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Reika [66]
2 years ago
5

Someone please answer this question !!! I’m sorry for spamming but I’m having a panic attack

Biology
1 answer:
VARVARA [1.3K]2 years ago
3 0

Answer:

if you're talking not apart of the theory, it would be b, I believe.

Explanation:

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Let's suppose you were interested in developing drugs to prevent epigenetic changes that may contribute to cancer. What cellular
Vaselesa [24]

Answer:

Potential targets:

1- DNA methyltransferases

2- Chromatin modifiers such as histone acetyltransferases, histone deacetylases, histone methyltransferases, etc.

3- Components of the RNA interference (RNAi) machinery such as Dicer, Argonaute, etc.

Explanation:

Epigenetics can be defined as the study of any heritable change in the phenotype that does not involve modifications in the DNA sequence. Epigenetic mechanisms can be classified into three major types: 1-DNA methylation, 2-histone modifications (e.g., acetylation, methylation, phosphorylation, etc), and 3-regulatory non-coding RNAs (e.g., miRNAs, lncRNAs, siRNAs, etc) that modulate target gene expression via the RNA interference pathway. There are different types of proteins that are involved in these complex epigenetic mechanisms, and those cited above represent only some examples that can be used as therapeutic targets.

5 0
3 years ago
Can someone help me with this please.​
Flura [38]
The answer to that would be B. This is because carrying capacity is the amount of something that can be handled.
4 0
3 years ago
In the space provided below draw electron dot diagram's for the following atoms nitrogen ,hydrogen , oxygen ,and carbon
earnstyle [38]
Here you go. Hopefully this helps

3 0
3 years ago
What is an aquifer??
Masja [62]
A body of permeable rock which can contain or transmit groundwater.
7 0
3 years ago
Explain how the random alignment of homologous chromosomes during metaphase I
borishaifa [10]

The randomness in the alignment of recombined chromosomes at the metaphase plate, coupled with the crossing over events between nonsister chromatids, are responsible for much of the genetic variation in the offspring. To clarify this further, remember that the homologous chromosomes of a sexually reproducing organism are originally inherited as two separate sets, one from each parent. Using humans as an example, one set of 23 chromosomes is present in the egg donated by the mother. The father provides the other set of 23 chromosomes in the sperm that fertilizes the egg. Every cell of the multicellular offspring has copies of the original two sets of homologous chromosomes. In prophase I of meiosis, the homologous chromosomes form the tetrads. In metaphase I, these pairs line up at the midway point between the two poles of the cell to form the metaphase plate. Because there is an equal chance that a microtubule fiber will encounter a maternally or paternally inherited chromosome, the arrangement of the tetrads at the metaphase plate is random. Thus, any maternally inherited chromosome may face either pole. Likewise, any paternally inherited chromosome may also face either pole. The orientation of each tetrad is independent of the orientation of the other 22 tetrads.

Explanation:

3 0
3 years ago
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