USMLE Step 1 Lecture notes 2018 Biochemistry and medical genetics 1st Edition by Sam Turco, Roger Lane, Ryan Harden ISBN 9781506239545 150623954X

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Product details:
ISBN 10: 150623954X
ISBN 13: 9781506239545
Author: Sam Turco, Roger Lane, Ryan Harden

a comprehensive study guide designed to help medical students prepare for the USMLE Step 1 exam. This edition provides a detailed overview of biochemistry and medical genetics, focusing on the essential concepts and principles needed for success on the exam. It covers topics such as molecular biology, metabolic pathways, genetics, and genetic disorders, with a clear emphasis on clinical relevance. The book is designed with high-yield content, easy-to-understand explanations, and numerous illustrations to enhance learning. Ideal for both review and in-depth study, this guide is a valuable resource for mastering the biochemistry and genetics components of the USMLE Step 1 exam.

USMLE Step 1 Lecture notes 2018 Biochemistry and medical genetics 1st Edition Table of contents:

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Part 1: Biochemistry

1. Basic Biochemistry Concepts

   • The Structure of Biomolecules
   • Chemical Bonding and Molecular Interactions
   • pH, Buffers, and Acid-Base Equilibria
   • Water, Solvents, and Solubility in Biological Systems

2. Enzyme Structure and Function

   • Enzyme Kinetics and Mechanisms
   • Regulation of Enzyme Activity
   • Enzyme Inhibition and Clinical Relevance
   • Cofactors and Coenzymes

3. Metabolism Overview

   • Metabolic Pathways and Their Regulation
   • Catabolic vs. Anabolic Pathways
   • Energy Production and Storage
   • ATP, NADH, and NADPH in Cellular Metabolism

4. Carbohydrate Metabolism

   • Glycolysis and Gluconeogenesis
   • Glycogen Metabolism
   • Pentose Phosphate Pathway
   • Regulation of Carbohydrate Metabolism in Health and Disease

5. Fat and Lipid Metabolism

   • Fatty Acid Synthesis and Beta-Oxidation
   • Cholesterol Metabolism and Transport
   • Lipoproteins and Lipid Disorders
   • Clinical Implications of Dyslipidemia

6. Amino Acid and Protein Metabolism

   • Amino Acid Catabolism and Urea Cycle
   • Protein Synthesis and Degradation
   • Genetic Disorders Related to Amino Acids
   • Inborn Errors of Metabolism

7. Nucleic Acid Metabolism

   • DNA Replication, Repair, and Recombination
   • RNA Synthesis and Processing
   • Genetic Code and Protein Synthesis
   • Disorders Related to Nucleic Acid Metabolism

8. Molecular Biology Techniques

   • PCR, Gel Electrophoresis, and Cloning
   • DNA Sequencing and Gene Expression Analysis
   • Applications in Diagnosis and Research

Part 2: Medical Genetics

9. Basic Genetic Principles

   • DNA Structure and Function
   • Mendelian Inheritance Patterns
   • Genetic Variation and Mutation
   • Chromosomal Abnormalities

10. Genetic Diseases and Inborn Errors of Metabolism

    • Autosomal Dominant and Recessive Disorders
    • X-Linked Disorders
    • Mitochondrial Inheritance and Disorders
    • Lysosomal Storage Diseases

11. Genetic Testing and Diagnostic Tools

    • Techniques for Genetic Diagnosis
    • Next-Generation Sequencing
    • Prenatal and Postnatal Genetic Screening
    • Carrier Screening and Genetic Counseling

12. Cancer Genetics

    • Oncogenes and Tumor Suppressor Genes
    • Genetic Syndromes Associated with Cancer
    • Genetic Testing in Cancer Diagnosis and Treatment
    • Pharmacogenomics and Personalized Medicine

13. Epigenetics

    • DNA Methylation and Histone Modification
    • Gene Expression Regulation
    • Role of Epigenetics in Disease and Development

14. Developmental Genetics

    • Role of Genetics in Embryogenesis
    • Developmental Disorders and Congenital Anomalies
    • Maternal and Paternal Genomic Imprinting

15. Pharmacogenetics

    • Genetic Variability in Drug Response
    • Genotype-Phenotype Correlations in Drug Metabolism
    • Implications for Personalized Medicine

16. Genetic Counseling and Ethical Issues

    • Principles of Genetic Counseling
    • Ethical Considerations in Genetic Testing
    • Gene Editing Technologies (CRISPR)