PLUNCs as potential modifier genes in Cystic Fibrosis

PLUNC 作为囊性纤维化的潜在修饰基因

• 批准号: 253082
• 负责人: Saferali Aabida
• 金额: $ 0.1万
• 依托单位: University of British Columbia
• 依托单位国家: 加拿大
• 财政年份: 2012
• 资助国家: 加拿大
• 起止时间: 2012-01-01 至 2012-02-01
• 项目状态: 已结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=253082&lang=en
• 关键词: Cystic Fibrosis; Modifier Genes; Pluncs

Cystic fibrosis (CF) is an inherited disease causing a build-up of thick, sticky mucus in the lung, digestive tract, and other areas of the body. This increases susceptibility to bacterial infection in the lung, leading to early death due to chronic lun

囊性纤维化（CF）是一种遗传性疾病，会导致肺、消化道和身体其他部位积聚粘稠的粘液。 这增加了肺部细菌感染的易感性，导致慢性肺结核导致的早期死亡。