Prophase
Metaphase
Anaphase
Telophase
Meiosis is the process of cell division by which involving gametes. Cell division is just the same for sperm and egg cells, but they have distinguishable descriptions and labels in the process. Spermatogenesis is for the males’ sperm cells and oogenesis is the process for females’ egg cells. The cell division of meiosis involves the two phases, respectively meiosis I and meiosis II. Meiosis I like mitosis is the cell division that produces diploid cells<span>. These diploid cells are cells that contain a complete pair of chromosomes which is 46. The result is two diploid cells after the first meiosis. To provide clear explanation, in contrast haploid cells only contain 23 chromosomes and are created after meiosis II which is 4 in number. </span>
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Answer:</h2>
Blue winged warblers are the popular species having distinct Buzz Buzz sounds. They are most likely to live in bushy fields and known as worm eater. Their favorite food is insects and spiders.
As the springs arrives, it will affect the blue winged warbles in a very positive way. They will be more likely to reproduce in spring. They will also find more food and shelter in spring.
Answer and Explanation:
The Huntington disease is caused by a mutation in the gene that codifies for the Huntingtin protein (Htt). The mutation produces an altered form of the protein leading to the neuron´s death in certain areas of the brain.
The Huntington disease characterizes for being,
- Hereditary, passing from generation to generation. To express the disease, a person must have been born with an altered gene.
- Autosomal, affecting men and women equally, because the mutated gene is located on an autosomal chromosome.
- Dominant, which means that by getting only one copy of the altered gene coming from any of the parents, the receiving person will express the disease. The mutation in the gene dominates over the normal gene copy.
- Expressed by heterozygosis. Most people affected by the disease are heterozygous, with a normal copy and a mutated copy.
There are just a few cases all around the world (3% approximately) in which the disease is expressed with no family history. The progenitors are not affected by the mutation. These cases are very rare and are called <u>"de-novo" mutations.</u> A new mutation is spontaneously produced and it is not inherited from any of the parentals. It consists of an increase in the number of CAG repetitions. In a normal person, the number of CAG repetitions is less than 35. When there are 40 or more repetitions it occurs the disease. But when there are between 35 and 39 repetitions, the penetrance of the disease is incomplete. This is a "gray zone". Those alleles that fall in the gray zone are unstable and might produce the HD. Individuals with these unstable alleles have a tendency to increase the number of repetitions from generation to generation until the number reaches 40 repetitions and the person expresses the disease. This <u>usually occurs in the paternal germinal line</u>, as it is particularly unstable in sperm and probably meiosis greatly affects their instability, causing an increase in the number of CAG repeats.
<span>Most likely result in the greatest decrease in the rate of a chemical reaction would come from the correct posting of all your answer choices available</span>
