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We found 16 genes down-regulated in tumor, inversely correlated with miR-21 and enriched (via KEGG) in the cell adhesion (CAM) pathway at p = 0.0006.
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CAM: cellular adhesion molecule; CAMs: cellular adhesion molecules; CI: Confidence Interval; eGFR: estimated glomerular filtration rate; HDL: high density lipoprotein; hsCRP: high sensitivity C reactive protein; ICAM: soluble intercellular CAM-1; VCAM: soluble vascular CAM-1.
As Calder elegantly revised [28, 29], these events include leukocyte chemotaxis, cellular adhesion molecule (CAM) expression, leukocyte endothelial adhesive interactions, production of ARA derived eicosanoids like PGs and LTs, production of inflammatory cytokines and T cell reactivity.
The specificity is due to a set of cell-surface glycoproteins called cell adhesion molecules (CAM).
Extracellular matrix (ECM) proteins and cell-cell adhesion molecules (CAM) play important roles in neuronal development and differentiation.
These cell adhesion molecules (CAM) are known to mediate blood cell (leukocyte, platelet -endothelial cell interactions that can occur in all segments of the microvasculature under certain platelet -endothelialmostasis) and pathologicell(eg, interactions) condithats.
The establishment of ordered neuronal connections is supposed to take place under the control of specific cell adhesion molecules (CAM) which guide neuroblasts and axons to their appropriate destination.
CHL1 gene (also known as CALL) on 3p26.3 encodes a one-pass trans-membrane cell adhesion molecule (CAM).
CHL1, located at 3p26.1, belongs to the family of cell adhesion molecules (CAM) – cell surface proteins mediating cell-cell and cell-matrix interactions.
Cell adhesion molecules (CAM) are believed to participate in fibrogenesis.
Most hPSC culture surfaces have been derived from extracellular matrix proteins (ECMPs) and their cell adhesion molecule (CAM) binding motifs.
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