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Tom [10]
3 years ago
8

An individual with (naturally) curly hair and an individual with (naturally) straight hair mate; all of their offspring have (na

turally) wavy hair. If an individual with wavy hair mates with an individual with straight hair, what is the probability that their child will have curly hair? An individual with (naturally) curly hair and an individual with (naturally) straight hair mate; all of their offspring have (naturally) wavy hair. If an individual with wavy hair mates with an individual with straight hair, what is the probability that their child will have curly hair? 50% 75% 0% 25%
Biology
2 answers:
vichka [17]3 years ago
6 0

If an individual with wavy hair mates with an individual with straight hair, what is the probability that their child will have curly hair? ... curly hair and an individual with (naturally) straight hair mate; all of their offspring have (naturally) wavy hair.

DochEvi [55]3 years ago
4 0

Answer:

If an individual with wavy hair mates with an individual with straight hair, what is the probability that their child will have curly hair? ... curly hair and an individual with (naturally) straight hair mate; all of their offspring have (naturally) wavy hair.

Explanation:

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A mutation creates a dominant negative allele of a particular gene. The normal allele of the gene encodes a protein that forms a
Wewaii [24]

Answer:

87.5% of the trimers in the cell will be inactive.

Explanation:

A monomer is a single subunit. Look at an easy comparison. If a monomer is a ball. For the protein to be functional, it needs to be a trimer .A trimer = 3 monomers joined / bound together with bonds. Therefore, if a monomer is a ball, we need 3 balls, we attach it together and that is the primer . if one ball becomes missing, that protein won't work .

In chemistry, a trimer is regarded as three molecules or ions of the same substance (that is, same type) which are associated together .

Double negative : Each gene has 2 alleles. So, for a positive protein, both allele needs to be same, let's say + means on. So for a x protein , if it's x+/x+ it means the protein is homozygous and active. If for some mutation, it's x+/x- , it's a heterozygous protein. Double negative means when it is x-/x- and this means the protein has lost is function . It's not functional at all.

The heterozygous cell will form one or more subunits has the mutant structure when the gene is expressed. From the question if there is a mutation in dominant negative allele, it will cause the inactivation of one trimer resulting in 87.5% inactive trimers for a heterozygous individual.

There are 87.5 % percent of the trimers present in the cell which will be inactive for a heterozygous individual, If at least one of the subunits has the mutant structure.

The probability for each individual subunit to be a mutant is 1/2

Gene codes for a protein that forms trimer so the percentage of the trimers present in the heterozygous individual is third power of 1/2 =1/8

1/8=0.125 will be active.

1- 0.125 will be inactive.

=0.875 will be inactive.

0.875 × 100= 87.5%

Therefore 87.5% will be inactive.

8 0
3 years ago
Please help help <br> its science
harina [27]

Answer:

plasma

Explanation:

3 0
2 years ago
how does the random alignment of homologous chromosomes contribute to genetic variation in a population
SCORPION-xisa [38]

The assortment of homologous chromosomes during meiosis is random and generates genetic variation, the raw material for evolution.

During metaphase I of meiosis, homologous chromosomes are lined up at the equator plate of the cell in order to be separated (assorted) in anaphase I.

The separation of homologous chromosomes during meiosis I is random. Daughter cells receive unique gene combinations from an original parent cell.

Subsequently, haploid cells got from two successive meiotic divisions fuse during fecundation to form a diploid (2n) zygote.

During prophase I, non-sister chromatids interchange genetic material by a process known as recombination. This genetic process also increases genetic variation in daughter cells.

In conclusion, the assortment of homologous chromosomes during meiosis is random and generates genetic variation.

8 0
2 years ago
Which hormone elevations indicate turner syndrome? select all that apply?
marusya05 [52]
Turner syndrome occurs among the females only because it has to do with the missing X chromosome. The effects of this syndrome is having a short height, ovary failure and heart defects. The female sex hormones, such as the estrogen and progesterone, are elevated.
6 0
3 years ago
Agouti is a type of coat-color pattern in mice that cannot be expressed in albinos (white mice). Non Albino mice without the dom
damaskus [11]

Answer:

37.5%

Explanation:

These here are

Black (AA or Aa) and albino (aa)

Agouti (Bb or BB)

Thus, a cross between

AaBb and aaBb

The percent of the progeny which are likely to be agouti would be

A. a. B. b

a. Aa. aa. B. BB. Bb

a. Aa. aa. b. Bb. bb

The probability of agouti would be

1/2 (Aa) * 3/4 (BB or Bb)

= 3/8

= 37.5%

5 0
3 years ago
Read 2 more answers
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