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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897618/
https://www.ncbi.nlm.nih.gov/pubmed/27272163
http://dx.doi.org/10.1038/srep27557

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897618/
https://www.ncbi.nlm.nih.gov/pubmed/27272163
http://dx.doi.org/10.1038/srep27557

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