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

Cytochrome P450 2D6 and glutathione S-transferase genotype in sudden infant death syndrome.

Journal of paediatrics and child health - 1 Feb 1997

Chen C L, Liu Q, Evans W E, Sander C H, Relling M V

Abstract excerpt

OBJECTIVES: The risk of sudden infant death syndrome (SIDS) has been linked with xenobiotic exposures, race and inheritance. Because cytochrome P450 2D6 (CYP2D6) and glutathione S-transferases (GSTM1 and GSTT1) are genetically regulated, polymorphically distributed, and responsible for detoxification of many centrally acting exogenous and endogenous bioactive compounds, our objective was to determine whether the...

Read the complete abstract on PubMed

Topics

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

Share to Cytochrome P-450 CYP2D6
Share to GSTM1 gene
Share to Genotype

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Glutathione Transferase

Share to Infant

Share to Mutation

Share to Phenotype

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 9069041
DOI: 10.1111/j.1440-1754.1997.tb00987.x

Genes

GSTM1
GSTT1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Cytochrome P450 2D6 and glutathione S-transferase genotype in sudden infant death syndrome.PMID 9069041Read ↗

Fatal intoxication cases: cytochrome P450 2D6 and 2C19 genotype distributions.Semantic proximity Read ↗

From Genotype to Phenotype: Cytochrome P450 2D6-Mediated Drug Clearance in Humans.Semantic proximity Read ↗

Detoxification genes polymorphisms in SIDS exposed to tobacco smoke.Semantic proximity Read ↗

Cytochrome P450 2D6 and glutathione S-transferase M1 genotypes and migraine.Semantic proximity Read ↗

Ontogeny of dextromethorphan O- and N-demethylation in the first year of life.Semantic proximity Read ↗

Polymorphism of dextromethorphan metabolism: relationships between phenotype, genotype and response to the administration of encainide in humans.Semantic proximity Read ↗

Discrepancy between CYP2D6 phenotype and genotype derived from post-mortem dextromethorphan blood level.Semantic proximity Read ↗

A fatal doxepin poisoning associated with a defective CYP2D6 genotype.Semantic proximity Read ↗

Developmental changes in human liver CYP2D6 expression.Semantic proximity Read ↗

No association of SIDS with two polymorphisms in genes relevant for the noradrenergic system: COMT and DBH.Semantic proximity Read ↗

Lack of association of the serotonin transporter polymorphism with the sudden infant death syndrome in the San Diego Dataset.Semantic proximity Read ↗

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