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We demonstrated that bile acids inhibit completion of autophagic process in hepatocytes by decreasing Rab7-mediated fusion of autophagosomes with lysosomes in hepatocytes, a process which is independent of FXR.
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When F-actin polymerization is inhibited, completion of oocyte meiotic maturation and embryo development are prevented [16].
Recent studies using laser microsurgery have proposed that Aurora B inhibits completion of cytokinesis when there is chromatin trapped in the cleavage furrow.
Mixing and combustion performance indicates that while flight conditions promote rapid mixing, high combustor temperatures inhibit the completion of reaction pathways, with reactant dissociation reducing chemical heat release by 16%.
Colchicine induces cytoskeletal alterations that inhibit the completion of mitosis.
Increased bile acids may inhibit the completion of autophagic degradation in hepatocytes.
In glioma cells, when combined with hypothermia, NO donors SNP (sodium nitroprusside), S-nitrosoglutathione or PAPA-NONOate (propylamine propylamine NONOate) inhibit the completion of autophagy, as is evident by LC3-II accumulation [ 107], whereas in primary neurons, NO induces Drp1 (dynamin-related protein 1 -mediated mitochondrial fission, which further causes an increase in mitophagy [ 1 -mediated
Since the primary interaction of proteasomes occurs with endogenous proteins, the signalling action of transcription factor NF-κB can be blocked by inhibition of proteasomes, thus inhibiting the completion of the cell cycle and mitotic proliferation of cancerous cells and ultimately leading to cell death.
This is the case for several standard treatments such as amphotericin B (partially inhibits the completion of the parasite's membrane), antimonials (decrease biosynthesis of energy in the amastigote), and itraconazole and pyrazolopyrimidines (inhibit the parasite growth).
These results further indicate that the ZF2 of KREPA3 is essential for editing progression, and mutation of ZF2 of KREPA3 inhibited the completion of editing in vivo as well as increasing the proportion of 'non-canonical' editing.
We were able to reproducibly identify compounds that affected wound healing with different effects including: inhibiting migration, affecting morphology, blocking completion of mitosis, and disrupting the cell monolayer.
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