How do cigarettes and radiation cause cancer? View Available Hint(s) How do cigarettes and radiation cause cancer? by destroying healthy cells by repressing the cell cycle by toxic chemicals (in smoke) or radiation that can damage the DNA in cells by destroying DNA by activating DNA mismatch-repair enzymes

B.  by toxic chemicals (in smoke) or radiation that can damage the DNA in cells.

Explanation:

The carcinogens presents in cigerates covalently bind to DNA and form DNA adducts which results into miscoding (e.g., insertion of the wrong base) during replication of DNA and this genetic mutation causes uncontrolled cellular growth which causes cancer.

Ionising radiation including X-rays, radioactive particles, and gamma rays,can cause cancer by damaging DNA. high-energy radiation damages DNA and cause genetic mutation same as cigerates and causes cancer.

Both toxic chemicals (in smoke) or radiation damages DNA inthe cells which leads to cancer.

Hence, the correct option is B.

1. (1.2kw)x(15/60hours) = .3kwh --> a

2. (5kw)x(90/60hours)x(8cents/kwh) = $0.60 --> d

3. microwave --> 1200 watts = (1.2kw)x(6/60hours) = .12kwh

coffee-maker --> 900 watts = (.9kw)x(10/60hours) = .15kwh

therefore, it requires more energy for the coffee-maker to do the same amount of work.

so the answer is a.

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.