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

Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA.

Transfusion - 1 Nov 2013

Lejon Crottet Sofia, Haer-Wigman Lonneke, Gowland Peter, Fontana Stefano, Niederhauser Christoph, Hustinx Hein

Abstract excerpt

BACKGROUND: The partial D variant DAR1 (weak D Type 4.2) is caused by three single-point mutations, 602C>G, 667T>G, and 1025T>C. Here we report a molecular study on different D variants belonging to the DAR category (DAR1, DAR1.2, DAR1.3, and DAR2) and their serologic data. STUDY DESIGN AND METHO...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Substitution
Share to Blood Grouping and Crossmatching
Share to Flow Cytometry

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Isoantibodies

Share to Rh-Hr Blood-Group System

Share to Rho(D) Immune Globulin

Share to Sequence Analysis, DNA

Share to Serologic Tests

Source

Identifiers

PMID: 23902153
DOI: 10.1111/trf.12363

Genes

RHD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23902153-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA.PMID 23902153Read ↗

Frequency and characterization of RHD variant alleles in a population of blood donors from southeastern Brazil: Comparison with other populations.Semantic proximity Read ↗

Weak D Type 4.2.2 (DAR1.2) in an African child: Serology and molecular characterization.Semantic proximity Read ↗

Serologic and molecular characterization of D variants in Brazilians: impact for typing and transfusion strategy.Semantic proximity Read ↗

Weak D types 38 and 11: determination of frequencies in a Brazilian population and validation of an easy molecular assay for detection.Semantic proximity Read ↗

High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype.Semantic proximity Read ↗

D category IV: a group of clinically relevant and phylogenetically diverse partial D.Semantic proximity Read ↗

RHD variants in Flanders, Belgium.Semantic proximity Read ↗

It's time to phase out "serologic weak D phenotype" and resolve D types with RHD genotyping including weak D type 4.Semantic proximity Read ↗

RHD alleles in Brazilian blood donors with weak D or D-negative phenotypes.Semantic proximity Read ↗

Standardization of a multiplex assay to identify weak D types in a mixed-race Brazilian population.Semantic proximity Read ↗

RhD variants in Caucasians: consequences for checking clinically relevant alleles.Semantic proximity Read ↗

RHCE variants inherited with altered RHD alleles in Brazilian blood donors.Semantic proximity Read ↗

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