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riadik2000 [5.3K]
4 years ago
9

Amniocentesis is a process in which amniotic fluid is taken from the mother's womb to identify any genetic abnormalities in the

fetus. How would the discovery of the human genome contribute to this process?
Biology
1 answer:
densk [106]4 years ago
5 0

Answer:

The correct option is <em>"the exact location of a particular disease-causing gene can be determined."</em>

Explanation:

The discovery of the human genome will let us know the sequence of normal genes in a human. By comparing to this sequence, one can easily know if there is any abnormality in the fetus. The exact location where a fault has occurred can be recognized if the sequence of the normal human genome is known. Hence, the discovery of the human genome is very beneficial to the process of amniocentesis.

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Black hole
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Provide brief overview of the nervous system and its role in the maintenance of homeostasis.
Alona [7]
Explanation:

The nervous system has two major anatomical subdivisions:

Central Nervous System: Composed of the brain (inside the skull) and the spinal cord (inside the spinal column).

The brain and spinal cord are responsible for processing and integrating the various sources of information to allow us to develop a response. Therefore, the main function of the somatic nervous system is to connect the Central Nervous System with the organs and skeletal muscle to carry out our daily functions.

Peripheral nervous system: it is everything that is outside the bone cavity and is formed by the nerves and nerve ganglia that extend outside the central nervous system.

The peripheral nervous system has a somatic component, which is associated with the voluntary control of body movements through the use of skeletal muscles. This means that it is responsible for all the functions that we are aware of, including the movement of our arms, legs, and other parts of our body.

On the other hand, the autonomic nervous system is a component of the peripheral nervous system that regulates involuntary physiological processes. These processes include heart rate, blood pressure, breathing, digestion, and sexual arousal. The autonomic nervous system contains three divisions: sympathetic, parasympathetic, and enteric.

Due to the above relationships and anatomical subdivisions we can say that the nervous system is responsible for regulating and maintaining homeostasis. In fact, through its receptors, neurotransmitters, nervous inputs, and outputs, the nervous system keeps us in touch with our environment, both external and internal.

We can conclude that the correct answer is:

Answer:

Overview of the nervous system:

The nervous system has two major anatomical subdivisions:

Central Nervous System: Composed of the brain (inside the skull) and the spinal cord (inside the spinal column).

The brain and spinal cord are responsible for processing and integrating the various sources of information to allow us to develop a response. Therefore, the main function of the somatic nervous system is to connect the Central Nervous System with the organs and skeletal muscle to carry out our daily functions.

Peripheral nervous system: it is everything that is outside the bone cavity and is formed by the nerves and nerve ganglia that extend outside the central nervous system.

The peripheral nervous system has a somatic component, which is associated with the voluntary control of body movements through the use of skeletal muscles. This means that it is responsible for all the functions that we are aware of, including the movement of our arms, legs, and other parts of our body.

On the other hand, the autonomic nervous system is a component of the peripheral nervous system that regulates involuntary physiological processes. These processes include heart rate, blood pressure, breathing, digestion, and sexual arousal. The autonomic nervous system contains three divisions: sympathetic, parasympathetic, and enteric.

Role in the maintenance of homeostasis:

Due to the above relationships and anatomical subdivisions we can say that the nervous system is responsible for regulating and maintaining homeostasis. In fact, through its receptors, neurotransmitters, nervous inputs, and outputs, the nervous system keeps us in touch with our environment, both external and internal.

6 0
1 year ago
Rosa drew a diagram to compare substitution mutation and insertion mutations. What label belongs in the area marked "Y"?
Bezzdna [24]

Answer:

Hey There!

_____________________________________

Answer:

_____________________________________

Mutations:

Mutations are the changes produced in the nucleotide sequence of the genome.

There are four main types of mutations

Substitution

Insertion

Deletion

Duplication.

_____________________________________

DELETION:

A small segment of chromosome mat be missing. This condition is known as deletion.

For example, Normal chromosome has A B C D E F G. If deletion mutation occurs then mutated chromosome has A D E F G and B C got deleted.

_____________________________________

DUPLICATION:

In this condition, a part of chromosome present in exec ess to the normal chromosome.

For example, Normal Chromosome has A B C D E F G. If duplication mutation occurs, then mutated chromosome had A B C B C D E F G and B C is duplicated.

_____________________________________

SUBSTITUTION MUTATION:

Substitution is a type of mutation where one base pair is replaced by a different base pair.

For example, in the sequence CAAGT, if C replaces G, it is a substitution mutation.

INSERTION MUTATION:

In genetics, an insertion is the addition of one or more nucleotide base pairs into a DNA sequence.

For example, in the sequence CAAGT, if extra base G gets inserted after C, the new sequence would be CGAAGT.

_____________________________________

Both substitution and insertion mutations change the position of nucleotide thus, the type of amino acid. Option A is correct because B and D are wrong as increase in number of bases and decrease in number of bases is because of deletion and duplication mutations here it asks for substitution and insertion mutations. C is wrong as In mutation there is always a change in bases or chromosome. So all the other choices seem incorrect as it is asking for substitution and insertion the base pair changes which results in the change in type of amino acid.

_____________________________________

Best Regards,

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