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Exams

NEET (PG)
CUET (PG)

Years

2022

Subjects

Biochemistry
Pathology
Pediatrics

Topics

Genetics
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
Biochemistry
Biomolecules
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
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 Endocrine System
Human Genome Project
Immunology
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
Physiological buffer systems
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
Proteinoids
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
Treatment of poisoning
Trinucleotide repeat disorders
Urea cycle and TCA cycle linkage
Urea cycle defects and hyperammonaemia
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
pH value

List of top Biochemistry Questions on Genetics asked in NEET (PG)

A 23-year-old female with a height of 4 feet has a karyotype, as shown in the image below. Which of the following conditions is the most likely etiology?

NEET (PG) - 2024
NEET (PG)
Biochemistry
Genetics

A single mutation in a nucleotide base pair resulting in a termination codon is known as ________?

NEET (PG) - 2022
NEET (PG)
Biochemistry
Genetics