Q38. The ΔF508 mutation of the CFTR gene is the cause of most cases of cystic fibrosis (CF). One focus of research into a cure for CF is "gene therapy" — inserting normal copies of the CFTR gene into the cells of CF patients. Which of the following areas of CF research is most likely to improve symptoms for CF patients? A. Inserting extra copies of genes that code for the proteosome. B. Studying the chaperone proteins of the endoplasmic reticulum (ER). C. Improving the lung function of people who are carriers of the CF allele (Cc). D. Stabilizing the plasma membrane were the ΔF508 form of the protein accumulates.
Q38. The ΔF508 mutation of the CFTR gene is the cause of most cases of cystic fibrosis (CF). One focus of research into a cure for CF is "gene therapy" — inserting normal copies of the CFTR gene into the cells of CF patients. Which of the following areas of CF research is most likely to improve symptoms for CF patients? A. Inserting extra copies of genes that code for the proteosome. B. Studying the chaperone proteins of the endoplasmic reticulum (ER). C. Improving the lung function of people who are carriers of the CF allele (Cc). D. Stabilizing the plasma membrane were the ΔF508 form of the protein accumulates.
Biology 2e
2nd Edition
ISBN:9781947172517
Author:Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:Matthew Douglas, Jung Choi, Mary Ann Clark
Chapter16: Gene Expression
Section: Chapter Questions
Problem 22RQ: Targeted therapies are used in patients with a set gene expression pattern. A targeted therapy that...
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Q38. The ΔF508 mutation of the CFTR gene is the cause of most cases of cystic fibrosis (CF). One focus of research into a cure for CF is "gene therapy" — inserting normal copies of the CFTR gene into the cells of CF patients.
Which of the following areas of CF research is most likely to improve symptoms for CF patients?
A. Inserting extra copies of genes that code for the proteosome.
B. Studying the chaperone proteins of the endoplasmic reticulum (ER).
C. Improving the lung function of people who are carriers of the CF allele (Cc).
D. Stabilizing the plasma membrane were the ΔF508 form of the protein accumulates.
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