Answer:
3/4
Explanation:
If we assume simple dominance and independent assortment for each trait, we can use Mendel's Law of Segregation to predict the phenotypic proportions in the offspring of the parental cross AABBCc x AabbCc.
<h3><u>Gene A</u></h3>
AA x Aa
- F1 genotypes: 1/2 AA, 1/2 Aa
- F1 phenotypes: all A
<h3 /><h3><u>Gene B</u></h3>
BB x bb
- F1 genotypes: 1 Bb
- F1 phenotypes: all B
<h3 /><h3><u>Gene C</u></h3>
Cc x Cc
- F1 genotypes: 1/4 CC, 2/4 Cc, 1/4 cc
- F1 phenotypes: 3/4 C, 1/4 cc
We want to know the proportion of progeny with all dominant phenotype (A_B_C_). Since the genes are independent, we can multiply the probabilities of each gene to obtain the overall probability of having a ABC progeny:
<h3>1 A_ x 1 B_ x 3/4 C_ = 3/4 A_B_C_</h3>
I would say it is true and if it isn’t then I’m sorry.
Answer:
Myogenic mechanisms
Hormones
Sympathetic nervous system
Explanation:
Myogenic mechanisms work in the arterioles that serve the glomerulus.
They cause the smooth muscle cells in the arterioles to contract and relax in response to blood pressure changes.
The sympathetic nervous system increases blood flow through the kidneys during resting conditions.
At times of stress, it decreases blood flow through the kidneys, making it more available to the rest of the body.
The hormones angiotensin and aldosterone regulate blood volume by controlling retention of Na⁺ and water.
C is wrong. The parasympathetic nervous system mainly controls visceral organs such as glands.
Answer:
Dorsal horn
Explanation:
The sensory neurons cell bodies are present in dorsal horns. The front side of spinal cord consist of two arms of it. The ventral horn is the centrally located grey matter with motor neurons cell bodies.
The dorsal horns are located at each spinal cord levels that are four in number. The sensory nuclei is present in dorsal horns that perceive somatosensory information. The information is then transferred to midbrain and diencephalon. Thus, Interneurons receiving input from sensory neurons are located in the dorsal horn.
Answer:
1- substitution.
2- neutral.
Explanation:
The change in the genetic sequence of the organisms known as mutation. Mutations might be sudden and heritable in nature. spontaneous mutation and induced mutation are types of mutation.
A change that causes a change in single base pair of a gene sequence is called substitution mutation. The original leucine sequence is GTT and the mutated sequence is GTG. Thus T has been substituted by G.
Mutation can be beneficial, detrimental or neutral. The neutral mutation is that does not affect the physical change. Both GTT and GTG code for the same amino acid so it would be neutral.
