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

SARA: a "new" low-frequency MNS antigen (MNS47) provides further evidence of the extreme diversity of the MNS blood group system.

Transfusion - 1 Jun 2015

McBean Rhiannon S, Hyland Catherine A, Hendry Julia L, Shabani-Rad Meer-Taher, Flower Robert L

Abstract excerpt

BACKGROUND: Until recently, SARAH (SARA) was a low-frequency antigen within the 700 series (700.052). SARA was discovered in Australia and subsequently described in Canada where anti-SARA was implicated in severe hemolytic disease of the fetus and newborn (HDFN). This study investigated whether SARA could be recategorized into an existing, or novel, blood group system. STUDY DESIGN AND METHODS: Serologically...

Read the complete abstract on PubMed

Topics

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

Share to Australia
Share to Canada
Share to Erythroblastosis, Fetal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family

Share to Infant, Newborn

Share to Isoantigens

Share to MNSs Blood-Group System

Share to Pregnancy

Source

Identifiers

PMID: 25523184
DOI: 10.1111/trf.12973

Genes

GYPA

Variants

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

SARA: a "new" low-frequency MNS antigen (MNS47) provides further evidence of the extreme diversity of the MNS blood group system.PMID 25523184Read ↗

A cold case of hemolytic disease of the fetus and newborn resolved by genomic sequencing and population studies to define a new antigen in the Rh system.Semantic proximity Read ↗

Resolving RH and GYP hybrid alleles while accessing the entire blood group genome with Nanopore adaptive samplingSemantic proximity Read ↗

Review: molecular basis of MNS blood group variants.Semantic proximity Read ↗

Hemolytic disease of the fetus and newborn caused by anti-sD antibody in a GP.Mur/Mur Thai mother and review of the prevalence of sD in Thai blood donors.Semantic proximity Read ↗

SCER and SCAN: two novel high-prevalence antigens in the Scianna blood group system.Semantic proximity Read ↗

Genetic landscape of human platelet antigen variants in the Indian population analysed from 1029 whole genomes.Semantic proximity Read ↗

Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemiaSemantic proximity Read ↗

Genetic landscape of human neutrophil antigen variants in India from population-scale genomes.Semantic proximity Read ↗

SCAR: The high-prevalence antigen 013.008 in the Scianna blood group system.Semantic proximity Read ↗

The Research of a Large-Scale Analysis Platform for MNS Blood Group Identification Based on Long-Read Sequencing.Semantic proximity Read ↗

High-throughput Kell, Kidd, and Duffy matrix-assisted laser desorption/ionization, time-of-flight mass spectrometry-based blood group genotyping of 4000 donors shows close to full concordance with serotyping and detects new alleles.Semantic proximity Read ↗

Genetic landscape of Human neutrophil antigen variants in India from population-scale genomesSemantic proximity Read ↗

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