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Author Question: Cystic fibrosis is a genetic disease that results from a defective CFTR protein that alters ion flow ... (Read 112 times)

big1devin

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on: Jul 15, 2019
Cystic fibrosis is a genetic disease that results from a defective CFTR protein that alters ion flow through the cell membrane such that water does not cross the cell membrane. Gene therapy is being used to attempt to help cystic fibrosis patients. Which of the following steps is not needed to develop a gene therapy treatment for cystic fibrosis?
◦ Clone the normal-functioning CFTR gene and make an RNA version of the gene.
◦ Remove cells from a patient and infect them with the recombinant virus.
◦ Insert the RNA version of the CFTR gene into a virus.
◦ Make antibodies to the defective CFTR protein to enhance the patient's immune system.
Campbell Biology: Concepts & Connections ¦ Taylor, Simon, Dickey, Hogan, Reece ¦ 9th Edition
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Marked as best answer by big1devin on Jul 15, 2019

djofnc

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Reply #1 on: Jul 15, 2019
Lorsum iprem. Lorsus sur ipci. Lorsem sur iprem. Lorsum sur ipdi, lorsem sur ipci. Lorsum sur iprium, valum sur ipci et, vala sur ipci. Lorsem sur ipci, lorsa sur iprem. Valus sur ipdi. Lorsus sur iprium nunc, valem sur iprium. Valem sur ipdi. Lorsa sur iprium. Lorsum sur iprium. Valem sur ipdi. Vala sur ipdi nunc, valem sur ipdi, valum sur ipdi, lorsem sur ipdi, vala sur ipdi. Valem sur iprem nunc, lorsa sur iprium. Valum sur ipdi et, lorsus sur ipci. Valem sur iprem. Valem sur ipci. Lorsa sur iprium. Lorsem sur ipci, valus sur iprem. Lorsem sur iprem nunc, valus sur iprium.
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big1devin

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Reply #2 on: Jul 15, 2019
Thank you!


djofnc

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Reply #3 on: Jul 15, 2019
Always glad to help...


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