Genetic variants in Apolipoprotein AV alter triglyceride concentrations in pregnancy (Q24797224)

6

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Andrew Tym Hattersley

5

object named as

Andrew T Hattersley

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author name string

Beverley Shields

2

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Beatrice Knight

3

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Maurice B Salzmann

Lipids in Health and Disease

4

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language of work or name

English

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publication date

5 November 2003

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published in

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volume

2

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issue

1

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page(s)

9

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exact match

https://scigraph.springernature.com/pub.10.1186/1476-511x-2-9

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cites work

Structure and interfacial properties of human apolipoprotein A-V

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Relative contribution of variation within the APOC3/A4/A5 gene cluster in determining plasma triglycerides

7 April 2017

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An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing

7 April 2017

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Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levels

7 April 2017

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Clinical significance of hypertriglyceridemia

7 April 2017

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Contribution of APOA5 gene variants to plasma triglyceride determination and to the response to both fat and glucose tolerance challenges

28 September 2017

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Genetic analysis of a polymorphism in the human apoA-V gene: effect on plasma lipids

28 November 2018

1 reference

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Effect of pregnancy on plasma lipid concentration in Trinidadian women. Result of a pilot study.

28 November 2018

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Lipoprotein lipase and apoE polymorphisms: relationship to hypertriglyceridemia during pregnancy

28 November 2018

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Fasting serum triglycerides, free fatty acids, and malondialdehyde are increased in preeclampsia, are positively correlated, and decrease within 48 hours post partum.

28 November 2018

1 reference

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Hyperlipidaemia during normal pregnancy, parturition and lactation

28 November 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/14613578

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Serum lipid concentrations change with serum alkaline phosphatase activity during pregnancy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/14613578

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

LDL receptor mutation genotype and vascular disease phenotype in heterozygous familial hypercholesterolaemia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/14613578