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We believe that the results described herein encourage further study of CNT constructs in vivo.
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The consolidated spectroscopic research described herein may encourage design of naphthalimide based pro-drugs for effective in vivo biodistribution using HSA-based drug delivery systems.
The experiences reported herein can encourage other countries to develop their own surveillance systems.
The reproducible experiments introduced herein are encouraged by the lack of a set of large, self-contained and easily reproducible experiments with the aim of replicating and confirming previously reported results.
Moreover, the main findings of our study based on Atlantic salmon SNP-chip were in line with those observed for human SNP-chips, and thus the technical approaches described herein are encouraging for employing allelotyping approach in other species using Illumina SNP-chips or other SNP genotyping systems and arrays.
Researchers interested in strengthening the evidence-based clinical applicability of the literature reviewed herein are encouraged to attempt to corroborate it in future research utilizing more rigorous methodology and more comprehensive as well as diverse samples (in terms of sexual orientation, disability status, and ethnic/racial/cultural diversity).
Herein reported results encourage further investigation of this class of compounds as novel antibacterial DNA binding agents.
We recognize that by selecting a well-defined group of patients, our cohort is relatively small thus we encourage independent confirmation of the results presented herein.
The results herein presented suggest that binary De Bruijn sequences, when properly selected, may compete with more consolidated options, and encourage further investigation activities, specifically focused on the generation of longer sequences, and the definition of correlation-based selection criteria.
Good concordance of FDCPmix with primary cells confirms its utility as a hematopoietic cell model amenable to systems-level analysis, and encourages confidence that the networks discussed herein have relevance to primary hematopoietic cells.
The examples described herein are not intended to be comprehensive, and readers are encouraged to examine previous reviews of fate-modulating compounds (8, 9).
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