A. Hexokinase
B. Phosphoglycerate kinase
C. Enolase
D. Phosphohexose isomerase
A. Glycolysis and citric acid cycle
B. Glycogenolysis and gluconeogenesis
C. Embden-meyerhof pathway and h.m.p shunt
D. Glycogenolysis and citric and cycle
A. 1
B. 2
C. 3
D. 4
A. G6 pd
B. 6 phosphogluconate dehydrogenase
C. Transketolase
D. Transaldolase
A. liver
B. wbc
C. lactating mammary gland
D. testes
A. Pomper’s disease
B. Von gierke’s disease
C. Mcardles syndrome
D. Downs syndrome
A. Atp
B. Adp
C. Acetyl coa
D. Nadph
A. Glucose 6 phosphate dehydrogenase
B. Glucose 1 phosphate dehydrogenase
C. Glucose 1,6 diphosphate dehydrogenase
D. All of the above
A. It usually exists in the furanose form
B. It is a ketose
C. It possessesan anomeric c-2 carbon atom
D. It formspart of the disaccharide sucrose