Which of the following factors act to bind cells together? which of the following factors act to bind cells together? glycoproteins, lipid-rafts, and cholesterol glycoproteins, specialized junctions, and cholesterol lipid-rafts, cholesterol, and glycolipids specialized junctions, wavy membrane contours, and glycoproteins

The cells are bound together by the glycoproteins, specialized junctions, and the wavy membranes contours. The glycolipids and the glycoproteins form the glycocalyx. This acts as the adhesive holding the cells together. The specialized junctions formed between the cells also function to hold the cells closely to each other. The wavy contours of the cells fit together with the contours of the other cells in the tongue-and-groove fashion.

Hence, the answer is glycoproteins, specialized junctions, and the wavy membranes contours.

The answer is glycoproteins and specialized junctions.

Explanation:

The cells are bound together by the glycoproteins, specific intersections, and the wavy layers shapes. The glycolipids and the glycoproteins frame the glycocalyx. This goes about as the cement holding the cells together. The particular intersections framed between the cells likewise capacity to hold the cells nearly to one another. The wavy forms of the cells fit together with the shapes of alternate cells in the tongue-and-furrow mold.

it's     c       this is a cell (b) with a nucleus (c) containing dna (a). the dna is organized into chromosomes (d). a section of the chromosome that codes for a trait is called a gene (e).

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.