Cortisol is a steroid hormone that can pass through the plasma membrane. complete the flowchart describing the interaction of cortisol with intracellular receptors. drag the labels to their appropriate locations in the flowchart. some labels will not be used.
1. cortisol passes through the plasma membrane into the cytoplasm.2. cortisol-receptor complex forms in the cytoplasm.3. cortisol-receptor complex enters the nucleus where it binds to genes.4. cortisol-receptor complex acts as a transcription factor.5. the transcribed mrna is translated into specific proteins.

1.Cortisol passes through the plasma membrane into the cytoplasm

2.Cortisol-receptor complex forms in the cytoplasm.

3.Cortisol-receptor complex enters the nucleus where it binds to genes

4.Cortisol-receptor complex acts as a transcription facto r

5.The transcribed mRNA is translated into a specific protein

Explanation:

Cortisol is a steroid hormone that is hydrophobic in nature and hence it can pass through the plasma membrane of cells. Cortisol receptors are found with in most cells in our body. These receptors receive and use the hormone in different ways. These  intracellular hormone receptors form a hormone-receptor complex  and then moves into the nucleus and acts as a transcription factor to activate the transcription of targeted genes into mRNA. Proteins is produced from these transcription mRNA. The amount of cortisol present in blood is regulated and checked by hypothalamus and pituitary gland  

Hence, the correct order is

1.Cortisol passes through the plasma membrane into the cytoplasm

2.Cortisol-receptor complex forms in the cytoplasm.

3.Cortisol-receptor complex enters the nucleus where it binds to genes

4.Cortisol-receptor complex acts as a transcription facto r

5.The transcribed mRNA is translated into a specific protein

can you give me more to work here with plzs and you

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.