Answer: Although both are X-linked recessive conditions, and therefore more likely in males, with the single X-chromosome. The recessive allele in colour blindness occurs at a higher frequency in the population and is a mild condition. Thus colour blindness does occur to a lesser extent in females because it needs the double recessive condition. DMD is a severe, disabling condition with a limited lifespan, and recessive allele frequency much lower, so the double recessive condition in females is very rare.
Explanation: DMD is an X-linked recessive, “nearly always in males” suggest that it also occurs due to a new mutation or some rare condition e.g. double recessive from an affected father and carrier mother, or inactivation of the normal gene in a heterozygote. It is also found that the defective allele is not completely recessive and that female carriers may exhibit mild to moderate effects.
colour blindness is polygenic, although the genes are all X-linked. It is more common in males than females. Females can carry two recessive alleles and so express the phenotype, but this is uncommon because the frequency of the recessive gene is low.
There are similarities in that both are X-linked recessives, therefore commonly expressed in males, who only have one X chromosome. The gene frequency of the colour blindness recessive is much higher than that of DMD, so the double recessive condition, which affects females, is more likely to be seen with colour blindness. In addition, DMD is a severe condition associated with disability and limited lifespan, which reduces the probability of mating between an affected male and carrier female
Explanation:
Homologous chromosomes are 2 physically different chromosomes that have the same genes but are not genetically identical. Sister chromatids are 2 copies of a single chromosome and so are genetically identical (they also are physically attached to one another).
Jimmy hole Tuesday went shopping on Tuesday and it’s pretty cool bcuz that’s where he got his name now go choke on a toenail
The virus' DNA becomes a part of the host cell's DNA, and every time the host cell copies and divides, it also copies viral DNA. The viral DNA may remain inactive (a provirus) for a long time, but it can become active when it frees itself from the host's chromosome, which triggers the lytic cycle.
I forget which one is the virus' DNA
Answer:
endocytosis
Explanation:
Endocytosis is a cellular process in which substances are brought into the cell. The material to be internalized is surrounded by an area of cell membrane, which then buds off inside the cell to form a vesicle containing the ingested material.
