When two lions compete for the same habitat, shelter, and food
The answer is A. a cell
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Answer: There is presence of tumor.
Explanation: The adhesion of cells to extracellular matrix (EMC) through integrins ( cell-EMC binding molecules, which are collagens, laminins and fibronectin) causes the activation of kinases in the cytoplasm.
However, kinanes helps in controlling the epithelial cell differentiation and upholding the epithelial tissues. This is done by the addition of phosphate groups to a substrate protein which is termed Protein phosporylation. Then, the kinases direct the affairs of the cell and it's activities. For example, it determines the cell division, anabolic and catabolic activities of the cell, movement of ions between the cell and it's environment (signal transduction), protein functions and etc.
Conclusively, since the activities of the cell like cell division and protein functions is dictated by the kinase, reduction in cell division that gave rise to rapid growth is put on hold. Hence, the tumor is been suppressed.
Note: the binding of cell-EMC is regulated by Transforming Growth Factor (TGF) β.
<span>Neutral mutations are neither harmful nor beneficial.
Therefore, they are invisible to natural selection. (Since they neither improve nor worsen one individual's chances of survival and reproduction over another.)
However neutral mutations can still spread into the population by just random replications and matings. This is called genetic drift.
In other words, they are 'silent'. They are mutations that exist and propagate in populations, but seem to have no effect at all.
The reason they can become important to evolution is that a day can come when they *do* have an effect. In other words, even though an individual mutation may have no immediate effect on survival or reproduction, a *combination* of neutral mutations may provide some new benefit or harm ... at which point natural selection *will* act on that combination.
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I believe the correct answer is chromosome.
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Explanation:</h2>
We inherit 23 chromosomes from our mother and another 23 chromosome pairs from our father. You have to inherit a defective chromosome for you to get the mutation. This is what is called germ line mutation usually carried in the sperm or ovum. Of the 23 chromosomes, 22 are autosomal and 1 is chromosomal meaning of the 23 one of them is X and another one is . You get the Y from your father and the X from your mother.
