QUESTION 1 The Wnt signaling pathway component, Dsh, effects the action of B catenin by: O A. inhibiting the function of axin in the destruction complex O B. blocking GSK-3B from joining the destruction complex OC. stimulating ubiquitination of B catenin O D. causing its release into the cytosol from the plasma membrane complex O E. causing an increase in phophorylation of B catenin

Biology 2e
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ISBN:9781947172517
Author:Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:Matthew Douglas, Jung Choi, Mary Ann Clark
Chapter9: Cell Communication
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QUESTION 1
The Wnt signaling pathway component, Dsh, effects the action of B catenin by:
O A. inhibiting the function of axin in the destruction complex
O B. blocking GSK-3B from joining the destruction complex
O C. stimulating ubiquitination of B catenin
O D. causing its release into the cytosol from the plasSma membrane complex
O E. causing an increase in phophorylation of B catenin
QUESTION 2
PCR can be used to identify the breakage points of mtDNA that are joined to form
a mitochondrial genome with a deletion.
This technique uses:
O A. two primers outside the deleted region; a long PCR extension segment.
O B. one primer within the deleted region and one primer outside the deleted region; a long PCR extension segment
O C. one primer within the deleted region and one primer outside the deleted region; a short PCR extension segment
O D. two primers outside the deleted region; a short PCR extension segment
O E. two primers within the deleted region; a short PCR extension segment
Transcribed Image Text:QUESTION 1 The Wnt signaling pathway component, Dsh, effects the action of B catenin by: O A. inhibiting the function of axin in the destruction complex O B. blocking GSK-3B from joining the destruction complex O C. stimulating ubiquitination of B catenin O D. causing its release into the cytosol from the plasSma membrane complex O E. causing an increase in phophorylation of B catenin QUESTION 2 PCR can be used to identify the breakage points of mtDNA that are joined to form a mitochondrial genome with a deletion. This technique uses: O A. two primers outside the deleted region; a long PCR extension segment. O B. one primer within the deleted region and one primer outside the deleted region; a long PCR extension segment O C. one primer within the deleted region and one primer outside the deleted region; a short PCR extension segment O D. two primers outside the deleted region; a short PCR extension segment O E. two primers within the deleted region; a short PCR extension segment
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