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Titlebook: Oxidative Phosphorylation in Health and Disease; Jan A. M. Smeitink,Rob C. A. Sengers,J. M. Frans T Book 2005 Springer-Verlag US 2005 DNA.

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書(shū)目名稱(chēng)Oxidative Phosphorylation in Health and Disease
編輯Jan A. M. Smeitink,Rob C. A. Sengers,J. M. Frans T
視頻videohttp://file.papertrans.cn/706/705303/705303.mp4
概述Oxidative Phosphorylation in Health and Disease includes up-to-date research on the normal structure, function, and molecular biology of the mitochondrial respiratory chain, information on traditional
叢書(shū)名稱(chēng)Medical Intelligence Unit
圖書(shū)封面Titlebook: Oxidative Phosphorylation in Health and Disease;  Jan A. M. Smeitink,Rob C. A. Sengers,J. M. Frans T Book 2005 Springer-Verlag US 2005 DNA.
描述Mitochondrial diseases are often hard to diagnose. From the time they were first researched without animal models, patients of mitochondrial diseases were of equal interest to both clinical and basic scientists. With the new research done, this book includes updates on the normal structure, function, and molecular biology of the mitochondrial respiratory chain, information on traditional diagnostical methodologies, and an overview of the diagnostic promise of new technologies. The hypermetabolism of Luft disease, although only seen twice, is also studied. There are critical reviews of symptoms and signs associated with syndromes, as well as updates on the genetic defects of either the mitochondrial or the nuclear genome responsible for many disorders.
出版日期Book 2005
關(guān)鍵詞DNA; RNA; biochemistry; biology; cell; development; diagnostics; genetics; genome; metabolism; mitochondria; mo
版次1
doihttps://doi.org/10.1007/b138432
isbn_softcover978-1-4419-3435-2
isbn_ebook978-0-387-26992-4
copyrightSpringer-Verlag US 2005
The information of publication is updating

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Nuclear DNA and Oxidative Phosphorylation, mitochondrial genetics all contribute to the extraordinary heterogeneity of clinical disorders associated with defects of oxidative phosphorylation (mitochondrial encephalomyopathies). Here, we review recent findings about nuclear gene defects in OXPHOS enzyme complex deficiency. This information s
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Therapeutic Options in OXPHOS Disorders,. We review available and experimental therapeutic approaches that fall into the following categories:.(a) Palliative therapy; (b) removal of noxious metabolites; (c) administration of artificial electron acceptors; (d) administration of metabolites and cofactors; (e) administration of oxygen radica
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