We hope that the scientific community can use this new knowledge to help design new drugs that will bind selectively to the defective protein to protect the body from its damaging effects.
我们希望,科学界可以使用这个新的知识,以帮助设计新的药物,将选择有缺陷的蛋白质结合,以保护身体的破坏性影响。
There are also genes that no longer make a protein; these defective remnants of evolution are called pseudogenes.
也有基因不再制造蛋白,这些进化中的残余物称为假基因。
BACKGROUND Increasing the activity of defective cystic fibrosis transmembrane conductance regulator (CFTR) protein is a potential treatment for cystic fibrosis.
背景提高有缺陷的囊性纤维化跨膜电导调节(CFTR)蛋白的活性是囊性纤维化的一种潜在治疗。
应用推荐