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We demonstrate that whole cell reflectance spectroscopy can be used to efficiently characterize the large numbers of mutants generated by engineering strategies that exploit saturation mutagenesis.
We further demonstrate that whole blood may serve as a convenient alternative to the isolated lymphocytes in mtDNA analysis.
The results of the present study demonstrate that whole walnuts have a beneficial effect in an animal model of PCa.
Our results demonstrate that whole organism-based, live vaccines against highly polymorphic apicomplexan parasites can be highly effective.
Our results demonstrate that whole genome shotgun sequencing combined with MS-directed determination of oligopeptides successfully can identify NRPS gene clusters and the corresponding oligopeptides.
These global regulatory patterns of transcript abundance demonstrate that whole regulatory and metabolic pathways are under clock control [ 8, 10, 11].
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These findings demonstrate that whole-genome (or exome) sequencing can be a valuable aid to diagnose genetic diseases, even in individual patients.
The Rorippa and Rumex studies demonstrate that whole-genome transcription profiling technologies can be successfully applied to non-model species to uncover novel tolerance genes and processes.
These results demonstrate that whole-genome transcriptome analysis during ciliogenesis is a powerful tool to gain insight into the molecular mechanism by which centrosomes and cilia are assembled.
Our data demonstrate that whole-genome sequencing of mutant strains is a rapid method to identify developmental genes in an organism that can be genetically crossed and where a reference genome sequence is available, even without prior mapping information.
Collectively, our results demonstrate that whole-genome resequencing data generated by NGS techniques can be highly useful for large-scale discovery of SNPs and development of SNP-based molecular markers.
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