HUMAN HEREDITY (LL)-W/MINDTAP ACCESS
HUMAN HEREDITY (LL)-W/MINDTAP ACCESS
11th Edition
ISBN: 9781305717022
Author: Cummings
Publisher: CENGAGE L
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Chapter 15, Problem 12QP

One unexpected result of the sequencing of the human genome was the finding that mutations in a single gene can be responsible for multiple distinct disorders. For example, mutations in the RET gene can cause two different types of multiple endocrine neoplasias, familial medullary thyroid carcinoma, and Hirschsprung disease. How do you think mutations in a single gene can have such diverse effects?

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For the a subunit of a trimeric G protein, A. a G-protein-coupled receptor GPCR) acts as a guanine nucleotide exchange factor (GEF), whereas a regulator of G protein signaling (RGS) can act as a GTPase-activating protein (GAP). B. a GPCR acts as a GAP, whereas an RGS can act as a GEF. C. both a GPCR and an RGS can act as a GEF. O D. both a GPCR and an RGS can act as a GAP OE. None of the above.
A cell expresses a transmembrane protein that is cleaved at the plasma membrane to release an extracellular fragment. The fragment binds to receptor proteins on nearby cells and activates signaling pathways resulting in altered gene expression patterns in the cells. What form of intercellular signaling does this represent? OA. Contact-dependent signaling B. Paracrine signaling OC. Synaptic signaling D. Endocrine signaling E. Autocrine signaling
Which of the following drive nuclearly encoded proteins import into the mitochondrial matrix? OA. ATP hydrolysis OB. Membrane Potential OC. K+ Ions OD. A and B OE. None of the above
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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY