View previous question(s) ON THE IMAGES TO ENLAGE THEM IF NEED. Question 40 of 68 (undefined) 40. Mark Patients with mut
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View previous question(s) ON THE IMAGES TO ENLAGE THEM IF NEED. Question 40 of 68 (undefined) 40. Mark Patients with mut
question(s) ON THE IMAGES TO ENLAGE THEM IF NEED. Question 40 of 68 (undefined) 40. Mark Patients with mutations in the recombination activating gene 1 (RAGI) frequently present with severe combined immunodeficiency and very low or undetectable levels of antibodies. A likely explanation for this defect could be: Scratch out (A) Scratch out (B) The inability of Ragl to form a complex with Rag2 and activate the transcription of the recombined immunoglobulin genes. The inability of the Ragl to form a complex with Rag2 and initiate V(D) recombination by binding and cleaving the RSS (also known as RS sequences). A defect in the secretion of the immunoglobulin genes The inability of the Rag1/2 complex to bind to the immunoglobulin encoding mRNA and splice out introns. Scratch out (C) Scratch out (D)
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