Answer: True
Explanation:
The neuron has leak channels in the cell body, axon and dendrite and cell body. This is because the trans membrane potential exists in all parts of the cell membrane.
Because of this reason the the leak channels are available at each part of the neuron.
The action potential, trans membrane potential should exits in all the parts of the cell so it should be located in all the parts of cell.
Answer:
C. metals
Explanation:
Elements in the periodic table are grouped into metal and non-metals depending on their characteristics. Metals usually possess the following characteristics:
- High melting and boiling point
- Brittle i.e. ability to break
- lustre i.e. ability to shine when polished.
- Good conductor of heat and electricity
Based on this above characteristics, element Q in this question is a METAL because it posseses the same qualities that a metal does.
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.
<h3>Answer:</h3>
- It's FALSE. Baby eyes are propotionallity larger than adult eyes.
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