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FOXN3 hyperglycemic risk allele and insulin sensitivity in humans

OBJECTIVE: The rs8004664 variation within the FOXN3 gene is significantly and independently associated with fasting blood glucose in humans. We have previously shown that the hyperglycemia risk allele (A) increases FOXN3 expression in primary human hepatocytes; over-expression of human FOXN3 in zebr...

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Détails bibliographiques
Publié dans:BMJ Open Diabetes Res Care
Auteurs principaux: Erickson, Melissa L, Karanth, Santhosh, Ravussin, Eric, Schlegel, Amnon
Format: Artigo
Langue:Inglês
Publié: BMJ Publishing Group 2019
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6731827/
https://ncbi.nlm.nih.gov/pubmed/31543974
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjdrc-2019-000688
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