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❶In , when the CFTR gene was discovered, scientists were intrigued, and in , gene therapy for cystic fibrosis patients began. Single high-dose oral vitamin D3 stoss therapy — A solution to vitamin D deficiency in children with cystic fibrosis?

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Cystic Fibrosis- Option 2 Justin Jang and Junior Suwannapeng Jasper High School Cystic fibrosis is an autosomal (not sex linked), hereditary disease caused by a mutation in the gene called the cystic fibrosis transmembrane conductance regulator gene, or the CFTR gene. This CFTR gene belongs to a group of genes called ABC (ATP-binding cassette). These are transport molecules for molecules such.

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In a group of parents founded the Cystic Fibrosis Foundation, which later became the National CF research Foundation in as well. In ,b The foundation created the Research Development Program, which is a network of research centers at top universities. Diet Health & Disease Cystic Fibrosis Essay Background on cystic fibrosis: Cystic fibrosis (CF) is a chronic disease that affects organs such as the liver, lungs, pancreas, and intestines. It disrupts the body's salt balance, leaving too little salt and water on the outside of cells and causing the.

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essay cystic fibrosis one out of every 2, births in the united states will be diagnosed with cystic fibrosis. this fact makes cystic fibrosis one of the most common genetic diseases in the nation. about 30, americans have the disease, but even though cystic fibrosis is the nations most common genetic disease the majority of americans know little about it. Cystic Fibrosis Research Paper. Cystic Fibrosis, a very serious inherited genetic disease, is also known as CF and sixty-five roses. This disease affects one in every 3, live births. It may first appear in a newborn, but can appear all the way up until a young adult.