In what way does translation change information?
a. from a nucleic acid code to an amino acid code
b. from an amino acid code to a nucleic acid code
c. from a rna code to a dna code
d. from a trna code to an mrna code

from nucleic acid code to an amino acid code

Explanation:

Actually, translation is a process when mRNA (messenger RNA) molecule comes from the nucleus and helps in the process of protein synthesis. This mRNA has a specific sequence of the amino acids upon which different amino acids attached and made protein molecules. So, in the process of translation nucleic acid code convert into amino acid code.

i'm sorry, but can you list the answers? i cannot with something i don't know the answers to

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chris

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.