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Exact(16)
In addition, CXCL-5, a chemotactic chemokine, and ICAM-1, an endothelial activation marker, were determined according to the recommendation of the manufacturer (R&D Systems, Wiesbaden, Germany).
Genomic position and expected PCR product size for each marker were determined based on the reference sequence of rice cultivar Nipponbare released by International Rice Genome Sequencing Program IRGSPP).
For comparison, expression of KDR/VEGFR-2, an angiogenic marker expressed by endothelial cells; CD11b, a monocyte/macrophage marker; and CD45, a pan-leukocyte marker were determined by immunohistochemistry on sequential frozen sections of a glioblastoma used for the in situ hybridization (Fig 5).
The genotypes of IL-8 (-251) T/A marker were determined as previously reported [ 30].
The mRNA levels of PPAR γ, FABP4 and RUNX2 (used as a bone marker) were determined by qRT-PCR.
The median, first and third quartile values for each molecular marker were determined using all informative samples.
Similar(44)
Similar results were also observed when serum pentosidine as another marker was determined.
The number of cells expressing a specific marker was determined as described in the ESM Methods.
For each marker from each sample, the percentage of viable cells positive for that marker was determined.
The favourable (unfavourable) allele of each marker was determined by the positive (negative) sign of the estimated marker effect.
Expression of the CD11b, differentiation-specific macrophage cell surface marker was determined by staining cells as previously described [ 26, 27].
More suggestions(15)
score were determined
marker were identified
benchmarks were determined
marker were normalized
marker were averaged
marker were explored
marker were analyzed
marker were extracted
marker were dissolved
marker were generated
marker were considered
marker were assembled
marker were calculated
marker were positioned
marker were counted
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