Explanation:
Ribosomes
The skeleton is an essential structural framework in vertebrates and protects organs allows for movement and acts as a storage site for minerals and immune cells.
Ribosomes are comprised of irony right when you click acid and proteins which are the two sections are called subunits the smaller of which facilitates mRNA binding while the larger incorporates or joins amino acids and manufactures proteins within the osteoid matrix such as collagen.
Osteoids comprise, significant sections of the entire bone matrix, and this includes fibers of collagen which give bone its flexibility and mechanical strength this allows born to resist stretching and twisting forces. Osteoblasts are highly specialized cells which formulate new bone through the production or secretion of parts of the organic matrix; this is referred to as the osteoid and mediate the calcification of osteoid during the formation of mature bone matrix.
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Answer:
If you can show me the answers I could help out but I can't see anything right now sorry
The difference in concentration between solutions on either side of a cell membrane is a concentration gradient.
In the field of biology, a concentration gradient can be described as a difference in the concentration of molecules inside and outside of a cell. It is due to concentration gradient that molecules move into and out of a cell through the cell membrane.
Some molecules move from an area of higher concentration gradient to an area of lower concentration along the concentration gradient. Diffusion is an example of such a process.
On the other hand, some molecules move from an area of lower concentration to an area of higher concentration against the concentration gradient. Active transport is an example of such a process.
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A carrier is a child who carries the genes of from parents but the gene doesn't show itself because of being masked by the dominant gene.
Answer: <em>D. Causes an accumulation of lipids in brain cells</em>
Explanation:
Tay-Sachs disease is caused by a genetic mutation in the <em>HEXA</em> gene. It is an autosomal recessive disease that causes the mutation on an enzyme, which metabolizes <em>GM2 Ganglioside</em> in nerve cells, this leads to a build-up of the molecule in brain cells. At the moment there is no cure for the disease, only support treatment is available.
