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two main pathways. Mutation in mitochondrial DNA causes diseases such as Kearns-Sayre syndrome and Pearson syndrome. Mutation in chromosomal;
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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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It was once assumed that mitochondrial diseases were rare and that few people were affected. As knowledge has grown about these organelles;
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It was once assumed that mitochondrial diseases were rare and that few people were affected. As knowledge has grown about these organelles;
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This book describes the author's work on the development of sequence-specific DNA binders for the therapy of mitochondrial diseases. In the;
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The book describes molecular principles and mechanisms by which mitochondrial DNA (mtDNA) can drive the occurrence of diseases and the;
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diseases are PCR and specific mutation analysis, southern blot and sequencing. Spindle therapy, embryonic mitochondrial transplant and protofection;
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of mitochondrial DNA, e.g. its in vivo conformational changes, and models of deletions and partition. Moreover, it discusses the involvement;
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during this process. It then discusses how diseases like cancer are initiated and regulated by mutations to mitochondrial DNA and dysfunctional;
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during this process. It then discusses how diseases like cancer are initiated and regulated by mutations to mitochondrial DNA and dysfunctional;
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, as well as the pathophysiology, diagnosis and treatment of mitochondrial diseases. Three all-inclusive sections examine the role;
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subunits of proton pumps (complexes I, III, IV and V), which are encoded on mitochondrial DNA. The nuclear encoded subunits have mostly a;
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of nonfunctional mitochondrial membranes in the most vulnerable cell. Free radicals induce downregulation of mitochondrial DNA, microRNA, AgNOR, and;
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of nonfunctional mitochondrial membranes in the most vulnerable cell. Free radicals induce downregulation of mitochondrial DNA, microRNA, AgNOR, and;
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Mitochondrial diseases comprise a clinically and genetically heterogeneous group of rare disorders that may affect virtually any system;
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of mitochondrial diseases are remarkably variable and heterogeneous. The laboratory and clinical methodologies used to evaluate dysfunction may vary widely;
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of mitochondrial diseases are remarkably variable and heterogeneous. The laboratory and clinical methodologies used to evaluate dysfunction may vary widely;
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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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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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manuscripts and review articles in this special issue covers a wide range of topics on G-quadruplex ribosomal DNA, impaired mitochondrial DNA function;
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diagnostically challenging clinical presentations of mitochondrial diseases and their pathophysiology.;
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generated during mitochondrial DNA replication, and more than 40 by DNA viruses. Consequently, a growing number of therapeutic drugs are targeted to;
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approach. Since mitochondrial diseases are diverse and influenced by genetic, environmental, and social-economic factors, this publication will;
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in pulmonary diseases and this volume focuses on the mitochondrial metabolism, redox signaling, and mechanisms of mitochondrial pathways in lung injury;
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partner NPAT and MCM4, respectively. Surveillance of the human DNA database has revealed that the numbers of DNA repairmitochondrial function;
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