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Future experiments should explore the possibility of making this Zika treatment safe for children.
Future experiments should explore mutagenesis of key sites within the Omp36 loopoop to decipher exactly which residues are interacting with each drug, and therefore, which aspects of the antibiotic molecular structure drives rapid transport.
Future experiments should explore this combination approach to studying other spinal injuries, e.g. contusion, to determine whether recovery of function is improved under these experimental conditions.
Future experiments should explore the effects of overexpressing IGFBP3 on IGF1 signalling, proliferation, survival and invasion and to investigate the level of IGFBP3 promoter methylation in this cell system.
Since cell fate transitions involve differential DNA methylation at enhancer regions [ 45], an attractive hypothesis is that PcG complexes and DNMTs synergize to regulate key enhancers relevant to neuroendocrine transdifferentiation. Consequently, future experiments should explore the distribution of DNA methylation in the context of genome-wide PRC1 and PRC2 chromatin binding in NEPC cells.
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Future experiments should assess this directly.
Future experiments should test these possibilities.
Future experiments should tackle this key question.
Future experiments should aim to confirm this hypothesis.
Future experiments should shed new light on this question.
Future research should explore whether international experiments with this model can provide lessons learned for the U.S. Future research is also needed to understand the precise conditions that contribute to the success and impacts of medical malls on costs and quality of care.
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CEO of Professional Science Editing for Scientists @ prosciediting.com