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

Mitochondrial tRNA genes and flanking regions in sudden infant death syndrome.

Acta paediatrica (Oslo, Norway : 1992) - 1 Feb 2007

Opdal Siri Hauge, Vege Ashild, Arnestad Marianne, Musse Musse Ahmed, Rognum Torleiv Ole

Abstract excerpt

AIM: Mitochondrial DNA (mtDNA) mutations have been proposed as a genetic risk factor for sudden infant death syndrome (SIDS). The aim of this study was to further investigate this issue, by sequencing the mitochondrial tRNA genes with flanking regions in SIDS cases and controls. METHOD: The selected genes were investigated in 24 cases of SIDS and 10 controls, the method used were direct sequencing. In addition,...

Read the complete abstract on PubMed

Topics

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

Share to 3' Flanking Region
Share to 5' Flanking Region

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Mitochondrial

Share to Infant, Newborn

Share to RNA, Mitochondrial

Share to RNA, Transfer

Share to Sudden Infant Death

Source

Identifiers

PMID: 17429907
DOI: 10.1111/j.1651-2227.2007.00085.x

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

Mitochondrial tRNA genes and flanking regions in sudden infant death syndrome.PMID 17429907Read ↗

Analysis of the mitochondrial genome in sudden infant death syndrome.Semantic proximity Read ↗

Mitochondrial deoxyribonucleic acid may play a role in a subset of sudden infant death syndrome cases.Semantic proximity Read ↗

A mitochondrial DNA polymorphism associated with cardiac arrhythmia investigated in sudden infant death syndrome.Semantic proximity Read ↗

Mutational Screening for Mitochondrial tRNA Genes in 100 Women with Pre-Eclampsia.Semantic proximity Read ↗

The sudden infant death syndrome gene: does it exist?Semantic proximity Read ↗

Genetic variation in the monoamine oxidase A and serotonin transporter genes in sudden infant death syndrome.Semantic proximity Read ↗

Sudden infant death syndrome (SIDS) and polymorphisms in Monoamine oxidase A gene (MAOA): a revisit.Semantic proximity Read ↗

Sudden infant death syndrome revisited: serotonin transporter gene, polymorphisms and promoter methylation.Semantic proximity Read ↗

Possible role of mtDNA mutations in sudden infant death.Semantic proximity Read ↗

Association between monoamine oxidase A promoter polymorphism and the risk of sudden infant death syndrome: a meta-analysis.Semantic proximity Read ↗

Tyrosine hydroxylase TH01 9.3 allele in the occurrence of sudden infant death syndrome in Swiss Caucasians.Semantic proximity Read ↗

Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland.Semantic proximity Read ↗

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