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BCH4024 101424 OC F24 E2 Q33: In the disease Cystic Fibrosis…
BCH4024 101424 OC F24 E2 Q33: In the disease Cystic Fibrosis (CF) a chloride channel (CFTR) is defective, which results in reduced Cl− and water movement across the plasma membrane. In the lungs, this is serious because mucus builds up leading to colonization by infectious bacteria. If you learn that the CFTR is a member of the family of ABC transporters, which of the following statements about CFTR and ABC transporters would be accurate? CFTR and other ABC transporters share a common mechanism of using ATP hydrolysis. CFTR operates exclusively in transporting organic substances. ABC transporters generally function via passive diffusion. Mutations in CFTR lead to abnormal ion movement
BCH4024 101424 OC F24 E2 Q33: In the disease Cystic Fibrosis…
Questions
BCH4024 101424 OC F24 E2 Q33: In the diseаse Cystic Fibrоsis (CF) а chlоride chаnnel (CFTR) is defective, which results in reduced Cl− and water mоvement across the plasma membrane. In the lungs, this is serious because mucus builds up leading to colonization by infectious bacteria. If you learn that the CFTR is a member of the family of ABC transporters, which of the following statements about CFTR and ABC transporters would be accurate? CFTR and other ABC transporters share a common mechanism of using ATP hydrolysis. CFTR operates exclusively in transporting organic substances. ABC transporters generally function via passive diffusion. Mutations in CFTR lead to abnormal ion movement
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