They would fall in the clumped or even category
Answer:
1. You will be unable to smell
3. Your olfactory receptor cells will no longer be able to respond to molecules trapped in the mucus.
Explanation:
The Olfactory receptors are the receptors present in the olfactory neurons which detect different odorants or smell.
The olfactory receptors are embedded in the epithelium or mucous lining of the nose in which one extension of the cell body reaches the epithelium surface and branches into cilia like structures which sense the odour.
If the axons of the olfactory cells are broken then the cells will not be able to respond to the molecules trapped in the mucus and thus no detection of odour. The signal will not be generated in response and thus will not be sent to the brain. Thus, the person will not be able to smell.
Thus, Options-1 and 3 are correct.
Ansa million. once you're staring at in ordinary terms one technology, it relatively is, all those fruit flies have been produced via 2 mum and dad, then the only plausible parental genotype that provide you a 50/50 ratio is that if the mummy is XwXw and the father is Xry... this gene is carried on the X chromosome, and w represents white eyes and r represents purple eyes. you are able to bypass forward and draw this out in case you like, even yet it provides 50% heterozygous women individuals (with purple eyes, provided that purple is dominant), and 50% white eyed men, who can in ordinary terms inherit Xw from their mom. The Y that they could inherit from the father could have not any effect on their eye shade. it relatively is comparable for women individuals, they are in a position to in ordinary terms inherit Xw from their mom and an Xr from their father, meaning they'll continually be heterozygous for the attention shade gene. 2. returned, set us the genotypes so which you will visualize it; we are going to say that this disease is carried on the X chrmsm (thats whats usually assumed), and the gene for customary creative and prescient is XB, yet for colorblindness its Xb. those are dominant/recessive to boot. So, if the girl is a provider, her genotype is XBXb, and if the male is colorblind, his genotype is XbY. in case you draw this out in a punett sq., you will get 25% heterozygous woman, 25% colorblind woman, 25% well-known male, and 25% colorblind male. so, there's a 50% risk that any baby they have would be colorblind, 50% risk if its a woman, or 50% risk if it relatively is male.wer:
Explanation:
You multiply 15,000 by .1, which equals 1,500. Then you add that to 15,000. This equals 16,500. That is your answer.
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