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portada Mutagenesis and Mitochondrial-Associated Pathologies
Type
Physical Book
Publisher
Language
English
Pages
116
Format
Hardcover
Dimensions
24.4x17x0.8 cm
Weight
0.39 kg.
ISBN13
9781803551715

Mutagenesis and Mitochondrial-Associated Pathologies

Catala, Angel ; Fasullo, Michael (Author) · Intechopen · Hardcover

Mutagenesis and Mitochondrial-Associated Pathologies - Catala, Angel ; Fasullo, Michael

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Synopsis "Mutagenesis and Mitochondrial-Associated Pathologies"

Reactive oxygen species (ROS) and DNA double-strand breaks can result from mitochondrial defects and external sources, such as ionizing radiation. If not repaired properly, pathogenic mutations are generated. Human diseases resulting from inherited mitochondrial defects manifest in organs that physiologically require a high level of ATP synthesis. These diseases are clinically challenging, but new experimental clinical therapies include gene editing and mitochondrial transplants. Pathogenic ROS-associated cellular damage includes DNA double-strand breaks, and mouse models are now available to study multiple repair pathways. This book discusses the clinical manifestations of mitochondrial diseases in both the eye and the kidney, and presents new insights into double-strand break repair pathways and developmental phenotypes of g-ray-associated ontogenic mutations of Drosophila melanogaste.

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