Disruption of Slc52a3 gene causes neonatal lethality with riboflavin deficiency in mice

Homeostasis of riboflavin should be maintained by transporters. Previous in vitro studies have elucidated basic information about riboflavin transporter RFVT3 encoded by SLC52A3 gene. However, the contribution of RFVT3 to the maintenance of riboflavin homeostasis and the significance in vivo remain...

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Bibliografische gegevens
Gepubliceerd in:Sci Rep
Hoofdauteurs: Yoshimatsu, Hiroki, Yonezawa, Atsushi, Yamanishi, Kaori, Yao, Yoshiaki, Sugano, Kumiko, Nakagawa, Shunsaku, Imai, Satoshi, Omura, Tomohiro, Nakagawa, Takayuki, Yano, Ikuko, Masuda, Satohiro, Inui, Ken-ichi, Matsubara, Kazuo
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Nature Publishing Group 2016
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Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4897618/
https://ncbi.nlm.nih.gov/pubmed/27272163
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep27557
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