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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)
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
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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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-
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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