{"id":37545,"date":"2020-08-17T04:30:22","date_gmt":"2020-08-17T04:30:22","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=37545"},"modified":"2020-08-17T04:30:22","modified_gmt":"2020-08-17T04:30:22","slug":"cystic-fibrosis-transmembrane-regulator-protein-cftr","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/cystic-fibrosis-transmembrane-regulator-protein-cftr\/","title":{"rendered":"Cystic fibrosis transmembrane regulator protein (CFTR)"},"content":{"rendered":"<p>A protein that regulates proper chloride ion transport across the cell membranes of human lung airway epithelial cells. When the gene that codes for CFTR protein is damaged or mutated, the (mutant) CFTR protein fails to function properly, which causes mucous (and bacteria) to accumulate in the lungs. This lung disease is known as Cystic Fibrosis.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>A protein that regulates proper chloride ion transport across the cell membranes of human lung airway epithelial cells. When the gene that codes for CFTR protein is damaged or mutated, the (mutant) CFTR protein fails to function properly, which causes mucous (and bacteria) to accumulate in the lungs. This lung disease is known as Cystic [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[3],"tags":[],"class_list":["post-37545","post","type-post","status-publish","format-standard","hentry","category-c"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Cystic fibrosis transmembrane regulator protein (CFTR) - Definition of Cystic fibrosis transmembrane regulator protein (CFTR)<\/title>\n<meta name=\"description\" content=\"A protein that regulates proper chloride ion transport across the cell membranes of human lung airway epithelial cells. When the gene that codes for CFTR protein is damaged or mutated, the (mutant) CFTR protein fails to function properly, which causes mucous (and bacteria) to accumulate in the lungs. This lung disease is known as Cystic Fibrosis.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.healthbenefitstimes.com\/glossary\/cystic-fibrosis-transmembrane-regulator-protein-cftr\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Cystic fibrosis transmembrane regulator protein (CFTR) - Definition of Cystic fibrosis transmembrane regulator protein (CFTR)\" \/>\n<meta property=\"og:description\" content=\"A protein that regulates proper chloride ion transport across the cell membranes of human lung airway epithelial cells. When the gene that codes for CFTR protein is damaged or mutated, the (mutant) CFTR protein fails to function properly, which causes mucous (and bacteria) to accumulate in the lungs. 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