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Article

Arylamine N-acetyltransferase (NAT2) gene mutations in children with allergic diseases.

Clinical pharmacology and therapeutics - 1 Dec 1997

Zielińska E, Niewiarowski W, Bodalski J, Stańczyk A, Bolanowski W, Rebowski G

Abstract excerpt

The overrepresentation of phenotypically slow acetylators among patients with atopic allergy has been reported in previous studies. The N-acetyltransferase coding gene has not yet been investigated in allergic diseases. This study was designed to determine the differences in the distribution of m...

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Source

Identifiers

PMID: 9433392
DOI: 10.1016/S0009-9236(97)90083-7

Genes

NAT2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-9433392-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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Arylamine N-acetyltransferase (NAT2) gene mutations in children with allergic diseases.PMID 9433392Read ↗

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N-acetyltransferase 2 acetylation polymorphism: prevalence of slow acetylators does not differ between atopic dermatitis patients and healthy subjects.Semantic proximity Read ↗

[Polymorphism of N-acetyltransferase-2 and pathogenesis of neoplastic diseases].Semantic proximity Read ↗

Genotype of N-acetyltransferase 2 (NAT2) polymorphism in children with immunoglobulin E-mediated food allergy.Semantic proximity Read ↗

Cloning, expression, and functional characterization of two mutant (NAT2(191) and NAT2(341/803)) and wild-type human polymorphic N-acetyltransferase (NAT2) alleles.Semantic proximity Read ↗

NAT2 slow acetylation genotypes contribute to asthma risk among Caucasians: evidence from 946 cases and 1,091 controls.Semantic proximity Read ↗

Association between the N-acetylation genetic polymorphism and bronchial asthma.Semantic proximity Read ↗

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