Answer:
Land use planning is about more than addressing the physical layout of development, how much it will cost, where it will be located and aesthetics. Land use planning also incorporates environmental impacts such as chemical pollution, noise pollution, flooding due to the loss of trees and plants, etc. In order to meet all these requirements land use planning must draw from a wide array of disciplines' expertise.
Explanation:
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D. Coal is naturally made and cannot be renewed by humans.
Answer:
The correct answer is A. Fat
Explanation:
Fat is one of the macronutrient that is present in our food and fat is accumulated in the body on the liver and in adipose tissue and provide storage form of energy to the body. So fat accumulation contributes to weight gain.
Fats contributes to more calory per gram than other macronutrient like carbohydrates and proteins, therefore, reducing the amount of fat by taking low calory diet which have less fat amount is important to reduce weight.
Therefore here to lose some weight by powerlifter fat will likely need to be monitored closely and possibly limited.
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.
