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Mama L [17]
3 years ago
7

A 4-year-old boy with a tracheostomy tube is experiencing respiratory distress. He has intercostal retractions, a heart rate of

80 beats/min, and an oxygen saturation of 85%. During his attempts to breathe, a gurgling sound is heard in the tracheostomy tube. You should:
Biology
1 answer:
creativ13 [48]3 years ago
4 0

Answer: carefully suction the tracheostomy tube.

Explanation:

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A sequence of three nitrogenous bases in a messenger-rna molecule is known as a.
sergejj [24]

Answer:

A sequence of three nitrogenous bases in a messenger-rna molecule is known as <em><u>Codon</u></em>

Explanation:

Codon is a triplet of three nitrogenous bases present in mRNA. It can be any three from uracil, adenine, guanine or cytosine. They are arranged in specific order and code for specific amino acids.

5 0
2 years ago
Which of the following is NOT an example of an anaerobic exercise?
nikdorinn [45]

Answer;

B. Jumping rope

Explanation;

Jumping rope is not an anaerobic exercise but an aerobic exercise.


Anaerobic exercise is a form of high intensity exercise that increase the oxygen debt. However since the muscles require oxygen to maintain prolonged exertion, anaerobic exercises can only last for short periods of time.

Examples of anaerobic activity sprinting, high-intensity interval training, power lifting and most athletic sports.



3 0
3 years ago
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PLEASE I REALLY NEED YOUR HELP I´LL GIVE BRAINLIEST
erma4kov [3.2K]

Answer:

D the train

Explanation:

The train is safe very fast and was the first built

4 0
3 years ago
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3. Describe three different ways to classify planets in our solar system.
klio [65]
You can classify them in what phase they are in: solid, liquid, gas
You can classify them in Sizes
You can classify them by the number of moons they have
You can classify them by distance from the sun
You can classify them all as heliocentric or orbiting/circling around the sun
You can classify them by color

8 0
3 years ago
Assume that a mutation occurs in the gene responsible for the production of hexosaminidase a, such that only about 50% of the en
zysi [14]

This statement is true.

In the case of autosomal dominant disease, the person is either homozygous (which is very rare) or heterozygous. On the molecular level, either the mutation produced a new deleterious protein for the organism, or the mutation affected an existing protein in the physiological state and that a 50% activity is not enough to compensate for the needs. of the body.

In case of autosomal recessive disease, the sick person is always homozygous. If the two loci each have a different mutant allele, it is called a "composite heterozygote". People with autosomal recessive inheritance disorder have "mandatory heterozygote" parents.

5 0
3 years ago
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