Evaluating on a collection of 202 full-text articles in which authors have ranked the figures based on importance, our best system achieved a weighted error rate of 0.2, which is significantly better than several other baseline systems we explored.
Using polysome fractionation and microarray methods, we were able to globally analyse differential mRNA translation, and through subsequent pathway analysis with Ingenuity IPA software (Ingenuity® Systems), we explored canonical pathways of potential interest and relevance in cases of hepatotoxicity.
With a need, in such settings, to understand how to appropriately adjust ANC sentinel surveillance estimates to represent HIV prevalence in general populations, and with evidence of possible biases inherent to both surveillance systems, we explore differences between the two systems.
Using a simple Au Bi model system, we explored experimentally whether such polymetallic melts can precipitate directly from a hydrothermal fluid, and investigated the ability of these melts to scavenge Au from the solution.
So, as to improve the system, we explored participants' user experiences, including their perceived ease of use, perceived usefulness, and how it could be improved.
Given the tremendous physiological and clinical importance of the Kp/GPR54 signaling system, we explored the contributions of the GPR54-coupled Gq/11 and β-arrestin pathways on the activation of a major downstream signaling molecule, ERK, using Gq/11 and β-arrestin knockout mouse embryonic fibroblasts.
To demonstrate the use of the eFIP system, we explored phosphorylation-dependent interactions involving 14-3-3 14-3-3 14-3-3
Using this high-throughput YTH system, we explored large-scale PPI analysis in the photoautotorophic cyanobacterium Synechocystis sp. PCC6803.
To gain insight into the behavior of the system, we explored the steady state solutions of the system using stability analysis.
Using transgenic mouse models of several diseases of the central nervous system, we explored whether a primary proteinopathy might secondarily drive TDP-43 proteinopathy.
Using E. coli fermentations as a model system, we explored the hypothesis that these phenolic amides might be direct inhibitors of bacterial metabolism.
