During metaphase 1 of meiosis of the cell cycle chromosomal translocation occur.
Explanation:
Chromosomal translocation is abnormal phenomenon when a fragment of chromosomes detaches and gets stick to the non-homologous chromosome in an individual. These are causative of aneuploid, cancer and infertility in organism.
In metaphase 1 of meiosis the chromosomes gets aligned on the metaphase plate. This leads to surety of equal number of chromosome in the cell.
Chromosomal translocation are seen in metaphase 1 because it is the phase of rearrangement of chromosomes where fragments easily gets attach to the other chromosome.
Answer:
The options are not given but they are gotten from another websites.
A. Capillaries surrounding the brain have no pores and are surrounded by membranes of astrocyte cells.
B. Capillaries surrounding the brain have pores and are surrounded by membranes of astrocyte cells.
C. Capillaries surrounding the brain have no pores and are not surrounded by membranes of astrocyte cells.
D. Capillaries surrounding the brain have pores and are not surrounded by membranes of astrocyte cells.
The correct answer is option A.
Capillaries surrounding the brain have no pores and are surrounded by membranes of astrocyte cells.
Explanation:
Capillaries surrounding the brain have no pores and are surrounded by membranes of astrocyte cells because
Capillaries are tiny blood vessels in the circulatory system that connect aterioles to venules. They are the most abundant or they are much blood vessels. They can penetrate the tissues of the body which allow passage of food nutrients, oxygen in the body thereby allowing exchange of nutrients and oxygen between the body tissues and the blood.
Capillaries surrounding the brain have no pores and are surrounded by membranes of astrocyte cells while capillaries in the periphery Capillaries surrounding the brain have pores and are not surrounded by membranes of astrocyte cells.
Answer:JuiceWrlds death
Explanation: Drugs seizure R.I.P
The disorder where the grandfather and the grandchild are affected is related with the X chromosome and is called Sex linked or X linked disorder.
<h3><u>Explanation:</u></h3>
All the sex linked disorders are recessive in character i.e the normal allele is dominant over the mutated allele. In females, there are 2 X chromosomes, so the mutated allele is only expressed when there are both the mutated alleles, else its masked by the dominant normal allele. But in males, there's only one X chromosome, so if a mutated allele is present, it's readily expressed.
If the Grandfather is diseased, then he must have that mutated allele in X chromosome. Through reproduction, its received by the mother, but she is normal because the other allele received from grandmother was normal. But mother has one of the X chromosomes with mutated allele, which is received by the grandson who again becomes diseased.
So the disorder must be X linked disorder
