Which cellular dysfunction is responsible for the manifestations of cystic fibrosis? abnormal chloride channel proteins allow increased sodium and water reabsorption. thickened peripheral proteins bind with phospholipids to block water absorption. extra integral proteins develop and block cellular fluid transport. transmembrane proteins transport additional water into cells?

Abnormal chloride channel proteins allow increased sodium and water reabsorption

Explanation:

Persons with cystic fibrosis have a defective CFTR gene. The causes the abnormal development of the cystic fibrosis transmembrane conductance regulator protein that is responsible for balancing water and salts across the membrane especially in epithelial cells that produce mucus and sweat and secretory enzymes. This causes the production of abnormally thick secretions that block the ducts.

hey there!

so, when you eat, your teeth chew and grind food into smaller pieces. this is mechanical digestion. then reactions aided by digestive enzymes break down large food molecules into smaller molecules. this is chemical digestion. the two processes change the food into simpler substances that can be used by the body for raw materials and energy.

hope this

tobey

it would be heredity