HMG-CoA is formed during metabolism of all except______________?

Related Mcqs:

1. HMG CoA reductase is inhibited by_____________?

   A. Clofibrate B. Gemfibrosil C. Lovastatin D. cholestyramine...

2. Which is not seen in HMG CoA pathway ?

   A. Pyruvate B. Cholesterol C. Mevalonate D. Acetyl CoA...

3. Acetyl CoA is produced from which fuel sources_____________?

   A. Carbohydrate B. Lipid C. Amino acids D. All of the above...

4. Direct filling gold formed by electrolytic precipitation is called by all the terms EXCEPT______________?

   A. Crystalline B. Granular gold C. Mat gold D. Sponge gold...

5. Ketone bodies are by products of metabolism of_____________?

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

6. All the following causes the secretion of gastric juice during cephalic phase EXCEPT______________?

   A. Food in the mouth B. Sight of food C. Food in the stomach D. Thought of food...

7. Which vitamin is related to a co-factor in glycine metabolism is______________?

   A. Vit E B. Folic acid C. Thiamine D. Cobalamine...

8. 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...

9. Albinism is a genetic disease that results in incomplete metabolism of______________?

   A. Histidine B. Cystine C. Tyrosine D. Alanine...

10. In the body, metabolism of 10 g of protein would produce approximately____________?

    A. 1 Kcal B. 41 Kcal C. 410 Kcal D. 4100 Kcal...