Cloning, sequencing and expression of NAT1 and NAT2 encoding genes from rapid and slow acetylator inbred rats

GSTM1 null and NAT2 slow acetylation genotypes, smoking intensity and bladder cancer risk: results from the New England bladder cancer study and NAT2 meta-analysis.

Carcinogenesis·2010

Acetyl CoA:arylamine N-acetyltransferase activity in rat hepatocytes cultured on different extracellular matrices.

Toxicology in vitro : an international journal published in association with BIBRA·2010

Para-phenylenediamine and allergic sensitization: risk modification by N-acetyltransferase 1 and 2 genotypes.

The British journal of dermatology·2009

Role of human CYP1A1 and NAT2 in 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine-induced mutagenicity and DNA adducts.

Xenobiotica; the fate of foreign compounds in biological systems·2009

Skin metabolism of aminophenols: human keratinocytes as a suitable in vitro model to qualitatively predict the dermal transformation of 4-amino-2-hydroxytoluene in vivo.

Toxicology and applied pharmacology·2008

Functional effects of single nucleotide polymorphisms in the coding region of human N-acetyltransferase 1.

The pharmacogenomics journal·2007

No evidence of a role for PPARgamma Pro12Ala polymorphism in endometrial cancer susceptibility.

Pharmacogenetics·2004

Pharmacogenetics and herb-drug interactions: experience with Ginkgo biloba and omeprazole.

Pharmacogenetics·2004

Functional comparison of the endothelial nitric oxide synthase Glu298Asp polymorphic variants in human endothelial cells.

Pharmacogenetics·2004

Response to micronized fenofibrate treatment is associated with the peroxisome-proliferator-activated receptors alpha G/C intron7 polymorphism in subjects with type 2 diabetes.

Pharmacogenetics·2004

Upstream and coding region CYP2C9 polymorphisms: correlation with warfarin dose and metabolism.

Pharmacogenetics·2004

The human serotonin receptor 2B: coding region polymorphisms and association with vulnerability to illegal drug abuse.

Pharmacogenetics·2004

A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans.

Clinical genetics·2026

Multivariate genetic analyses test for the presence of a general 'n' factor underlying neurodevelopmental conditions.

JCPP advances·2026

Functional profiling of STXBP1 missense variants using a novel dual-readout fluorometric assay.

Epilepsia·2026

The association of neighborhood socioeconomic status with birth weight is not confounded by ambient air pollution in twin pregnancies: a retrospective cohort study.

Neonatology·2026

Don't miss this treatable neurogenetic disease!

Pediatric radiology·2026

Large-scale genetic profiling of hereditary ataxias in China: implications for a stepwise molecular diagnostic strategy.

Translational neurodegeneration·2026

Related Experiment Videos

Cloning, sequencing and expression of NAT1 and NAT2 encoding genes from rapid and slow acetylator inbred rats

Related Concept Videos

GSTM1 null and NAT2 slow acetylation genotypes, smoking intensity and bladder cancer risk: results from the New England bladder cancer study and NAT2 meta-analysis.

Acetyl CoA:arylamine N-acetyltransferase activity in rat hepatocytes cultured on different extracellular matrices.

Para-phenylenediamine and allergic sensitization: risk modification by N-acetyltransferase 1 and 2 genotypes.

Role of human CYP1A1 and NAT2 in 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine-induced mutagenicity and DNA adducts.

Skin metabolism of aminophenols: human keratinocytes as a suitable in vitro model to qualitatively predict the dermal transformation of 4-amino-2-hydroxytoluene in vivo.

Functional effects of single nucleotide polymorphisms in the coding region of human N-acetyltransferase 1.

No evidence of a role for PPARgamma Pro12Ala polymorphism in endometrial cancer susceptibility.

Pharmacogenetics and herb-drug interactions: experience with Ginkgo biloba and omeprazole.

Functional comparison of the endothelial nitric oxide synthase Glu298Asp polymorphic variants in human endothelial cells.

Response to micronized fenofibrate treatment is associated with the peroxisome-proliferator-activated receptors alpha G/C intron7 polymorphism in subjects with type 2 diabetes.

Upstream and coding region CYP2C9 polymorphisms: correlation with warfarin dose and metabolism.

The human serotonin receptor 2B: coding region polymorphisms and association with vulnerability to illegal drug abuse.

A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans.

Multivariate genetic analyses test for the presence of a general 'n' factor underlying neurodevelopmental conditions.

Functional profiling of STXBP1 missense variants using a novel dual-readout fluorometric assay.

The association of neighborhood socioeconomic status with birth weight is not confounded by ambient air pollution in twin pregnancies: a retrospective cohort study.

Don't miss this treatable neurogenetic disease!

Large-scale genetic profiling of hereditary ataxias in China: implications for a stepwise molecular diagnostic strategy.

Related Experiment Videos

Cloning, sequencing and expression of NAT1 and NAT2 encoding genes from rapid and slow acetylator inbred rats

Related Concept Videos

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