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 Mechanism of a Rhesus D Variant Individual with RHD*845A/1227A].

Zhongguo shi yan xue ye xue za zhi - 1 Aug 2023

Xie Xiu-Hua, Wu Fan, Deng Qing, Zhuang Nai-Bao

Abstract excerpt

OBJECTIVE: To explore the genetic mutation mechanism of a rare Rhesus D variant individual. METHODS: Regular serological assay was used for determination of Rh type for the sample. Indirect anti-human globulin test (IAT) was used to confirm the RhD antigen and screen the antibodies. D-screen reagent was used to analyze the RhD epitopes of the sample. RHD genotype and RHD zygosity testing of the sample were...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Blood Group Antigens
Share to Genotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Phenotype

Share to Polymerase Chain Reaction

Share to Rh-Hr Blood-Group System

Source

Identifiers

PMID: 37551491
DOI: 10.19746/j.cnki.issn.1009-2137.2023.04.034

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Molecular Mechanism of a Rhesus D Variant Individual with RHD*845A/1227A].PMID 37551491Read ↗

[Phenotype Types and Genetic Mutation Mechanism of Rhesus D Variant Individuals].Semantic proximity Read ↗

[Molecular genetic analysis of two individuals with weak D variant of the Rh blood type].Semantic proximity Read ↗

[Molecular genetic analysis of four cases with weak D variant of Rh blood type].Semantic proximity Read ↗

[Family investigation of a RHD 845A/1227A genotype individual].Semantic proximity Read ↗

[Molecular genetic analysis of a weak D phenotype].Semantic proximity Read ↗

[Molecular Mechanism Study of One Case of Novel Allele of RhD Blood Group].Semantic proximity Read ↗

[Identification of Weak D Type 1 in Rh Blood Group System and Discussion of Transfusion Strategy].Semantic proximity Read ↗

[Molecular mechanism of 101A>G and 845G>A mutations of RHD gene responsible for a weak RhD].Semantic proximity Read ↗

[Investigation of RHD 1227A allele in five pedigrees in Zhejiang Han population].Semantic proximity Read ↗

Molecular basis of weak D phenotypes.Semantic proximity Read ↗

[Blood Typing and Pedigree Analysis of a Novel RHD Allele with c.179T>C and c.1154-31T>C Mutations].Semantic proximity Read ↗

Gene symbol: RHD. Disease: Rhesus blood group variation.Semantic proximity Read ↗

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