Carnitine content and expression of mitochondrial beta-oxidation enzymes in placentas of wild-type (OCTN2(+/+)) and OCTN2 Null (OCTN2(-/-)) Mice (Q28507159)

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English	Carnitine content and expression of mitochondrial beta-oxidation enzymes in placentas of wild-type (OCTN2(+/+)) and OCTN2 Null (OCTN2(-/-)) Mice	scientific journal article

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scholarly article

1 reference

PubMed publication ID

24 January 2017

Carnitine content and expression of mitochondrial beta-oxidation enzymes in placentas of wild-type (OCTN2(+/+)) and OCTN2 Null (OCTN2(-/-)) Mice (English)

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PubMed publication ID

24 January 2017

Hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta

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GOA release 2020-03-11

Hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha

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GOA release 2020-03-11

Hydroxyacyl-Coenzyme A dehydrogenase

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GOA release 2020-03-11

Solute carrier family 22 (organic cation transporter), member 5

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GOA release 2020-03-11

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based on heuristic

inferred from title

Vadivel Ganapathy

7

object named as

Vadivel Ganapathy

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author name string

Prem S. Shekhawat

1

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PubMed publication ID

24 January 2017

Han-Soo Yang

2

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PubMed publication ID

24 January 2017

Michael J. Bennett

3

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PubMed publication ID

24 January 2017

Alva Lee Carter

4

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24 January 2017

Dietrich Matern

5

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PubMed publication ID

24 January 2017

Ikumi Tamai

6

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PubMed publication ID

24 January 2017

language of work or name

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publication date

1 September 2004

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PubMed publication ID

24 January 2017

Pediatric Research

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PubMed publication ID

24 January 2017

56

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24 January 2017

3

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24 January 2017

323–328

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24 January 2017

Fatty acid oxidation disorders

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https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

Inborn errors of mitochondrial fatty acid oxidation

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https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

Molecular and functional identification of sodium ion-dependent, high affinity human carnitine transporter OCTN2

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https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

Carnitine transport: pathophysiology and metabolism of known molecular defects

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https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

Role of intrapartum hypoxia in carnitine nutritional status during the early neonatal period

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https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

Glucose transporters in the human placenta

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https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

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

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https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

Liver disease in pregnancy and fetal fatty acid oxidation defects

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https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

Prenatal diagnosis of disorders of fatty acid transport and mitochondrial oxidation

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https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

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

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https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

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

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21 January 2018

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

1 reference

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21 January 2018

Suppressed expression of the urea cycle enzyme genes in the liver of carnitine-deficient juvenile visceral steatosis (JVS) mice in infancy and during starvation in adulthood.

1 reference

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21 January 2018

A novel gene suppressed in the ventricle of carnitine-deficient juvenile visceral steatosis mice

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

L-carnitine modifies the humoral immune response in mice after in vitro or in vivo treatment

1 reference

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21 January 2018

Feeding acetyl-L-carnitine and lipoic acid to old rats significantly improves metabolic function while decreasing oxidative stress

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

L-carnitine reduces brain injury after hypoxia-ischemia in newborn rats

1 reference

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21 January 2018

Na+- and Cl--coupled active transport of carnitine by the amino acid transporter ATB(0,+) from mouse colon expressed in HRPE cells and Xenopus oocytes

1 reference

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21 January 2018

Reminiscences of Sidney Carter, MD.

1 reference

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21 January 2018

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

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000134252.02876.55

21 January 2018

Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Fatty acid synthesis is essential in embryonic development: fatty acid synthase null mutants and most of the heterozygotes die in utero

1 reference

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21 January 2018

Disruption of mitochondrial beta -oxidation of unsaturated fatty acids in the 3,2-trans-enoyl-CoA isomerase-deficient mouse

1 reference

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21 January 2018

A null mutation in murine CD36 reveals an important role in fatty acid and lipoprotein metabolism.

1 reference

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21 January 2018

Prospective screening for pediatric mitochondrial trifunctional protein defects in pregnancies complicated by liver disease

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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10.1203/01.PDR.0000134252.02876.55

1 reference

PubMed publication ID

24 January 2017

Dimensions Publication ID

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PubMed publication ID

1 reference

PubMed publication ID

24 January 2017

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