J
Julie E Reed
Researcher at Imperial College London
Publications - 62
Citations - 3393
Julie E Reed is an academic researcher from Imperial College London. The author has contributed to research in topics: Health care & Quality management. The author has an hindex of 20, co-authored 57 publications receiving 2519 citations. Previous affiliations of Julie E Reed include Halmstad University & University of Bath.
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Systematic review of the application of the plan–do–study–act method to improve quality in healthcare
TL;DR: A theoretical framework for assessing the quality of application of PDSA cycles is proposed and the consistency with which the method has been applied in peer-reviewed literature against this framework is explored.
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Stabilization of G-quadruplex DNA and inhibition of telomerase activity by square-planar nickel(II) complexes.
TL;DR: Two new alkylamine-substituted nickel(II)-salphen complexes have been prepared and their interactions with DNA investigated and TRAP/Taq assays have shown that these complexes inhibit telomerase at low micromolar concentrations.
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The problem with Plan-Do-Study-Act cycles
Julie E Reed,Alan J. Card +1 more
TL;DR: It is argued that the problem with PDSA is the oversimplification of the method as it has been translated into healthcare and the failure to invest in a rigorous and tailored application of the approach.
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Navigating the sustainability landscape: a systematic review of sustainability approaches in healthcare
TL;DR: This work aimed to identify what approaches are available to assess and influence sustainability in healthcare and to describe the different perspectives, applications and constructs within these approaches to guide their future use.
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Stabilisation of human telomeric quadruplex DNA and inhibition of telomerase by a platinum–phenanthroline complex
TL;DR: Two new mono-substituted phenanthroline ligands and their platinum(II) square planar complexes have been prepared and one of the complexes has been shown to induce a high degree of quadruplex DNA stabilisation and to inhibit telomerase.