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PhysiologyNerve & Muscle Physiology
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Q5783. Immediate energy supply for muscle contraction ?

A.GTP
B.ATP
C.Creatine phosphate
D.Fatty acid

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NEET-PG
2014
Repeats: N/A
MedicineNephrology
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Q5784. Main source of energy in 1 min is ?

A.Glycogen
B.FFA
C.Phosphates
D.Glucose

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BiochemistryLipid Metabolism
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Q5785. Which of the following is increased in lipoprotein lipase deficiency?

A.VLDL
B.LDL
C.HDL
D.Chylomicrons

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BiochemistryEnzymes & Proteins
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Q5786. Major source of energy for brain in fasting/ starvation ?

A.Glucose
B.Glycogen
C.Fatty acids
D.Ketone bodies

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ENTEar
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Q5787. Defect in type II hyperlipidemia

A.Apo-E
B.Lipoprotein lipase
C.LDL receptor
D.None

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BiochemistryCarbohydrate Metabolism
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Q5788. Rate limiting step in fatty acid synthesis is ?

A.Production of acetyl CoA
B.Production of oxaloacetate
C.Production of malonyl-CoA
D.Production of citrate

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DermatologyGeneral Dermatology
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Q5790. Mineral required for cholesterol biosynthesis ?

A.Fe
B.Mn
C.Mg
D.Cu

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BiochemistryLipid Metabolism
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Q5791. Lipoprotein involved in reverse cholesterol transport?

A.LDL
B.VLDL
C.IDL
D.HDL

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BiochemistryLipid Metabolism
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Q5792. Lipoprotein associated with carrying cholesterol from peripheral tissues to liver is ?

A.HDL
B.LDL
C.VLDL
D.IDL

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BiochemistryHeme & Porphyrin
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Q5793. Enzyme deficient in gangliosidoses ?

A.β-glucuronidase
B.Iduronidase
C.β-galactosidase
D.Hyaluronidase

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BiochemistryLipid Metabolism
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Q5794. Hunter syndrome is due to deficiency of

A.Beta galactosidase
B.Sphingomyelinase
C.Iduronate Sulfatase
D.Hyaluronidase

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BiochemistryLipid Metabolism
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Q5795. Tay-Sach disease is due to deficiency of

A.Hexosaminidase A
B.Hexosaminidase B
C.Sphingomyelinase
D.α-galactosidase

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MicrobiologyBacteriology
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Q5796. Alcohol is metabolized by ?

A.Alcohol dehydrogenase
B.MEOS
C.Catalase
D.All of the above

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BiochemistryNucleotide Metabolism
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Q5797. Oxidation of very long chain fatty acids takes place in ?

A.Cytosol
B.Mitochondria
C.Ribosomes
D.Peroxisomes

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BiochemistryCarbohydrate Metabolism
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Q5798. which of the following occurs only in mitochondria

A.ECT
B.Ketogenesis
C.Urea cycle
D.Steroid synthesis

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BiochemistryLipid Metabolism
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Q5799. Which of the following is not a glycerosphingolipid?

A.Lecithin
B.Cardiolipin
C.Plasmalogens
D.Sphingomyelin

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BiochemistryLipid Metabolism
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Q5800. Highest mobility on electrophoresis

A.HDL
B.VLDL
C.LDL
D.Chylomicrons

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BiochemistryProtein & Amino Acid
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Q5801. In argininosuccinase deficiency, what should be supplemented to continue the urea cycle ?

A.Aspartate
B.Arginine
C.Citrullin
D.Argininosuccinate

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PharmacologyCardiovascular Drugs
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Q5802. Immediate precursor of creatine

A.Carbamoyl phosphate
B.Arginosuccinate
C.Guanidoacetate
D.Citrulline

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BiochemistryProtein & Amino Acid Metabolism
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Q5803. Which one of the following can be a homologous substitution for isoleucine in a protein sequence?

A.Methionine
B.Aspartic acid
C.Valine
D.Arginine

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