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In our study, we have identified a truncated N-terminal peptide, LL-25, that acts as a potent inhibitor of both LL-37 signalling and of LL-37-induced migration and alteration of cancer cell colony morphology.
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The pathology detected in 92% of the autistic brains reflects focal modifications of neurogenesis, migration, and alterations of the cytoarchitecture.
The effects of transfection were subsequently assessed on cell viability patterns, cell migration and alterations in gene and protein expression by real-time quantitative PCR and immunocytochemistry respectively.
At the cellular level, we show that FAK deletion causes reduced endothelial cell proliferation, migration and alterations in cell signalling, all biological processes that are likely responsible for the observed decrease in tumour angiogenesis.
The (a) detected changes within the subependymal cell layer with subependymal nodular dysplasia, (b) subcortical and periventricular heterotopias and (c) neocortex, archicortex, dentate gyrus, cornu Ammonis and cerebellar dysplasia reflect focal modification of neurogenesis, migration and alterations of the cytoarchitecture of brain cortex, subcortical structures and cerebellum in autism.
Based on the present data and existing literature, we proposed this model as a mechanism that could explain the focal modification of neurogenesis, migration, and alterations of the cytoarchitecture of brain cortex, subcortical structures and cerebellum observed in individuals with autism.
The aim is to elucidate their origin and migration and their alteration by thermochemical sulfate reduction (TSR) and water-rock interactions.
In this study, we perform laboratory corefloods using aqueous solutions with different salinities in engineered rocks with different kaolinite content, yielding fines migration and permeability alteration.
We reported for the first time that hesperidin reduced SCF-induced mast cell migration and morphological alteration.
Actin polymerization and cytoskeleton rearrangement induced by topographical and chemical cues present in the growing surface are known to serve as driving forces for directional migration and morphological alterations.
Hence, the binding of a specific ECM ligand by an integrin may elicit the activation of intracellular signaling pathways, cytoskeletal reorganisations and changes in cell adhesion or migration; and conversely, alterations in the intracellular environment and signaling can result in the activation or inhibition of ligand binding by the extracellular domain of an integrin [ 1, 2].
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