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A total 108 of NSCLC patients were identified for analysis of prognostic evaluation.
A total 109 of cervical cancer patients were identified for analysis of prognostic evaluation, of which 51 were early stage cervical cancers and 58 were late stage.
The "healthy cartilage" and "repair tissue" regions were readily identified for analysis of the other quantitative parameters (thickness, repair tissue area, and surface roughness).
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Tissue sections were imaged using a ScanScope digital scanner (Aperio, Oxford, UK), regions of interest identified for analysis to exclude areas of background staining or poor sample quality, and the mean vessel density (MVD) per mm was assessed using the microvessel analysis algorithm running under ImageScope (Aperio).
Fig. 1 Summary of vehicles identified for analysis Table 1 Vehicle characteristics by DRL status Std.
Thirteen eligible studies were identified for the analysis of the effect of prophylaxis on mutation (21 – 33 ) and five for the analysis of mutation effect on treatment outcome (Table 1) (25 – 27, 34, 35 ).
A total of 50 consecutive patients (25 men and 25 women) without a history of dream enactment or nocturnal behaviors seen from 2010 to 2012 were identified for retrospective analysis of RSWA from the polysomnographic (PSG) database at the Mayo Clinic Center for Sleep Medicine.
Five investigations were identified for the analysis of association between ACE I/D gene polymorphism and steroid-resistant nephrotic syndrome (SRNS) risk in Asian children and seven studies were included to explore the relationship between ACE I/D gene polymorphism and steroid-sensitive nephrotic syndrome (SSNS) susceptibility.
Altogether, 1,642 TSSs in the upstream regions of annotated genes were identified and used for analysis of the 5′-UTR length distribution and the detection of 75 cis-regulatory RNA elements.
A total of 36 SNPs were finally identified for further analysis (Table S3), out of which, four SNPs (ROCK2 SNP rs10929728, MYLK SNPs rs11717814, rs40305, and rs820336) emerged significant among the study groups (P<0.05).
For each SNP the majority allele within each infection was identified for use in analysis of population allele frequencies and examination of long range haplotypes.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com