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

Compound heterozygosity induces a rare Gerbich-negative phenotype in an immunized blood donor.

Transfusion - 1 Feb 2024

Petermann Sarah, Mayer Vanessa, Carbol Alexander, Opitz Andreas, Flesch Brigitte K

Abstract excerpt

BACKGROUND: Antibodies to Gerbich blood group antigens are exceedingly rare and can cause moderate transfusion reactions. Several deletional variants of the GE-gene, that harbors long sequence repeats, enable alloimmunization and formation of naturally occurring antibodies. SUBJECT AND METHODS: A female blood donor and soldier of the German Army without history of pregnancy or transfusion showed an antibody...

Read the complete abstract on PubMed

Topics

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

Share to Anemia, Hemolytic, Autoimmune
Share to Antibodies
Share to Blood Donors

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Blood Group Antigens

Share to Blood Transfusion

Share to Phenotype

Share to Pregnancy

Source

Identifiers

PMID: 38235836
DOI: 10.1111/trf.17711

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Compound heterozygosity induces a rare Gerbich-negative phenotype in an immunized blood donor.PMID 38235836Read ↗

Genetic diversity of Gerbich alleles in Brazilians reveals an unexpected prevalence of the GE:-2,-3,4 phenotype.Semantic proximity Read ↗

An update on the GE (Gerbich) blood group system.Semantic proximity Read ↗

Co-presence of a point mutation and a deletion of exon 3 in the glycophorin C gene and concomitant production of a Gerbich-related antibody.Semantic proximity Read ↗

Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles.Semantic proximity Read ↗

Molecular basis of glycophorin C variants and their associated blood group antigens.Semantic proximity Read ↗

Analysis of RhCE variants among 806 individuals in France: considerations for transfusion safety, with emphasis on patients with sickle cell disease.Semantic proximity Read ↗

(C)ce(s) haplotype screening in Tunisian blood donors.Semantic proximity Read ↗

The low prevalence Rh antigen Be(a) (Rh36) is associated with RHCE*ce 662C>G in exon 5, which is predicted to encode Rhce 221Arg.Semantic proximity Read ↗

Compound heterozygosity of two novel RHAG alleles leads to a considerable disruption of the Rh complex.Semantic proximity Read ↗

RHCE variant allele: RHCE*ce254G,733G.Semantic proximity Read ↗

[Analysis of RhC Antigen Weak Expression Combined with Mimicking Autoanti-Ce and Homologous Anti-Jkb Causing Mismatch].Semantic proximity Read ↗

RhCE protein variants in Southwestern Germany detected by serologic routine testing.Semantic proximity Read ↗

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