How does curcumin treatment lead to a normalization of chloride transport in mice with the cystic fibrosis transmembrane conductance regulator (CFTR) DF508 mutation?
A) It causes skipping of the mutated codon
B) It is a cofactor for the CFTR protein
C) It prevents retention and degradation of CFTR in the endoplasmic reticulum
D) It prevents transport of the mutant CFTR to the lysosome
E) It inhibits the proteasome
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