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I propose an hypothesis of a developmental phase of oligogenic expression that is followed by positive and negative selection resulting usually in cells with one expressed receptor.
Sometimes, H. pylori bodies or remnants were found inside PaCSs (Figure 2C and D), usually in cells also showing H. pylori outside PaCS, in membrane-enclosed vacuoles of the supranuclear cytoplasm (Figure 2E).
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Because the conventional method of in vitro expansion and MSC delivery involves cell culture on 2D tissue culture plastic monolayers (usually in cell stacks), we compared the osteogenic potential of 3D MC-bound cells to 2D MNL-harv cells.
Fine needle aspirations of MCT are usually rich in cells as these exfoliate easily and cytology is usually sufficient for a diagnosis of MCT.
As cells live in a watery environment, this adhesive mechanism is usually absent in cells.
These targets are all genes usually expressed in cells of mesenchymal or neuronal origin.
FGFR1-IIIb usually expressed in cells of epithelial origin is almost absent in PDAC (Kornmann et al, 2002).
Apical secretory snouts are usually found in cells of the apocrine metaplasia, and intra-cytoplasmic vacuoles are present.
HMGB1 release usually occurs in cells that are undergoing classical necrotic cell death marked by abrupt membrane lysis and the release of soluble proteins (16).
Usually, in unstimulated cells, COX-2 and iNOS proteins are undetectable, but in response to immunostimulators like LPS, COX-2 and iNOS genes are strongly induced.
This method requires the transfection, usually in a cell culture, of the potential interacting protein pair, one with a donor chromophore and the other with an acceptor chromophore.
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