Your answer would happen to be <span>Distortion</span>
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.
Hi! What are the possible answers?
The correct answer is "regulating important involuntary bodily functions such as blood pressure, heart rate, breathing and swallowing".
The area highlighted in this example is the posterior part of the brain, called the brainstem. The brainstem is comprised of three important parts, the medulla, the pons and the midbrain. The basic functions of this brain area include breathing, heart rate and sleeping.
Answer:
The correct answer is option D.
Explanation:
The process of translation, that is, synthesis of proteins takes place until the occurrence of the termination process. The termination takes place when the ribosome encounters a stop codon. These are UAG, UAA, and UGA. As there are no molecules of tRNA, which can identify these codons, the ribosome determines that the process of protein synthesis is complete. The formed protein then get discharged and the complex of translation move away from each other.
