Human placenta metabolizes fatty acids: implications for fetal fatty acid oxidation disorders and maternal liver diseases (Q44312288)

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title

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

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Prem Shekhawat

1

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Michael J Bennett

2

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Yoel Sadovsky

3

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D Michael Nelson

4

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Dinesh Rakheja

5

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Arnold W Strauss

6

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publication date

11 February 2003

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American Journal of Physiology - Endocrinology and Metabolism

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published in

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volume

284

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issue

6

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page(s)

E1098-105

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Mitochondrial short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: a new defect of fatty acid oxidation.

1 December 2017

cites work

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https://api.crossref.org/works/10.1152%2FAJPENDO.00481.2002

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Plasma membrane fatty-acid-binding protein in human placenta: identification and characterization

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

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Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndrome.

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A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women

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

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Molecular prenatal diagnosis in families with fetal mitochondrial trifunctional protein mutations.

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Glucose transporters in the human placenta

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Lipoprotein metabolism in pregnancy, fat transport to the fetus, and the effects of diabetes

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Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation

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Reduced food intake and body weight in mice treated with fatty acid synthase inhibitors

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Complementation analysis of fatty acid oxidation disorders

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Hypoxia limits differentiation and up-regulates expression and activity of prostaglandin H synthase 2 in cultured trophoblast from term human placenta

21 January 2018

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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

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Metabolic disease in the fetus predisposes to maternal hepatic complications of pregnancy

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Effect of Reye's syndrome serum on isolated chinchilla liver mitochondria

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Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of thirteen patients.

21 January 2018

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

21 January 2018

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Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency

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10.1152/AJPENDO.00481.2002

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Identifiers

DOI

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1 December 2017

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