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 novel mitochondrial DNA-like sequence insertion polymorphism in Intron I of the FOXO1A gene.

Gene - 3 Mar 2004

Giampieri Claudia, Centurelli Matteo, Bonafè Massimiliano, Olivieri Fabiola, Cardelli Maurizio, Marchegiani Francesca, Cavallone Luca, Giovagnetti Simona, Mugianesi Elena, Carrieri Giuseppina, Lisa Rosamaria, Cenerelli Stefano, Testa Roberto, Boemi Massimo, Petropoulou Chariklia, Gonos Efstathios S, Franceschi Claudio

Abstract excerpt

The human forkhead box O1A (FOXO1A) gene belongs to the human forkhead gene family and acts downstream of the human insulin signalling pathway. In this study, polymorphisms of the Intron I of FOXO1A gene were studied in Italian healthy people and insulin resistant subjects. No significant associa...

Read the complete abstract on PubMed

Topics

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

Share to Adenosine Triphosphatases
Share to Forkhead Box Protein O1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Forkhead Transcription Factors

Share to Insulin Resistance

Share to Introns

Share to Mutagenesis, Insertional

Share to Sequence Deletion

Source

Identifiers

PMID: 14980718
DOI: 10.1016/j.gene.2003.11.003

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-14980718-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel mitochondrial DNA-like sequence insertion polymorphism in Intron I of the FOXO1A gene.PMID 14980718Read ↗

Analysis of FOXO1A as a candidate gene for type 2 diabetes.Semantic proximity Read ↗

A SNP haplotype of the forkhead transcription factor FOXO1A gene may have a protective effect against type 2 diabetes in German Caucasians.Semantic proximity Read ↗

A common polymorphism in exon 16 of the human insulin-like growth factor-1 receptor gene (IGF1R).Semantic proximity Read ↗

Genomics complement of FOXO1 gene prevents Type 2 DiabetesSemantic proximity Read ↗

Early-onset Type II diabetes mellitus in Italian families due to mutations in the genes encoding hepatic nuclear factor 1 alpha and glucokinase.Semantic proximity Read ↗

Genetic variation in insulin/IGF-1 signaling pathways and longevity.Semantic proximity Read ↗

Association between genetic variations in the insulin/insulin-like growth factor (Igf-1) signaling pathway and longevity: a systematic review and meta-analysis.Semantic proximity Read ↗

Characterization of genetic variation in the Forkhead box class O3 gene (FOXO3) in sheep.Semantic proximity Read ↗

Candidate gene study of FOXO1, FOXO4, and FOXO6 reveals no association with human longevity in GermansSemantic proximity Read ↗

Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity.Semantic proximity Read ↗

A newly identified mutation in an IPF1 binding site of the insulin gene promoter may predispose to type 2 diabetes mellitus.Semantic proximity Read ↗

Genetic investigation of FOXO3A requires special attention due to sequence homology with FOXO3B.Semantic proximity Read ↗

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