DNA diagnosis revolution 基因研究帶來診斷革命
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Comparing variations in genetic code will allow the development of targeted medicines to treat cancer
一項由英國國民保健服務(NHS) 設(shè)立的基因工程研究項目有可能破解一系列致命疾病的發(fā)病秘密。此研究項目將通過分布設(shè)立在英格蘭醫(yī)院的十一所基因醫(yī)學中心來收集 DNA 樣本，用于幫助制定對一系列疾病有針對性的療程，尤其是對癌癥的治療。請聽 BBC 記者 James Gallapher 的報道：
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The NHS is aiming to be at the forefront of a new era of genomic medicine. Cancer treatment will be targeted at the precise mutations in DNA that are causing the patient’s tumour.
Genetic diseases will be identified by finding mistakes in the 3bn pairs of letters that make up our genetic code. Eleven genomic medicine centres will open in hospitals from Newcastle to Exeter in February. Their challenge is to sequence 100,000 genomes within three years.
It could improve treatment for some patients but all that data will be made available to drugs companies and researchers to help them create precision drugs for future generations.
Glossary 詞匯表 （點擊單詞收聽發(fā)音）
- to sequence確定… 的順序（編排）
- drug companies制藥公司
- precision精確的
