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ohaa [14]
3 years ago
14

SCIENCE QUESTION

Health
1 answer:
Natasha_Volkova [10]3 years ago
4 0
C it would die no way or survival without food and water
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During infancy, abnormal levels of hormones can cause children to behave. true false
Hitman42 [59]
True. During the period of early infancy, the effects of androgen (testosterone/male hormones) is questioned due to behavior. In a male's first few weeks of life, their testosterone levels rise.
8 0
3 years ago
How are progression and variation similar?
White raven [17]

Answer:

The answer is C.

Explanation:

Both represent major components of the FITT principle. Plato.

<em>Hope this helped and good luck!</em>

4 0
4 years ago
How do molecules from food and air get to the cells in the body?
AURORKA [14]

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Molecules from food and molecules of oxygen move from the mouth and the nose to cells of the body through a series of blood vessels, including veins, arteries, and microscopically small blood vessels (capillaries), that extend throughout the body.Explanation:

8 0
3 years ago
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Which statement about the endocrine system is true?
Alona [7]
Correct answer choice is:

The endocrine system controls the growth rate.

The endocrine system comprises certain glands, producing and secreting hormones. They produce <span>chemical substances in our body which are responsible for the regulation of the cells and organs activity. These </span>hormones<span> regulate the body's </span>growth<span>, </span>metabolism<span>, and sexual development and </span>function<span>.</span>
5 0
4 years ago
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If already serving as a member of the IRB, a clinical investigator can participate in the review of her own clinical protocol
Nastasia [14]

Yes, If already serving as a member of the IRB, a clinical investigator can participate in the review of her own clinical protocol.

<h3>What is IRB?</h3>

An Institutional Review Board (IRB) is group that has been formally designated to review and monitor biomedical research involving human subjects.

<h3>Can a clinical investigator can participate in the review of her own clinical protocol?</h3>

Yes, a clinical investigator can participate in the review of her own clinical protocol.

However, the Institutional Review Board regulations prohibit any member from participating in the IRB's initial or continuing review of any study in which the member has a conflicting interest, except to provide information requested by the IRB.

Thus, we can conclude that a clinical investigator can participate in the review of her own clinical protocol.

Learn more about IRB here: brainly.com/question/8905808

#SPJ1

8 0
2 years ago
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