Alkaptonuria, an inherited metabolic disorder of L0tyrosine metabolism is due to lack of_____________?

Related Mcqs:

1. Alkaptonuria an inherited metabolic disorder is due to the deficiency of____________?

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

2. During phagocytosis, the metabolic process called respiratory burst involves the activation of_____________?

   A. Oxidase B. Hydrolase C. Peroxidase D. Dehydrogenase...

3. During phagocytosis the metabolic process called respiratory burst involves activation of_____________?

   A. Oxidase B. Hydrolase C. Peroxidase D. Dehydrogenase...

4. 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...

5. Ketone bodies are by products of metabolism of_____________?

   A. Carbohydrate B. Protein C. Fat D. All of the above...

6. Under metabolic conditions associated with a high rate of fatty acid oxidation liver produces________________?

   A. Glutamate B. Acetoacetate C. Cholesterol D. Glycine...

7. Most importent compansatory mechanism in metabolic acidosis______________?

   A. Hyperventilation B. Increased NH3 excretion by kidneys C. Increased urinary phosphates D. Increased HCO3 Production...

8. Amelogenesis imperfecta is a disorder of_____________?

   A. Ectoderm B. Mesoderm C. Endoderm D. Ecto and Mesoderm...

9. Decreased basal metabolic rate is seen in_______________?

   A. Obesity B. Hyperthyroidism C. Feeding D. Exercise...

10. Basic metabolic unit of bone is_______________?

    A. Osteon B. Osteoblast C. Osteocyte D. Osteoclast...