Answer:
c. Two sister chromatids did not separate into the proper daughter cells during anaphase.
Explanation:
The observed cell is undergoing mitosis which does not include separation of homologous chromosomes. During anaphase of mitosis, two sister chromatids of each chromosome separate from each other. They move to opposite poles. This results in equal distribution of two complete sets of chromosomes to each daughter cell.
However, the failure of two sister chromatids of a chromosome during anaphase would lead to the formation of two abnormal daughter cells. One of the daughter cells would have one extra chromosome (2n+1) while the other would lack one chromosome from the diploid set (2n-1).
Answer:
external
Explanation:
<em>Through the process of photosynthesis, plants use the sun's energy to make sugars to function. External means from an outside force, while internal means from within. Since the sun isn't inside a plant, they gather it from outside, thus it's external.</em>
<span>A major difference between the eccrine sweat glands and the appocrine sweat glands is that eccrine glands empty into/onto the skin surface while apocrine glands empty into/onto the hair follicle.
There are two types of sweat gland, eccrine and apocrine. As the eccrine glands empty into the skin surface, they are present all over the body particularly on forehead, palms and feet. That's why we feel more sweat on these parts of the body. while apocrine glands empty into/onto the hair follicles so they are mostly armpits.</span>
They both contain a Nucleus, the part of the cell designed to dictate the cells operations.
Answer:
The correct answer is d) genomic imprinting.
Explanation:
Genomic imprinting is a biological process by which specific modifications in the germ line that produce differences in the expression of the genetic material that is biochemically marked indicating its parental origin. The Prader-Willi syndrome is one of the best known and most studied examples in relation to pathologies produced by genomic imprinting. Prader-Willi syndrome is a complex genetic disease that is fundamentally neurological. Its appearance is due to a deletion of a fragment of chromosome 15 derived from the father.
