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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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NEET-PG
2014
Repeats: N/A
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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PsychiatryMood Disorders
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Q5804. Bond involved in formation of primary structure of protein/polypeptide ?

A.Hydrogen
B.Peptide
C.Disulfide
D.a and b both

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RadiologyGeneral Radiology
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Q5805. Urea is synthesized in all except

A.Liver
B.Brain
C.Kidney
D.Spleen

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BiochemistryProtein & Amino Acid
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Q5806. Rate limiting step in urea cycle is catalyzed by ?

A.Arginase
B.Argininosuccinase
C.Carbamoyl-phosphate synthase
D.Ornithine transcarbamylase

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PharmacologyCardiovascular Drugs
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Q5807. Citrullinemia is due to deficiency of ?

A.Argininosuccinate lyase
B.Argininosuccinate synthase
C.Arginase
D.Ornithine transcarbamylase

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BiochemistryProtein & Amino Acid
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Q5808. Amino acid carrying ammonia from muscle to liver?

A.Alanine
B.Glutamine
C.Arginine
D.Lysine

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PaediatricsCongenital
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Q5809. Mousy odor of urine is seen in ?

A.Alkaptunuria
B.Phenylketonuria
C.Hartnup disease
D.Albinism

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PaediatricsCongenital
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Q5810. Cabbage-like odour is seen in ?

A.Alkaptonuria
B.Phenylketonuria
C.Hartnup disease
D.Tyrosinemia

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ENTEar
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Q5811. If urine sample darkens on standing: the most likely conditions is ?

A.Phenylketonuria
B.Alkaptonuria
C.Maple syrup disease
D.Tyrosinemia

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PhysiologyEndocrine
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Q5812. Derivative of POMC

A.Norepinephrine
B.Dopamine
C.ACTH
D.Acetylcholine

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BiochemistryEnzymes
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Q5813. Cofactor for dopamine hydroxylase ?

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

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BiochemistryProtein & Amino Acid
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Q5814. Not an essential amino acid ?

A.Arginine
B.Histidine
C.Glutamate
D.Lysine

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BiochemistryProtein & Amino Acid Metabolism
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Q5815. Nicotinic acid is derived from ?

A.Glutamine
B.Tryptophan
C.Glutathione
D.Phenylalanine

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BiochemistryProtein & Amino Acid Metabolism
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Q5816. Amino acids with extra NH2 (amino group) in structure-

A.Aspartate
B.Glutamate
C.Histidine
D.Alanine

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BiochemistryProtein & Amino Acid Metabolism
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Q5817. Neutral amino acid is ?

A.Aspartate
B.Arginine
C.Glycine
D.Histidine

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BiochemistryProtein & Amino Acid Metabolism
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Q5818. Which of the following amino acids is purely ketogenic?

A.Phenylalanine
B.Leucine
C.Proline
D.Tyrosine

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BiochemistryProtein & Amino Acid Metabolism
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Q5819. Amino acid which is optically inert ?

A.Valine
B.Alanine
C.Glycine
D.Threonine

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