A. Homogentisate oxidase
B. Cystathionase
C. Pheylalanine hydroxylase
D. Tyrosine transaminase
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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 ā Dās 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...
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