ビタミン
Online ISSN : 2424-080X
Print ISSN : 0006-386X
レチノイン酸の代謝と機能にかかわる遺伝子多型 : ALDH1A2とRARβの場合(<特集>「ビタミンと遺伝子多型」-ビタミンA-)
四童子 好廣
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ジャーナル フリー

2013 年 87 巻 10 号 p. 551-556

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Few association studies on vitamin A and genetic polymorphism have been conducted so far, even though brilliant success has been achieved in translational researches on vitamin D receptor or methylene tetrahydrofolate reductase gene polymorphism. Recently, a couple of epoch-making papers have been published in vitamin A and genetic polymorphism field: 1) a common intronic single nucleotide polymorphism (SNP) (rs12591551 A/C) of the aldehyde dehydrogenase 1A2 (ALDH1A2) gene was shown to be associated with individual variations of retinoic acid concentrations in umbilical cord blood, and 2) two common intronic SNPs (rs6800566, rs13070407) of the retinoic acid receptor β (RARβ) gene were shown to be associated with individual variations of adaptive immune responses to measles vaccine. In this mini-review, these 2 pioneering works are introduced and discussed briefly.
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© 2013 日本ビタミン学会

この記事はクリエイティブ・コモンズ [表示 - 非営利 - 改変禁止 4.0 国際]ライセンスの下に提供されています。
https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja
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