A. Homogentisate oxidase
B. Cystathionase
C. Pheylalanine hydroxylase
D. Tyrosine transaminase
Related Mcqs:
- Alkaptonuria, an inherited metabolic disorder of L0tyrosine metabolism is due to lack of_____________?
A. Parahydroxy phenyl pyruvate Hydroxylase
B. Tyrosine transaminase
C. Homogentisate oxidase
D. Tyrosine oxidase - Type II glycogen storage disorder is due to deficiency of______________?
A. Alpha -Glucosidase
B. Alpha galactosidase
C. Muscle phosphorylase
D. Acid Lipase - Scurvy is the result of deficiency of____________?
A. Vitamin A
B. Vitamin C
C. Vitamin B
D. Vitamin D - The 3 – D’s dermatitis, diarrhoea and dementia are seen in deficiency of____________?
A. Thiamin
B. Riboflavin
C. Niacin
D. Pyridoxine - Under metabolic conditions associated with a high rate of fatty acid oxidation liver produces________________?
A. Glutamate
B. Acetoacetate
C. Cholesterol
D. Glycine - 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 - Most importent compansatory mechanism in metabolic acidosis______________?
A. Hyperventilation
B. Increased NH3 excretion by kidneys
C. Increased urinary phosphates
D. Increased HCO3 Production - Acromegaly is a disorder of____________?
A. Excess growth hormone secreting
B. Excess thyroxine secretion
C. Excess ACTH secretion
D. Excess FSH secretion - Decreased basal metabolic rate is seen in_______________?
A. Obesity
B. Hyperthyroidism
C. Feeding
D. Exercise
