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NEET (PG)

2014
2019

Biochemistry

Urea cycle defects and hyperammonaemia
Amine metabolism - trimethylaminuria
Amino Acids
Amino acid chemical reactions and tests
Amino acid chemistry and coagulation proteins
Amino acid metabolism
Amino acid metabolism - tyrosine catabolism disorders
Amino acid properties and UV absorption
Amino acid transport - Cystinuria
Aminoacidopathies
Antioxidants and vitamins
Bilirubin metabolism
Biochemical Markers in Clinical Diagnosis
Cancer
Cancer Cell Metabolism - Warburg Effect
Carbohydrate chemistry - aldose vs ketose
Carbohydrate metabolism
Carbohydrates
Cardiac biomarkers / LDH isoenzymes
Catecholamine synthesis
Cell Biology
Cell Biology - Clathrin Mediated Endocytosis
Cell organelles - peroxisome biogenesis disorders
Chemical bonds and molecular interactions
Cholesterol metabolism and gallstones
Collagen types and distribution
Concepts and regulation of metabolism of amino acids
Copper metabolism and collagen cross-linking
DNA Repair / Xeroderma Pigmentosum
DNA Replication
DNA Structure
Diagnostic Enzymes - CPK
Dietary fiber
Dietary fiber fermentation and short-chain fatty acids
Electron transport chain inhibitors
Enzyme Kinetics - Michaelis-Menten Equation
Enzyme inhibition
Enzyme kinetics
Enzymes
Enzymes - protease classification
Fat-soluble vitamins
Free radical injury and the Fenton reaction
G6PD deficiency genetics / X-linked inheritance
GLUT4 transporter and exercise in type 2 diabetes
Galactosemia
Gene expression
Gluconeogenesis
Gluconeogenesis and blood glucose regulation
Glucose homeostasis and hypoglycemia
Glucose transporters
Glycogen storage disease type I and hyperuricemia
Glycolysis
Glycolysis - phosphofructokinase cofactor
Glycosaminoglycans and Proteoglycans
HDL function
Hemoglobin Structure and Ligand Binding
Homocystinuria
Homocystinuria - Inborn Error of Metabolism
Hormones
Human Genome Project
Inborn errors of metabolism - urine odours
Insulin biosynthesis - proinsulin and C-peptide
Ion-exchange chromatography
Iron metabolism
LDH isoenzymes and cardiac markers
Lipid Metabolism and Hyperlipoproteinemias
Lipid absorption
Lipid metabolism - fatty acid synthesis
Lipids
Lipoprotein electrophoresis
Liver enzyme location: AST
Lysosomal storage disorders
Maple syrup urine disease
Metabolic pathways and their regulation
Metabolic syndrome
Microbiology
Molecular Biology
Molecular Biology Techniques (Blotting Methods)
Molecular biology - DNA replication enzymes
Monoamine neurotransmitters - serotonin
Monoclonal antibody and cell fusion
Nucleic acid chemistry (bases, nucleosides, nucleotides)
Nutrition
Pentose phosphate pathway
Plasma proteins - Alpha-1 antitrypsin and elastase inhibition
Plasma proteins and liver function
Prenatal diagnosis of hemophilia
Protein degradation
Protein structure
Protein structure - chaperones and folding
Purine metabolism - salvage pathway defects
Purine nucleotide biosynthesis
RNA catalysis and ribozymes
Regulation of major metabolic pathways
Renal tubular transport
Rothera's test for ketones
Sphingolipidoses
Structure Of Proteins
TCA cycle
Telomerase / Cell Immortalisation in Cancer
Trinucleotide repeat disorders
Urea cycle and TCA cycle linkage
Urine sugar detection tests
Vitamin K and clotting factors
Vitamin deficiencies
Vitamins
Vitamins - Niacin Deficiency and Pellagra
Vitamins and Coenzymes
Vitamins and Nutrition
Wilson disease / copper metabolism
Wilson's Disease

List of top Biochemistry Questions on Urea cycle defects and hyperammonaemia asked in NEET (PG)

Glutamine is increased in CSF, blood, and urine. This is due to deficiency of which enzyme?

The rate limiting step in the urea cycle is catalyzed by which enzyme?