Imprinting, habituation, and conditioning are all examples of
A. canalization
B. fixation
C. maturation
D. learning
Answer: D. learning
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At an autosomal gene locus in humans, the allele for brown eyes is dominant over the allele for blue eyes. At another gene locus, located on the X chromosome, a recessive allele produces colorblindness while the dominant allele produces normal color vision. A heterozygous brown-eyed woman who is a carrier of colorblindness has a child with a blue-eyed man who is not colorblind. An ultrasound test shows that the child is a girl. What is the probability that she will be colorblind? (Enter the probability as a percent. Enter the number only without the percent sign. For example, enter 100% as 100 and enter 12.5% as 12.5)
What will be an ideal response? Clarify Question · What is the key concept addressed by the question? · What type of thinking is required? · What key words does the question contain? Gather Content · What do you already know about X-linked and autosomal inheritance? Consider Possibilities · What other information is related to the question? Which information is most useful? Choose Answer · Given what you now know, what information and/or problem solving approach is most likely to produce the correct answer? Reflect on Process · Did your problem-solving process lead you to the correct answer? If not, where did the process break down or lead you astray? How can you revise your approach to produce a more desirable result?
Helicase PcrA follows classic Michaelis-Menten kinetics. In this reaction, ATP serves as a substrate for hydrolysis, while the DNA is most appropriately called the _____________
A. product. B. substrate. C. intermediate. D. coenzyme. E. ligand.
Variolation is a procedure once used to protect against
A. measles. B. bubonic plague. C. rabies. D. smallpox.
Jerry is six years old. His sister Hanah has the autosomal recessive condition neuronal ceroid lipofuscinosis that affects learning and coordination. Their parents are healthy. Given that Jerry has a normal phenotype and is not affected by the disorder, the probability that Jerry is a homozygote for the wild type allele of the gene that causes the condition is
A) 1/8. B) 1/4. C) 1/3. D) 2/3.