Answer: genetic mutation maybe?
Explanation: i know that it is a genetic mutation and that it is passed from mothers to children, not from the father. the queen held the trait in her DNA and all the male children had it but the queen never showed any signs of having hemophilia
I think the correct answer from the choices listed above is option A. Sickle cell disease is caused by a change in allele. It is a disorder of the blood caused by an inherited abnormal hemoglobin. Hope this answers the question. Have a nice day.
“D” would be the best answer choice for me.... not sure if it’s correct though
<h2>a) is the correct option </h2>
Explanation:
The extracellular domain of the transmembrane receptor protein acts as binding site for primary messenger molecule whereas the transmembrane domain holds the receptor within membrane and the cytosolic domain has intrinsic tyrosine kinase activity, all these helps in proper cell signaling
If because of any mutation there is change in shape of the extracellular domain then that molecule that normally binds to the receptor protein will no longer attach hence cellular response will be deactivated
Ancient organism remains, fossil layers, similarities among organisms alive today, similarities in DNA and similarities of embryos.
