Biochemistry Snapshots
150+ NEETPG Mind Maps
Analyze, Summarize, Visualize
1500 High Yield Facts
1st Edition
March 2024
Dr Murali Bharadwaz MD
Mentored 300,000 Medical Students to become
Toppers in PG Medical Entrance in past 25 Years
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Incus Quiz Private Limited
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Biochemistry Snapshots
Dr Murali Bharadwaz MD
First Edition March 2024
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Biochemistry Mind Maps for NEEPG Rapid Revision
1. Vitamin A
2. Hypervitaminosis A
3. Vitamin B1 (Thiamine)
4. Vitamin B5, B6, B7
5. Vitamin B12, Vitamin C
6. Vitamin C, Vitamin D
7. Vitamin E
8. Vitamin K
9. Rate-Limiting Enzymes in Metabolic Pathways
10. Metabolism Sites in the Cell
11. ATP Production
12. Activated Carriers and Their Groups
13. Universal Electron Acceptors
14. Hexokinase vs Glucokinase
15. Net glycolysis
16. Regulation of Glycolysis by Fructose-2,6-Bisphosphate
17. Pyruvate Dehydrogenase Complex
18. Pyruvate dehydrogenase complex deficiency
19. Pyruvate Metabolism Pathways and Cofactors
20. TCA Cycle
21. Electron Transport Chain and Oxidative Phosphorylation
22. Oxidative Phosphorylation Poisons
23. Gluconeogenesis
24. Odd-Chain Fatty Acids
25. Gluconeogenesis, irreversible enzymes
26. Essential Fatty Acids
27. Vitamin B2 (Riboflavin)
28. Vitamin B3 (Niacin)
29. Niacin Deficiency
30. Hartnup Disease
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31. Vitamin B9 (Folate)
32. Vitamin B12 Deficiency.png
33. Pentose Phosphate Pathway (PPP)
34. Glucose-6-phosphate Dehydrogenase Deficiency
35. Disorders of Fructose Metabolism
36. Essential Fructosuria & Hereditary Fructose Intolerance
37. Disorders of galactose metabolism
38. Sorbitol Metabolism
39. Lactase Deficiency
40. Amino Acids
41. Urea Cycle
42. Enzymes in Urea Cycle are Mitochondrial
43. Hyperammonaemia
44. Ornithine Transcarbamylase Deficiency
45. Phenylketonuria (PKU)
46. Maple Syrup Urine Disease (MSUD)
47. Alkaptonuria
48. Homocystinuria
49. Cystinuria
50. Organic acidemias
51. Glycogen
52. Activation Cascade for Glycogen Metabolism upon Epinephrine Stimulation
53. Glycogen Storage Diseases (GSDs)
54. Lysosomal Storage Diseases
55. Fatty Acid Metabolism
56. Ketone Bodies
57. Fasting and Starvation
58. Key Enzymes in Lipid Transport
59. Apolipoproteins and Their Functions
60. Lipoproteins
61. Abetalipoproteinemia
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62. Chromatin Structure
63. DNA methylation
64. Nucleotides
65. De novo Pyrimidine base production
66. Purine Synthesis Pathways
67. Drugs Affecting Nucleotide Synthesis
68. Adenosine Deaminase (ADA) Deficiency
69. Purine Synthesis Salvage Pathway
70. Features of the Genetic Code
71. DNA Replication
72. Key Enzymes in DNA Replication
73. Telomerase and DNA Repair Mechanisms
74. Double Strand DNA Repair Mechanisms
75. Single Strand DNA Repair Mechanisms
76. Types of DNA Mutations and Their Consequences
77. Lac operon
78. Regulation of Gene Expression
79. RNA Processing in Eukaryotes
80. RNA Polymerases
81. RNA Polymerase Inhibitors
82. DNA to Protein Pathway and Pre-mRNA Splicing.png
83. Introns vs. Exons
84. Introns vs Exons and tRNA Structure
85. tRNA Charging Process and Accuracy
86. tRNA Charging
87. Start and stop codons
88. Protein Synthesis Overview
89. Eukaryotes vs. Prokaryotes
90. Chaperone Proteins
91. Cell Cycle Phases
92. Cell Cycle Regulation
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93. Rough endoplasmic reticulum
94. I-cell disease inclusion cell disease
95. Cellular Trafficking Mechanisms
96. Peroxisome
97. Peroxisomal Disorders
98. Proteasome Function and Disease Association
99. Cytoskeletal Elements
100. Microtubules Structure and Function
101. Molecular motor proteins
102. Cilia structure
103. Primary Ciliary Dyskinesia
104. Sodium-Potassium Pump
105. Collagen Characteristics and Types
106. Collagen Types and Functions
107. Collagen Synthesis and Structure
108. Osteogenesis Imperfecta
109. Ehlers-Danlos Syndrome
110. Menkes Disease
111. Elastin
112. Marfan Syndrome
113. Homocystinuria & Metabolic Issue
114. Polymerase Chain Reaction (PCR)
115. CRISPRCas9 Genome Editing
116. Blotting procedures
117. Flow Cytometry
118. Microarrays Overview
119. Enzyme-linked immunosorbent assay
120. Karyotyping
121. Fluorescence in situ hybridization (FISH)
122. Molecular cloning
123. Gene expression modifications in mice
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124. RNA interference (RNAi)
125. Dominant negative mutation
126. Loss of heterozygosity
127. Genetic Concepts (continued)
128. Locus heterogeneity
129. Heteroplasmy
130. Uniparental Disomy
131. Hardy-Weinberg Population Genetics
132. Prader-Willi Syndrome
133. Autosomal Dominant Inheritance
134. Autosomal Recessive Inheritance
135. X-Linked Recessive Inheritance
136. X-linked dominant
137. Mitochondrial Inheritance
138. Cystic Fibrosis
139. Complications of Cystic Fibrosis
140. Treatment of Cystic Fibrosis
141. Muscular Dystrophies
142. Gowers Sign
143. Duchenne Muscular Dystrophy
144. Mitochondrial diseases
145. Rett syndrome
146. Fragile X syndrome
147. Trinucleotide repeat expansion diseases
148. Autosomal trisomies
149. Robertsonian translocation
150. Down syndrome (trisomy 21)
151. Edwards syndrome (trisomy 18)
152. Patau syndrome (trisomy 13)
153. Genetic disorders by chromosome
