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METABOLISM
CHAPTER 1 CARBOHYDRATES
1.1 – Glycolysis Part 1
1.2 – Glycolysis Part 2
1.3 – Regulation of PFK-1 and FBPase-1 by F-2,6-BP and During the Fed and Fasting State
1.4 – Gluconeogenesis
1.5 – Pyruvate Dehydrogenase Complex
1.6 – Fates of Pyruvate
1.7 – Pyruvate Dehydrogenase Deficiency and Arsenic Poisoning
1.8 – Hormonal Regulation of Glycogen by Insulin, Glucagon, and Epinephrine
1.9 – TCA Cycle
1.10 – Glycogen Synthesis (Glycogenesis) and Degradation (Glycogenolysis)
1.11 – Malate-Aspartate and Glycerol-Phosphate Shuttles
1.12 – Pentose Phosphate Pathway, G6PD Deficiency
1.13 – Electron Transport Chain/Oxidative Phosphorylation
1.14 – Metabolism and Disorders of Galactose
1.15 – Metabolism and Disorders of Fructose and Sorbitol
1.16 – Lactase Deficiency
1.17 – Glycogen Storage Diseases
CHAPTER 2 AMINO ACIDS AND PROTEINS
2.1 – Amino Acids (Overview)
2.2 – Amino Acid Derivatives
2.3 – Catecholamine Synthesis and Degradation
2.4 – Inborn Errors of Amino Acid Metabolism (Overview), Phenylketonuria (PKU)
2.6 – Disorders of Tyrosine Catabolism, Alkaptonuria
2.7 – Branched-Chain Amino Acid Catabolism, Maple Syrup Urine Disease
2.8 – Urea Cycle, Hyperammonemia, Ornithine Transcarbamylase Deficiency
2.9 – The Cahill and Cori Cycles
2.10 – Organic Acidemias
2.11 – Homocystinuria
CHAPTER 3 LIPIDS
3.1 – Triglyceride Catabolism, Beta Oxidation of Even-Chain Fatty Acids
3.2 – Beta Oxidation of Odd-Chain Fatty Acids (VOMIT Pathway)
3.3 – Ketone Bodies
3.4 – Fatty Acid Synthesis
CHAPTER 4 ALCOHOL METABOLISM
4.1 – Alcohol Metabolism
CELL BIOLOGY
CHAPTER 1 PARTS OF CELL
1.1 – Collagen (Overview and Synthesis)
CHAPTER 2 LYSOSOMAL STORAGE DISEASES
2.1 – Sphingolipidoses Part 1: Tay-Sachs Disease, Niemann-Pick Disease
2.2 – Sphingolipidoses Part 2: Gaucher Disease, Metachromatic Leukodystrophy, Krabbe Disease
2.3 – Sphingolipidoses Part 3: Fabry Disease
2.4 – Mucopolysaccharidoses: Hurler Syndrome, Hunter Syndrome
MOLECULAR BIOLOGY
CHAPTER 1 DNA
1.1 – Chromatin Structure
1.2 – Purine (De-Novo) and Pyrimidine Synthesis
1.3 – Purine Salvage Pathway
1.4 – Purine Salvage Deficiencies (Adenosine Deaminase Deficiency, Lesch-Nyhan Syndrome)
1.5 – Lac Operon
VITAMINS & MINERALS
CHAPTER 1 WATER SOLUBLE VITAMINS
1.1 – Vitamin B1 (Thiamine)
1.2 – Vitamin B2 (Riboflavin)
1.3 – Vitamin B3 (Niacin)
1.4 – Vitamin B5 (Pantothenic Acid)
1.5 – Vitamin B6 (Pyridoxine)
1.6 – Vitamin B7 (Biotin)
1.7 – Vitamin B9 (Folate)
1.8 – Vitamin B12 (Cobalamin)
1.9 – Vitamin C
CHAPTER 2 FAT SOLUBLE VITAMINS
2.1 – Vitamin A
2.2 – Vitamin D
2.3 – Vitamin E
2.4 – Vitamin K
CLINICAL GENETICS
CHAPTER 1 POPULATION GENETICS
1.1 – Hardy-Weinberg Population Genetics
CHAPTER 2 X-LINKED DOMINANT DISEASES
2.1 – Rett Syndrome
CHAPTER 3 TRINUCLEOTIDE REPEAT DISEASES
3.1 – Fragile-X Syndrome
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