基因疗法曾经由于缺少安全和有效的方法将治疗性基因转导入细胞内部而被认为没什么发展前景。
The promise of gene therapy has long been held up by the lack of a safe and effective way to insert the desired therapeutic genes into the right cells.
人们希望,改构后的腺病毒在基因治疗方面能起到重要的作用,例如,作为载体基因携带治疗性基因到达细胞内。
The hope is that modified adenovirus could play a role in gene therapy, used as a vector (carrier) for delivering therapeutic genes to the interior of cells.
她从1990年开始接受治疗,采用了一种革命性的新疗法,试图从她白细胞基因的源头纠正缺陷。
She was treated beginning in 1990 with a revolutionary new therapy that sought to correct the defect at its very source, in the genes of her white blood cells.
Another example of using this technique is to produce therapeutic proteins from cloned DNA and I'm going to describe this one.
另一个运用到此技术的例子就是,从克隆的基因中制造治疗性的蛋白质,我会具体说这个例子
Because of this, because cystic fibrosis is a disease that's caused by a single gene defect, there's been great interest in trying to treat cystic fibrosis with gene therapy.
就是因为如此,就因为囊胞性纤维症,是一种单基因病,人们对于用基因治疗,治愈囊胞性纤维症产生了很大的兴趣
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