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kotegsom [21]
2 years ago
10

***please help.***

Biology
1 answer:
Fantom [35]2 years ago
4 0

Answer:

1.  first part Gene expression is the process by which the instructions in our DNA are converted into a functional product, such as a protein. When the information stored in our DNA? is converted into instructions for making proteins or other molecules, it is called gene expression.  second part Double-stranded DNA consists of two polynucleotides that are arranged such that the nitrogenous bases within one polynucleotide are attached to the nitrogenous bases within another polynucleotide by way of special chemical bonds called hydrogen bonds.

2. Gene regulation is an important part of normal development. Genes are turned on and off in different patterns during development to make a brain cell look and act different from a liver cell or a muscle cell, for example. Gene regulation also allows cells to react quickly to changes in their environments.

3. Non-coding DNA sequences do not code for amino acids. Most non-coding DNA lies between genes on the chromosome and has no known function. Other non-coding DNA, called introns, is found within genes. Some non-coding DNA plays a role in the regulation of gene expression.

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10. Researchers observe a large population of birds on a remote island. Birds in the population are found to have either red cre
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Suppose that the proportion of the white crest alleles (r) is given by w and that of the Red crest allele (R) is given by p. We have that p+w=1. The probability that an individual has 2 r alleles is given by w*w since for each allele position the probability is w. Only these individuals have a White phenotype. Hence, we get that w^2=\frac{1759}{1759+11088}; the right hand side is the proportion of white birds in the total population. Doing the calculations, this yields that w=0.37. From this, we calculate that p=0.63. The possible ways we have heterozygous individuals are the combinations Rr and rR. The probability for each of those is p*w. Thus, the total probability is 2pw. This is equal to 0.466=0.47. This is the fraction of the future population that is going to be heterozygous assuming the conditions of the Handy-Weinberg equilibrium like random reproductive matching etc.
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3 years ago
The nutrient availability of aquatic ecosystems is the .....
Elden [556K]
<span>amount of nitrogen, oxygen, and other elements dissolved in the water. Hope this helps!</span>
8 0
2 years ago
An example of a value is...
Artist 52 [7]

Answer:

d) all of the above

Explanation:

5 0
2 years ago
Read 2 more answers
2) How many solutions does the equation 4x + 2(x-5) = 3(2x - 4) have? Write down the final form as well as if it has no solution
Brilliant_brown [7]

Answer:

0 = -2, hence no solution.

Explanation:

4x + 2(x-5) = 3(2x-4)

4x + 2x - 10 = 6x - 12

     6x - 6x = -12 + 10

               0 = -2

3 0
2 years ago
Achondroplasia is an autosomal dominant genetic disorder in humans. If a man with Achondroplasia ( heterozygous) and a normal wo
tresset_1 [31]

Answer and Explanation:

Achondroplasia is a form of dwarfism that affects the formation of cartilage; early in development, most of the skeleton is comprised of cartilage. Cartilage is a type of flexible, tough tissue; in achondroplasia ossification (conversion of cartilage to bone) is affected. Symptoms include an enlarged head, shorter upper and lower limbs, and limited motion at the elbow.

Punnett squares are illustrations that display the product of hybrid trait crosses by genetic breeding.

For this cross...

Assuming Achondroplasia= dominant

Parent generation or P generation:

gametes: An → Achondroplasia dominant (A), No Achondroplasia recessive (n)

Heterozygousity describes the allelic makeup; these traits comprise two varying forms of a  gene. However, homozygous traits comprise identical forms of the gene.

Male: An  →  with Achondroplasia

Female: nn → without Achondroplasia

genotypes and phenotypes for parent and offspring...

Assuming heterozygousity of the male , for the cross

P generation:                         An × nn

                          Achondroplasia   × No Achondroplasia

F1 generation:

genotype:                      An × nn       ...(from punnet square)

phenotype:          2 with Achondroplasia ; 2 without

∴ 50% are genotypically heterozygous while 50% is homozygous , 2 with Achondroplasia ; 2 without

8 0
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