Results 71 to 80 of about 17,285 (228)

Neonatal Ontogeny of Murine Arylamine N-Acetyltransferases: Implications for Arylamine Genotoxicity [PDF]

open access: yesToxicological Sciences, 2003
Age-related changes in the expression of xenobiotic biotransformation enzymes can result in differences in the rates of chemical activation and detoxification, affecting responses to the therapeutic and/or toxic effects of chemicals. Despite recognition that children and adults may exhibit differences in susceptibility to chemicals, information about ...
Binh Chau, Charlene A. McQueen
openaire   +3 more sources

Structure and Mechanism of Arylamine N-Acetyltransferases

open access: yesCurrent Topics in Medicinal Chemistry, 2006
Arylamine N-acetyltransferases (NATs) are a family of phase II drug-metabolising enzymes which are important in the biotransformation of various aromatic and heterocyclic amines and hydroxylamines, arylhydrazines and arylhydrazides. NATs are present in a wide range of eukaryotes and prokaryotes.
Westwood, I M   +5 more
openaire   +3 more sources

Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene [PDF]

open access: yes, 2015
Journal ArticleDecreased insulin sensitivity, also referred to as insulin resistance (IR), is a fundamental abnormality in patients with type 2 diabetes and a risk factor for cardiovascular disease. While IR predisposition is heritable, the genetic basis
Alan Sinaiko   +48 more
core   +1 more source

Asociación entre polimorfismos del gen NAT2 y fisura labiopalatina no sindrómica en Argentina [PDF]

open access: yes, 2015
Background: NAT genes are considered candidate genes for the genetic predisposition to non-syndromic Cleft lip with or without cleft palate (NSCLP), since they codify for N-acetyltransferases, enzymes responsible for the biotransformation of arylamines ...
Bailliet, Graciela   +4 more
core   +5 more sources

Exploration of Piperidinols as Potential Antitubercular Agents

open access: yesMolecules, 2014
Novel drugs to treat tuberculosis are required and the identification of potential targets is important. Piperidinols have been identified as potential antimycobacterial agents (MIC < 5 μg/mL), which also inhibit mycobacterial arylamine N ...
Areej Abuhammad   +6 more
doaj   +1 more source

Human Arylamine N-Acetyltransferase 1 Is Inhibited by the Dithiocarbamate Pesticide Thiram

open access: bronzeMolecular Pharmacology, 2017
Ximing Xu   +7 more
openalex   +2 more sources

Determination of Human NAT2 Acetylator Genotype by Oligonucleotide Ligation Assay

open access: yesBioTechniques, 1997
The oligonucleotide ligation assay (OLA) was adapted to the genotyping of the N-arylamine-acetyltransferase (NAT2) gene. This assay allows the use of 96-well microplates and robotic workstations for high sample throughput.
Jeannette Bigler   +2 more
doaj   +1 more source

Identification of new arylamine N-acetyltransferases and enhancing 2-acetamidophenol production in Pseudomonas chlororaphis HT66

open access: yesMicrobial Cell Factories, 2020
Background 2-Acetamidophenol (AAP) is an aromatic compound with the potential for antifungal, anti-inflammatory, antitumor, anti-platelet, and anti-arthritic activities.
Shuqi Guo   +4 more
doaj   +1 more source

Polymorphisms in GSTT1, GSTM1, NAT1 and NAT2 genes and bladder cancer risk in men and women [PDF]

open access: yes, 2011
Background: Cigarette smoking is an established risk factor for bladder cancer. Epidemiological and biological data suggest that genetic polymorphisms in activating and detoxifying enzymes may play a role in determining an individual's susceptibility to ...
De Vivo, Immaculata   +2 more
core   +1 more source

Characterisation of a putative AraC transcriptional regulator from Mycobacterium smegmatis [PDF]

open access: yes, 2014
MSMEG_0307 is annotated as a transcriptional regulator belonging to the AraC protein family and is located adjacent to the arylamine N-acetyltransferase (nat) gene in Mycobacterium smegmatis, in a gene cluster, conserved in most environmental ...
Abuhammad   +48 more
core   +1 more source

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