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

[C742T mutation of α1, 3 N-acetyl-D-galactosaminyltransferase gene is responsible for A2 subgroup].

Zhongguo shi yan xue ye xue za zhi - 1 Jun 2011

Hong Xiao-Zhen, Yin Yan-Ling, Xu Xian-Guo, Ma Kai-Rong, Lan Xiao-Fei, Liu Ying, Zhu Fa-Ming, Lü Hang-Jun, Yan Li-Xing

Abstract excerpt

The objective of this study was to analyze the molecular genetic basis for 2 individuals with A2B phenotype of ABO subtype. The ABO group antigens on red blood cells were identified by monoclonal antibodies and the ABO antibodies in serum were detected by the standard A, B, O cells. The exon 5 to exon 7 coding region of ABO gene was amplified by polymerase chain reaction (PCR) and the PCR product was sequenced...

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 Alleles

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Antibodies, Anti-Idiotypic

Share to Blood Donors

Share to Heterozygote

Share to N-Acetylgalactosaminyltransferases

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 21729554

Genes

ABO

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[C742T mutation of α1, 3 N-acetyl-D-galactosaminyltransferase gene is responsible for A2 subgroup].PMID 21729554Read ↗

[Variants 467C > T and 539G > C of the alpha-1,3-N-acetylgalactosaminyltransferase allele responsible for A2 subgroup].Semantic proximity Read ↗

α-1,3-N-acetylgalactose aminotransferase gene 539G>C mutation leads to the A2B isoform.Semantic proximity Read ↗

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

[Study of 467C>T and 745C>T variants of alpha-1, 3-N-acetylgalactoseaminotransferase gene].Semantic proximity Read ↗

[Study of the molecular basis of an individual with Aw43 subtype of the ABO blood group].Semantic proximity Read ↗

[Study on a 905A to G mutation of α 1,3 galactosyltransferase gene].Semantic proximity Read ↗

[Genetic analysis of a case with A subtype of the ABO blood type].Semantic proximity Read ↗

[Ael subgroup due to alpha-1,3-N-acetylgalactoseaminotransferase gene 467C>T and 804insG variants].Semantic proximity Read ↗

[Study of a Chinese pedigree carrying a novel variant of α-1, 3-N-acetyl galactosaminyl transferase gene].Semantic proximity Read ↗

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

[A case of Bw39 subtype caused by 562C to T mutation of exon 7 of α -1,3-D-galactosyltransferase gene].Semantic proximity Read ↗

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

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