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Hepatic deletion of Mboat7 (LPIAT1) causes activation of SREBP-1c and fatty liver
Genetic variants that increase the risk of fatty liver disease and cirrhosis have recently been identified in the proximity of membrane-bound O-acyltransferase domain-containing 7 (MBOAT7). To elucidate the link between these variants and fatty liver disease, we characterized Mboat7 liver-specific K...
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| Publicat a: | J Lipid Res |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Biochemistry and Molecular Biology
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8022244/ https://ncbi.nlm.nih.gov/pubmed/32859645 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1194/jlr.RA120000856 |
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