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 Study on Fucosyltransferase 2 Gene Polymorphism and Secretion Status Related to Neonatal Necrotizing Enterocolitis.

Journal of healthcare engineering - 1 Jan 2021

Ye Qing, Yu Jialin

Abstract excerpt

Objective: To detect the single nucleotide polymorphism (SNP) of alpha-(1,2) fucosyltransferase 2 gene (FUT2) and the secretion status in the newborns of Chongqing China and explore the relationship between genotype or phenotype of FUT2 and neonatal necrotizing enterocolitis (NEC). Methods: Newborns who were hospitalized in Children's Hospital of Chongqing Medical University from August 2014 to December 2015 and...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Fucosyltransferases
Share to Galactoside 2-alpha-L-fucosyltransferase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn

Share to Polymorphism, Genetic

Source

Open in PubMed Open full text

Identifiers

PMID: 34336165
DOI: 10.1155/2021/7219850
PMCID: PMC8321722

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Study on Fucosyltransferase 2 Gene Polymorphism and Secretion Status Related to Neonatal Necrotizing Enterocolitis.PMID 34336165Read ↗

Clinical significance of the fucosyltransferase 2 (FUT2) secretor status in children hospitalized with acute gastroenteritis in Taiwan.Semantic proximity Read ↗

Fucosyltransferase 2 non-secretor and low secretor status predicts severe outcomes in premature infants.Semantic proximity Read ↗

Association of fucosyltransferase 2 gene polymorphism with the susceptibility to norovirus infection in Han Chinese population.Semantic proximity Read ↗

Association of fucosyltransferase 2 gene with norovirus infection: A systematic review and meta-analysis.Semantic proximity Read ↗

Fucosyltransferase 2: A Genetic Risk Factor for Intestinal DiseasesSemantic proximity Read ↗

FUT2 secretor genotype and susceptibility to infections and chronic conditions in the ALSPAC cohortSemantic proximity Read ↗

Fucosyltransferase 2: a genetic risk factor for primary sclerosing cholangitis and Crohn's disease--a comprehensive review.Semantic proximity Read ↗

FUT 2 polymorphism and outcome in very-low-birth-weight infants.Semantic proximity Read ↗

The fusion allele of the FUT2 (secretor type alpha(1,2)-fucosyltransferase) gene at a high frequency and a new se385 allele in a Korean population.Semantic proximity Read ↗

Systematic sequence analysis of the human fucosyltransferase 2 (FUT2) gene identifies novel sequence variations and alleles.Semantic proximity Read ↗

Molecular characterization of secretor type alpha(1, 2)-fucosyltransferase gene deficiency in the Philippine population.Semantic proximity Read ↗

A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.Semantic proximity Read ↗

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