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

Sudden infant death syndrome: rare mutation in the serotonin system FEV gene.

Pediatric research - 1 Aug 2007

Rand Casey M, Berry-Kravis Elizabeth M, Zhou Lili, Fan Wenqing, Weese-Mayer Debra E

Abstract excerpt

Recent studies have identified abnormalities in the development and function of medullary serotonin (5-HT) pathways in postmortem brain from sudden infant death syndrome (SIDS) cases, suggesting 5-HT-mediated dysregulation of the autonomic nervous system (ANS) in SIDS. The human fifth Ewing variant (FEV) gene is specifically expressed in central 5-HT neurons in the brain, with a predicted role in specification...

Read the complete abstract on PubMed

Topics

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

Share to Black or African American
Share to Introns
Share to Mutagenesis, Insertional

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Neurons

Share to Nuclear Proteins

Share to Serotonin

Share to Sudden Infant Death

Share to White People

Source

Identifiers

PMID: 17597646
DOI: 10.1203/PDR.0b013e3180a725a0

Genes

FEV

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

Sudden infant death syndrome: rare mutation in the serotonin system FEV gene.PMID 17597646Read ↗

Serotonin-related FEV gene variant in the sudden infant death syndrome is a common polymorphism in the African-American population.Semantic proximity Read ↗

High serum serotonin in sudden infant death syndrome.Semantic proximity Read ↗

HTR2A variation and sudden infant death syndrome: a case-control analysis.Semantic proximity Read ↗

Multiple serotonergic brainstem abnormalities in sudden infant death syndrome.Semantic proximity Read ↗

Serotonin gene variants are unlikely to play a significant role in the pathogenesis of the sudden infant death syndrome.Semantic proximity Read ↗

Sudden Infant Death Syndrome: review of implicated genetic factors.Semantic proximity Read ↗

The expression of the transcription factor FEV in adult human brain and its association with affective disorders.Semantic proximity Read ↗

Identifying infants at risk for sudden infant death syndrome.Semantic proximity Read ↗

Genomic risk factors in sudden infant death syndromeSemantic proximity Read ↗

Sudden infant death syndrome: another year of new hope but no cure.Semantic proximity Read ↗

Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis.Semantic proximity Read ↗

Sudden infant death syndrome and sudden intrauterine unexplained death: correlation between hypoplasia of raphé nuclei and serotonin transporter gene promoter polymorphism.Semantic proximity Read ↗

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