Answer:
Hemophilia and color blindness are two common sex-linked conditions.
Explanation:
In humans, certain hereditary defects are linked to the X chromosome. The most important ones are colour blindness and haemophilia. Color blindness is a vision defect that is transmitted by a recessive gene carried on the X chromosome. The disease is more common in men than in women. Haemophilia is a serious disease in which blood take an abnormally long time to clot which leads to uncontrolled bleeding.
<span>The antigen-antibody that is deposited in the dermis is known as T-cells. These are protein cells that divide excessively causing the development of thick and calloused skin.
The overproduction of these cells on the dermis area causes the overproduction of collagen fibers on the skin. As the skin pushes its way up to the epridermis, the overproduction of these cells result to the symptoms that are observable for diagnosis.<span>
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Enzymes are biological catalysts. ... Thus enzymes speed up reactions by lowering activation energy. Many enzymes change shape when substrates bind. This is termed "induced fit", meaning that the precise orientation of the enzyme required for catalytic activity can be induced by the binding of the substrate.on:
Answer: mitochondria, i think
Explanation:
I'm so sorry if its wrong!
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