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Firdavs [7]
3 years ago
12

From these results, determine the relationship between the mutant allele and its corresponding wild-type allele in each line.

Biology
1 answer:
Lynna [10]3 years ago
8 0
Please provide complete details
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Where are proteins
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Answer:

B

Explanation:

Protein synthesis occurs in the cytoplasm on ribonucleoprotein particles, the ribosomes.

HOPE IT HELPS!

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3 years ago
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The function of the heart and blood vessels that supplies oxygen and nutrients to the entire body is known as:
MAXImum [283]
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4 0
3 years ago
PLEASE HELP GIVING BRAINLIEST
Anestetic [448]

Answer:

C. 50%

Explanation:

for this problem i'm unsure of what the graph is called exactly but it starts with a p and you make a chart and it's to help you decide what the genes will create. and here if there is both Rr for the two plants, then that means the offspring has a 50% chance for wrinkled seeds

3 0
3 years ago
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Suppose a person is homozygous recessive for a
sleet_krkn [62]

Answer:

Has the genetic disorder

Explanation:

Recessive gene are genes that are expressed phenotypically only in the homozygous condition. Homozygous is a condition where an organism contains identical alleles in homologous chromosomes. When a person is homozygous recessive for a recessive genetic disorder, then this genotype means that person has the genetic disorder since they have the identical allele.

8 0
2 years ago
Describe how mutations lead to genetic variations.
pickupchik [31]

Describe how mutations lead to genetic variations.

Mutations are changes in the DNA sequence of any organism. These DNA sequence comprise genes which control all the traits of an organism such as height, weight, eye color or which specific protein will be formed in body at which time. Everything is controlled by tiny pieces of DNA. If there occurs any change in the DNA sequence of an organism, it can be lethal to it, for example: In case of cancerous mutations where proteins controlling cell division are badly affected. Other mutations are simply passed to the offspring leading to genetic variations in the offspring. This is how mutations leads to the changes in genetic of an organism.

Which appears to be more dangerous: the BRC1 or BRC2 mutation?

The BRC1 and BRC2 are mutations or changes in the BRCA gene of humans mostly females. BRCA gene is basically a tumor suppressor gene which in some cases undergo mutations of different types. Some of which can be unharmful while BRC1 and BRC2 are typically very dangerous mutations because they increase the chances of a woman to develop breast cancer. Woman with BRC1 and BRC2 mutations have five times more risk of developing the breast cancer than other women. Studies suggest that BRC1 mutation is more dangerous than BRC2 mutations because a greater number of patients seen have BRC1 kind of mutation. Moreover, BRCA1 is associated with triple-negative breast cancer response in which a person cannot be fully treated with some drugs like which does not respond to hormonal trastuzumab and hormonal treatments.  

Analyze a woman’s risk of dying of cancer if she carries a mutated BRC1 gene.

The risk of a woman to die with cancer due to with BRC1 mutation are quite high. This is because 18 percent of the women which develop breast cancer due to BRC1 mutation die while only 2.8 percent of the women who develop breast cancer due to BRC2 mutations die. This indicates substantially higher risk of BRC1 patients of dying as compared to BRC2 patients.

How do heredity and inheritance relate to the data presented in these charts?

Please add charts.

What data would you need to see in order to draw conclusions about the effectiveness of preventive surgeries?

There are several preventive surgeries used to prevent the chances of breast cancer in women. However, the genetic history of a person and her family’s genetic history is important to see before drawing some effective preventive surgery.

What does the age at diagnosis tell you about the mutation?

By looking at different cases of breast cancers and analyzing the data of different countries, we noticed that,  the onset of disease takes several years because it is a genetic level mutation and the onset of mutation starts in earlier years of a woman’s life however she fully becomes a victim and notices it in late years of her life. This is why it cannot be easily diagnosed in early years even it is present there.

Explain how breast-cancer genes are still present in the population, despite cancer-related surgeries and deaths.

The genes responsible for breast cancer such as BRC1 and BRC2 are inherited from parents to offspring in a dominant fashion which means only one copy of gene is enough for the onset of the disease. Also because the disease is caused due to genetic level mutations, even if the doctors remove the cancers through surgeries they are not able to remove each and every affected gene from an organism which is passed from parents to offspring and still present in population.

Hope it helps!

7 0
3 years ago
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