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51– 53 A phase II study of oral etoposide and bendamustine was conducted in thirty-eight pretreated (n = 12) and previously untreated patients with indolent NHL and CLL.
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There was no significant difference between the mortality rate in the sham treated mice and the fasudil pre- or posttreated mice (n = 25 (fasudil pretreated) and n = 30 (fasudil posttreated); P > 0.05 for both, Kaplan-Meier analysis; Figure 1(b)).
The red arrows indicated episodes of Ca2+ release from ER. (C ) The bar graphs represent the normalized changes of YPet/ECFP emission ratio of the D3ER in HMSCs upon force application without extracellular Ca2+ in the untreated cells as the control group (n = 3) or cells pretreated with CytoD (n = 5), Noc (n = 5), ML-7 (n = 6), Bleb (n = 5), or TRPM7 siRNA (n = 9) as indicated.
This polymer was inorganically modified incorporating different amounts of zirconium phosphate (ZrPh) pretreated with n-propylamine and polybenzimidazole (PBI).
Purified human CD14+ monocytes and CD4+ T cells were pretreated with N-acetyl cysteine (NAC), a well-known ROS quenching agent [34], prior to ZnO NP exposure.
(A) HCT116 cells were pretreated with N-6 (10 μmol/L) for 2 h in serum free medium before being exposed to TNFα (10 ng/mL) for an additional 30 min.
(C and D) H292 cells (C) or A549 cells (D) pretreated with N-6 (10 μmol/L) for 2 h in serum free medium before being exposed to TNFα (10 ng/mL) for an additional 30 min were analyzed for p85α/tRXRα interaction by co-immunoprecipitation assay using anti-RXRα antibodies of D20 or ΔN197.
Further study showed that these effects were significantly blocked when the cells were pretreated with N-acetyl cysteine (NAC), a specific ROS inhibitor.
The role of lipid peroxidation in the mechanism of arsenic toxicity was investigated in female rats pretreated with N-acetylcysteine (NAC, a glutathione [GSH] inducer) or with buthionine sulfoximine (BSO, a GSH depletor).
From the histological observation, lymphocyte infiltration and marked necrosis were observed in PCM-treated groups (negative control), whereas maintenance of hepatic structure was observed in group pretreated with N-acetylcysteine and MEMC.
Consistent with this, a marked reduction of tumoricidal activity of splenocytes was observed when B16 cells were pretreated with N-glycosidase, whereas O-glycosidase treatment did not affect this activity.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com