Cystic fibrosis is the most common fatal genetic disease in the United States. 囊性纤维化(CF)是美国最常见的致命遗传疾病。
Health researchers use them in the study of cancer, heart disease, multiple sclerosis, and cystic fibrosis. 健康研究人员利用他们在癌症,心脏疾病,多发性硬化症,囊性纤维化(CF)的研究。
In some patients with cystic fibrosis, this approach has reversed a disease once thought unstoppable. 对一些患有囊肿性纤维化疾病的病人来说,这一方式战胜了曾经被认为无法治愈的疾病。
This research was funded by the National Institutes of Health, National Science Foundation and Cystic Fibrosis(CF) Foundation. 美国国立卫生研究院和美国国家科学基金与囊性纤维化(CF)基金为该项研究提供资金支持。
Children with CF have an abnormality in the function of a cell protein called the cystic fibrosis transmembrane regulator. 患有囊性纤维化(CF)的儿童有异常的细胞蛋白功能,这个细胞蛋白叫囊性纤维化(CF)跨膜蛋白调节因子。