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Genetic study of ICAM1 in clinical malaria in Senegal.

机译:塞内加尔临床疟疾中ICAM1的遗传研究。

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摘要

Many genes have been implicated in the risk of severe malaria, generally based on candidate gene studies in case/control populations. Among these genes, there has been conflicting reports for the implication of a variant of the intercellular adhesion molecule 1 (ICAM1), ICAM1(Kilifi), in the risk of severe malaria, while in vitro studies provided independent support for a functional role of this variant. In order to explore the possible implication of ICAM1 in the susceptibility/resistance to malaria and to try to understand its clinical relevance in the disease process, we have conducted linkage and association studies of ICAM1 in two Senegalese villages located in regions of endemic malaria. We explored the full genetic variability of ICAM1, and tested it on several clinical malarial traits which are under genetic control, focusing principally on variables related to the parasite density and the number of malarial attacks. Our study provides no evidence for a role of ICAM1 variability on the malarialphenotypes studied.
机译:通常根据病例/对照人群的候选基因研究,许多基因与严重疟疾风险有关。在这些基因中,关于细胞间粘附分子1(ICAM1),ICAM1(Kilifi)的变体在严重疟疾中的隐含作用存在矛盾的报道,而体外研究对此功能的作用提供了独立的支持。变体。为了探索ICAM1对疟疾的敏感性/耐药性并试图了解其在疾病过程中的临床意义,我们在位于疟疾流行地区的两个塞内加尔村庄进行了ICAM1的关联研究。我们探索了ICAM1的完整遗传变异性,并在遗传控制下的几种临床疟疾特征上对其进行了测试,主要关注与寄生虫密度和疟疾发作次数有关的变量。我们的研究没有证据表明ICAM1变异在研究的疟疾表型中的作用。

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