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
Answers: 2
Biology, 21.06.2019 17:00
Q: a pair of homologous chromosomesa) always has the same genes and the same allows b)always has the same genes c)always has the same alleles d)never has the same genes
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Biology, 22.06.2019 13:00
Pulmonary arteries carry highly oxygenated blood. true or false?
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Biology, 23.06.2019 01:30
Acertain species of fish can have either long or short fins. the allele for long fins is dominant over the allele for short fins. a heterozygous, long-finned fish is crossed with a homozygous, short-finned fish. of the offspring, will have long fins and be , and will have short fins and be .
Answers: 1
A group of scientists were using CRISPR to treat a mouse with cystic fibrosis, a disease caused by a...
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