A. Parahydroxy phenyl pyruvate Hydroxylase
B. Tyrosine transaminase
C. Homogentisate oxidase
D. Tyrosine oxidase
Related Mcqs:
- Alkaptonuria an inherited metabolic disorder is due to the deficiency of____________?
A. Homogentisate oxidase
B. Cystathionase
C. Pheylalanine hydroxylase
D. Tyrosine transaminase - During phagocytosis, the metabolic process called respiratory burst involves the activation of_____________?
A. Oxidase
B. Hydrolase
C. Peroxidase
D. Dehydrogenase - During phagocytosis the metabolic process called respiratory burst involves activation of_____________?
A. Oxidase
B. Hydrolase
C. Peroxidase
D. Dehydrogenase - Blood glucose level cannot be augmented by mobilization of muscle glycogen due to lack of_____________?
A. G-6-P dehydrogenase
B. G-6-P phydrogenase
C. Aldolase
D. Glucokinase - Ketone bodies are by products of metabolism of_____________?
A. Carbohydrate
B. Protein
C. Fat
D. All of the above - Under metabolic conditions associated with a high rate of fatty acid oxidation liver produces________________?
A. Glutamate
B. Acetoacetate
C. Cholesterol
D. Glycine - Most importent compansatory mechanism in metabolic acidosis______________?
A. Hyperventilation
B. Increased NH3 excretion by kidneys
C. Increased urinary phosphates
D. Increased HCO3 Production - Amelogenesis imperfecta is a disorder of_____________?
A. Ectoderm
B. Mesoderm
C. Endoderm
D. Ecto and Mesoderm - Decreased basal metabolic rate is seen in_______________?
A. Obesity
B. Hyperthyroidism
C. Feeding
D. Exercise - Basic metabolic unit of bone is_______________?
A. Osteon
B. Osteoblast
C. Osteocyte
D. Osteoclast
