What are the intercellular communication types at a synapse? Select all that apply. a. soups - chemical synaptic transmission

b. sparks - chemical synaptic transmission

c. soups - direct electrical communication

d. sparks - direct electrical communication

Option A and D.

Soups chemical synaptic transmission.

Sparks direct electrical transmission.

Explanation:

Intercellular communication refers to the communication and interaction that exists between two cells in the body. It could be hormonal or synaptic transmission.

Synapse is the site where electric nerve impulses are transmitted between two nerve impulses.

There are two synapse possibilities which are electrical and chemical.

The Sparks and soups mean that the scientific discovery over the transmission of nerve impulses as to whether they are electrical impulses (Sparks) or chemical impulses(soup).

Chemical synaptic transmission means there is no physical touch in the space chemical are released and move to the neighbouring cells.

Electrical transmission means neuron physically touch and give way for flow of impulses between cells.

a

explanation:

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.