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Pharmacogenetics of asthma.

机译:哮喘的药物遗传学。

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摘要

Recent advances in the extent of knowledge regarding interindividual genetic variation in drug treatment targets and drug metabolizing enzymes has resulted in studies designed to assess the contribution of genetic variability to treatment response in a range of diseases. This review describes the current state of knowledge of genetic variability in key airway targets important in the treatment of asthma. Whilst the genes coding for some key treatment targets contain little polymorphic variation (e.g. the muscarinic M2 and M3 receptors) other genes whose products are important targets in the treatment of asthma contain extensive genetic variation. The best examples of the latter are the beta2-adrenoceptor and the 5-lipoxygenase genes. Genetic variability in both of these genes may account in part for interindividual variability in treatment response. Finally, a number of key targets within the airways remain to be adequately screened for polymorphic variation.
机译:关于药物治疗靶标和药物代谢酶中个体间遗传变异的知识范围的最新进展,导致了旨在评估遗传变异对多种疾病治疗反应的贡献的研究。这篇综述描述了在哮喘治疗中重要的关键气道靶标中遗传变异性的当前知识状态。虽然编码某些关键治疗靶标的基因几乎没有多态性变异(例如毒蕈碱M2和M3受体),但其产物在哮喘治疗中是重要靶标的其他基因却具有广泛的遗传变异。后者的最佳例子是β2-肾上腺素能受体和5-脂氧合酶基因。这两个基因的遗传变异可能部分解释了治疗反应的个体差异。最后,仍然需要对气道内的许多关键目标进行适当的多态变异筛选。

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