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SKETCHY Biochem Videos & Review 2021

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SKETCHY USMLE Biochemistry is an engaging educational resource designed to help medical students master biochemistry concepts through visual mnemonics and storytelling. This series simplifies complex biochemical pathways and processes, making them more accessible and memorable for exams like the USMLE Step 1. Sketchy USMLE Biochemistry is a valuable resource for mastering the complexities of biochemistry, providing a unique and effective approach to understanding biochemical processes in a clinical context.

SKETCHY USMLE Biochemistry – Benefits:

  • Enhanced Memory Retention: Engaging visuals and stories improve recall of complex biochemical concepts.
  • Motivating Learning Experience: Humor and creativity in the content keep students engaged and focused.
  • Exam-Focused Content: Emphasizes high-yield information that is crucial for success on the USMLE Step 1.

SKETCHYBIOCHEM VIDEOS 2021 – UPDATED 02/2021

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SKETCHY USMLE BIOCHEMISTRY TOPICS 2021

Chapter 1: Carbohydrates (17)

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

.15 – Metabolism and Disorders of Fructose and Sorbitol

1.16 – Lactase Deficiency

1.17 – Glycogen Storage Diseases

Chapter 2 Amino Acids And Proteins (10)

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 (4)

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 (1)

4.1 – Alcohol Metabolism

Chapter 1: Parts of Cell (1)

1.1 – Collagen (Overview and Synthesis)

Chapter 2: Lysosomal Storage Diseases (4)

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

Chapter 1: DNA

1.1 – Chromatin Structure

1.2 – Purine (De-Novo) and Pyrimidine Synthesis

1.3 – Purine Salvage Pathway

1.5 – Purine Salvage Deficiencies (Adenosine Deaminase Deficiency, Lesch-Nyhan Syndrome)

1.6 – Lac Operon

Chapter 1: Water Soluble Vitamins (9)

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 (4)

2.1 – Vitamin A

2.2 – Vitamin D

2.3 – Vitamin E

2.4 – Vitamin K

Chapter 1: Population Genetics (1)

1.1 – Hardy-Weinberg Population Genetics

Chapter 2: X-linked Dominant Diseases (1)

2.1 – Rett Syndrome

Chapter 3: Trinucleotide Repeat Diseases (1)

3.1 – Fragile-X Syndrome

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