b. insertion
<span>
</span><span>The Klinefelter syndrome is caused by an insertion mutation. It occurs
when there is an existence of an excess or extra X chromosome in each cell that
may cause an abnormality in the development of males. It usually affects the
physical and cognitive development of male with symptoms varying from one
person to another. Kids with these type
of disorder may experience learning
disabilities and even speech and language
problems. These kids tend to be
quiet and very sensitive. They can also be very passive.
</span>
<h2>Flagging pathway EGFR development </h2>
Explanation:
- The epidermal development factor (EGF) receptor (EGFR) is a receptor tyrosine kinase associated with the guideline of cell development, wound mending, and tissue fix. When EGF ties to the EGFR, a course of downstream occasions makes the cell develop and isolate. In the event that EGFR is actuated at improper occasions, uncontrolled cell development (malignancy) may happen.
- After the ligand ties to the phone surface receptor, the initiation of the receptor's intracellular parts sets off a chain of occasions that is known as a flagging pathway, here and there called a flagging course. In a flagging pathway, second delivery people catalysts and enacted proteins interface with explicit proteins, which are thus initiated in a chain response that in the long run prompts an adjustment in the cell's condition
- For example, an expansion in digestion or explicit quality articulation. The occasions in the course happen in an arrangement, much like an ebb and flow streams in a waterway. Collaborations that happen before a specific point are characterized as upstream occasions, and occasions after that point are called downstream occasions.
Answer:
C. 22
Explanation:
I just studied this last week
