Answer:
a series of mitochondrial proteins that transport electrons of hydrogen, released in the Krebs cycle, from acetyl coenzyme A to inhaled oxygen to form H2O: the energy released in the process is conserved as ATP.
Explanation:
Each person carries 23 pairs of chromosomes in every cell that makes up their body, with the exception of gametes, which contain 23 SINGLE chromosomes. So when a sperm and egg meet, they then have 23 pairs. In the process of meiosis 'crossing-over' occurs, which means that the chromosomes get "shuffled". This means that the child can receive random traits not only from the parents, but also the grandparents. so there is about 2⁴⁶ possible pairings, excluding the risk for things such as Down-Syndrome
<span>it occurs during the gamete formation</span>
Answer:
See the answer below
Explanation:
<em>Hemophilia typically affects more males than females because the disorder is </em><em>X-linked </em><em>and </em><em>recessive</em><em>. </em>
<u>Females have two X chromosomes (XX) while males only have one X and one Y chromosome (XY). The two X chromosomes in females are capable of carrying alleles while the Y chromosome in males is hypothesized not able to carry alleles. </u>
Consequently, the two X chromosomes in females will both need to carry the recessive allele of hemophilia in order for any female to be affected for hemophilia while the males only need their single X chromosome to carry the recessive allele in order to be affected.
In order words, the presence of a single recessive allele is not enough for a female to be affected while it is more than enough for a male to be affected. Hence, more males are affected b hemophilia disorder than females.
