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Sav [38]
3 years ago
15

Recent research indicates fcrl4 is to b-cells as glutathione is to t-cells. what is fcrl4

Biology
2 answers:
Varvara68 [4.7K]3 years ago
6 0
FCRL4 is a type of immunoregulatory receptor. It is expressed by memory B cells (MBCs) localized in sub-epithelial regions of lymphoid tissues. Both FCRL4 and Glutathione function as pro-inflammatory for b-cells and t-cells respectively during the event of autoimmune disease responses.
Mkey [24]3 years ago
5 0
FCRL4  is an immuno-regulatory receptor that is usually expressed by memory cells that are located in the lymphoid tissues in a region called the sub-epithelial region. During  the time of autoimmune disease responses, the glutathione and the FCRL4 function as pro-inflammatory for t-cells and b-cells respectively.
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Duchenne Muscular Dystrophy (DMD) is an X-linked recessive trait that causes muscular weakness, deterioration of muscle tissue,
Ronch [10]

Answer:

The correct answer is - XDXd and XD Y

Explanation:

Sex-linked disorders are the disorders that are expressed only when there is two copy of the mutated allele or have not masked by the dominant allele of the gene. In DMD, the dominant allele is XD and the mutated allele is Xd. To express it there are the following genotype possible-

in women XdXd, and in men XdY, so these two genotypes are not possible for the parents in this case. If a mutated allele is present with the dominant allele it will be considered as carrier women but diseased will not be found in them.

So the correct genotype would be

mother: XDXd ( a carrier woman)

father : XDY (normal man)

7 0
2 years ago
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Answer el agua es acido

Explanation:

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Trade winds (D) is the answer
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8 0
2 years ago
Color-blindness is a x-linked recessive disease. Under what circumstances will this condition manifest in a child? (2 points)
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I think the correct answer from the choices listed above is the first option. The circumstances that this condition would manifest would be if  the child is a male and its mother has the recessive allele. X-linked recessive inheritance<span> is a mode of </span>inheritance<span> in which a </span>mutation<span> in a </span>gene<span> on the </span>X chromosome<span> causes the phenotype to be expressed in males </span><span>and in females who are homozygous for the gene mutation</span>
8 0
2 years ago
Read 2 more answers
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