Explanation:
the release of an egg from the ovary
Answer:
Fats would accumulate in the liver and the individual would show hypocholesterolemia
Explanation:
Familial hypercholesterolemia is a genetic disorder caused by a reduction and/or defect in the low-density lipoprotein (LDL) receptor. Moreover, apolipoprotein B is the unique protein component of LDL, which plays a critical role in lipid metabolism by binding the LDL receptor. Familial defective apolipoprotein B-100 refers to an inherited disorder associated with mutations of the apolipoprotein B-100 that leads to moderate or severe cases of hypercholesterolemia. Mutations in apolipoprotein B-100 are associated with a reduction in the binding capacity of LDL to the LDL receptor, thereby leading to hypercholesterolemia.
Answer:
T T C O C T
Explanation:
Each eukaryotic chromosome usually has repeated telomere sequences ranging from 2 to as many as 2000.
There is normally just one specialized DNA sequence called the centromere per eukaryotic chromosomal DNA molecule.
The origin of replication is the site where DNA duplication starts in S phase.
The centromere attaches the chromosome to the mitotic spindle via the kinetochore structure.
Teleomere contains repeateted sequences at the ends of the chromosomes.