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Is obesity genetic disease?

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dc.contributor.author Duran, Tugce
dc.contributor.author Zainalbden, Hasanain Akram
dc.contributor.author Kocak, Nadir
dc.date.accessioned 2022-02-17T11:17:41Z
dc.date.available 2022-02-17T11:17:41Z
dc.date.issued 2017
dc.identifier.citation Duran, T., Akram Zainalbden, H., & Kocak, N. (2021). Is obesity genetic disease? . Annals of Medical Research, 24(4), 0531–0534. Retrieved from https://annalsmedres.org/index.php/aomr/article/view/1568 en_US
dc.identifier.uri http://hdl.handle.net/11616/47403
dc.description.abstract Obesity is a complex disease that has unfavorable impacts for all ethnic populations in worldwide. Genetics, environment and lifestyle are among aetiological factors of this disease. Genetic contribution associated with this disease is generally classified into 2 types: monogenic syndromes that display severe obesity, and the polygenic model of common obesity. Single-gene mutations can cause severe obesity resulting from alteration in central and peripheral appetite control mechanisms. Candidate gene and genome-wide association studies have led to the identification of nine loci associated with Mendelian forms of obesity and 58 loci contributing to polygenic obesity. These loci explain a small fraction of the heritability for obesity and many genes remain to be identified. The interaction of several polymorphisms and epigenetic modifications open a new research field for common obesity. As a result, still remains to be a mystery en_US
dc.language.iso eng en_US
dc.relation.isversionof 10.5455/jtomc.2017.03.032 2017; 24(4):531-4 en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title Is obesity genetic disease? en_US
dc.type article en_US
dc.relation.journal Annals of Medical Research en_US
dc.contributor.department İnönü Üniversitesi en_US


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