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

The genotype and expression of the TGFβ2 gene in children with congenital conotruncal defects.

Pediatric cardiology - 1 Jan 2013

Meng Yingying, Ma Xiaojing, Zhang Jing, Wang Huijun, Ma Duan, Huang Guoying

Abstract excerpt

Animal studies have shown that knockout of the transforming growth factor beta-2 (TGFβ2) gene results in diverse cardiovascular malformations and that its unregulated expression is involved in the pathogenesis of heart defects. However, little information is available on the genetic and expressio...

Read the complete abstract on PubMed

Topics

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

Share to Gene Expression Regulation, Developmental
Share to Heart Defects, Congenital
Share to Immunohistochemistry

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Infant, Newborn

Share to Real-Time Polymerase Chain Reaction

Share to Transforming Growth Factor beta2

Source

Identifiers

PMID: 23712828
DOI: 10.1007/s00246-013-0696-2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23712828-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

The genotype and expression of the TGFβ2 gene in children with congenital conotruncal defects.PMID 23712828Read ↗

Genetic variance of transforming growth factor β2 gene in conotruncal heart defects.Semantic proximity Read ↗

Polymorphisms of VEGF, TGFβ1, TGFβR2 and conotruncal heart defects in a Chinese population.Semantic proximity Read ↗

Association between TGFBR2 gene polymorphisms and congenital heart defects in Han Chinese population.Semantic proximity Read ↗

TGFbeta2 knockout mice have multiple developmental defects that are non-overlapping with other TGFbeta knockout phenotypes.Semantic proximity Read ↗

Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients.Semantic proximity Read ↗

Association of TGFBR2 rs6785358 Polymorphism with Increased Risk of Congenital Ventricular Septal Defect in a Chinese Population.Semantic proximity Read ↗

[Association between rs6658835 polymorphism of transforming growth factor beta 2 gene and congenital heart diseases in Chinese Han population].Semantic proximity Read ↗

Cloning of TgfβR1 and TgfβR2 and Likely Exclusion as Loci of Origin in a Rabbit Craniosynostotic Model.Semantic proximity Read ↗

DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 gene.Semantic proximity Read ↗

Contribution of TGFB1 and TNF-α genes in one of twin pregnancies with congenital complete heart block phenotype.Semantic proximity Read ↗

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