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首页> 外文期刊>Lancet Neurology >DNA microarrays: translation of the genome from laboratory to clinic.
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DNA microarrays: translation of the genome from laboratory to clinic.

机译:DNA微阵列:从实验室到临床的基因组翻译。

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摘要

As the complete sequences of human and other mammalian genomes become available we are faced with the challenge of understanding how variation in sequence and gene expression contributes to neurological and psychiatric disorders. DNA microarrays, or DNA chips, provide the means to measure simultaneously where and when thousands of genes are expressed. Microarrays are changing the way that researchers approach work at the bench and have already yielded new insights into brain tumours, multiple sclerosis, acute neurological insults such as stroke and seizures, and schizophrenia. The study of disease-related changes in gene expression is the first step in the long process in translation of genome research to the clinic. Eventually, the changes observed in microarray studies will need to be independently confirmed and we wil need to understand how gene expression changes translate into functional effects at the cellular level in the nervous system. Progress in these studies will translate into array-based disease classification schemes and help optimise therapy for individual patients based on gene expression patterns or their genetic background.
机译:随着人类和其他哺乳动物基因组的完整序列变得可用,我们面临着挑战,即了解序列和基因表达的变化如何导致神经系统疾病和精神疾病的挑战。 DNA微阵列或DNA芯片提供了同时测量数千个基因在何处和何时表达的方法。微阵列正在改变研究人员在替补席上工作的方式,并且已经对脑肿瘤,多发性硬化症,中风和癫痫发作等急性神经系统损伤以及精神分裂症产生了新见解。与疾病相关的基因表达变化的研究是将基因组研究转化为临床的漫长过程中的第一步。最终,需要独立确认在微阵列研究中观察到的变化,我们将需要了解基因表达的变化如何在神经系统的细胞水平上转化为功能作用。这些研究的进展将转化为基于阵列的疾病分类方案,并有助于根据基因表达模式或遗传背景针对个别患者优化治疗。

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