Answer:
Cellular Fluids and Organelles
Explanation:
Hope this helped
Answer:
Women who carry one copy of the mutated gene still have normal color vision because they have another copy, which is not mutated, in the other X chromosome that will be the dominant one. As a result, the women are carriers of the mutated gene but not color blind.
Explanation:
Colorblindness is a sex-linked mutation. A woman has two X chromosomes, while a man has one X chromosome and one Y chromosome. The mutated gene that causes color blindness is on the X chromosome, and it is OPN1LW. So if a woman has one mutated OPN1LW in one of her two X chromosomes, the OPN1LW gene in the other X chromosome will be the dominant one stopping the woman from being colorblind.
In the case of men, as they only have one X chromosome, if there is a mutation on the OPN1LW in the X chromosome, the men will be colorblind because there is no extra copy of the gene, as it is in women.
Answer:
D.electrical signals and chemical neurotransmitters
Explanation:
chemical transmitters are the language that neurons use to connect eachother.
Answer:
outside the nucleus in the cytoplasm
Explanation:
Yes, I think I have some genetic traits which is similar to my grandparents.
Explanation:
Genes are blue print of our body. The 25% gene of Grandparent is similar to their grandchildren. This gene effects the look. It may affect the color of hair and color of eyes.
Each gene is responsible for different change of our body. Genes pass from one generation to other so it is passed through grandparents to parents and reaches to us.
