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Titlebook: Nutrigenomics: How Science Works; Carsten Carlberg,Stine Marie Ulven,Ferdinand Molná Textbook 2020 Springer Nature Switzerland AG 2020 Nut

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书目名称Nutrigenomics: How Science Works
编辑Carsten Carlberg,Stine Marie Ulven,Ferdinand Molná
视频video
概述Written by experts with more than 15 years of lecturing experience on the topic.Presents an updated and simplified view of the first textbook on nutrigenomics.Includes a high figure to text ratio
图书封面Titlebook: Nutrigenomics: How Science Works;  Carsten Carlberg,Stine Marie Ulven,Ferdinand Molná Textbook 2020 Springer Nature Switzerland AG 2020 Nut
描述.The fascinating area of .Nutrigenomics. describes this daily communication between our diet and our genome. This book describes how nutrition shapes human evolution and demonstrates its consequences for our susceptibility to diseases, such as diabetes and atherosclerosis. Inappropriate diet can yield stress for our cells, tissues and organs and then it is often associated with low-grade chronic inflammation. Overnutrition paired with physical inactivity leads to overweight and obesity and results in increased burden for a body that originally was adapted for a life in the savannahs of East Africa. Therefore, this textbook does not discuss a theoretical topic in science, but it talks about real life and our life-long “chat” with diet. We are all food consumers, thus each of us is concerned by the topic of this book and should be aware of its mechanisms..The purpose of this book is to provide an overview on the principles of nutrigenomics and their relation to health or disease. The content of this book is based on the lecture course “Nutrigenomics”, which is held since 2003 once per year by Prof. Carlberg at the University of Eastern Finland in Kuopio. The book represents an update
出版日期Textbook 2020
关键词Nutrition; Genomics; Molecular Medicine; Metabolic Syndrome; Epigenetics; Evolution; gene expression
版次1
doihttps://doi.org/10.1007/978-3-030-36948-4
isbn_softcover978-3-030-47663-2
isbn_ebook978-3-030-36948-4
copyrightSpringer Nature Switzerland AG 2020
The information of publication is updating

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Human Genomic Variation,rtia, such as the .. Genome-wide genotyping and whole genome sequencing allows the study and analysis of complex diseases, such as T2D and CVDs, on the basis of dozens to hundreds of genetic variants, such as SNPs and CNVs (copy number variations).
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Nutritional Epigenetics,tal supplementation in mice as well as natural human experiments provide insight into the concepts of epigenetic programming during embryogenesis and epigenetic drift during adult life. This may explain some of the susceptibility for complex metabolic diseases, such as T2D.
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