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Many different types of mutations can occur within the body. Cystic fibrosis is a genetic disorder that is caused by different mutations within the CFTR gene. One mutation in the CFTR gene that leads to cystic fibrosis causes translation to end earlier in the gene sequence. Which type of mutation causes this translation error that leads to cystic fibrosis?
silent
missense
nonsense
deletion

q: compare the parts of a cell and the cell as a whole to another common nonliving system (i.e., a car, a city,

a:

comparing this to the inside of a food building/company.

all cells are surrounded by a plasma membrane, which protects the cell from its environment, keeping toxic substances out of the cell. it regulates which molecules are allowed to enter and exit the cell.

regulates all cell activity such as cellular metabolism, and growth in addition to storing and maintaining the cell's dna for transcription and replication. determines what proteins to make.

contains the organelles; site of most cell activity

the place where ribosomes do their working activity.

builds the proteins.

prepares proteins for use or export.

responsible for breaking down and absorbing materials taken in by the cell.

maintains cell shape.

transforms one form of energy into another.

homeostasis is the tendency towards a relatively stable equilibrium between interdependent elements, especially as maintained by physiological processes. and this is how it applies to the integumentary system. back to top. skin functions in homeostasis include protection, regulation of body temperature, sensory reception, water balance, synthesis of vitamins and hormones, and absorption of materials. when body temperature falls, the sweat glands constrict and sweat production decreases.

a. 35°c

b. 25°c

c. 10°c

d. 40°c

osteogenesis imperfecta (oi) refers to a congenital ailment of bones. in the condition, the bones become brittle or fragile. this ailment is a general result of the defect or mutations in the genes (colia1 or colia2). this mutation results in imperfect collagen formation either in quantity or quality wise.  

there are eight kinds of oi defects, and each kind varies with certain distinctions in symptoms. the usual symptoms include frequent bone fractures, loss of hearing in infants, protruding eyes, discoloration of the white in the eyes, respiratory issues, loosening of the joints, short stature, and other symptoms.