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

Relationship between TBX20 gene polymorphism and congenital heart disease.

Genetics and molecular research : GMR - 2 Jun 2016

Yang X F, Zhang Y F, Zhao C F, Liu M M, Si J P, Fang Y F, Xing W W, Wang F L

Abstract excerpt

Congenital heart disease in children is a type of birth defect. Previous studies have suggested that the transcription factor, TBX20, is involved in the occurrence and development of congenital heart disease in children; however, the specific regulatory mechanisms are yet to be evaluated. Hence, this study aimed to evaluate the relationship between the TBX20 polymorphism and the occurrence and development of...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Case-Control Studies
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heart Defects, Congenital

Share to Polymorphism, Single Nucleotide

Share to T-Box Domain Proteins

Source

Identifiers

PMID: 27323105
DOI: 10.4238/gmr.15027374

Genes

TBX20

Variants

rs3999950

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

Relationship between TBX20 gene polymorphism and congenital heart disease.PMID 27323105Read ↗

Association of TBX20 gene polymorphism with congenital heart disease in Han Chinese neonates.Semantic proximity Read ↗

The Role of TBX20 Gene Mutations in the Pathogenesis of Congenital Heart Disease: Functional Analysis and Genetic Association Study.Semantic proximity Read ↗

T-box transcription factor TBX20 mutations in Chinese patients with congenital heart disease.Semantic proximity Read ↗

Mild decrease in TBX20 promoter activity is a potentially protective factor against congenital heart defects in the Han Chinese population.Semantic proximity Read ↗

[Association between Tbx20 gene polymorphism and congenital atrial septal defects].Semantic proximity Read ↗

[Association between the SNPs of human Tbx20 gene and congenital atrial septal defects in Uygur population of Xinjiang region].Semantic proximity Read ↗

Association Analysis of Nonsyndromic Congenital Heart Disease and Tag Single Nucleotide Polymorphisms of TBX20 and Genes in the Ras-MAPK Pathway.Semantic proximity Read ↗

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.Semantic proximity Read ↗

Familial cardiac septal defect due to a novel nine-base deletion in TBX20.Semantic proximity Read ↗

Upregulation of TBX1 by genetic variants are associated with human congenital heart diseaseSemantic proximity Read ↗

Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy.Semantic proximity Read ↗

Screening and evaluation of TBX20 and CITED2 mutations in children with congenital cardiac septal defects: Correlation with cardiac troponin T and caspase-3.Semantic proximity Read ↗

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