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

Revisiting the association of sudden infant death syndrome (SIDS) with polymorphisms of NHE3 and IL13.

International journal of legal medicine - 1 May 2024

Qu Dong, Schürmann Peter, Rothämel Thomas, Fleßner Jessica, Rehberg Daniela, Dörk Thilo, Klintschar Michael

Abstract excerpt

OBJECTIVES: Disturbances of the central nervous system and immune system are thought to play a role in sudden infant death syndrome (SIDS). Dysregulated expression of sodium (Na+)/hydrogen (H+) exchanger 3 (NHE3) in the brainstem and of interleukin 13 (IL13) in the lungs has been observed in SIDS. An association of single-nucleotide polymorphisms (SNPs) in NHE3 and IL13 with SIDS has been proposed, but...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Predisposition to Disease
Share to Infant

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Interleukin-13

Share to Polymorphism, Single Nucleotide

Share to Sudden Infant Death

Source

Open in PubMed Open full text

Identifiers

PMID: 38091065
DOI: 10.1007/s00414-023-03139-2
PMCID: PMC11003888

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Revisiting the association of sudden infant death syndrome (SIDS) with polymorphisms of NHE3 and IL13.PMID 38091065Read ↗

Sodium/proton exchanger 3 (NHE3) and sudden infant death syndrome (SIDS).Semantic proximity Read ↗

Impact of sodium/proton exchanger 3 gene variants on sudden infant death syndrome.Semantic proximity Read ↗

Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.Semantic proximity Read ↗

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

Aquaporin-1 and aquaporin-9 gene variations in sudden infant death syndrome.Semantic proximity Read ↗

Gene variants predisposing to SIDS: current knowledge.Semantic proximity Read ↗

Candidate gene variants of the immune system and sudden infant death syndrome.Semantic proximity Read ↗

The gene encoding the inwardly rectifying potassium channel Kir4.1 may be involved in sudden infant death syndrome.Semantic proximity Read ↗

Altered gene expression and possible immunodeficiency in cases of sudden infant death syndrome.Semantic proximity Read ↗

Genetic Association Study of Acetylcholinesterase (ACHE) and Butyrylcholinesterase (BCHE) Variants in Sudden Infant Death Syndrome (SIDS).Semantic proximity Read ↗

Cytokine gene polymorphisms and sudden infant death syndrome.Semantic proximity Read ↗

Aquaporin 4 expression in the hippocampus in sudden infant death syndrome and sudden unexplained death in childhoodSemantic proximity Read ↗

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