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.
Weather conditions such as wind, the path of the flow
They can enter your blood stream (via breathing/ingesting) and once in your bloodstream they can enter cells and mutate your dna, which can cause cancer/birth defects/ reproductive harm
... termed "hypotonic," meaning less solids (or more diluted) than inside the cell. For fluid movement in/out of cells, water will diffuse (via osmosis) from the hypotonic solution to the hypertonic one, assuming a permeable barrier (i.e. cell membrane) allows it. With this case, water will flow into the cell from outside.
