01969nam 2200373 450 991068818390332120230626213347.0(CKB)5850000000050203(NjHacI)995850000000050203(EXLCZ)99585000000005020320230626d2022 uy 0engur|||||||||||txtrdacontentcrdamediacrrdacarrierMutagenesis and Mitochondrial-Associated Pathologies /Michael Fasullo, Angel Catala, editorsLondon :IntechOpen,2022.1 online resource (116 pages)1-80355-173-9 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.DNA damageMutagenicity testingDNA damage.Mutagenicity testing.616.042Catala AngelFasullo MichaelNjHacINjHaclBOOK9910688183903321Mutagenesis and Mitochondrial-Associated Pathologies2903154UNINA