The first one is a atom
The second one is a compound
The third one is molecules that are not compounds
The last one is a atom
Answer:
Explanation:
This question is incomplete. However, what is described in this question is a method of DNA damage repair mechanism. The method described is called base excision repair. Generally, glycosylases play important roles in base excision repair (as they detect and remove these damaged bases).
One thing that can be considered while identifying the bond to be broken is the codon that will be formed after the removal of base. If this codon (a three base sequence) will still produce the same protein as when a normal cytosine was present.
NOTE: During this base excision repair, a glycosylase will detect and remove the damaged cytosine. Once removed, the remaining nucleotide backbone (of the removed cytosine) is also removed and the gap is filled and sealed by other enzymes in this repair mechanism.
<span>John could make some simple changes to his breakfast to increase his fiber intake. Instead of orange juice, he could drink juice with added fiber such as V8 juice or fiber added grape juice. Instead of corn flakes, he could eat a high fiber cereal such as Grape Nuts. Instead of white toast, he could eat a slice of high fiber whole wheat bread. He can make some simple substitutions that will really impact his diet and his health.</span>
100% shore its B hope that helps you good luck
Answer:
Genetic mapping for unequivocal identification of the potentially causative mutation
Explanation:
Galactosemia is a genetic disorder caused by mutations in the Galactose-1-phosphate uridylyltransferase (GALT) gene, which encodes an enzyme involved in the metabolism of galactose. Gene mapping is a technique widely used in genetics to identify the position of one locus a chromosome by using molecular markers to estimate genetic distances. Genetic mapping provides useful evidence in order to identify when a disease that is transmitted from parent to offspring can be associated with one or more genes and then determine which gene/s is/are responsible for this condition.
