A. Histidine
B. Cystine
C. Tyrosine
D. Alanine
Related Mcqs:
- All are genetic amino acid deficiency disease except___________?
A. Phenyl ketonuria
B. Alkaptonuria
C. Homocystinuria
D. 6alactosemia - Which vitamin is related to a co-factor in glycine metabolism is______________?
A. Vit E
B. Folic acid
C. Thiamine
D. Cobalamine - 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 - In the body, metabolism of 10 g of protein would produce approximately____________?
A. 1 Kcal
B. 41 Kcal
C. 410 Kcal
D. 4100 Kcal - Incomplete casting is the result of_____________?
A. More porous investment in the mould
B. Narrow sprue diameter
C. Hollow sprue pin
D. Large reservoir - Incomplete fractures of the bone are called___________?
A. Comminuted fracture
B. Compound fracture
C. Simple fracture
D. Green stick fracture - In conn’s disease, there is an excess of______________?
A. Adrenaline
B. Aldosterone
C. Cortisol
D. Noradrenaline - Hansen’s disease is another name of______________?
A. Leprosy
B. Tuberculosis
C. Diabetes
D. Lichen planus - Letterer seiwe disease is a disturbance of______________?
A. protein metabolism
B. histiocytic disorder
C. Mucopolysaccharide metabolism
D. Carbohydrate metabolism - Ketone bodies are by products of metabolism of_____________?
A. Carbohydrate
B. Protein
C. Fat
D. All of the above