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Degger [83]
3 years ago
14

How do cells replace themselves?

Biology
1 answer:
Romashka [77]3 years ago
3 0
By undergoing mitosis.
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Suppose a new data pair with an x-coordinate of 30 was entered into the data set below. If the new data pair followed the same t
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<span>{(45, 18), (62, 13), (72, 11), (55, 15), (38, 21), (26, 31), (93, 9), (64, 13), (29, 28), (33, 25), (49, 17)}</span>
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3 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
Meaning of transparent<br>​
Charra [1.4K]

fine or sheer enough to be seen through

5 0
2 years ago
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Which of the following features is not unique to either prokaryotic or eukaryotic cells? A. a nucleoid. B. a nucleus. C. a mitoc
11Alexandr11 [23.1K]
D. a cell wall.

reasoning: in a prokaryotic cell, they have no nucleus or organelles. a cell wall is the only answer that is neither of those.
6 0
3 years ago
In peas, tall plants (T) are completely dominant over short plants (t). You cross two heterozygous pea plants Use a Punnett squa
Nikitich [7]

Answers and Explanation:

Find enclosed the Punnet square.

T= dominant allele

t= recessive allele

Tt= heterozygous genotype

TT and tt= homozygous genotype

- The male pea plant's genotype is Tt (heterozygous)

- The female pea plant's genotype is Tt (heterozygous)

- Male gametes: T and t

- Female gametes: T and t

- The expected genotypic ratio of the offpring will be:

TT: Tt: tt ⇒ 1: 2: 1

1/4 of the offpring will be TT genotype (dominant homozygous), 1/2 of the offpring will be Tt (heterozygous) genotype and 1/4 of the offpring will be tt genotype (recessive homozygous).

- The expected phenotypic ratio of the offpring will be:

tall : short ⇒ 3 : 1

3/4 of the offpring will be tall (TT and Tt) and the restant 1/4 will be short (tt).

4 0
3 years ago
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