33. Which of the following is a typical hotspot for mutations? a. often located where adenine is methylated b. often located where thymine is methylated c. often located where guanine is methylated d. often located where cytosine is methylated 34. In Garrod's study, mutation in gene lead to accumulation of
33. Which of the following is a typical hotspot for mutations? a. often located where adenine is methylated b. often located where thymine is methylated c. often located where guanine is methylated d. often located where cytosine is methylated 34. In Garrod's study, mutation in gene lead to accumulation of
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
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
Transcribed Image Text:33. Which of the following is a typical hotspot for mutations?
a. often located where adenine is methylated
b. often located where thymine is methylated
c. often located where guanine is methylated
d. often located where cytosine is methylated
34. In Garrod's study, mutation in
causing alkaptonuria.
a. homogentisic acid oxidase; phenylalanine
b. phenylalanine hydrolase; homogentisic acid
c. phenylalanine hydrolase; phenylalanine
d. homogentisic acid oxidase; homogentisic acid
35. In the sickle cell disease, the mutations in the
red blood cells.
a. 8-globin
b. y-globin
gene lead to accumulation of
c. a-globin
d. ß-globin
36. A silent mutation in a kinase leads to problems with
translational modification.
a. proteolysis
b. glycolysis
c. phosphorylation
d. none of the above
gene causes dysfunctional
a type of post-
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