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Which of the following statements about mutations and genetic disease are correct?
Mutations can result from spontaneous events or external mutagens.
A change in DNA sequence may change the pattern of protein folding, resulting in genetic disease.
Some genetic diseases may be caused by the substitution of only one incorrect amino acid in a protein.
It is possible for the substitution of one base for another to have no effect on an organism.
What else can I help you with?
Which of the following statements defines the association between a risk factor and the development of a disease?
The more risk factors for a disease, the greater the chance of developing that disease.
How can mutations in different genes contribute to the development of a single disease?
Mutations in different genes can contribute to the development of a single disease by affecting various biological pathways or processes that are involved in the disease. These mutations can interact with each other or with environmental factors to disrupt normal cellular functions, leading to the manifestation of the disease.
What chromosome does tay-sachs disease affect?
Tay-Sachs disease is caused by mutations in the HEXA gene located on chromosome 15. These mutations result in the absence or deficiency of the enzyme hexosaminidase A, leading to the accumulation of harmful substances in the brain and nervous system.
Psychosocial interventions have been shown to do which of the following in patients with coronary heart disease?
All options are correct.
What type of disease can occur from mutations that can disrupt the control of cell reproduction?
Cancer is a disease that can occur from mutations that disrupt the control of cell reproduction. Mutations in genes involved in cell cycle regulation and growth can lead to uncontrolled cell division and the formation of tumors.
An example of all human cells and mutations?
Sickle-cell disease
What causes Pick disease?
The molecular cause of Pick disease are a series of mutations linked to chromosomes 17, 9 and 3
What is the mutated gene of the Charcot-Marie-Tooth disease?
CMT is caused by mutations in genes that produce proteins involved in the structure and function of either the peripheral nerve axon or the myelin sheath. Although different proteins are abnormal in different forms of CMT disease, all of the mutations affect the normal function of the peripheral nerves. The gene mutations in CMT disease are usually inherited.
Did you ever hear of sweets diseace maybe not the correct spelling?
disease is the correct spelling disease is the correct spelling
What is a genetically linked disease?
A genetically linked disease is a condition that has a known genetic basis, meaning that it is caused by mutations in specific genes or variations in the DNA sequence. These mutations can be inherited from one or both parents and can increase the risk of developing the disease. Examples include cystic fibrosis, Huntington's disease, and sickle cell anemia.
How do you spell desies?
The correct spelling is "disease."
How do you spell disese?
The correct spelling is "disease."
