RESPIRATORY
CYSTIC FIBROSIS
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Question
[CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
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Amount of surfactant produced to keep a structure hydrated and stable.
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The chloride (salt) levels of surfactants.
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Regulates the conductivity of proteins.
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It controls you.
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Detailed explanation-1: -The cystic fibrosis transmembrane conductance regulator (CFTR) protein helps to maintain the balance of salt and water on many surfaces in the body, such as the surface of the lung. When the protein is not working correctly, chloride-a component of salt-becomes trapped in cells.
Detailed explanation-2: -The cystic fibrosis transmembrane conductance regulator (CFTR) belongs to a superfamily of proteins implicated in the transport of ions, proteins, and hydrophobic substances.
Detailed explanation-3: -The CFTR gene provides instructions for making a protein called the CF transmembrane conductance regulator (CFTR). This protein functions as a channel across the membrane of cells that produce mucus, sweat, saliva, tears, and digestive enzymes.
Detailed explanation-4: -Cystic fibrosis transmembrane conductance regulator (CFTR) is a phosphorylation-dependent epithelial Cl− channel. It is located primarily in the apical membrane, where it provides a pathway for Cl− movement across epithelia and regulates the rate of Cl− flow.
Detailed explanation-5: -Cystic fibrosis (CF) is a recessive genetic disease caused by mutations in a gene encoding a protein called Cystic Fibrosis Transmembrane Conductance Regulator (CFTR).