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Loss of CTRP5 improves insulin action and hepatic steatosis
The gene that encodes C1q/TNF-related protein 5 (CTRP5), a secreted protein of the C1q family, is mutated in individuals with late-onset retinal degeneration. CTRP5 is widely expressed outside the eye and also circulates in plasma. Its physiological role in peripheral tissues, however, has yet to be...
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| Vydáno v: | Am J Physiol Endocrinol Metab |
|---|---|
| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Physiological Society
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4935138/ https://ncbi.nlm.nih.gov/pubmed/27143553 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpendo.00010.2016 |
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