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Alternately, active bile acid synthesis within the follicle could result in a higher follicular content compared to serum.
Thus elevated GGT immediately after transplantation indicates an active bile flow.
Gd-EOB-DTPA-enhanced MRC allows detection of active bile leakage by direct visualisation of contrast material extravasation into fluid collections in addition to demonstrating the anatomical site of the leakage and the type of bile duct injury.
De Rooij et al. found significant decreases in active bile acid uptake when examining ileal brush border membrane vesicles [ 11] and proposed that altered viscosity of the ileal mucus was likely not a factor in ileal bile acid malabsorption associated with cystic fibrosis.
It has been proposed that the specific induction of HO-1 by various forms of oxidative stress, for example, different heavy metals, CCL4, and aminoacetophenone, was part of the defensive mechanism mounted by cells against stress injury, to decrease the levels of potential pro-oxidants and to increase the concentrations of active bile pigments that can act as antioxidants [ 126, 127].
Gd-EOB-DTPA-enhanced MRC allows detection of active bile leakage and cysto-biliary communication by direct visualisation of contrast material extravasation into fluid collections and also demonstrates the anatomical site of the leakage and the type of bile duct injury [ 10– 10].
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Main histopathological findings in groups 1 and 3 were the lesions in the liver, characterised by a severe active fibrosis, bile duct proliferation, haemosiderosis and mild necroses.
One should take into consideration that solubilization of interfacially active molecules by bile is only possible in the duodenum.
For instance, H. hepaticus can cause chronic active infection of bile canaliculi that progresses to liver carcinoma in A/JCr laboratory strains of mice (Ward et al, 1994).
The extent of digestion of human DNA by micrococcal nuclease was compared, as shown in Figure 2. The result showed that micrococcal nuclease remained active at the bile concentration up to 9%.
During apoptosis induced by ESC-3, an active ingredient of crocodile bile, in human cholangiocarcinoma Mz-ChA-1 cells, PHB1 is dramatically downregulated, and the region of co-localization between PHB1 and AIF, p53, Rb, and c-fos shifted from the cytoplasm to the nucleus.
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