Answer:
a the graph of a function I hope it will help you please follow me
<span>Cells control cell division in order to maintain normal cell function. If something happens to the control of the cell division, the healthy cells will divide uncontrollably. These new cells are cancer cells. </span>
The mutations in three genes are responsible for development of cancers:
1. Mutation in proto-oncogenes. Proto-oncogenes normally signal cells to grow and differentiate. Proto-oncogenes can become oncogenes due to mutations which result in the uncontrollable division of the cells.
2. Mutation in tumor suppressor genes. In normal cells, tumor suppressor genes suppress genes essential for cell cycle and that way they prevent uncontrollable cell division. However, after a mutation in these genes, suppression is lost and the cell may progress to cancer.
3. Mutation in stability genes. In normal cells, they have no role either in cell death or growth, but they control mutation rate. Mutation in stability genes results in situation where all genes, including proto-oncogenes and tumor suppression genes, are more frequently mutated.
<span>The nurse conducting wound care should choose a dressing that
keeps the periwound skin dry and the surgical wound bed moist to contribute
healing. The dressing used for wound care should control exudate from the
wound, but it should not desiccate the wound bed. There must be a pressure in
application while cleaning the periwound and wound may deepend the wound bed. Using
sterile normal saline and a sterile gauze to clean the surgical wound reduces
the incidences of infection.</span>
Your answer is leukocytes.
Answer:
The answer is mother in meiosis II
Explanation:
nondisjunction can be defined as the failure of the segregation of the child chromosomes in meiosis I and meiosis II resulting in gametogenes. This results in abnormal gametes with some chromosomal imbalance being formed and subsequent fertilization of these gametes results in a generation of abnormal individuals.
According to exercise, red-green color blindness follows an X-linked recessive pattern and the phenotype is only expressed. the father cannot bring the possibility of color blindness to his children, and the nondisjunction, defined earlier, cannot occur in either meiosis I or meiosis II. As a conclusion we can say that it may have a place in meiosis I or meiosis II corresponding to the mother and although the mother's condition may be normal, the first child would be compromised with color blindness, therefore, the mother is the carrier.
