Enhanced placental cholesterol efflux by fetal HDL in Smith-Lemli-Opitz syndrome (Q34566372)

3 August 2017

title

Enhanced placental cholesterol efflux by fetal HDL in Smith-Lemli-Opitz syndrome (English)

1 reference

3 August 2017

0 references

Katie T Jenkins

1

1 reference

3 August 2017

Louise S Merkens

2

1 reference

3 August 2017

Matthew R Tubb

3

1 reference

3 August 2017

Leslie Myatt

4

1 reference

3 August 2017

W Sean Davidson

5

1 reference

3 August 2017

Robert D Steiner

6

1 reference

3 August 2017

Laura A Woollett

7

1 reference

3 August 2017

publication date

17 March 2008

1 reference

Molecular Genetics and Metabolism

3 August 2017

published in

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3 August 2017

volume

94

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3 August 2017

issue

2

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3 August 2017

page(s)

240-247

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Adverse birth outcome among mothers with low serum cholesterol

3 August 2017

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Uterine Glands Provide Histiotrophic Nutrition for the Human Fetus during the First Trimester of Pregnancy

7 July 2018

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Smith-Lemli-Opitz (RHS) syndrome: holoprosencephaly and homozygous IVS8-1G-->C genotype

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Carrier frequency of the common mutation IVS8-1G>C in DHCR7 and estimate of the expected incidence of Smith-Lemli-Opitz syndrome.

7 July 2018

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Onset of maternal arterial blood flow and placental oxidative stress. A possible factor in human early pregnancy failure

7 July 2018

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RSH/Smith-Lemli-Opitz syndrome: a multiple congenital anomaly/mental retardation syndrome due to an inborn error of cholesterol biosynthesis

7 July 2018

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Smith-Lemli-Opitz syndrome: the first malformation syndrome associated with defective cholesterol synthesis

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Fetal demise with Smith-Lemli-Opitz syndrome confirmed by tissue sterol analysis and the absence of measurable 7-dehydrocholesterol Delta(7)-reductase activity in chorionic villi

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene

7 July 2018

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Mutations in the Delta7-sterol reductase gene in patients with the Smith-Lemli-Opitz syndrome

7 July 2018

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Mutations in the human sterol delta7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome.

7 July 2018

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Fatty streak formation occurs in human fetal aortas and is greatly enhanced by maternal hypercholesterolemia. Intimal accumulation of low density lipoprotein and its oxidation precede monocyte recruitment into early atherosclerotic lesions

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Markedly inhibited 7-dehydrocholesterol-delta 7-reductase activity in liver microsomes from Smith-Lemli-Opitz homozygotes

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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27 October 2018

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7 January 2021

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7 January 2021

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7 January 2021

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PubMed

https://pubmed.ncbi.nlm.nih.gov/18346920

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.YMGME.2008.01.015

1 reference

3 August 2017

1 reference

3 August 2017

1 reference