Answer:
By designing suitable gene therapies in order to restore target gene expression.
Explanation:
Cystic fibrosis and muscular dystrophy are inherited genetic disorders associated with serious health problems. Cystic fibrosis is caused by mutations in the gene that encodes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein, and it is a condition associated with abnormal production of sticky mucus that leads to problems in the lungs and the digestive systems. On the other hand, muscular dystrophy is produced by mutations in genes localized on the X chromosome such as, for example, the gene 'dystrophin'. Gene therapy is an experimental approach used to compensate abnormal gene function by introducing exogenous genetic material and thus restore their altered protein products. Consequently, personalized gene therapies can be useful to treat inherited disorders such as cystic fibrosis and muscular dystrophy.
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<span>The answer to this question would be: tissues; decrease
Oxygen is delivered to the tissue by the heart. It will be unloaded in the tissue, causing the oxygen level in the blood to be decreased. After that, the blood also picks up the carbon dioxide so its level will be increased.
In lungs, the carbon dioxide will be unloaded and oxygen will be loaded back into the blood.</span>
simple mules are a mix of hourse and donky and are born infertle they cant BREED.
