Publication for Dhcr7 and Nsdhl
Species | Symbol | Function* | Entrez Gene ID* | Other ID | Gene coexpression |
CoexViewer |
---|---|---|---|---|---|---|
mmu | Dhcr7 | 7-dehydrocholesterol reductase | 13360 | [link] | ||
mmu | Nsdhl | NAD(P) dependent steroid dehydrogenase-like | 18194 |
Pubmed ID | Priority | Text |
---|---|---|
22394543 | 0.98 | Nsdhl, Tm7sf2, Dhcr7, Hsd17b7) were found consistently upregulated in the intestinal tissue. |
0.97 | Dhcr7), the hydroxysteroid (17-beta) dehydrogenase 7 (Hsd17b7), the NAD(P) dependent steroid dehydrogenase-like (Nsdhl) and the transmembrane 7 superfamily member 2 (Tm7sf2) genes. | |
22252456 | 0.98 | Nsdhl, Idi1, Sc4mol, Cyp51, and Dhcr7). |
25393872 | 0.98 | Nsdhl and Dhcr7 in females and again Dhcr24 in males (Figure S2 B). |
27878435 | 0.98 | DHCR7, HSD17B7, NSDHL, DHCR24, FDPS, SIGMAR1, SQLE, MVK, that are expressed in the lens. |
29352187 | 0.98 | sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating (Nsdhl), 3-keto-steroid reductase (Hsd17b7) and 7-dehydrocholesterol reductase (Dhcr7), were increased in AB mice compared with vehicle control mice, and this increase was reversed by secondary bile acid supplementation (Fig. 4A-F). |
30069000 | 0.98 | Dhcr7, Fdft1, Fdps, Hmgcr, Hmgcs1, Hsd17b7, Idi1, Lss, Mvd, Mvk, Msmo1, Nsdhl, Pmvk, Sc5d, Sqle, and Tm7sf2 were significantly decreased in HFD livers. |
30271348 | 0.98 | Nsdhl (NAD(P) dependent steroid dehydrogenase-like), Hsd17b7, Ebp, Sc5d, and Dhcr7] exhibited reduced expression compared to ad libitum mice (Figure 8A). |
31549781 | 0.97 | Nsdhl, Fdft1, Fdps, Dhcr7, and Mvd) were upregulated with sleep in young and old mice. |
19183246 | 0.96 | DHCR7, DHCR24, FDFT1, FDPS, IDI1, NSDHL and SQLE are members of the mevalonate pathway downstream of the 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase and represent potent therapeutic targets for cholesterol-lowering agents. |
0.73 | DHCR7, FDPS, NSDHL) displayed q-values above the 0.01 threshold employed in significance analysis, highlighting the fact that both approaches use independent criteria for pathway selection. | |
19631568 | 0.96 | Dhcr7, in contrast to the much earlier embryonic lethality of mutations in enzymes such as squalene synthase and NSDHL that block earlier steps in the pathway. |
31998465 | 0.96 | DHCR7, DHCR24, LSS, NSDHL). |
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