Although dating of some foods is required by more than 20 states, there are areas of the country where much of the food supply has some type of open date and other areas where almost no food is dated. Open dating is found primarily on perishable foods such as meat, poultry, eggs and dairy products.
Of the total amount of glucose energy consumed by the body each day, about 20% is used by the brain and nerve cells.
The brain constitutes about 2% of the total body but it is one of the main consumers of energy derived from glucose.
The energy provided by glucose is used for the proper functioning of the brain. It generates ATP which is an energy source that is responsible for r neuronal and non-neuronal cellular maintenance and generates neurotransmitters.
Thus glucose-derived energy is critical for the health of the brain. Lack of energy can cause several brain diseases.
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Answer: The mother of the man can be either XHXH or XHXh and pass her normal allele to the son and his father can be either XHY or XhY, he only passes his Y chromosome. The mother of the woman can be XHXH or XHXh and the father could be XhY, then she could have inherited the normal allele from the mother and the affected allele from the father. But also, the mother of the woman could be XHXh or XhXh and the father could be XHY, so in this case she could have inherited the normal alele from the father and the affected allele from the mother.
Explanation:
Hemophilia is an inherited bleeding disorder in which the blood does not clot properly. This can cause bleeding either spontaneously or after an injury.
<u>It is related to the X chromosome and it is recessive for females</u>, this mean they need both affected alleles to develop the trait. <u>Males only need one recessive allele because they only have one X chromosome</u>. This means that females need both parents to be at least carriers (although one or both can also have the disease or both recessive alleles). While males inherit it only from the mother, either she is a carrier (one recessive allele) or she has the disease (both recessive alleles). Then the mother passes the X chromosome with the affected allele to the son, and that son only receives the Y chromosome from the father, which does not have the gene that determines this disease.
If the mother is a carrier, her genotype is XHXh, being XH the normal allele and Xh the affected allele. She does not have hemophilia because she has a dominant allele. The father is XHY, so he does not have the disease because his only allele is normal (dominant)
The mother of the man can be either XHXH (she can only pass a normal allele) or XHXh and pass her normal allele to the son (in this case, the recessive allele is not inherited by chance.) His father can be either XHY or XhY, he only passes his Y chromosome which is not related to the disease. The mother of the woman can be XHXH or XHXh and the father could be XhY, then she could have inherited the normal allele from the mother and the affected allele from the father. But also, the mother of the woman could be XHXh or XhXh and the father could be XHY, so in this case she could have inherited the normal alele from the father and the affected allele from the mother.
Answer: they damage proteins and DNA
<span>Oxidative stress and other cell processes induce the formation of highly reactive aldehydes that react directly with DNA of a microbial organism, forming aldehyde-derived DNA </span>adducts lead to proteins and DNA damage. DNA damage causes deregulation of cell homeostasis and thus contributes to the disease phenotype.
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The degree to which chromatin is compacted greatly affects its accessibility for transcription, and thus, gene expression.
<h3>What is Transcription?</h3>
This is the process which involves copying a segment of DNA into RNA in organisms.
When chromatin is condensed, DNA becomes less accessible for transcription factors and vice versa which was why it was chosen as the most appropriate choice.
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