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A genetic approach to understanding auditory function.

机译:一种了解听觉功能的遗传方法。

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摘要

Little is known of the molecular basis of normal auditory function. In contrast to the visual or olfactory senses, in which reasonable amounts of sensory tissue can be gathered, the auditory system has proven difficult to access through biochemical routes, mainly because such small amounts of tissue are available for analysis. Key molecules, such as the transduction channel, may be present in only a few tens of copies per sensory hair cell, compounding the difficulty. Moreover, fundamental differences in the mechanism of stimulation and, most importantly, the speed of response of audition compared with other senses means that we have no well-understood models to provide good candidate molecules for investigation. For these reasons, a genetic approach is useful for identifying the key components of auditory transduction, as it makes no assumptions about the nature or expression level of molecules essential for hearing. We review here some of the major advances in our understanding of auditory function resulting from the recent rapid progress in identification of genes involved in deafness.
机译:正常听觉功能的分子基础知之甚少。与视觉或嗅觉可以收集到合理数量的感觉组织相反,事实证明,听觉系统很难通过生化途径进入,主要是因为这种少量组织可用于分析。每个感官毛细胞可能仅以几十个拷贝存在关键分子,例如转导通道,这增加了难度。此外,刺激机制的根本差异,最重要的是,与其他感觉相比,听觉的反应速度也不同,这意味着我们没有充分理解的模型来提供良好的候选分子进行研究。由于这些原因,遗传方法可用于确定听觉转导的关键组成部分,因为它不对听力必不可少的分子的性质或表达水平做出任何假设。我们在这里回顾了我们对听觉功能的理解方面的一些主要进展,这些进展是由于最近鉴定耳聋相关基因的快速进展而产生的。

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