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 rare Pk phenotype caused by a 433 C>T mutation of the β-1,3-N-acetylgalactosyltransferase gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 1 Jun 2015

Lan Xiaofei, Hong Xiaozhen, Xu Xianguo, Chen Shu, Ma Kairong, Liu Ying, He Ji, Zhu Faming, Lyu Hangjun

Abstract excerpt

OBJECTIVE: To study the serological characteristics and molecular mechanism for a rare Pk phenotype of the P1Pk blood group system. METHODS: The blood group of the proband was identified by serological techniques. The coding region and flanking intronic sequences of the β-1,3-N-acetylgalactosyltransferase gene (B3GALANT1) associated with the Pk phenotype were analyzed using polymerase chain reaction...

Read the complete abstract on PubMed

Topics

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

Share to ABO Blood-Group System
Share to Base Sequence

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

Share to Blood Grouping and Crossmatching

Share to Genotype

Share to Molecular Sequence Data

Share to N-Acetylgalactosaminyltransferases

Share to Pedigree

Share to Point Mutation

Source

Identifiers

PMID: 26037356
DOI: 10.3760/cma.j.issn.1003-9406.2015.03.018

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

[A rare Pk phenotype caused by a 433 C>T mutation of the β-1,3-N-acetylgalactosyltransferase gene].PMID 26037356Read ↗

[Molecular basis for an individual with rare p phenotype in P1Pk blood group system].Semantic proximity Read ↗

[A rare p phenotype caused by a 26-bp deletion in α 1,4-galactosyltransferase gene].Semantic proximity Read ↗

[Pedigree investigation and genetic analysis of a case with p blood group].Semantic proximity Read ↗

[Serological and genetic study of a pedigree featuring a rare p phenotype].Semantic proximity Read ↗

[A A311 blood group gene subtype caused by a-1-3-N-acetylgalactosaminyltransferase gene exon 7 mutations].Semantic proximity Read ↗

[Serological characteristics and molecular mechanism of an individual with p phenotype].Semantic proximity Read ↗

[One base deletion of the alpha(1,4) galactosyltransferase gene responsible for p phenotype].Semantic proximity Read ↗

Two previously proposed P1/P2-differentiating and nine novel polymorphisms at the A4GALT (Pk) locus do not correlate with the presence of the P1 blood group antigen.Semantic proximity Read ↗

[Serological feature and molecular mechanism for a case with A307 subgroup].Semantic proximity Read ↗

[Serological and Molecular Biological Analysis of Rare Cases of p-Blood Type].Semantic proximity Read ↗

Additional molecular bases of the clinically important p blood group phenotype.Semantic proximity Read ↗

[Identification of a novel T421C mutation of α-1,3-N-acetylgalactosaminyltransferase allele responsible for an A variant].Semantic proximity Read ↗

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