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Biology
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Human Heredity Principles Study Set 1
Exam 10: From Proteins to Phenotypes
Path 4
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Question 21
Multiple Choice
The nervous system damage symptomatic of untreated PKU is due to
Question 22
Short Answer
The study of genetic variations that affect people's responses to environmental chemicals is called _____________.
Question 23
Multiple Choice
What is the nature of the genetic mutation that causes lactose intolerance?
Question 24
Multiple Choice
Supertasters for the chemical PTC are ____________.
Question 25
Multiple Choice
PKU is a recessive disorder. If a woman who has PKU has a child, what is the child's possible genotype?
Question 26
Essay
Certain traits in humans are incompletely penetrant, or show variations in expressivity. Can you suggest a biochemical explanation for these observations in such cases caused by a metabolic error?
Question 27
True/False
An essential amino acid is defined as one that is not produced by the body.
Question 28
Short Answer
Garrod called enzyme defects ____________________.
Question 29
True/False
The uptake of neutral amino acids such as leucine, histidine, and valine is inhibited in brain cells of PKU individuals.
Question 30
Multiple Choice
The hemoglobin molecule
Question 31
Multiple Choice
What actually happens to the blood cells of people with sickle cell anemia that causes the cells to change their shape ("sickle") ?
Question 32
True/False
PKU results from a failure to convert tyrosine to phenylalanine.
Question 33
Short Answer
The symptoms of alkaptonuria result from a build-up of ____________________ in the blood.
Question 34
Short Answer
Why must dietary therapy for PKU be instituted soon after birth?
Question 35
Essay
In most cases, mutations in metabolic pathways produce a recessive trait. Suggest how a mutation in a metabolic pathway might produce a dominant condition.
Question 36
Short Answer
Some success has been achieved in efforts to treat sickle cell disease by the process of ____________________.
Question 37
True/False
Large scale alterations of the amino acid structure in alpha globin are the cause of sickle cell anemia.
Question 38
Multiple Choice
Results from the study of globin variants indicate that
Question 39
Essay
In Chapter 4, two forms of bleeder's disease (hemophilia A and hemophilia B) were described. Each is deficient in a clotting factor. What would you predict are the clotting capacities of a mixture of blood from these two disorders? Why?