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

Retinoid Pathway and Congenital Diaphragmatic Hernia: Hypothesis from the Analysis of Chromosomal Abnormalities

1 Jan 2010

Abstract excerpt

BACKGROUND/OBJECTIVES: Although there is strong evidence implicating genetic factors in congenital diaphragmatic hernia (CDH) pathogenesis, few causal genes have been identified. Many studies suggest that early disruption of the retinoid signaling pathway during gestation may contribute to CDH etiology. Chromosome abnormalities are detected in 10-20% of CDH cases. Chromosomal regions that are involved in balanced...

Read the complete abstract on PubMed

Topics

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

Share to Congenital Diaphragmatic Hernia Studies
Share to Neonatal Health and Biochemistry
Share to Neuroblastoma Research and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 20501978
DOI: 10.1159/000313331

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Retinoid Pathway and Congenital Diaphragmatic Hernia: Hypothesis from the Analysis of Chromosomal AbnormalitiesPMID 20501978Read ↗

The etiology of congenital diaphragmatic hernia: the retinoid hypothesis 20 years laterSemantic proximity Read ↗

Congenital diaphragmatic hernia (CDH) etiology as revealed by pathway geneticsSemantic proximity Read ↗

Congenital diaphragmatic hernia and retinoids: searching for an etiologySemantic proximity Read ↗

Metabolic disturbances of the vitamin A pathway in human diaphragmatic herniaSemantic proximity Read ↗

Congenital diaphragmatic hernia: A retinoid‐signaling pathway disruption during lung development?Semantic proximity Read ↗

Congenital diaphragmatic hernias: from genes to mechanisms to therapies.Semantic proximity Read ↗

Gene ontology enrichment analysis of congenital diaphragmatic hernia-associated genesSemantic proximity Read ↗

The role of genes and environment in the etiology of congenital diaphragmatic hernias.Semantic proximity Read ↗

De novo copy number variants are associated with congenital diaphragmatic hernia.Semantic proximity Read ↗

Linking animal models to human congenital diaphragmatic herniaSemantic proximity Read ↗

Developmental and genetic aspects of congenital diaphragmatic hernia.Semantic proximity Read ↗

Genetic aspects of human congenital diaphragmatic herniaSemantic proximity Read ↗

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