Answer:
c. Would have deviated from the 9:3:3:1 phenotypic ratio
Explanation:
<em>If two genes are linked together on the same chromosome, the phenotype of the F2 generation would have deviated from 9:3:3:1.</em>
Two genes whose loci are close on the same chromosome are said to be linked. Linked genes have higher frequency of recombination than genes that are not linked.
<u>Hence, while genes that are not linked assort independently to produce 9:3:3:1 phenotypic ratio at F2, linked genes do not assort independently and the higher frequency of recombination ensures that they standard phenotypic ratio is deviated from.</u>
The correct option is c.
Answer:
other guy is wrong its sensory organ
Explanation
Answer:
False.
Explanation:
Neurotransmitter release occurs from the nervous terminal or varicosities in the neuronal axon. When an action potential reaches the nervous terminal, the neurotransmitter is released by exocytose. The molecule binds to its receptor in the postsynaptic neuron, triggering an answer. As long as the signal molecule is in the synaptic space, it keeps linking to its receptor and causing a postsynaptic response. To stop this process the neurotransmitter must be taken out from the synaptic space. There are two mechanisms by which the neurotransmitter can be eliminated:
• Enzymatic degradation/deactivation: There are specific enzymes in the synaptic space, which are in charge of inactivating the neurotransmitter by breaking or degrading it. The enzyme acetylcholinesterase prevents ACh from continuing to stimulate contraction.
• Reuptake: Receptors located in the presynaptic membrane can capture de molecule to store it back in new vesicles for posterior use. These transporters are active transport proteins that easily recognize the neurotransmitter.
The medical term for this is the endicrine.
Conventional genetic analyses of prions involving rrna sequences are impossible because Prions do not contain nucleic acids
The name "prions" refers to aberrant, pathogenic agents that are transmissible and capable of inducing improper folding of specific normal cellular proteins known as prion proteins, which are abundant in the brain.
Prions are virus-like creatures that contain a prion protein. These elongated fibrils (green) are thought to be protein aggregations from the infectious prion. Prions cause neurodegenerative brain illness by attacking nerve cells. Symptoms of "mad cow" include glassy eyes and uncontrollable bodily trembling.
Prion disorders develop when normal prion protein, which is found on the surface of many cells, becomes aberrant and clumps in the brain, causing harm to the brain.
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