Zoning laws establish

Biology

2 answers:

dexar [7]3 years ago

5 0

Answer:

b. the uses an area of land can be put to

MaRussiya [10]3 years ago

3 0

99% sure the answer is B

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How is blood different after it is pumped through the capillaries in the intestines?

kumpel [21]

Answer:

Explanation:

7 0

3 years ago

Each of the four pedigrees that follow represents a human family within which a genetic disease is segregating. Affected individ

Ne4ueva [31]

Answer:

The following four traits are -:

Pedigree 1 - A recessive trait (autosomal recessive) is expressed by pedigree 1.
Pedigree 2- Recessive inheritance is defined by Pedigree 2.
Pedigree 3 - The inheritance of the dominant trait (autosomal dominant) is illustrated by Pedigree 3.
Pedigree 4- An X-like dominant trait is expressed by Pedigree 4.

Explanation:

Explaination of each pedigree chart-

Pedigree 1 demonstrates the recessive trait since their children have been affected by two unaffected individuals. If the characteristics were X-linked, in order to have an affected daughter, I-1 would have to be affected. $X^A$ In this, both parents are autosomal recessive trait carriers, so the child will be affected by a 1/4 (aa)
Recessive inheritance is defined by Pedigree 2. This is X-related inheritance as autosomal recessive inheritance has already been accounted for in part 1. This inference is confirmed by evidence showing that the father (I-1) is unaffected and that only the sons exhibit the characteristic in generation II, suggesting that the mother must be the carrier. The individual I-2 is a carrier for this X-linked trait. A typical Xa chromosome is attached to the unaffected father (I-1), so the chance of carrier II-5 is 1/2. Probability of an affected son = 1/2 (probability II-5 is a carrier) x 1/2 (probability II -5 contributes ( $X^A$ ) x 1/2 (probability of Y from father II-6) = 1/8. An affected daughter's likelihood is 0 because a typical $X^A$ must be contributed by II-6.
The inheritance of the dominant trait is demonstrated by Pedigree 3 because affected children still have affected parents (remember that all four diseases are rare). The trait must be autosomal dominant because it is passed down to the son by the affected father. There is a 1/2 risk that the heterozygous mother (II-5) would pass on mutant alleles to a child of either sex for an autosomal dominant feature.
Pedigree 4 is an X-linked dominant function characterized by the transmission to all of his daughters from the affected father but none of his son. On the mutant X chromosome, the father (I-1) passes on to all his daughters and none of his sons. As seen by his normal phenotype, II-6 therefore does not bear the mutation. An affected child's likelihood is 0.

In the question the pedigree chart was missing ,hence it is given below.

7 0

3 years ago

When an ADP molecule gains a phosphate, it becomes an ATP molecule. This process is called _____.

disa [49]

The correct answer is phosphorylation. When an ADP (Adenine Diphosphate) molecule gains a phosphate, it becomes an (Adenine Triphosphate) molecule. This process is called a phosphorylation. Phosphorylation and its counterpart dephosphorylation change many proteins in terms of its functions and activities.

6 0

3 years ago

Read 2 more answers

Hou many codons code for PRO?

mart [117]

Answer:Three codons: Ile, STOP (“nonsense”). Four codons: Ala, Gly, Pro, Thr, Val

Explanation:

6 0

2 years ago

Sometimes a population cannot grow to its biotic potential due to environmental conditions called ____________.

strojnjashka [21]

C because limiting factor can’t grow to it’s biotic!