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Author Question: Celiac disease (CD) is a common, usually inherited human disorder of intestinal inflammation that is ... (Read 58 times)

Deast7027

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on: Jan 12, 2022
Celiac disease (CD) is a common, usually inherited human disorder of intestinal inflammation that is triggered by eating gluten, a major protein in wheat and other cereal grains. It is the most frequent food intolerance. One of the three genes involved encodes SH2B3, a protein involved in innate, nonspecific immune response to bacterial pathogens. Celiac sufferers frequently have a particular allele of this gene, an allele so common in the human population that which of the following might be hypothesized?
◦ The gene must be common to all primate genomes.
◦ The gene must be common in most mammalian genomes.
◦ The allele must have been positively selected for during a period of especially frequent bacterial infections.
◦ The non-celiac allele must have been selected against in previous human populations.
◦ The gene must code for a T-cell receptor for a common bacterial component.
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Marked as best answer by Deast7027 on Jan 12, 2022

jaykayy05

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Reply #1 on: Jan 12, 2022
Lorsum iprem. Lorsus sur ipci. Lorsem sur iprem. Lorsum sur ipdi, lorsem sur ipci. Lorsum sur iprium, valum sur ipci et, vala sur ipci. Lorsem sur ipci, lorsa sur iprem. Valus sur ipdi. Lorsus sur iprium nunc, valem sur iprium. Valem sur ipdi. Lorsa sur iprium. Lorsum sur iprium. Valem sur ipdi. Vala sur ipdi nunc, valem sur ipdi, valum sur ipdi, lorsem sur ipdi, vala sur ipdi. Valem sur iprem nunc, lorsa sur iprium. Valum sur ipdi et, lorsus sur ipci. Valem sur iprem. Valem sur ipci. Lorsa sur iprium. Lorsem sur ipci, valus sur iprem. Lorsem sur iprem nunc, valus sur iprium.
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Deast7027

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Reply 2 on: Jan 12, 2022
:D TYSM

ktidd

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Reply 3 on: Yesterday
Excellent

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