Publications by authors named "Jacqueline J Chritton"

Article Synopsis
  • The study investigates the effectiveness of a procalcitonin-based antibiotic stewardship program in community hospitals to reduce inappropriate antibiotic use, addressing the global concern of antimicrobial resistance.
  • Conducted as a matched cohort study, the research compared patients from hospitals implementing the procalcitonin protocol with those from hospitals without it, focusing on various demographic and clinical factors.
  • Results indicated that patients in procalcitonin cohort hospitals received 1.47 fewer days of antibiotic therapy, though there was a noted increase in acute kidney injury, but no significant differences in length of stay or other adverse outcomes.
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Objective: Procalcitonin (PCT) is a biomarker that may help providers optimize antibiotic (AB) therapy. Numerous clinical trials have demonstrated the utility of PCT-guided decision algorithms in treating lower respiratory tract infections and sepsis, but evidence from real-world studies is limited. This study sought to evaluate the effects of PCT on select clinical outcomes in community hospitals.

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PUF proteins regulate translation and mRNA stability throughout eukaryotes. Using a cell-free translation assay, we examined the mechanisms of translational repression of PUF proteins in the budding yeast Saccharomyces cerevisiae. We demonstrate that the poly(A)-binding protein Pab1p is required for PUF-mediated translational repression for two distantly related PUF proteins: S.

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PUF proteins bind mRNAs and regulate their translation, stability, and localization. Each PUF protein binds a selective group of mRNAs, enabling their coordinate control. We focus here on the specificity of Puf2p and Puf1p of Saccharomyces cerevisiae, which copurify with overlapping groups of mRNAs.

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PUF (Pumilio and FBF) proteins provide a paradigm for mRNA regulatory proteins. They interact with specific sequences in the 3' untranslated regions (UTRs) of target mRNAs and cause changes in RNA stability or translational activity. Here we describe an in vitro translation assay that reconstitutes the translational repression activity of canonical PUF proteins.

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