Answer:
Men express all the X-linked genes present in their genome.
Explanation:
Human males have one copy of X and one copy of Y chromosomes. They express all the alleles present on their X chromosome irrespective of its dominant or recessive nature. This occurs because males do not have a second copy of the X chromosome to carry another allele for the same gene. Color blindness is caused by a recessive allele present on the X chromosome. Males carrying one copy of this allele exhibit the disease while females need two copies of the allele of color blindness to express the disease. Therefore, males are more frequently affected by this disease. 
 
        
             
        
        
        
Answer.
Actually all of these are involved.
Explanation:
Transcription is the process where genetic material or DNA is copied into RNA by the enzyme RNA polymerase. The transcription unit is made up of a promoter, a protein-coding sequence an attenuation sequence, a termination sequence. The rotein coding sequence contain the structural genes which Consist of two strands which is known as template strand and coding strand. Attenuator sequence can be as a result of stop signal which can also lead to transcription.
 
        
             
        
        
        
Answer:
electron microscope
Explanation:
An electron microscope is a microscope that uses a beam of accelerated electrons as a source of illumination. As the wavelength of an electron can be up to 100,000 times shorter than that of visible light photons, electron microscopes have a higher resolving power than light microscopes and can reveal the structure of smaller objects.
 
        
             
        
        
        
Answer is B 
 Explanation : Plant cells are enclosed by a rigid cell wall. When the plant cell is placed in a hypotonic solution , it takes up water by osmosis and starts to swell, but the cell wall prevents it from bursting. ... This liquid or hydrostatic pressure called the turgor pressure prevents further net intake of water .
 
        
             
        
        
        
Answer:
chromosomes
Explanation:
Genomics refers to the scientific study of genes (DNA) found in living organisms such as humans and animals.
A genome can be defined as the complete set of hereditary instructions that is typically found in the deoxyribonucleic acid (DNA). 
The complex structures of deoxyribonucleic acid (DNA) and protein found in the cell nucleus are generally referred to as chromosomes.
In sexual reproduction, the chromosomes from parents are found in the cell nucleus and are comprised of deoxyribonucleic acid (DNA), histone proteins, etc. Thus, they are used to store genetic informations in living organisms.
Basically, the human somatic cell is made up of 46 chromosomes which are sub-divided into 22 pairs of autosomes and a pair of sex chromosomes (X and Y). An autosome is one of the numbered chromosome that is typically not a sex chromosome. 
On the other hand, sex chromosomes (X and Y) are responsible for determining the gender or sex of living organisms such as humans.