Explanation:
(a) After vis friends comforted him he went back to school.
(b) No. HIV can only be caught by another person of they come in contact with your blood or through sexual intercourse. So it is not possible for others to become infected if they didn't come in contact with the person's blood or have unprotected intercourse. There is no reason for a HIV+ve person to isolate themself from the outside world. They are people just as we are but they only have something that can cause them to be really sick.
Answer: option A, B and D
Explanation:
The telomeres found at the terminal ends of eukaryotic chromosomes are long repetitive sequences that protects the DNA from being identify as a damage molecule to encourage fusion with other chromosomes. Since replication does not extend down to these 3' ends, the cell recruits the telomerase enzyme which is a ribonucleoprotein that helps to add telomeric repeats using its own RNA component as template to extend this end. Thus if mutation like a large deletion occurs in the gene encoding for this enzyme, the telomerase would not be able to associate correctly with the telomere, the catalytic center also encoding for its RNA polymerase would be altered and the enzymes will not be able to synthesize new telomeric repeats sequences
It is a White Blood Cell hope this helps! ^0^
Answer:
A histone modification mechanism proliferate through a process that includes post translational modification procedure. The methylation, acetylation as well as ubiquitylation are one of the main modifiers that help in activation of silent genes and ultimately these covalently bonded histone modifiers help in regulating chromatin. The PTM has a main role in altering histone structure by these modifier's recruitment....
Answer:
a. Trisomic
Explanation:
A trisomy is a genomic phenomenon whereby a particular chromosome is present in three copies. In this case, the trisomy involves the chromosome P, being this species a tetraploid with 5 pairs of homologous chromosomes (2n = 10). In humans, the trisomy for chromosome 21 is one of the most common types of aneuploidies that lead to the Down syndrome by producing alterations in gene expression patterns that are associated with changes in the phenotype
