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

A novel RHD (c.509T>G, p.Met170Arg) allele shows weakened D expression.

Transfusion - 1 Mar 2022

Ding Mengyuan, Li Qin, Zhang Hui, Wang Mingyuan

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Genotype
Share to Phenotype
Share to Rh-Hr Blood-Group System

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34921421
DOI: 10.1111/trf.16773

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel RHD (c.509T>G, p.Met170Arg) allele shows weakened D expression.PMID 34921421Read ↗

A new RHD variant allele (RHD Gly339Val) shows weakened D expression compared to RHD Gly339Glu and Gly339Arg mutants.Semantic proximity Read ↗

An intron c.149-2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype.Semantic proximity Read ↗

The c.254C>A change (p.Ala85Glu) in RHD causing a weak D phenotype.Semantic proximity Read ↗

A novel RHD allele, RHD c.56C>G (p.Thr19Arg), with Del phenotype identified in a Chinese family.Semantic proximity Read ↗

Identification of a novel missense mutation (p.Ser230Asn) in RHD allele in a Chinese individual with partial D phenotype.Semantic proximity Read ↗

A novel RHD allele, RHD*1166delA, with D-negative phenotype identified in a Chinese family.Semantic proximity Read ↗

Identification of four novel RHD alleles with altered expression of D in Brazilians.Semantic proximity Read ↗

Novel RHD allele with c.333C>G change predicted to encode p.Phe111Leu.Semantic proximity Read ↗

New RHD variant alleles.Semantic proximity Read ↗

The novel RHD c.325A>G single nucleotide variation found in Argentineans leads to a partial D phenotype.Semantic proximity Read ↗

A novel RHD allele caused by c.687_689delAAG variant.Semantic proximity Read ↗

A novel RHD allele caused by c.767 C>T mutation was identified in a Chinese individual.Semantic proximity Read ↗

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