Development of CFTR activators from Chinese medicinal plants to improve pulmonary adaptation to altitude/hypoxia stress
Introduction CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) is a chloride channel on the airway epithelia, playing a major role in electrolyte and fluid transport. It is well documented that cystic fibrosis, the most common genetic respiratory disease, is caused by mutations in the CFTR gene that lead to dysfunction and/or improper localization of the protein. Approximately one in every 25 Caucasians carries one mutant version of this gene as a heterozygote.
Li Canhui Viirre Russell Marshall John
The Hospital for Sick Children in Toronto, Canada Ryerson University, Canada Ryerson University, Canada
国际会议
广州
英文
995-996
2008-08-01(万方平台首次上网日期,不代表论文的发表时间)