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Extracellular ATP is an important signaling molecule for vascular adaptation to limited oxygen availability (hypoxia).
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The upregulated genes in long term cocultures of OECs and pOBs included growth factors, their receptors, chemokines, cytokines, matrix molecules, and adhesion molecules, for example, vascular endothelial growth factor beta.
The phosphoserines equip the molecule with strong affinity for vascular calcification, thereby causing a decrease in the plasma circulating levels of t-ucMGP, leading to lower t-ucMGP levels at higher levels of calcification (21).
Advances in understanding the basic mechanisms of the formation and remodeling of blood vessels have led to the identification of several signaling molecules that are critical for vascular development.
No significant changes were observed for vascular adhesion molecule and high-sensitivity C-reactive protein levels in any treatment group.
Primers (Invitrogen) were designed to match intron-spanning probes within the Roche Universal Probe Library for vascular cell adhesion molecule 1 (VCAM-1), intercellular adhesion molecule-1 (ICAM-1), chemokine (C-C motif) receptor 2 (CCR2), fractalkine receptor (CX3CR1), β-actin, leptin, inducible nitric oxide synthase (iNOS), resistin-like molecule-α (Relm-α), and mannose receptor (Table 1 ).
After two, four and 24 hours, fluorescence activated cell sorter (FACS) analysis for vascular cell adhesion molecule-1, intercellular adhesion molecule-1 and E-selectin was performed.
The intra- and inter-assay CV were 5·8 and 7·9 % for E-selectin and 3·1 and 7·0 % for vascular cell adhesion molecule-1, respectively.
The renal tubular epithelium shows increased expression of inducible nitric oxide (NO) synthase and 3-nitrotyrosine, as well as increased staining for vascular cell adhesion molecule-1 (VCAM-1) in the interstitial capillary cells and tubular epithelial cells compared with normal control mice.
Intercellular adhesion molecule 1-positive cells increased between 1 minute and 10 minutes, and neutralizing antibodies for intercellular adhesion molecule 1, vascular cell adhesion molecule 1 and activated leukocyte-cell adhesion molecule inhibited the attachment.
Vascular endothelial growth factor (VEGF) a well-known mitogen for vascular endothelial cells and a fundamental molecule for the EPCs recruitment from bone marrow, was greatly repressed in SSc patients (FC -36.08) but highly induced (F.C. + 5.58) after iloprost treatment.
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