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Putative miRNAs for the diagnosis of dyslexia, dyspraxia, and specific language impairment

机译:推定的miRNA用于阅读障碍,阅读障碍和特定语言障碍的诊断

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摘要

Disorders of human communication abilities can be classified into speech and language disorders. Speech disorders (e.g., dyspraxia) affect the sound generation and sequencing, while language disorders (e.g., dyslexia and specific language impairment, or SLI) are deficits in the encoding and decoding of language according to its rules (reading, spelling, grammar). The diagnosis of such disorders is often complicated, especially when a patient presents more than one disorder at the same time. The present review focuses on these challenges. We have combined data available from the literature with an in silico approach in an attempt to identify putative miRNAs that may have a key role in dyspraxia, dyslexia and SLI. We suggest the use of new miRNAs, which could have an important impact on the three diseases. Further, we relate those miRNAs to the axon guidance pathway and discuss possible interactions and the role of likely deregulated proteins. In addition, we describe potential differences in expressional deregulation and its role in the improvement of diagnosis. We encourage experimental investigations to test the data obtained in silico.
机译:人类交流能力障碍可分为言语障碍和语言障碍。言语障碍(例如,阅读障碍)会影响声音的生成和排序,而语言障碍(例如,阅读障碍和特定的语言障碍或SLI)会根据其规则(阅读,拼写,语法)对语言进行编码和解码。这种疾病的诊断通常很复杂,尤其是当患者同时出现一种以上疾病时。本审查着重于这些挑战。我们将文献中的数据与计算机方法相结合,以试图鉴定可能在阅读障碍,阅读障碍和SLI中起关键作用的推定miRNA。我们建议使用新的miRNA,这可能会对这三种疾病产生重要影响。此外,我们将那些miRNA与轴突引导途径联系起来,并讨论可能的相互作用和可能的失控蛋白的作用。此外,我们描述了表达失调的潜在差异及其在改善诊断中的作用。我们鼓励进行实验研究,以测试通过计算机获得的数据。

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