Abstract:
:Genetic polymorphism of drug metabolizing enzymes (DME) can lead to severe toxicity or therapeutic failure of pharmacotherapy. Additionally, genetically determined differences in the activity of the metabolic enzymes can increase an individual's susceptibility to certain types of chemically induced cancers and possibly other diseases. Cytochrome P450 is one of the most important metabolic systems of the organism involved in the oxidation of different xenobiotics. This contribution summarizes and updates the information concerning the genetic polymorphism of the CYP2A6 isoform of the cytochrome P450. A special emphasis is put upon the genotyping techniques of CYP2A6 with a comparative analysis of their predictable sensitivity and specificity given on the example of the German population.
journal_name
Toxicologyjournal_title
Toxicologyauthors
Bourian M,Gullstén H,Legrum Wdoi
10.1016/s0300-483x(99)00199-7keywords:
subject
Has Abstractpub_date
2000-04-03 00:00:00pages
129-37issue
1-3eissn
0300-483Xissn
1879-3185pii
S0300483X99001997journal_volume
144pub_type
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