Publication for Hmgcr and Aacs
| Species | Symbol | Function* | Entrez Gene ID* | Other ID | Gene coexpression |
CoexViewer |
|---|---|---|---|---|---|---|
| mmu | Hmgcr | 3-hydroxy-3-methylglutaryl-Coenzyme A reductase | 15357 | [link] | ||
| mmu | Aacs | acetoacetyl-CoA synthetase | 78894 |
| Pubmed ID | Priority | Text |
|---|---|---|
| 27200103 | 0.98 | AACS gene, which encodes the ketone body-utilizing enzyme, is transcriptionally regulated by SREBP-2 and the knockdown of SREBP-2 induced downregulation of AACS and HMGCR gene expression. |
| 0.97 | AACS, and HMGCR mRNA levels were dramatically suppressed in the mice that were fed FAVA (Figures 5(b) and 5(c)). | |
| 0.97 | AACS, and HMGCR mRNA levels. | |
| 0.95 | AACS, and HMGCR RNA in the mouse liver were induced by FAVA. | |
| 19721697 | 0.98 | AACS and HMGCR are key enzymes in cholesterol synthesis, and LDLR is responsible for the uptake of low-density lipoprotein (LDL)-cholesterol from the blood. |
| 0.97 | Hmgcr, Low density lipoprotein receptor (Ldlr), and Acetoacetyl-CoA synthetase (Aacs) in Rev-KO and TgRev animals suggested that the activity of SREBP2 was affected in these animals as well (Figure 1D), in spite of the apparently normal Srebp2 mRNA accumulation (Figure S4A). | |
| 31139087 | 0.98 | 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR), and fatty acid elongase family members (ELOVL), the low-density lipoprotein receptor (LDLr), and acetoacetyl-CoA synthetase (AACS) to modulate daily lipid metabolism in the liver. |
| 27185526 | 0.97 | Aacs (acetoacetyl-CoA synthetase), Hmgcr (3-hydroxy-3-methylglutaryl-Coenzyme A reductase), and Lss (Lanosterol synthase), were also increased (Figure 5D). |
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