Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A population-wide applicable HLA-DQ2 and DQ8 genotyping using DNA from dried blood spots and duplex allele-specific qPCR amplification.

Scandinavian journal of clinical and laboratory investigation - 1 Nov 2016

Aguayo-Patrón Sandra, Beltrán-Sauceda Lizbeth, Calderón de la Barca Ana María

Abstract excerpt

Genotyping of HLA-DQ2 and DQ8 haplotypes is important for diagnosis or for screening of early risk detection of celiac disease or type 1 diabetes. Usually, venous blood DNA extraction and expensive and time consuming amplification are used, that hinder population-wide studies. We assayed a friendly HLA-DQ2 and DQ8 genotyping procedure using a combination of DNA from dried blood spot (DBS) and duplex...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Benzothiazoles
Share to Celiac Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Diamines

Share to Dried Blood Spot Testing

Share to HLA-DQ Antigens

Share to Multiplex Polymerase Chain Reaction

Share to Organic Chemicals

Share to Quinolines

Source

Identifiers

PMID: 27670799
DOI: 10.1080/00365513.2016.1230773

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A population-wide applicable HLA-DQ2 and DQ8 genotyping using DNA from dried blood spots and duplex allele-specific qPCR amplification.PMID 27670799Read ↗

Saliva direct PCR protocol for HLA-DQB1*02 genotypingSemantic proximity Read ↗

Celiac Disease Risk Allele Frequencies in San Luis (Argentina) and Evaluation of a Saliva Direct PCR Genotyping ApproachSemantic proximity Read ↗

Saliva direct PCR protocol for HLA-DQB1*02 genotyping.Semantic proximity Read ↗

A new automated human leukocyte antigen genotyping strategy to identify DR-DQ risk alleles for celiac disease and type 1 diabetes mellitus.Semantic proximity Read ↗

Genotyping of celiac disease-related-risk haplotypes using a closed-tube polymerase chain reaction analysis of dried blood and saliva disk samples.Semantic proximity Read ↗

Simplifying celiac disease predisposing HLA-DQ alleles determination by the real time PCR method.Semantic proximity Read ↗

HLA Genotyping: Methods for the Identification of the HLA-DQ2,-DQ8 Heterodimers Implicated in Celiac Disease (CD) Susceptibility.Semantic proximity Read ↗

HLA DR-DQ genotyping by capillary electrophoresis for risk assessment for celiac disease.Semantic proximity Read ↗

HLA-DQ2/DQ8 and HLA-DQB1*02 homozygosity typing by real-time polymerase chain reaction for the assessment of celiac disease genetic risk: evaluation of a Spanish celiac population.Semantic proximity Read ↗

A novel duplex SSP-PCR typing method for KIR gene profiling.Semantic proximity Read ↗

Tag-single nucleotide polymorphism-based human leukocyte antigen genotyping in celiac disease patients from northeastern Italy.Semantic proximity Read ↗

Human leukocyte antigen typing using buccal swabs as accurate and non-invasive substitute for venipuncture in children at risk for celiac disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.