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Sarah R. Hart

Researcher at Keele University

Publications -  25
Citations -  1457

Sarah R. Hart is an academic researcher from Keele University. The author has contributed to research in topics: Electron-transfer dissociation & Tandem mass spectrometry. The author has an hindex of 14, co-authored 25 publications receiving 1369 citations. Previous affiliations of Sarah R. Hart include University of Manchester & University of Bristol.

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Flagellar motility is required for the viability of the bloodstream trypanosome

TL;DR: It is shown that RNAi-mediated ablation of various proteins identified in the trypanosome flagellar proteome leads to a rapid and marked failure of cytokinesis in bloodstream-form (but not procyclic insect-form)trypanosomes, suggesting that impairment of flageLLar function may provide a method of disease control.
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Growth control of the eukaryote cell: a systems biology study in yeast

TL;DR: This work constitutes a first comprehensive systems biology study on growth-rate control in the eukaryotic cell and has direct implications for advanced studies on cell growth, in vivo regulation of metabolic fluxes for comprehensive metabolic engineering, and for the design of genome-scale systems biology models of the eUKaryoticcell.
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PEDRo: A database for storing, searching and disseminating experimental proteomics data

TL;DR: The PEDRo database provides access to a collection of comprehensive descriptions of experimental data sets in proteomics and serves to extend the debate on the level of detail at which proteomics data should be captured, the sorts of facilities that should be provided by proteome data management systems, and the techniques by which such facilities can be made available.
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Characterization of Protein Phosphorylation by Mass Spectrometry Using Immobilized Metal Ion Affinity Chromatography with On-Resin β-Elimination and Michael Addition

TL;DR: The combined protocol enabled the detection and sequencing of phosphopeptides from protein digests at low femtomole concentrations of initial sample and was employed to identify novel phosphorylation sites on the cell adhesion protein p120 catenin and the glycoprotein fetuin.