Daily Bugle's Biochem Test evaluates key biochemical concepts and their clinical applications, focusing on enzyme deficiencies, metabolic pathways, and diagnostic markers relevant to diseases like diabetes and myeloma.
Insulin
Glucagon
Aldosterone
Adrenalin
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7,0
14,0
9,4
4,7
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Citric
Oxaloacetic
Isocitric
Fumaric
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Saccharose
Maltose
Fructose
Lactose
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Cretinism
Acromegalia
Pituitary nanism
Gigantism
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Glucagon
Adrenaline
Insulin
Thyroid hormones
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It inhibits GP and activates GS
It inhibits both GP and GS
It activates both GP and GS
It activates GP and inhibits GS
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Hypoactivation of pepsin by hydrochloric acid
Obturation of bile duct
Cholaemia
Bilirubinuria
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Lack of linoleic acid, vitamins A, D, E, K
Lack of vitamins PP, H
Low caloric value of diet
Lack of palmitic acid
Lack of oleic acid
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Inhibition of cytochrome oxidase
Chemical bounding to the substrates of TCA
Blockage of succinate dehydrogenase
Inactivation of oxygen molecule
Inhibition of cytochrome b
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Bilirubin
Bence Jones protein
Ceruloplasmin
Antitrypsin
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Gierke’s disease
Acquired immunodeficiency syndrome
Cushing’s basophilism
Lesch-Nyhan syndrome
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UDP-glucose pyrophosphorylase
UDP-glucuronyl transferase
UDP-glycogen transferase
Mido phosphoribosyl transferase
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3.3 mM/1
5.5 mM/1
8.0 mM/1
1.5 mM/1
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Thrombin formation
Fibrin formation
Clot retraction
Thromboplastin formation
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Metabolic calcification
Osteomalacia
Dystrophic calcification
Rickets
Metastatic calcification
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Cyclooxygenase
Phospholipase A2
Arginase
Phospholipase C
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Succinyl-CoA
Acyl-CoA
Acetyl-CoA
Malonate
Citrate
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Anion and cation forms of amino acids are balanced
Cation forms of amino acids are prevalent
Certain protein aggregates are formed
Irreversible protein precipitation occurs
Anion forms of amino acids are prevalent
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Urea cycle
Oxidative decarboxylation of keto acids
Pentose-phosphate pathway
Anaerobic glycolysis
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Gout
Phenylketonuria
Wilson disease
Tay-Sachs disease
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Chromogenic
Protein synthesizing
Detoxication
Glycogen synthesizing
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Lysozyme
Interleukin
Interferon
Complement
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Vitamin D
Vitamin Е
Vitamin K
Vitamin K1
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Nongaseous acidosis
Nongaseous alkalosis
Gaseous acidosis
Gaseous alkalosis
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NH3 attachment to glutamate
NH3 detachment from glutamine
CO2 attachment to pyruvate
Beta-oxidation of fatty acids
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Increase in thromboplastin production
Decrease in thrombin production
Fibrinolysis intensification
Decrease in fibrin production
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Arachidonic acid
Methionine
Alanine
Cholesterol
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Alimentary hyperlipemia
Retention hyperlipemia
Transport hyperlipemia
Hyperplastic obesity
Hypertrophic obesity
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Unconjugated bilrubin
Stercobilin
Conjugated bilirubin
Ketone bodies
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Thiamine and pyridoxine
Calciferol and ascorbic acid
Ascorbic acid and rutin
Folic acid and cobalamin
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Phosphopentose isomerase
Transketolase Lactonase
Transketolase
Transaldolase
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B6
C
B12
K
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Biliverdine reductase
Heme oxygenase
Aminolevulinate synthase
UDP-glucuronyl transferase
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Glycogen phosphorylase
γ-amylase
Glucose 6-phosphate dehydrogenase
α-amylase
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Conjugated bilirubin
Unconjugated bilirubin
Stercobilinogen
Biliverdin
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Specific transfer RNA
Adenosine triphosphate
Specific ribosomal RNA
Specific messenger RNA
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Sphingosine
Glycosyltransferase
Sphingomyelinase
Gangliosides
Ceramides
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Gilbert’s syndrome
Parenchymatous
Mechanic
Crigler-Najjar syndrome
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