Functional Consequences of Mutations and Polymorphisms in the Coding Region of the PAF Acetylhydrolase (PAF-AH) Gene (Q37689865)

22 August 2017

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title

Functional Consequences of Mutations and Polymorphisms in the Coding Region of the PAF Acetylhydrolase (PAF-AH) Gene (English)

1 reference

22 August 2017

Diana M Stafforini

1

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22 August 2017

20 November 2009

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22 August 2017

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22 August 2017

2

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22 August 2017

94-117

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22 August 2017

3

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Creative Commons Attribution 4.0 International

22 August 2017

start time

20 November 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Genotyping of single nucleotide polymorphisms using base-quenched probe: a method does not invariably depend on the deoxyguanosine nucleotide

1 September 2018

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1 September 2018

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Association of platelet-activating factor acetylhydrolase gene polymorphism with premature coronary artery disease in Turkish patients

1 September 2018

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Lp-PLA2 activity and PLA2G7 A379V genotype in patients with diabetes mellitus

1 September 2018

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1 September 2018

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1 September 2018

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Platelet-activating factor acetylhydrolase gene polymorphism and its activity in Japanese patients with multiple sclerosis.

1 September 2018

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Altered distribution of plasma PAF-AH between HDLs and other lipoproteins in hyperlipidemia and diabetes mellitus

1 September 2018

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Association between the Ala379Val variant of the lipoprotein associated phospholipase A2 and risk of myocardial infarction in the north and south of Europe

1 September 2018

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Association of a G994 --> T (Val279 --> Phe) polymorphism of the plasma platelet-activating factor acetylhydrolase gene with myocardial damage in Japanese patients with nonfamilial hypertrophic cardiomyopathy

1 September 2018

1 reference

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Evidence for the existence of the PAF acetylhydrolase mutation (Val279Phe) in non-Japanese populations: a preliminary study in Turkey, Azerbaijan, and Kyrgyzstan.

1 September 2018

1 reference

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Role of platelet-activating factor acetylhydrolase gene mutation in Japanese childhood IgA nephropathy

1 September 2018

1 reference

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1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978535

A mutation in plasma platelet-activating factor acetylhydrolase (Val279Phe) is a genetic risk factor for cerebral hemorrhage but not for hypertension.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3978535

Association of sixty-one non-synonymous polymorphisms in forty-one hypertension candidate genes with blood pressure variation and hypertension

1 September 2018

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The Val279Phe Variant of the Lipoprotein-Associated Phospholipase A2 Gene Is Associated with Catalytic Activities and Cardiovascular Disease in Korean Men

2 October 2018

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Crossref

https://api.crossref.org/works/10.3390%2FPH2030094

Lipoprotein-associated phospholipase A2 A379V variant is associated with body composition changes in response to exercise training

21 January 2018

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Crossref

https://api.crossref.org/works/10.3390%2FPH2030094

Relationship between the platelet activating factor acetylhydrolase gene and intractability of ulcerative colitis

21 January 2018

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12 December 2020

The platelet-activating factor acetylhydrolase from human plasma prevents oxidative modification of low-density lipoprotein

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12 December 2020

Exploration of associations between phospholipase A2 gene family polymorphisms and AIDS progression using the SNPlex method

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12 December 2020

Associations of PLA2G7 gene polymorphisms with plasma lipoprotein-associated phospholipase A2 activity and coronary heart disease in a Chinese Han population: the Beijing atherosclerosis study

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12 December 2020

Plasma platelet-activating factor acetylhydrolase deficiency in Japanese patients with asthma

1 reference

12 December 2020

Evidence for an association between plasma platelet-activating factor acetylhydrolase deficiency and increased risk of childhood atopic asthma

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12 December 2020

Systematic screening of the LDL-PLA2 gene for polymorphic variants and case-control analysis in schizophrenia

1 reference

12 December 2020

Platelet-activating factor-acetylhydrolase A379V (exon 11) gene polymorphism is an independent and functional risk factor for premature myocardial infarction

1 reference

12 December 2020

Association of plasma PAF acetylhydrolase gene polymorphism with IMT of carotid arteries in Japanese type 2 diabetic patients

1 reference

12 December 2020

Plasma platelet-activating factor acetylhydrolase deficiency is associated with atherosclerotic occlusive disease in japan

1 reference

12 December 2020

[Plasma platelet-activating factor acetylhydrolase (PAF-AH) deficiency as a risk factor for stroke]

1 reference

12 December 2020

Correlations between plasma platelet-activating factor acetylhydrolase (PAF-AH) activity and PAF-AH genotype, age, and atherosclerosis in a Japanese population

1 reference

12 December 2020

Single nucleotide polymorphism (G994-->T) in the plasma platelet-activating factor-acetylhydrolase gene is associated with graft patency of femoropopliteal bypass

1 reference

12 December 2020

Association of a G994-->T missense mutation in the plasma platelet-activating factor acetylhydrolase gene with genetic susceptibility to nonfamilial dilated cardiomyopathy in Japanese

1 reference

12 December 2020

Identifiers

DOI

10.3390/PH2030094

1 reference

22 August 2017

1 reference

22 August 2017

1 reference

PMCID

3978535