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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...
Uloženo v:
| Vydáno v: | BMJ Open Diabetes Res Care |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2019
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| Témata: | |
| On-line přístup: | 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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