Answer:
Cystic fibrosis (CF) is more common in Caucasian individuals and is inherited with an autosomal recessive inheritance pattern.
Explanation:
Cystic fibrosis (CF) is a condition of genetic origin, which affects organs such as the lungs, pancreas, intestine and liver. CF is characterized by the production of very thick and viscous mucus, and promotes the formation of cysts and fibrosis of the affected organs.
CF is an inherited disease that is transmitted in an autosomal recessive pattern, that is, the altered gene is required to be on both chromosomes of the allelic pair, in order to be expressed.
It is a very common disease in Caucasian individuals, especially those of European descent.
Water is needed to break the hydrogen bonds in the starch aggregates, allowing ready access to stored energy.
Answer:
How can you determine experimentally whether a bacterium is a psychrophile or a mesophile? incubate two cultures, one around 10°C and the other around 35°C. If it grows in the lower temperature incubator, it is a psychrophile. If it grows in the higher temperature incubator, it is a mesophile.
Explanation:
I am pretty sure it is glycogenesis<span>. Please tell me if I'm wrong.</span>
Answer:
a) Yes
b) Yes
c) Yes
d) Yes
Explanation:
a.
In the exons?
Yes mutant site will be expected. It will transcript-ed as well and it can be a polypeptide depending on the mutation type.
b.
In the intron?
Yes mutant site will be expected. It will be transcript-ed as well and it cannot be a polypeptide
c.
In the promoter?
Yes mutant site will be expected. It will not be transcript-ed and it cannot be a polypeptide
d.
In the intron-exon boundary?
Yes mutant site will be expected. It will be transcript-ed and it cannot be a polypeptide
