Answer:
Option-C
Explanation:
Mitophagy refers to the process which is evolutionarily conserved in the organisms to remove the dysfunctional mitochondria in the cell.
The mitochondrial is degraded by the digestive organelles by engulfing the mitochondria.
The mitochondria are engulfed by the lysosome and then phagosome is formed which is double membrane structure.
This phagosome matures into the autophagosome and now has the mitochondria engulfed.
Since the mitochondria contain toe layer and during mitophagy engulfed by the phagosome, therefore, there is a total of four-layer.These four layers separate the matric of the mitochondria with the cytosol.
Thus, Option-C is the correct answer.
Answer:
Intestine is the lower part of the alimentary canal from the end of the stomach to the anus.
Explanation:
Answer:
d. Monosomy X is the only viable monosomy known to occur in humans.
Explanation:
Human have 22 pair of homologous chromosomoses and an extra pair of sex chromosomes. While in males the sex chromosomes are X and Y , females have two chromosomes X . Anyway, in normal conditions the total number of chromosomomes that humans have in their cells is 46 (23 pair of chromosomes).
Aneuploidy is a biological condition where an individual have an abnormal number of chromosomes in their cells. In humans for examples, this would be a human having more or less than 46 chromosomes.
The Turner syndrome also called monosomy X is an aneuploidy where one of the X chromosomes is missing in a female. Although under constant supervision, people with Turner syndrome have viable healthy lives. However this is the only monosomy that occur in humans that is compatible with life.
Answer:
The change in time for the first quarter is 2.07 seconds.
The change in time for the second quarter is 1.09 seconds.
The change in time for the third quarter is 0.95 seconds.
The change in time for the fourth quarter is 0.81 seconds.
Explanation:
This is for table C
Answer:
Dihybrid
Explanation:
A dihybrid cross explores the interaction of two traits in affecting the genotype of the offsping
