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10.0 MB
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44F91DA1C9BE5FB1A78C4017E7EABF5FB3A54742
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Nov. 14, 2025, 4:53 a.m.
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(Last updated: Nov. 14, 2025, 4:54 a.m.)
| File | Size |
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| Goodwin J. Mitochondrial Biology. New Perspectives 2023.pdf | 10.0 MB |
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355.5 MB
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2023-12-13
| Uploaded by mainlyclassical | Size 355.5 MB | Health [ 23 /15 ] | Added 2023-12-13 |
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363.7 MB
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2023-08-27
| Uploaded by mainlyclassical | Size 363.7 MB | Health [ 0 /0 ] | Added 2023-08-27 |
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6.9 MB
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2023-07-01
| Uploaded by FreeCourseWeb | Size 6.9 MB | Health [ 18 /6 ] | Added 2023-07-01 |
NOTE
SOURCE: Goodwin J. Mitochondrial Biology. New Perspectives 2023
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COVER
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MEDIAINFO
Textbook in PDF format Mitochondria are best known as the sites for production of respiratory ATP and are essential for eukaryotic life. Mitochondria are extremely active organelles that perform a variety of roles in the cell including energy production, regulation of calcium homeostasis, apoptosis, and population maintenance through fission and fusion. Mitochondrial dysfunction in the form of oxidative stress and mutations can contribute to the pathogenesis of various neurodegenerative diseases such as Parkinson’s (PD), Alzheimer’s (AD), and Huntington’s diseases (HD). Abnormalities of Complex I function in the electron transport chain have been implicated in some neurodegenerative diseases, inhibiting ATP production and generating reactive oxygen species that can cause major damage to mitochondria. They have their own genome but the great majority of the mitochondrial proteins are encoded by the nuclear genome and are imported into the mitochondria. The mitochondria participate in critical central metabolic pathways and they are fully integrated into the intracellular signalling networks that regulate diverse cellular functions. It is not surprising then that mitochondrial defects or dysregulation have emerged as having key roles in ageing and in the cytopathological mechanisms underlying cancer, neurodegenerative and other diseases. This book covers diverse areas of mitochondrial biology and function and how defects in these areas can lead to disease. In addition, the chapters in this book highlight how model organisms have contributed to our understanding of these processes. Human mitochondria are complex and highly dynamic biological systems, comprised of over a thousand parts and evolved to fully integrate into the specialized intracellular signaling networks and metabolic requirements of each cell and organ. Over the last two decades, several complementary, top-down computational and experimental approaches havebeen developed to identify, characterize and modulate the human mitochondrial system, demonstrating the power of integrating classical reductionist and discovery-driven analyses in order to de-orphanize hitherto unknown molecular components of mitochondrial machineries and pathways. To this goal, systematic, multiomics-based surveys of proteome composition, protein networks, and phenotype-to-pathway associations at the tissue, cell and organellar level have been largely exploited to predict the full complement of mitochondrial proteins and their functional interactions, therefore catalyzing data-driven hypotheses. Mitochondrial biology reinvented itself and became a new world that has attracted new scientists influencing every field of biomedical research. This fully updated edition explores the different pathways that converge into the regulation of mitochondrial function
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