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BiochemistryCarbohydrate Metabolism
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Q2443. Methionine can entre the TCA cycle at which level?

A.Fumarate
B.Oxabacetate
C.Succinyl - CoA
D.Citrate

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NEET-PG
2012
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PharmacologyCardiovascular Drugs
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Q2444. Rate limiting steps in TCA cycle ?

A.a–Ketoglutarate Succinyl CoA
B.Citrate - Isocitrate
C.Succinyl CoA 4 Succinate
D.Succinate - Fumarate

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BiochemistryCarbohydrate Metabolism
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Q2445. Rate limiting step in TCA cycle is catalyzed by -

A.a-ketoglotarate synthase
B.Fumarase
C.Aconitase
D.Thiokinase

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BiochemistryCarbohydrate Metabolism
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Q2446. Fluroacetate inhibits ?

A.Citrate synthetase
B.Aconitase
C.Succinate dehydrogenase
D.Alphaketoglutarate dehydrogenase

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BiochemistryCarbohydrate Metabolism
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Q2447. Inhibitors of glycolysis are all except ?

A.Fluoride
B.Fluoroacetate
C.Arsenite
D.Iodoacetate

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BiochemistryCarbohydrate Metabolism
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Q2448. The biosynthesis of the enzyme pyruvate carboxylase is repressed by ?

A.Insulin
B.Glucagon
C.Cortisol
D.Epinephrine

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BiochemistryCarbohydrate Metabolism
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Q2449. Where can glucose 6 phosphate not be converted to glucose ?

A.Muscle
B.Liver
C.Adipose tissue
D.Kidney

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BiochemistryCarbohydrate Metabolism
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Q2450. Common intermediate between gluconeogenesis and fatty acid synthesis ?

A.Glucose-6-phosphate
B.Acetyl-CoA
C.Citrate
D.Succinyl-CoA

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NEET-PG2012Repeats: N/A
BiochemistryGeneral Biochemistry
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Q2451. Glycogen synthase is activated by ?

A.Insulin
B.Glucagon
C.Epinophrine
D.AMP

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BiochemistryCarbohydrate Metabolism
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Q2452. Glycogen storage disease which presents as lysosomal storage disease ?

A.Von gierke's disease
B.Pompes disease
C.Mcardle's disease
D.Andersen's disease

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BiochemistryCarbohydrate Metabolism
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Q2453. Aldolase-B is involved in metabolism of ?

A.Galactose
B.Fructose
C.Sucrose
D.None

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PaediatricsGeneral Pediatrics
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Q2454. In humans, ascorbic acid cannot be synthesized because of ?

A.Deficiency of G6PD
B.Deficiency of xylulose kinase
C.Deficiency of L-gulonolactone oxidase
D.Deficiency of phosphoglucomutase

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BiochemistryHeme & Porphyrin
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Q2455. Glucose oxidase converts glucose to?

A.Gluconic acid
B.Glucuronic acid
C.Iduronic acid
D.Galactic acid

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MicrobiologyGeneral Microbiology
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Q2456. Glucose is converted to glucuronate by ?

A.Oxidation of aldehyde group
B.Oxidation of terminal alcohol
C.Oxidation of both
D.None

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BiochemistryCarbohydrate Metabolism
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Q2457. Increased uric acid levels are seen in which glycogen storage disease ?

A.Type I
B.Type II
C.Type III
D.Type IV

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BiochemistryVitamins & Minerals
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Q2458. Gulonate dehydrogenase requires ?

A.NADP
B.NAD
C.FAD
D.FMN

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PsychiatryMood Disorders
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Q2459. All are reducing sugars except-

A.Sucrose
B.Lactose
C.Glucose
D.Fructose

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BiochemistryNucleotide Metabolism
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Q2460. Mutation in GLUT-2 causes ?

A.Dandy walker syndrome
B.Fanconi becker syndrome
C.Beckwith syndrome
D.Menke's disease

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ENTNose
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Q2461. Amino sugar are formed forms ?

A.Glucose- 1 -phosphate
B.Glucose-6-phosphate
C.Fructose- 1 -phosphate
D.Fructose-6-phosphate

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PharmacologyCardiovascular Drugs
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Q2462. Difference between ganglioside & cerebroside, all except?

A.Charge
B.Presence of NANA
C.Presence of carbohydrate
D.Native tissue

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