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GO analysis showed that when the clusters are ripening, the activity of the nucleus, cytoplasmic, cytosol, membrane and chloroplast genes in the cluster architecture cells decreases.
In the proposed architecture, cells are used to store the current frame and compare the current frame with a reference frame to achieve the low-power by reusing the block.
Surprisingly, despite the dramatic changes in their architecture, cells remain alive and the epithelial monolayer maintains a normal barrier function.
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In this architecture, cell-edge is further partitioned into three sectors.
Here, we first uncover changes in intestinal architecture, cell number, and cell composition upon aging.
FGFs especially FGF8 promoted sheet-like architecture, cell proliferation, and survival as compared to the control.
The selected genes included biological features central to bladder cancer biology, eg, cell cycle activity, cellular architecture, cell-cell interactions, and key receptor tyrosine kinases.
No changes in intestinal architecture, cell differentiation, or lineage selection were observed with expression of the transgene.
Subtypes of HL and NHL are defined based on tumor architecture, cell morphology and differentiation, surface markers and genetic aberrations.
These proteins are variously involved in organisation of the actin cytoskeleton, membrane cytoskeleton architecture, cell adhesion, and contractile apparatus.
Recent hippocampus research has yielded a wealth of data on network architecture, cell types, the anatomy and membrane properties of pyramidal cells and interneurons, and synaptic plasticity.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com