Answer:
mutations can affect an organism by changing its physical characteristics (or phenotype) or it can impact the way dna codes the genetic information (genotype). when mutations occur they can cause termination (death) of an organism or they can be partially lethal.
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Cell division is the process essential for growth and repair in multi-cellular organisms.
Injury to the tissue can activate surrounding cells to undergo cell division with the help of mitogens. Mitogens are the chemical substances which help in escalating mitotic divisions in the cells.
They act by activating the signal-transduction pathway which involve mitogen-activated protein kinase (MAPK).
Other possible manner could be the loss of density which could lead to the inactivation of contact inhibition. As there is a loss of cells during the injury, it makes an empty space which could also trigger or activate surrounding cell to start cell division.
In addition, at injury site the flow of blood also increases to transport various nutrients, clotting factors, growth factors etc. These increased nutrition and growth factors also speed up the process of mitosis.
<span>Animals with a monogastric digestive system are able to digest and use a high percentage of the fats and proteins that they take in from their foods and therefore exhibit high levels of energy.</span>
Explanation:
Hemophilia is a disease that is characterized by an abnormal blood clotting process. There are many different proteins that are involved in the clotting process and a single mutation or change in one of them could result in serious effects. Hemophilia is characterized by an abnormal version of one of the many proteins involved in the clotting process, the proteins that are commonly affected are the coagulation factor 8 or 9 (VIII or IX). These abnormal proteins are caused by a mutation in the gene (within the DNA) that codifies for the production of each protein. In other words, a mutation in the part of the DNA, (gene F8) will lead to a dysfunctional coagulation factor VIII and a mutation in the gene F9 will lead to a dysfunctional coagulation factor IX. Importantly, these mutations could be inherited and could cause hemophilia. Therefore, an error in the DNA and subsequently, an error in the protein will cause hemophilia. Finally, it is important to mention that there are other types of hemophilia that are not caused by the above-mentioned mutations, such as acquired hemophilia.
Inside the seed there are is an embryo the baby plan and cotyledons. When the seed begins to grow, one part of the embryo becomes the plant while the other part becomes the root of the plant.
