It is killing of population forcing us to self quarantine and stay away from people. Quarantine is marking many people depressed because we can’t talk or visit people face to face and it’s harming many people with anxiety and depression it’s making them worse.
Explanation:
1.What is the probability that a sperm from the father will contain the PKU allele?
Probability = ½
2.What is the probability that an egg from the mother will contain the PKU allele?
Probability = ½
3.What is the probability that their next child will have PKU?
Probability = ¼ (because each parent has ½ chance ½ X ½ = ¼)
4.What is the probability that their next child will be heterozygous for the PKU gene?
Probability = ½ (because each parent has ½ chance of donating the ‘P’ allele and ½ chance of donating the ‘p’ allele (½ x ½) + (½ x ½) = ½
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.
Hello.
The answer is interphase and <span>mitosis.
</span>interphase is the resting phase between successive mitotic divisions of a cell, or between the first and second divisions of meiosis.
mitosis is a type of cell division that results in two daughter cells each having the same number and kind of chromosomes as the parent nucleus, typical of ordinary tissue growth.
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Tribrachidium was originally described by Martin Glaessner as a problematic organism, one that is excluded from all known major groups of animals by its tri-radial symmetry. ... Tribrachidium was a soft-bodied benthic organism that temporarily attached (but did not accrete) to the substrate of its habitat (microbial mats).
