Molecular Diseases
eBook - PDF

Molecular Diseases

FEBS Federation of European Biochemical Societies: 12th Meeting, Dresden, 1978

  1. 112 pages
  2. English
  3. PDF
  4. Available on iOS & Android
eBook - PDF

Molecular Diseases

FEBS Federation of European Biochemical Societies: 12th Meeting, Dresden, 1978

About this book

Molecular Diseases, Volume 56 presents the interrelated problems of synthesis, assembly, and breakdown of the various organelles of the cell for which powerful methods have been developed. This book discusses the processing of virus-coded proteins. Organized into nine chapters, this volume begins with an overview of the primary causes that can account for the hereditary defects of enzyme activity. This text then examines the basic methodological aspects of the assessment of protein turnover in a complex intact mammalian organism. Other chapters consider the method of desialylation of erythrocytes and their in vivo and in vitro behavior after this treatment. This book discusses as well the interrelationship between the peroxidatic enzymes and superoxide dismutase in the red cell. The final chapter deals with the use of liposomes as enzyme carriers in the treatment of lysosomal storage diseases. This book is a valuable resource for biological and medical students in various fields.

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Yes, you can access Molecular Diseases by G. Jacobasch,S. Rapoport in PDF and/or ePUB format, as well as other popular books in Medicine & Clinical Medicine. We have over one million books available in our catalogue for you to explore.

Information

Publisher
Pergamon
Year
2017
Print ISBN
9780080231808
eBook ISBN
9781483188553
Topic
Medicine
Subtopic
Clinical Medicine

Table of contents

  1. Front Cover
  2. Molecular Diseases
  3. Copyright Page
  4. Table of Contents
  5. PREFACE
  6. CHAPTER 1. MOLECULAR BASIS OF THE HEREDITARY DEFECTS OF ENZYME ACTIVITY
  7. CHAPTER 2. HAEMOLYTIC ANAEMIA IN PYRUVATE KINASE DEFICIENCY: POSSIBILITIES OF THERAPY
  8. CHAPTER 3. MEMBRANE DESIALYLATION AND ELIMINATION OF ERYTHROCYTES
  9. CHAPTER 4. REACTIVE OXYGEN METABOLITES AND HEMOLYSIS
  10. CHAPTER 5. RED BLOOD CELL MEMBRANE DEFECTS IN β THALASSEMIA AND THE THERAPEUTIC ROLE OF α-TOCOPHEROL (VITAMIN E)
  11. CHAPTER 6. HAEMOGLOBIN PRECIPITATION AND RED CELL HAEMOLYSIS
  12. CHAPTER 7. REVERSION OP HGPRT DEFICIENCY OP SKIN FIBROBLASTS FROM LESCH-NYHAN PATIENTS
  13. CHAPTER 8. SUBSTITUTION THERAPY IN LYSOSOMAL STORAGE DISEASES
  14. CHAPTER 9. INTRODUCTION OF ENZYMES INTO LIVER CELLS BY MEANS OF LIPOSOMES
  15. AUTHOR INDEX
  16. SUBJECT INDEX