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

Molecular background of novel silent RHCE alleles.

Transfusion - 1 Nov 2013

Pham Bach-Nga, Ramelet Stéphanie, Wibaut Bénédicte, Juszczak Genevieve, Loukil Chawki, Dubeaux Isabelle, Gien Dominique, Kappler-Gratias Sandrine, Rouger Philippe, Le Pennec Pierre-Yves

Abstract excerpt

BACKGROUND: The absence of expression of C/c and E/e antigens has been associated with rare variant RHCE alleles, referred to as silent RHCE alleles, classically identified among individuals with a rare D- - or Rhnull phenotype. This work reports on different molecular mechanisms identified in three novel silent RHCE alleles. STUDY DESIGN AND METHODS: Samples from D- - or Rhnull individuals and their family...

Read the complete abstract on PubMed

Topics

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

Share to Child, Preschool
Share to Family

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Expression Regulation

Share to Gene Silencing

Share to Heterozygote

Share to Mutation, Missense

Share to Pedigree

Share to Rh-Hr Blood-Group System

Source

Identifiers

PMID: 23252593
DOI: 10.1111/trf.12023

Genes

RHCE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular background of novel silent RHCE alleles.PMID 23252593Read ↗

Heterogeneous molecular background of the weak C, VS+, hr B-, Hr B- phenotype in black persons.Semantic proximity Read ↗

A novel nonsense variant in RHAG underlies a Nordic Rhnull phenotype.Semantic proximity Read ↗

Identification of a novel RHCE*Ce (829G > A) allele associated with absence of C and e antigens expression.Semantic proximity Read ↗

New RHCE variant alleles encoding the D- - phenotype.Semantic proximity Read ↗

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

RHCE*cE734C allele encodes an altered c antigen and a suppressed E antigen not detected with standard reagents.Semantic proximity Read ↗

A Dc- phenotype encoded by an RHCE-D(5-7/8)-CE hybrid allele.Semantic proximity Read ↗

A Novel RHCE*cE (c.827C>A) Allele, Containing the Single-Nucleotide Change, Encodes Altered c/E Antigens.Semantic proximity Read ↗

Rhnull syndrome: identification of a novel mutation in RHce.Semantic proximity Read ↗

Identification of a novel frequent RHCE*ce308T variant allele in Chinese D- individuals, resulting in a C+c- phenotype.Semantic proximity Read ↗

Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29.Semantic proximity Read ↗

RHCE-D-CE hybrid genes can cause false-negative DNA typing of the Rh e antigen.Semantic proximity Read ↗

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