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Titlebook: Circadian Rhythms and Their Impact on Aging; S. Michal Jazwinski,Victoria P Belancio,Steven M H Book 2017 The Editor(s) (if applicable) an

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發(fā)表于 2025-3-21 19:49:06 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Circadian Rhythms and Their Impact on Aging
編輯S. Michal Jazwinski,Victoria P Belancio,Steven M H
視頻videohttp://file.papertrans.cn/227/226575/226575.mp4
概述Deals in a multi-faceted way with an emerging area in longevity and healthy aging research.A book on this topic is not currently on the market.Summarizes the current state of the art and outlines futu
叢書名稱Healthy Ageing and Longevity
圖書封面Titlebook: Circadian Rhythms and Their Impact on Aging;  S. Michal Jazwinski,Victoria P Belancio,Steven M H Book 2017 The Editor(s) (if applicable) an
描述Biological rhythms time the ebb and flow of virtually every physiological process, and their mutual coordination guarantees the integrity of the organism over space and time. Aging leads to the disintegration of this coordination, as well as to changes in the amplitude and/or frequency of the underlying rhythms. The results of this are accelerated loss of health during aging, and in experimental model systems curtailed lifespan occurs. This book will examine the machinery that constitutes circadian systems and how they impact physiologic processes. It will also discuss how disturbances of circadian rhythms can lead to complex diseases associated with aging. Much of this treatment will focus on metabolism and genome stability. Importantly, the chapters in this book will encompass work in several different models, in addition to human. The book will conclude with a discussion of modeling approaches to biologic cycles and chronotherapy, for future research and translation.
出版日期Book 2017
關(guān)鍵詞Circadian rhythms; Healthy aging; Diseases of aging; Metabolism; Genome stability
版次1
doihttps://doi.org/10.1007/978-3-319-64543-8
isbn_softcover978-3-319-87816-4
isbn_ebook978-3-319-64543-8Series ISSN 2199-9007 Series E-ISSN 2199-9015
issn_series 2199-9007
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerl
The information of publication is updating

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發(fā)表于 2025-3-21 20:50:44 | 只看該作者
Siedlungsstrukturen und Stadtsysteme,gression of age-related lung diseases, and the underlying molecular mechanisms, are still largely unknown. The chronobiology of the lung and the role of the circadian clock in the pathophysiology of age-related lung disease will be discussed in this chapter. We describe the molecular links between t
板凳
發(fā)表于 2025-3-22 00:50:54 | 只看該作者
Phasenmodelle der Stadtentwicklung,sleep, and eating at irregular hours. This is causing more stress and less time to spend outdoors. All of these factors are contributing to circadian disruption “in general” but more importantly?to circadian disruption of bone rhythms. Bone metabolism displays circadian variation that is coincident
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發(fā)表于 2025-3-22 05:04:21 | 只看該作者
Gunther Maier,Franz T?dtling,Michaela Trippltrointestinal aging is reviewed. Although we know quite a lot about the physiological and molecular mechanisms of circadian clocks in mammals, we know very little about the mechanisms of food-entrainable rhythmicity. The role played by the pineal hormone melatonin has been posited as a key to unders
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發(fā)表于 2025-3-22 11:56:22 | 只看該作者
Gunther Maier,Franz T?dtling,Michaela Tripplgical or cellular level. However, in mammals internal clock becomes less rhythmic and more vulnerable to external disturbing stimuli with age. In this chapter we briefly describe rodent circadian system physiology, rhythms and clock genes disturbance in aging and age-related diseases, models of gene
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發(fā)表于 2025-3-22 13:44:17 | 只看該作者
Gunther Maier,Franz T?dtling,Michaela Trippl-autonomous and consists of molecular negative feedback loops that turn over with an endogenous circa 24?h period. While daily oscillations in the activity of clock genes and proteins are well understood in young fruit flies ., much less is known about how the clock mechanism changes during organism
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發(fā)表于 2025-3-23 00:08:14 | 只看該作者
https://doi.org/10.1007/3-211-31908-5 decreased proteostasis. Indeed, the two main intracellular protein degradation systems, autophagy and proteasome, have been shown to generally decline with age while age-related alterations of redox homeostasis has also been reported. Both antioxidant defenses and autophagy have been shown to be re
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