Cancer|May 14, 1998
Functional retinoid and thyroid hormone receptors in human thyroid-carcinoma cell lines and tissuesC schmutzler, J Brtko, R Winzer, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Valproate inhibits the mitochondrial pyruvate-driven oxidative phosphorylation in vitroM F Silva, J P Ruiter, L Illst, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Molecular basis of Refsum disease: identification of new mutations in the phytanoyl-CoA hydroxylase cDNAG A Jansen, S Ferdinandusse, O H Skjeldal, et al.
European Journal of Pediatrics|April 1, 1986
Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus materialE A Kvittingen, P P Guibaud, P Divry, et al.
Molecular Genetics and Metabolism|April 4, 2006
High cerebral guanidinoacetate and variable creatine concentrations in argininosuccinate synthetase and lyase deficiency: implications for treatment?F J van Spronsen, D J Reijngoud, N M Verhoeven, et al.
Fertility and Sterility|December 16, 1998
Randomized, double-blind, placebo-controlled study of the effects of raloxifene and conjugated equine estrogen on plasma homocysteine levels in healthy postmenopausal womenV Mijatovic, C Netelenbos, M J van der Mooren, et al.
Biochimica Et Biophysica Acta|October 16, 1999
Phytanic acid alpha-oxidation: identification of 2-hydroxyphytanoyl-CoA lyase in rat liver and its localisation in peroxisomesG A Jansen, N M Verhoeven, S Denis, et al.
Journal of Medical Genetics|July 13, 2002
Breakpoint analysis of a familial balanced translocation t(2;8)(q31;p21) associated with mesomelic dysplasiaH Sugawara, M Egashira, N Harada, et al.
The Netherlands Journal of Medicine|April 29, 1998
The effect of renal transplantation on hyperhomocysteinaemia in dialysis patients, and the estimation of renal homocysteine extraction in patients with normal renal functionC van Guldener, M J Janssen, C D Stehouwer, et al.
Journal of Inherited Metabolic Disease|February 24, 2001
Plasma creatinine assessment in creatine deficiency: A diagnostic pitfallN M Verhoeven, W S Guérand, E A Struys, et al.
Pageof 42

Showing results (271-280 of 417) with videos related to

Sort By:
Pageof 42
International Journal of Cancer|May 14, 1998
Functional retinoid and thyroid hormone receptors in human thyroid-carcinoma cell lines and tissuesC schmutzler, J Brtko, R Winzer, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Valproate inhibits the mitochondrial pyruvate-driven oxidative phosphorylation in vitroM F Silva, J P Ruiter, L Illst, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Molecular basis of Refsum disease: identification of new mutations in the phytanoyl-CoA hydroxylase cDNAG A Jansen, S Ferdinandusse, O H Skjeldal, et al.
European Journal of Pediatrics|April 1, 1986
Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus materialE A Kvittingen, P P Guibaud, P Divry, et al.
Molecular Genetics and Metabolism|April 4, 2006
High cerebral guanidinoacetate and variable creatine concentrations in argininosuccinate synthetase and lyase deficiency: implications for treatment?F J van Spronsen, D J Reijngoud, N M Verhoeven, et al.
Fertility and Sterility|December 16, 1998
Randomized, double-blind, placebo-controlled study of the effects of raloxifene and conjugated equine estrogen on plasma homocysteine levels in healthy postmenopausal womenV Mijatovic, C Netelenbos, M J van der Mooren, et al.
Biochimica Et Biophysica Acta|October 16, 1999
Phytanic acid alpha-oxidation: identification of 2-hydroxyphytanoyl-CoA lyase in rat liver and its localisation in peroxisomesG A Jansen, N M Verhoeven, S Denis, et al.
Journal of Medical Genetics|July 13, 2002
Breakpoint analysis of a familial balanced translocation t(2;8)(q31;p21) associated with mesomelic dysplasiaH Sugawara, M Egashira, N Harada, et al.
The Netherlands Journal of Medicine|April 29, 1998
The effect of renal transplantation on hyperhomocysteinaemia in dialysis patients, and the estimation of renal homocysteine extraction in patients with normal renal functionC van Guldener, M J Janssen, C D Stehouwer, et al.
Journal of Inherited Metabolic Disease|February 24, 2001
Plasma creatinine assessment in creatine deficiency: A diagnostic pitfallN M Verhoeven, W S Guérand, E A Struys, et al.
Pageof 42