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

Differential duplication of an intronic region in the NFATC1 gene in patients with congenital heart disease.

Genome - 1 Sept 2006

Yehya Amin, Souki Ramzi, Bitar Fadi, Nemer Georges

Abstract excerpt

Most forms of congenital heart disease (CHD) result from aberrations in cardiac morphogenesis including errors in septation, valve formation, and proper patterning of the great vessels. Transcription factors are key proteins that dictate mRNA synthesis rate and subsequent protein production in mo...

Read the complete abstract on PubMed

Topics

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

Share to Alternative Splicing
Share to Gene Duplication
Share to Heart Defects, Congenital

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heart Septal Defects, Ventricular

Share to Lebanon

Share to NFATC Transcription Factors

Share to Protein Isoforms

Share to Tandem Repeat Sequences

Source

Identifiers

PMID: 17110989
DOI: 10.1139/g06-072

Genes

NFATC1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17110989-2026-09-02.2. 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

Differential duplication of an intronic region in the NFATC1 gene in patients with congenital heart disease.PMID 17110989Read ↗

Two heterozygous mutations in NFATC1 in a patient with Tricuspid Atresia.Semantic proximity Read ↗

Association Between Single Nucleotide Polymorphisms in NFATC1 Signaling Pathway Genes and Susceptibility to Congenital Heart Disease in the Chinese Population.Semantic proximity Read ↗

Association of NFATc1 gene polymorphism with ventricular septal defect in the Chinese Han population.Semantic proximity Read ↗

Genetic and functional analyses detect one pathological NFATC1 mutation in a Chinese tricuspid atresia family.Semantic proximity Read ↗

The NFKB1 -94 ATTG insertion/deletion polymorphism (rs28362491) contributes to the susceptibility of congenital heart disease in a Chinese population.Semantic proximity Read ↗

Absence of association between length variation of an intronic region in the NFATC1 gene and congenital heart defects in a Han Chinese population.Semantic proximity Read ↗

A novel mutation in exon 1 of GATA4 in Egyptian patients with congenital heart disease.Semantic proximity Read ↗

Correlation between NFATC1 gene polymorphisms and congenital heart disease in children.Semantic proximity Read ↗

Mutations of transcription factors in human with heart disease for understanding the development and mechanisms of congenital cardiovascular heart disease.Semantic proximity Read ↗

Novel and functional sequence variants within the TBX2 gene promoter in ventricular septal defects.Semantic proximity Read ↗

Study of variants associated with ventricular septal defects (VSDs) highlights the unique genetic structure of the Pakistani population.Semantic proximity Read ↗

[Novel GATA4 mutations identified in patients with congenital atrial septal defects].Semantic proximity Read ↗

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