I believe it relates because as we know the cell membrane is permeable meaning that allows oxygen, carbohydrates, food to enter the cell but it doesn't allow the entrance of large molecules that harm the cells.
After all the movement around it, matters because for example without food the mitochondria won't be able to create the energy and then with that energy, the nucleus to use it to complete the main the activities of the cell.
Hopefully this what you meant when you asked the question. Have a nice day/evening
Answer:
The disease is autosomal dominant.
Explanation:
Huntigton's disease is an autosomal dominant disease because the allele for this disease is present on an autosomal chromosome and the person with even one mutated allele (H) can develop the disease even if he has one normal allele (h) too. If a person is affected with Huntigton's disease, there are 50 percent chances that the children will also suffer from the disease.
For example: A father is suffering from Huntigton's disease but mother is normal. Let us see how it will be passed to kids.
P1: Hh : hh
Gametes: H : h: h: h
Offspring: Hh: Hh: hh: hh
50% : 50%
Therefore, 50 percent chances are there that the kids will have disease even if only parent suffers from it.
