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The Sav1-deficient livers exhibit a marked expansion of oval cells, however in contrast to the Mst1/Mst2-deficient livers, the Sav1 null livers do not show a parallel overproliferation of adult hepatocytes (Le et al, 2010).
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However, when Cyclin B1 expression was examined, we discovered that MYC ON/DDC and MYC ON/CCl4 livers exhibited a 250 and 150 percent increase in Cyclin B1 mRNA, respectively, compared to MYC OFF/DDC and MYC OFF/CCl4 livers (Figure 7D).
As measured by Ki67, MYC ON/DDC and MYC ON/CCl4 livers exhibited a 30 and 40 percent increase in hepatocyte proliferation, respectively, as compared to DDC and CCl4-treated MYC OFF livers (Figure 6A).
After 5 weeks of MCD diet, livers exhibited an increase both in the sphingomyelin and ceramide concentrations for all mice.
The developmental expression profile of chicken MAC structural genes shows that their transcripts initially appear in the 12th embryonic day in the liver, exhibiting a pick in the 17th, while no expression was detected in the early whole embryo (day 4 and 6), as well as in the 2-day old neonate chicken liver.
In particular, the liver exhibited a severe diffuse congestion of sinusoids with prominent compression of hepatocytes, accompanied by a multifocal macro-vacuolar steatosis that was prominent around portal triads.
Whereas primary tumors did not exhibit E-cadherin staining in cell membranes, a subset of tumor cells that had metastasized to the lung and the liver exhibited a re-distribution of E-cadherin to the membrane.
In addition to the observation that transgenic mice constitutively expressing SHP in the liver exhibited an enhanced expression of SREBP-1c mRNA levels and a concomitant accumulation of hepatic triglycerides [33], these data suggest that also a SHP-independent mechanism is activated by FXR ligands.
These results indicate that few PBP/MED1 expressing hepatocytes present in PBP/MED1ΔLiv mouse livers exhibit profound growth advantage in a milieu where the majority of hepatocytes do not express this coactivator.
Downstream of Atg1, FIP200- (Atg17 homologue) knockout livers exhibit significant increases in mitochondrial mass and ROS [ 139].
Downstream of Atg1, FIP200(Atg17 homolog) knockout livers exhibit significantly increase in the mitochondrial mass and ROS.
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