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We determined the pattern agreement between histoPET and in vivo PET using coefficients of determination (R 2) as a new voxel-based method for quantitative comparison of histopathologic data and PET signal.
The objective of this study was to develop a new real time PCR-based method for quantitative detection of topoisomerase II alpha (TOP2A) aberrations and to evaluate its clinical utility in breast cancer.
The aim of the present study was to identify conserved sequences among the genomes of major species of vaginal lactobacilli that could be used for the development of a PCR-based method for quantitative determination of vaginal microbiota-specific lactobacilli.
Recently, a magnetic resonance image (MRI -based MRI -based quantitative analysis of methodus size, shape and position has been presented [ 17] and shows satisfortory intra-observer [ 17] and inter-observer precision in vivo [ 18].
Expression of pH dependent senescence associated β-galactosidase (SA-β-gal) activity was analyzed with a fluorescence-based method for quantitative and sensitive analysis by flow-cytometry as described before [ 70].
This novel AgNPs-based colorimetric method for quantitative determination of trypsin has a linear detection range from 2.5 to 200 ng mL−1 and a rather low detection limit down to 2 ng mL−1.
In both real-time PCR based methods an adoption to a quantitative approach was not performed.
Sometimes DNA based methods may be needed for unambiguous authentication [ 82], but do not yield any information on the qualitative and quantitative chemical profiles.
They are quantitative model-based methods, qualitative model-based methods, and process history based methods.
Based on this model, a method for quantitative assessment of both mode-I and mode-II crack shielding is proposed.
We emphasize that metabolic flux analysis based on material balance is a critical method for quantitative investigations into cell metabolism.
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