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We measured two markers for late endosomes and exosomes: CD63 and LAMP2.
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We measured two surrogate markers of insulin resistance: HDL-cholesterol levels and waist circumference.
We measured two serum bone formation markers: osteocalcin and bone-specific alkaline phosphatase (BSAP).
Furthermore, accurate and standardized methods to measure these two markers by quantitative real-time PCR (qPCR) have been described [9], [10].
The interrelated values may also be a consequence of the methodology used in measuring the two markers.
The MultiTox-Fluor Assay simultaneously measures two protease activities; one is a marker of cell viability, and the other is a marker of cytotoxicity.
Three tracks, the front caster, the large wheel, and the drive wheel, are measured by three markers.
The same NAF and plasma samples were used to measure all three markers so that we could determine celecoxib's coordinate effect on them.
Allele sequence divergence between the DIP chromosome and non- DIP homolog's was measured at six marker regions at different distances from DIP.
The plasmatic levels of the two markers, measured at the patients' first clinical presentation, are plotted in Figure 1.
We measured cell-free DNA, two markers of nuclear DNA, and two markers of mitochondrial DNA (mtDNA) at the 0, 12, and 24 h time points.
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CEO of Professional Science Editing for Scientists @ prosciediting.com