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BiochemistryProtein & Amino Acid Metabolism
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Q9624. The most abundant aminoacid of collagen is -

A.Glycine
B.Proline
C.Lysine
D.Tryptophan

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2016
Repeats: N/A
BiochemistryVitamins & Minerals
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Q9626. Heme synthesis requires

A.Ferrous iron
B.Glycine
C.Succhyl CoA
D.All

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BiochemistryProtein & Amino Acid
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Q9627. Heme is which porphyrin ?

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

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BiochemistryLipid Metabolism
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Q9629. Genetically mediated VLDL overproduction is a feature of all except ?

A.Familial combined hyperlipidemia
B.Hypoapobetalipoproteinemia
C.Familial dyslipidemic hypertension
D.LDL subclass B

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BiochemistryVitamins & Minerals
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Q9637. Vitamin A deficiency leads to metaplasia of?

A.Squamous epithelium
B.Columnar epithelium
C.Both
D.None

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BiochemistryProtein & Amino Acid Metabolism
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Q9648. Vasodilatation following endothelial damage is due to ?

A.Histamine
B.IL-2
C.TGF-3
D.FGF

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BiochemistryProtein & Enzyme Metabolism
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Q9650. Primary granules contain which enzyme?

A.Myeloperoxidase
B.Hydrolases
C.Lactoferrin
D.Phospholipase A2

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BiochemistryProtein & Enzyme Metabolism
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Q9652. Peroxidase enzyme found in neutrophills is used for -

A.Macrophage activation
B.Chemotactic agent
C.Microbial killing
D.Vasodilatation

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BiochemistryNucleotide & DNA Metabolism
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Q9677. Expression of a gene is known as?

A.Genotype
B.Phenotype
C.Genome
D.Morphology

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BiochemistryNucleotide & DNA Metabolism
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Q9679. Acute intermittent porphyria is associated with which type of inheritance?

A.Autosomal dominant
B.Autosomal recessive
C.X-linked dominant
D.X-linked recessive

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BiochemistryNucleotide & DNA Metabolism
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Q9681. Inheritance associated with fragile X- syndrome is-

A.Autosomal dominant
B.Autosomal recessive
C.X-linked dominant
D.X-linked recessive

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BiochemistryNucleotide & DNA Metabolism
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Q9682. HOX gene is associated with

A.Cranio-caudal development
B.Brain development
C.Teeth formation
D.All of the above

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BiochemistryNucleotide & DNA Metabolism
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Q9683. Chromosome for ABO gene is?

A.9q
B.10p
C.11 q
D.12p

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BiochemistryNucleotide & DNA Metabolism
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Q9685. Trinucleotide sequence associated with spino-cerebellar ataxia is?

A.CTG
B.CUG
C.GGG
D.CAG

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BiochemistryNucleotide Metabolism
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Q9687. Li-fraumani syndrome occurs due to mutation in gene?

A.p53
B.p16
C.p41
D.p12

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BiochemistryNucleotide Metabolism
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Q9702. In patients with hypertrophic cardiomyopathy maximum mutations are found in which gene:

A.. β - myosin heavy chain
B.Elastin
C.. α - tropomyosin
D.Troponin T

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BiochemistryNucleotide Metabolism
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Q9703. Mutation in protein associated with restrictive cardiomyopathy?

A.Myosin regulatory proteins
B.Myosin binding protein-C
C.Troponin I
D.Tropomyosin

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BiochemistryNucleotide Metabolism
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Q9732. Deficiency of p53 mutation is maximum in which lung carcinoma?

A.Small cell carcinoma
B.Squamous cell carcinoma
C.Adenocarcinoma
D.Lymphoma

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BiochemistryVitamins & Minerals
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Q9749. Autoimmune gastritis is associated with deficiency of vitamin?

A.A
B.B12
C.C
D.D

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BiochemistryVitamins & Minerals
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Q9755. Vitamin deficiency associated with cystic fibrosis is

A.K
B.B6
C.C
D.B12

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