Biology
4th Edition
ISBN: 9781259188121
Author: Peter Stiling, Robert Brooker, Linda Graham, Eric Widmaier
Publisher: McGraw-Hill Education
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Textbook Question
Chapter 12.1, Problem 1CC
What disease would result if a person inherited two defective copies of the gene that encodes phenylalanine hydroxylase?
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Chapter 12 Solutions
Biology
Ch. 12.1 - What disease would result if a person inherited...Ch. 12.1 - Prob. 2CCCh. 12.1 - What is the direction of flow of genetic...Ch. 12.2 - Prob. 1CCCh. 12.2 - Core Skill: Connections Look back at the role of...Ch. 12.3 - Prob. 1CCCh. 12.4 - Prob. 1CCCh. 12.4 - Prob. 2CCCh. 12.4 - Prob. 1EQCh. 12.4 - Prob. 2EQ
Ch. 12.4 - Prob. 3EQCh. 12.5 - Prob. 1CCCh. 12.5 - Core Skill: Connections Look back at Figure 6.3,...Ch. 12.5 -
Figure 12.17 Comparison of small subunit rRNA...Ch. 12.6 - Prob. 1CCCh. 12 - Which of the following best represents the central...Ch. 12 - A mutation prevents a gene from being transcribed...Ch. 12 - Prob. 3TYCh. 12 - Prob. 4TYCh. 12 - If a eukaryotic mRNA failed to have a cap attached...Ch. 12 - Prob. 6TYCh. 12 - Prob. 7TYCh. 12 - During the initiation of translation, the first...Ch. 12 - Prob. 9TYCh. 12 - Prob. 10TYCh. 12 - Prob. 1CQCh. 12 - Prob. 2CQCh. 12 - Prob. 3CQCh. 12 - Prob. 1COQCh. 12 - Prob. 2COQ
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- Describe two reasons why the reaction glutamine synthetase performs is important to the body.arrow_forwardGlucose-6-phosphatase deficiency (G6PD), also known as von Gierke disease, is glycogen storage disease. It is an autosomal recessive disease occurring most frequently in males of African or Middle Eastern descent. G6PD is involved in many reactions, but we will focus on the following simplified pathway: The conversion of glycogen to glucose is called:arrow_forwardWhat type of bond is hydrolyzed by alpha Amylase?arrow_forward
- Choose the CORRECT sequence of glycine formation. transamination of 3-phosphoglycerate → hydrolysis of 3-phosphohydroxypyruvate → hydrolysis of 3-phosphoserine → transfer of the side-chain methylene group of cysteine to tetrahydrofolate → glycine transamination of 3-phosphohydroxypyruvate → oxidation of 3-phosphoglycerate → transfer of the side-chain amino group of serine to tetrahydrofolate → glycine oxidation of 3-phosphoglycerate → oxidation of 3-phosphohydroxypyruvate → hydrolysis of 3-phosphoserine → glycine transamination of 3-phosphohydroxypyruvate → hydrolysis of 3-phosphoserine → oxidation of 3-phosphoglycerate →transfer of the side-chain methylene group of serine to tetrahydrofolate → glycine oxidation of 3-phosphoglycerate → transamination of 3-phosphohydroxypyruvate → hydrolysis of 3-phosphoserine → transfer of the side-chain methylene group of serine to tetrahydrofolate → glycinearrow_forwardWhen transaminated, the three branched-chain amino acids (valine, leucine, and isoleucine) form compounds that have the characteristic odor of maple syrup. An enzyme known as branched-chain a-keto acid dehydrogenase converts these compounds into CoA esters. People who do not have this enzyme have the genetic disease known as maple syrup urine disease, so called because their urine smells like maple syrup. a. Draw the compounds that smell like maple syrup.b. Draw the CoA esters.c. Branched-chain a-keto acid dehydrogenase has five coenzymes. Identify them.d. Suggest a way to treat maple syrup urine disease.arrow_forwardWhat is the major activator (non-allosteric, direct-activator) of phosphorylase? How does this activator activate phosphorylase (type of regulation)?arrow_forward
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