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The Human Mitochondrial Genome cover

The Human Mitochondrial Genome

From Basic Biology to Disease

by Giuseppe Gasparre, Anna Maria Porcelli

1st Edition

Publisher: Academic Press

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Book Details

Print ISBN9780128196564
eText ISBN9780128226421
PublisherAcademic Press
Publishing Year2020
Edition1st Edition
LanguageEnglish
Pages596

The Human Mitochondrial Genome: From Basic Biology to Disease, 1st Edition, connects basic research in mitochondrial genetics to translational medicine. The volume provides an overview of mitochondrial genome function across normal cellular processes and human disease contexts.

Core biological coverage examines the maintenance, repair, segregation, and heredity of human mitochondrial DNA. The book addresses diverse pathologies, including cancer, neurodegenerative conditions, age-related diseases, and disorders characterized by mitochondrial DNA depletion, deletion, and point mutations.

The work outlines experimental research protocols and perspectives intended for early-career scientists. It serves active researchers and clinician-scientists working across biochemistry, molecular biology, cell biology, oncology, neurology, neuroscience, and pharmacology.

Table of Contents

  1. Chapter 1: MtDNA replication, maintenance and nucleoid organization

  2. Chapter 2: Human mitochondrial transcription and translation

  3. Chapter 3: Epigenetic features of mitochondrial DNA

  4. Chapter 4: Heredity and Segregation of mtDNA

  5. Chapter 5: Haplogroups and the history of human evolution through mtDNA

  6. Chapter 6: Human Nuclear mitochondrial Sequences (NumtS)

  7. Chapter 7: MtDNA exploitation in forensics

  8. Chapter 8: Human mitochondrial DNA repair

  9. Chapter 9: Mechanisms of onset and accumulation of mtDNA mutations

  10. Chapter 10: Mitochondrial DNA mutations and ageing

  11. Chapter 11: Methods for the identification of mitochondrial DNA variants

  12. Chapter 12: Bioinformatics resources, databases, and tools for human mtDNA

  13. Chapter 13: Methods and models for functional studies on mtDNA mutations

  14. Chapter 14: Mitochondrial DNA point mutation diseases

  15. Chapter 15: Nuclear genetic disorders of mitochondrial DNA gene expression

  16. Chapter 16: mtDNA maintenance: disease and therapy

  17. Chapter 17: MtDNA mutations in cancer

  18. Chapter 18: MitoTALENs for mtDNA editing

  19. Chapter 19: Mitochondrially-Targeted Zinc Finger Nucleases

  20. Chapter 20: Mitochondrial movement between mammalian cells: an emerging physiological phenomenon

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