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.
Answer:
Activated
Explanation:
In the presence of lactose, and in the absence of glucose, lactose will bind to a protein called a "repressor," deactivating it. Through this, RNA polymerase has a free way to synthesize the mRNA that will give enzymes for lactose degradation.
I'm try
Explanation:
originality and creativity im pretty sure
The answer is cellular respiration.
The answer to your question is:
C. 22 pairs of autosomal chromosomes, 1 X chromosome, and 1 Y chromosome.
I hope this helps!
