Concise writing, a focus on clinical applications, and superb illustrations make Netter’s Essential Biochemistry, by Peter Ronner, PhD, the perfect choice for a basic understanding of biochemistry.. A single expert voice, informed by the insights of a team of reviewers, provides continuity throughout the text, presenting essentials of biochemical principles step by step. Summary diagrams help you grasp key concepts quickly, and end-of-chapter questions reinforce key concepts.
1. Cover image - p. i 2. Title page - p. ii 3. Table of Contents - p. iii 4. Copyright - p. iii 5. Dedication - p. iii 6. About the Author - p. iii 7. Acknowledgments - p. iii 8. Coauthors and Chapter Reviewers - p. iii 9. About the Artist - p. iii 10. Preface - p. iii 11. List of Tables - p. iii 12. Chapter 1: Human Karyotype and the Structure of DNA - p. iii 13. Chapter 2: DNA Repair and Therapy of Cancer - p. iii 14. Chapter 3: DNA Replication - p. iii 15. Chapter 4: Clinical Tests Based on DNA or RNA - p. iii 16. Chapter 5: Basic Genetics for Biochemistry - p. iii 17. Chapter 6: Transcription and RNA Processing - p. iii 18. Chapter 7: Translation and Posttranslational Protein Processing - p. iii 19. Chapter 8: Cell Cycle and Cancer - p. iii 20. Chapter 9: Structure of Proteins and Protein Aggregates in Degenerative Diseases - p. iii 21. Chapter 10: Enzymes and Consequences of Enzyme Deficiencies - p. iii 22. Chapter 11: Biological Membranes - p. iii 23. Chapter 12: Collagen, Collagenopathies, and Diseases of Mineralization - p. iii 24. Chapter 13: Pathologic Alterations of the Extracellular Matrix That Involve Fibrillin, Elastin, or Proteoglycans - p. iii 25. Chapter 14: Heme Metabolism, Porphyrias, and Hyperbilirubinemia - p. iii 26. Chapter 15: Iron Metabolism: Iron-Deficiency Anemia and Iron Overload - p. iii 27. Chapter 16: Erythropoiesis, Hemoglobin Function, and the Complete Blood Count - p. iii 28. Chapter 17: Hemoglobinopathies - p. iii 29. Chapter 18: Carbohydrate Transport, Carbohydrate Malabsorption, and Lactose Intolerance - p. iii 30. Chapter 19: Glycolysis and Its Regulation by Hormones and Hypoxia - p. iii 31. Chapter 20: Fructose and Galactose Metabolism: Hereditary Fructose Intolerance and Galactosemia - p. iii 32. Chapter 21: Pentose Phosphate Pathway, Oxidative Stress, and Glucose 6-Phosphate Dehydrogenase Deficiency - p. iii 33. Chapter 22: Citric Acid Cycle and Thiamine Deficiency - p. iii 34. Chapter 23: Oxidative Phosphorylation and Mitochondrial Diseases - p. iii 35. Chapter 24: Glycogen Metabolism and Glycogen Storage Diseases - p. iii 36. Chapter 25: Gluconeogenesis and Fasting Hypoglycemia - p. iii 37. Chapter 26: Insulin and Counterregulatory Hormones - p. iii 38. Chapter 27: Fatty Acids, Ketone Bodies, and Ketoacidosis - p. iii 39. Chapter 28: Triglycerides and Hypertriglyceridemia - p. iii 40. Chapter 29: Cholesterol Metabolism and Hypercholesterolemia - p. iii 41. Chapter 30: Metabolism of Ethanol and the Consequences of Alcohol Dependence Syndrome - p. iii 42. Chapter 31: Steroid Hormones and Vitamin D - p. iii 43. Chapter 32: Eicosanoids - p. iii 44. Chapter 33: Signaling - p. iii 45. Chapter 34: Digestion of Dietary Protein and Net Synthesis of Protein in the Body - p. iii 46. Chapter 35: Protein Degradation, Amino Acid Metabolism, and Nitrogen Balance - p. iii 47. Chapter 36: One-Carbon Metabolism, Folate Deficiency, and Cobalamin Deficiency - p. iii 48. Chapter 37: Pyrimidine Nucleotides and Chemotherapy - p. iii 49. Chapter 38: Gout and Other Diseases Related to the Metabolism of Purine Nucleotides - p. iii 50. Chapter 39: Diabetes - p. iii 51. Answers to Review Questions - p. iii 52. Index - p. iii
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Concise writing, a focus on clinical applications, and superb illustrations make Netter’s Essential Biochemistry, by Peter Ronner, PhD, the perfect choice for a basic understanding of biochemistry.. A single expert voice, informed by the insights of a team of reviewers, provides continuity throughout the text, presenting essentials of biochemical principles step by step. Summary diagrams help you grasp key concepts quickly, and end-of-chapter questions reinforce key concepts.
1. Cover image - p. i 2. Title page - p. ii 3. Table of Contents - p. iii 4. Copyright - p. iii 5. Dedication - p. iii 6. About the Author - p. iii 7. Acknowledgments - p. iii 8. Coauthors and Chapter Reviewers - p. iii 9. About the Artist - p. iii 10. Preface - p. iii 11. List of Tables - p. iii 12. Chapter 1: Human Karyotype and the Structure of DNA - p. iii 13. Chapter 2: DNA Repair and Therapy of Cancer - p. iii 14. Chapter 3: DNA Replication - p. iii 15. Chapter 4: Clinical Tests Based on DNA or RNA - p. iii 16. Chapter 5: Basic Genetics for Biochemistry - p. iii 17. Chapter 6: Transcription and RNA Processing - p. iii 18. Chapter 7: Translation and Posttranslational Protein Processing - p. iii 19. Chapter 8: Cell Cycle and Cancer - p. iii 20. Chapter 9: Structure of Proteins and Protein Aggregates in Degenerative Diseases - p. iii 21. Chapter 10: Enzymes and Consequences of Enzyme Deficiencies - p. iii 22. Chapter 11: Biological Membranes - p. iii 23. Chapter 12: Collagen, Collagenopathies, and Diseases of Mineralization - p. iii 24. Chapter 13: Pathologic Alterations of the Extracellular Matrix That Involve Fibrillin, Elastin, or Proteoglycans - p. iii 25. Chapter 14: Heme Metabolism, Porphyrias, and Hyperbilirubinemia - p. iii 26. Chapter 15: Iron Metabolism: Iron-Deficiency Anemia and Iron Overload - p. iii 27. Chapter 16: Erythropoiesis, Hemoglobin Function, and the Complete Blood Count - p. iii 28. Chapter 17: Hemoglobinopathies - p. iii 29. Chapter 18: Carbohydrate Transport, Carbohydrate Malabsorption, and Lactose Intolerance - p. iii 30. Chapter 19: Glycolysis and Its Regulation by Hormones and Hypoxia - p. iii 31. Chapter 20: Fructose and Galactose Metabolism: Hereditary Fructose Intolerance and Galactosemia - p. iii 32. Chapter 21: Pentose Phosphate Pathway, Oxidative Stress, and Glucose 6-Phosphate Dehydrogenase Deficiency - p. iii 33. Chapter 22: Citric Acid Cycle and Thiamine Deficiency - p. iii 34. Chapter 23: Oxidative Phosphorylation and Mitochondrial Diseases - p. iii 35. Chapter 24: Glycogen Metabolism and Glycogen Storage Diseases - p. iii 36. Chapter 25: Gluconeogenesis and Fasting Hypoglycemia - p. iii 37. Chapter 26: Insulin and Counterregulatory Hormones - p. iii 38. Chapter 27: Fatty Acids, Ketone Bodies, and Ketoacidosis - p. iii 39. Chapter 28: Triglycerides and Hypertriglyceridemia - p. iii 40. Chapter 29: Cholesterol Metabolism and Hypercholesterolemia - p. iii 41. Chapter 30: Metabolism of Ethanol and the Consequences of Alcohol Dependence Syndrome - p. iii 42. Chapter 31: Steroid Hormones and Vitamin D - p. iii 43. Chapter 32: Eicosanoids - p. iii 44. Chapter 33: Signaling - p. iii 45. Chapter 34: Digestion of Dietary Protein and Net Synthesis of Protein in the Body - p. iii 46. Chapter 35: Protein Degradation, Amino Acid Metabolism, and Nitrogen Balance - p. iii 47. Chapter 36: One-Carbon Metabolism, Folate Deficiency, and Cobalamin Deficiency - p. iii 48. Chapter 37: Pyrimidine Nucleotides and Chemotherapy - p. iii 49. Chapter 38: Gout and Other Diseases Related to the Metabolism of Purine Nucleotides - p. iii 50. Chapter 39: Diabetes - p. iii 51. Answers to Review Questions - p. iii 52. Index - p. iii
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