Biology, 09.03.2021 05:00 clonetrooper099
A group of scientists were using CRISPR to treat a mouse with cystic fibrosis, a disease caused by a defective Cl- channel protein called CFTR. The most common cause of cystic fibrosis in humans is the absence of a phenylalanine, an amino acid, in the CFTR protein, which prevents CFTR from achieving the correct 3-D structure. If the scientists wished to repair this mutation, how would they alter the mutated CFTR gene before using CRISPR to insert the DNA into the mice
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This organism is not capable of performing photosynthesis. (horseshoe crab) true false
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What volume of a 0.25 m solution can be made using 0.55 moles of ca(oh)2
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A group of scientists were using CRISPR to treat a mouse with cystic fibrosis, a disease caused by a...
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