I believe the answer is comparative anatomy. It is the study of the similarities and differences in the structures of different species. Similar body parts may be homologies or analogies, such that both provide evidence of evolution. Similarities in embryos are evidence of common ancestry. For example all vertebrates embryos have gill slits and tails.
Answer:
The correct answer is "both Cdc6 and Cdt1"
Explanation:
The replisome is a complex molecular system that allows for the replication of DNA in yeast. There are multiple genes that participate in the replisome function, however if a researcher finds out that a yeast strain fails to properly form replisomes it is very likely that the genes that might be mutated are both Cdc6 and Cdt1. Cdc6 and ORC are the genes that send the signal to the yeast to start the replisome formation, and Cdt1 is a DNA replication factor that if it is mutated it could cause that yeast is not able to form the replisome.
It is expected to see in the offspring of a woman who has DMD and a man who does not have the disease that all of their sons and none of their daughters will have the disease
Option A.
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Duchene muscular dystrophy, also known as DMD is a recessive, x-linked disease. It occurs when there is a mutation in the dystrophin gene. This mutation further affects the muscles of the body leading it to degenerate and ultimately death.
When a woman with DMD and a man without DMD have an offspring, their daughters and the sons will get the mutated gene signature from the mother as she is the carrier. But since the father has normal genes, the daughters will become the carriers and will not be afflicted by it. This is because the normal X chromosome from the father will be passed on to them. The sons on the other hand will have the disease as they will get one of their mother's X chromosome which would be carrying the mutated gene.
