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

Human fetal heart specific coexpression network involves congenital heart disease/defect candidate genes.

Scientific reports - 24 Apr 2017

Wang Bo, You Guoling, Fu Qihua

Abstract excerpt

Heart development is a complex process requiring dynamic transcriptional regulation. Disturbance of this process will lead to severe developmental defects such as congenital heart disease/defect (CHD). CHD is a group of complex disorder with high genetic heterogeneity, common pathways associated with CHD remains largely unknown. In the manuscript, we focused on the tissue specific genes in human fetal heart...

Read the complete abstract on PubMed

Topics

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

Share to Cluster Analysis
Share to Evolution, Molecular
Share to Fetal Heart

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Expression Profiling

Share to Gene Expression Regulation, Developmental

Share to Gene Ontology

Share to Gene Regulatory Networks

Share to Heart Defects, Congenital

Source

Open in PubMed Open full text

Identifiers

PMID: 28436429
DOI: 10.1038/srep46760
PMCID: PMC5402266

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Human fetal heart specific coexpression network involves congenital heart disease/defect candidate genes.PMID 28436429Read ↗

Molecular convergence of risk variants for congenital heart defects leveraging a regulatory map of the human fetal heartSemantic proximity Read ↗

Systems Analysis of de novo Mutations in Congenital Heart Diseases Identified a Molecular Network in Hypoplastic Left Heart SyndromeSemantic proximity Read ↗

CHDTEPDB: Transcriptome Expression Profile Database and Interactive Analysis Platform for Congenital Heart DiseaseSemantic proximity Read ↗

Systems analysis of de novo mutations in congenital heart diseases identified a protein network in the hypoplastic left heart syndrome.Semantic proximity Read ↗

Gene regulatory networks in the evolution and development of the heart.Semantic proximity Read ↗

Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart development.Semantic proximity Read ↗

Analysis of commonly expressed genes between first trimester fetal heart and placenta cell types in the context of congenital heart diseaseSemantic proximity Read ↗

Exploration and Validation of Hub Genes and Pathways in the Progression of Hypoplastic Left Heart Syndrome via Weighted Gene Co-Expression Network AnalysisSemantic proximity Read ↗

Analysis of commonly expressed genes between first trimester fetal heart and placenta cell types in the context of congenital heart diseaseSemantic proximity Read ↗

Exploration and validation of hub genes and pathways in the progression of hypoplastic left heart syndrome via weighted gene co-expression network analysis.Semantic proximity Read ↗

Deciphering transcriptional networks during human cardiac developmentSemantic proximity Read ↗

Gene expression and transcriptional regulation driven by transcription factors involved in congenital heart defects.Semantic proximity Read ↗

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