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DCTAs of 15 patients, who presented with signs of acute cerebral ischemia, were derived from 320-slice CT perfusion scans using both the standard subtraction method and the proposed ToBE method.
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Four hundred seventy-seven subjects underwent scans using both imaging sequences, and the remainder (including all subjects with knee OA and all who underwent two scans) underwent only the T1-weighted scan sequence.
The corresponding GH3 promoters (−1000 to −1 bp) were scanned using both Watson and Crick words for the consensus AuxRE motif (TGTCTC core sequence) [ 35], which we call AUX1, and its less stringent variant, named AUX2 (TGTCYS) [ 28, 29].
The persons were scanned in supine position using both the neck coil and the attachable anterior element from the head coil.
Here, we present a software package called Prismatic for parallelized simulation of image formation in scanning transmission electron microscopy (STEM) using both the PRISM and multislice methods.
Retention times (Rt) of the targeted compounds were determined with the help of the NIST08 library, using both the full scan and SIM chromatograms of the standard solutions.
Therefore the GATA-3 motif was scanned using the original PWM in both strands.
Both groups were scanned using the same equipment, analyses and stimuli which included written English words (with both low-frequency regular and irregular spellings), their Italian translations, and pseudowords.
The chips were scanned using the GeneArray scanner (Affymetrix).
The arrays were scanned using the BeadStation 500 Instrument (Illumina Inc).
The GeneChips were scanned using the GeneChip Scanner 3000 (Affymetrix).
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