(Q38313706)

English

Allelic drop-out may occur with a primer binding site polymorphism for the commonly used RFLP assay for the -1131T>C polymorphism of the Apolipoprotein AV gene

scientific article published on 02 May 2006

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

Allelic drop-out may occur with a primer binding site polymorphism for the commonly used RFLP assay for the -1131T>C polymorphism of the Apolipoprotein AV gene (English)

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

object named as

Kirsten J Ward

1

0 references

Giriraj R Chandak

object named as

Giriraj R Chandak

7

0 references

object named as

Sian Ellard

2

0 references

Andrew Tym Hattersley

5

object named as

Andrew T Hattersley

1 reference

Europe PubMed Central

2 September 2017

PMC publication ID

4

object named as

Timothy M Frayling

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

Chittaranjan Yajnik

3

object named as

Chittaranjan S Yajnik

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

author name string

Prathyusha N S Venigalla

6

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

publication date

2 May 2006

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

Lipids in Health and Disease

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

5

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

11

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

https://scigraph.springernature.com/pub.10.1186/1476-511x-5-11

0 references

Hyperlipidemia in patients with apolipoprotein E 2/2 phenotype: apolipoprotein A5 S19W mutation as a cofactor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

Allelic drop-out in the STR system ACTBP2 (SE33) as a result of mutations in the primer binding region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

Mechanism of triglyceride lowering in mice expressing human apolipoprotein A5

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

Genetic variants in Apolipoprotein AV alter triglyceride concentrations in pregnancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

Ser19-->Trp polymorphism within the apolipoprotein AV gene in hypertriglyceridaemic people

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

T-1131-->C polymorphism within the apolipoprotein AV gene in hypertriglyceridemic individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

Structure and interfacial properties of human apolipoprotein A-V

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

The genetic effect of the apoprotein AV gene on the serum triglyceride level in Japanese

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

Detection of a primer-binding site polymorphism for the STR locus D16S539 using the Powerplex 1.1 system and validation of a degenerate primer to correct for the polymorphism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

Apolipoprotein A-V: a novel apolipoprotein associated with an early phase of liver regeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

Insulin resistance syndrome in 8-year-old Indian children: small at birth, big at 8 years, or both?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

6 September 2017

Allele specific amplification by tetra-primer PCR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

14 September 2017

Fetal growth and glucose and insulin metabolism in four-year-old Indian children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

23 June 2018

Allelic drop-out and preferential amplification in single cells and human blastomeres: implications for preimplantation diagnosis of sex and cystic fibrosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

23 June 2018

[Association of APOA5 gene single nucleotide polymorphism with levels of lipids and coronary heart disease in Chinese].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

31 August 2018

Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

31 August 2018

A Single Nucleotide Polymorphism Under the Reverse Primer Binding Site May Lead to BsmI Mis-Genotyping in the Vitamin D Receptor Gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

31 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

31 August 2018

The relative contributions of birth weight, weight change, and current weight to insulin resistance in contemporary 5-year-olds: the EarlyBird Study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1513378

31 August 2018

A single nucleotide polymorphism -1131T>C in the apolipoprotein A5 gene is associated with an increased risk of coronary artery disease and alters triglyceride metabolism in Chinese

1 reference

https://pubmed.ncbi.nlm.nih.gov/16670016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association found between the promoter region polymorphism in the apolipoprotein A-V gene and the serum triglyceride level in Japanese schoolchildren

1 reference

https://pubmed.ncbi.nlm.nih.gov/16670016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apolipoprotein A5 and hypertriglyceridemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16670016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

APOA5-1131T>C polymorphism is associated with triglyceride levels in Chinese men

1 reference

https://pubmed.ncbi.nlm.nih.gov/16670016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

APOA5polymorphisms influence plasma triglycerides in young, healthy African Americans and whites of the CARDIA Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16670016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic drop-out in exon 2 of the hepatocyte nuclear factor-1alpha gene hinders the identification of mutations in three families with maturity-onset diabetes of the young

1 reference

https://pubmed.ncbi.nlm.nih.gov/16670016

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1476-511X-5-11

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q38313706&oldid=1948781230"