(Q57199604)

5

object named as

Ronald J. A. Wanders

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author name string

Nadia A. Oey

1

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Jos P. N. Ruiter

2

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Lodewijk IJlst

4

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Frits A. Wijburg

Journal of Inherited Metabolic Disease

6

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publication date

February 2006

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published in

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volume

29

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issue

1

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page(s)

71-75

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exact match

https://scigraph.springernature.com/pub.10.1007/s10545-006-0199-x

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cites work

Tissue specific and developmental expression of rat long-and medium-chain acyl-CoA dehydrogenases.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10545-006-0199-X

Evidence that the sensitivity of carnitine palmitoyltransferase I to inhibition by malonyl-CoA is an important site of regulation of hepatic fatty acid oxidation in the fetal and newborn rabbit. Perinatal development and effects of pancreatic hormon

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10545-006-0199-X

Human placenta metabolizes fatty acids: implications for fetal fatty acid oxidation disorders and maternal liver diseases

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10545-006-0199-X

IUGR alters postnatal rat skeletal muscle peroxisome proliferator-activated receptor-gamma coactivator-1 gene expression in a fiber specific manner.

21 January 2018

1 reference

12 December 2020

Myocardial gene expression of glucose transporter 1 and glucose transporter 4 in response to uteroplacental insufficiency in the rat.

1 reference

12 December 2020

Control of mitochondrial beta-oxidation flux

1 reference

12 December 2020

PPAR gamma is required for placental, cardiac, and adipose tissue development

1 reference

12 December 2020

Mitochondrial trifunctional protein deficiency: a severe fatty acid oxidation disorder with cardiac and neurologic involvement

1 reference

12 December 2020

Evidence for fatty acid oxidation in human placenta, and the relationship of fatty acid oxidation enzyme activities with gestational age

1 reference

12 December 2020

Cyclo-oxygenase-2-derived prostacyclin mediates embryo implantation in the mouse via PPARdelta

1 reference

12 December 2020

Intrauterine growth retardation leads to the development of type 2 diabetes in the rat.

1 reference

12 December 2020

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients

1 reference

12 December 2020

Mitochondrial fatty acid beta-oxidation in the human eye and brain: implications for the retinopathy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

1 reference

12 December 2020

Phosphorylation of rat liver mitochondrial carnitine palmitoyltransferase-I: effect on the kinetic properties of the enzyme

1 reference

12 December 2020

High activity of fatty acid oxidation enzymes in human placenta: implications for fetal-maternal disease

1 reference

12 December 2020

Long-Chain Fatty Acid Oxidation during Early Human Development

1 reference

12 December 2020

Perinatal changes in myocardial metabolism in lambs

1 reference

12 December 2020

Living with the past: evolution, development, and patterns of disease

1 reference

12 December 2020

Effects of peroxisome proliferator-activated receptor delta on placentation, adiposity, and colorectal cancer

1 reference

12 December 2020

Disorders of mitochondrial fatty acyl-CoA beta-oxidation

1 reference

12 December 2020

Complete deficiency of mitochondrial trifunctional protein due to a novel mutation within the beta-subunit of the mitochondrial trifunctional protein gene leads to failure of long-chain fatty acid beta-oxidation with fatal outcome

1 reference

12 December 2020

Characterization of carnitine and fatty acid metabolism in the long-chain acyl-CoA dehydrogenase-deficient mouse

1 reference

12 December 2020

Disrupted blastocoele formation reveals a critical developmental role for long-chain acyl-CoA dehydrogenase.

1 reference

12 December 2020

Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death

1 reference

12 December 2020

Thinness at birth and insulin resistance in adult life.

1 reference

12 December 2020

Fetal genotypes and pregnancy outcomes in 35 families with mitochondrial trifunctional protein mutations

1 reference

12 December 2020

dif-1 and colt, both implicated in early embryonic development, encode carnitine acylcarnitine translocase.

1 reference

12 December 2020

Trifunctional protein deficiency: three families with significant maternal hepatic dysfunction in pregnancy not associated with E474Q mutation

1 reference

12 December 2020

Molecular basis of hepatic carnitine palmitoyltransferase I deficiency

1 reference

12 December 2020

Carnitine deficiency with cardiomyopathy presenting as neonatal hydrops: successful response to carnitine therapy.

1 reference

12 December 2020

Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation

1 reference

12 December 2020

Fetal and infant growth and impaired glucose tolerance at age 64.

1 reference

12 December 2020