(Q44312288)

1 December 2017

title

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

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1 December 2017

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Prem Shekhawat

1

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1 December 2017

Michael J Bennett

2

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1 December 2017

Yoel Sadovsky

3

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1 December 2017

D Michael Nelson

4

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1 December 2017

Dinesh Rakheja

5

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1 December 2017

Arnold W Strauss

6

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1 December 2017

publication date

11 February 2003

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American Journal of Physiology - Endocrinology and Metabolism

1 December 2017

published in

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1 December 2017

volume

284

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1 December 2017

issue

6

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1 December 2017

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

Detection and cellular localization of plasma membrane-associated and cytoplasmic fatty acid-binding proteins in human placenta

21 January 2018

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

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

21 January 2018

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

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

21 January 2018

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

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

21 January 2018

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

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

21 January 2018

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

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

21 January 2018

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

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

21 January 2018

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

Glucose transporters in the human placenta

21 January 2018

1 reference

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

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

21 January 2018

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

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

21 January 2018

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

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

21 January 2018

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

Complementation analysis of fatty acid oxidation disorders

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

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

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

21 January 2018

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

10.1152/AJPENDO.00481.2002

21 January 2018

Identifiers

DOI

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1 December 2017

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