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This book will describe the nuclear encoded genes and their expressed proteins of mitochondrial oxidative phosphorylation. Most of these;
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Mitochondria, often referred to as the powerhouses of the cell, generate adenosine triphosphate (ATP) by oxidative phosphorylation or;
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Despite the fact that over 200 phosphorylation sites have been mapped on the mitochondrial oxidative phosphorylation (OxPhos) complexes;
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With the recent renaissance in mitochondrial biology and increasing recognition of their role in many diseases, this book provides a timely;
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bioactivation; identification of mitochondria as the key target site for oxidative stress; involvement of mitochondrial respiratory chain in the;
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phosphorylation. This unique reference will inform specialized biochemistry courses and researchers in their understanding of the role biochemistry has;
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formation of reactive oxygen species due to electron leakage from the electron transport chain during oxidative phosphorylation. In simple terms;
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in different response to oxidative stress. Special attention should be devoted to the topic of oxidative nuclear and mitochondrial DNA damage and its;
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abnormalities that lead to hyperactivation of cellular and mitochondrial pathways that ultimately result in oxidative and nitrosative stress that left;
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of environmental pollutants and inflammatory responses, and explores mitochondrial dysfunction. It then describes the protective abilities of antioxidants;
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of environmental pollutants and inflammatory responses, and explores mitochondrial dysfunction. It then describes the protective abilities of antioxidants;
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age-related metabolic pathways, mitochondrial nutrients, neurodegeneration and micronutrients, cell signaling, and neuronal functions. General;
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underlie the condition, including studies that implicate dysfunction of mitochondrial proteins such as parkin and pink1.;
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The book focuses on the current research of the relation between protein phosphorylation and meat quality, reviews the influence mechanism;
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during pathogenesis of plant peroxidases; phospholipids and peroxidases in mitochondrial apoptosis; glutathione peroxidases in stem, cancer, and;
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mitochondrial dysfunction in FA patients has so far been an unexplored field warranting ad hoc investigations. This book provides the readers with up-to;
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methodologies for mitochondrial DNA analysis. of Mitochondrial DNA: Methods and Protocols describes protocols for detecting mutations in mitochondrial;
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Mitochondrial Neuropathies, Volume 146, brings together experts in a range of diseases that damage the nervous system to present the role;
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equally elaborate array of protein phosphatases can remove phosphate groups from proteins. It is now well established that protein phosphorylation;
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field of Mitochondrial Medicine. Volume II guides readers through chapters on mitochondrial dysfunction, functional' mitochondria, mitochondrial;
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Regulation of Electron Transport and Proton Translocation in Mammalian Cytochrome c Oxidase by ATP, Palmitate, and Protein Phosphorylation;
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Mitochondrial Case Studies: Underlying Mechanisms and Diagnosis offers the science behind mitochondrial disease with a case studies;
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organelles in cell signaling, cell survival, and cell death. Mitochondrial dysfunction is a factor in a myriad of pathophysiological conditions;
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