Answer;
-Association areas
The association areas of the cerebral cortex are not involved in primary motor or sensory functions; rather, they are involved in learning, remembering, thinking, and speaking.
Explanation;
-The cerebral cortex is divided into sensory, motor and association areas. Sensory areas receive and interpret impulses from sensory receptors , motor areas control movement of muscles (initiate impulses to skeletal muscles). Association areas are involved with more complex functions such as learning, decision making and complex movements such as writing.
-Association cortex is the cerebral cortex outside the primary areas, The majority of the cortex is composed of this area. It is essential for mental functions that are more complex than detecting basic dimensions of sensory stimulation.
The came too fast.
During the 20th century the canal water efforts to create major changes in South Florida landscape. The leeve-canal in Evergrade failed to improve the wetland habitat, a canal was constructed to drain and reclaim the wetlands.
Answer:
3
Explanation:
when the climate changes sometimes it can make drought occur
<span>The molecules that provoke a specific immune response are called antigens.
</span>This molecule initiates the production of an antibody and causes an immune response. T<span>oxins, chemicals, bacteria, viruses, or other substances that come from outside the body can be part of the antigens.
</span>
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.
