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

The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes.

Transfusion - 1 Nov 2014

Scott Stacy A, Nagl Lisa, Tilley Louise, Liew Yew-Wah, Condon Jenny, Flower Robert, Hyland Catherine A

Abstract excerpt

BACKGROUND: Red blood cells (RBCs) with D antigen levels only detected by anti-D adsorption-elution and an antiglobulin test express a DEL phenotype. For two DEL types, including RHD(1227G>A), immunization of D- recipients has been reported. This study's aim was to measure the prevalence of DEL-associated RHD alleles in a cohort of Australian D- donors to develop a model to estimate alloimmunization risk. STUDY...

Read the complete abstract on PubMed

Topics

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

Share to Australia
Share to Blood Donors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Blood Group Incompatibility

Share to Erythrocyte Transfusion

Share to Point Mutation

Share to Prevalence

Share to Rh-Hr Blood-Group System

Share to Sequence Deletion

Source

Identifiers

PMID: 24894016
DOI: 10.1111/trf.12701

Genes

RHD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes.PMID 24894016Read ↗

Molecular basis of DEL phenotype in the Indian population: Insights from next-generation sequencing analysis of two cases.Semantic proximity Read ↗

DEL variants: review of molecular mechanisms, clinical consequences and molecular testing strategy.Semantic proximity Read ↗

Transitioning a multiethnic donor pool from serologic D-negative to molecularly RHD-negative at a hospital-based blood donor service.Semantic proximity Read ↗

Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles.Semantic proximity Read ↗

Evaluation of the applicability and effectiveness of a molecular strategy for identifying weak D and DEL phenotype among D- blood donors of mixed origin exhibiting high frequency of RHD*Ψ.Semantic proximity Read ↗

Characterization of novel RHD alleles: relationship between phenotype, genotype, and trimeric architecture.Semantic proximity Read ↗

Anti-D alloimmunisation in pregnant women with DEL phenotype in China.Semantic proximity Read ↗

Identification and pedigree analysis of a hidden partial D antigen with rare RHD*DV.1 allele.Semantic proximity Read ↗

Is current serologic RhD typing of blood donors sufficient for avoiding immunization of recipients?Semantic proximity Read ↗

Overview of the serologic and molecular basis of D variants with a focus on D variants in the Indian population.Semantic proximity Read ↗

RHD positive haplotypes in D negative Europeans.Semantic proximity Read ↗

Identification of RHD alleles with the potential of anti-D immunization among seemingly D- blood donors in Upper Austria.Semantic proximity Read ↗

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