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

[Study of a case with homozygous 35C>T and 658C>T mutations of FUT1 gene leading to a para-Bombay phenotype].

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

Lin Fengqiu, Sun Changping, Wang Hui, Zhang Xu, Li Jianping

Abstract excerpt

OBJECTIVE: To explore the molecular mechanism for a case with para-Bombay phenotype caused by α-1,2-fucosyltransferase (FUT1) gene mutations. METHODS: Blood phenotype of the propositus was determined by standard serological testing. Polymerase chain reaction-sequence specific primer (PCR-SSP) and direct sequencing of PCR product were used to analyze its ABO genotype. The PCR product of FUT1 gene was sequenced and...

Read the complete abstract on PubMed

Topics

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

Share to DNA Primers
Share to ABO Blood-Group System

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

Share to DNA Mutational Analysis

Share to Fucosyltransferases

Share to Galactoside 2-alpha-L-fucosyltransferase

Share to Homozygote

Share to Point Mutation

Share to Polymerase Chain Reaction

Source

Identifiers

PMID: 26663060
DOI: 10.3760/cma.j.issn.1003-9406.2015.06.018

Genes

FUT1
ABO

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

[Study of a case with homozygous 35C>T and 658C>T mutations of FUT1 gene leading to a para-Bombay phenotype].PMID 26663060Read ↗

[Serological and molecular biological analysis of an individual with para-Bombay blood group due to homozygous c.948C>A variant of FUT1 gene].Semantic proximity Read ↗

[Para-Bombay phenotype due to bi-allelic heterozygous base deletions of FUT1 gene].Semantic proximity Read ↗

[Genetic analysis of an individual with para-Bombay phenotype].Semantic proximity Read ↗

[Para-Bombay phenotype caused by combined heterozygote of two bases deletion on fut1 alleles].Semantic proximity Read ↗

[Analysis of alpha-1,2-fucosyltransferase gene mutations in a Chinese family with para-Bombay phenotype].Semantic proximity Read ↗

[Analysis of two novel variants of FUT1 gene in a Chinese family with para-Bombay phenotype].Semantic proximity Read ↗

Analysis of the molecular mechanism and pedigree investigation of para-Bombay phenotype caused by combined mutations at position h649 and h768 of FUT1 gene.Semantic proximity Read ↗

[Molecular genetic basis for para-Bombay phenotypes in two cases].Semantic proximity Read ↗

Two novel FUT1 alleles that cause para-Bombay phenotype in a Chinese individual.Semantic proximity Read ↗

Genetic and mechanistic evaluation of an individual with para-Bombay phenotype associated with a compound heterozygote comprising two novel FUT1 variants.Semantic proximity Read ↗

[Identification of a novel FUT1 allele in a Chinese individual featuring para-Bombay phenotype].Semantic proximity Read ↗

[Sequence analysis for a case with Para-Bombay AB blood type].Semantic proximity Read ↗

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