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Douglas B. Kell

Researcher at University of Liverpool

Publications -  657
Citations -  55792

Douglas B. Kell is an academic researcher from University of Liverpool. The author has contributed to research in topics: Systems biology & Dielectric. The author has an hindex of 111, co-authored 634 publications receiving 50335 citations. Previous affiliations of Douglas B. Kell include Max Planck Society & University of Wales.

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A 'rule of 0.5' for the metabolite-likeness of approved pharmaceutical drugs.

TL;DR: This work exploits the recent availability of a community reconstruction of the human metabolic network to study how close in structural terms are marketed drugs to the nearest known metabolite(s) that Recon2 contains, and suggests a ‘rule of 0.5’ mnemonic for assessing the metabolite-like properties that characterise successful, marketed drugs.
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Poorly controlled type 2 diabetes is accompanied by significant morphological and ultrastructural changes in both erythrocytes and in thrombin-generated fibrin: implications for diagnostics

TL;DR: The axial ratio of the erythrocytes of poorly controlled type 2 diabetics was significantly increased, and that their fibrin morphologies were again highly aberrant, but these could be reversed, to some degree, by the addition of the iron chelators deferoxamine (DFO) or deferasirox (DFX).
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Viscoelastic and ultrastructural characteristics of whole blood and plasma in Alzheimer-type dementia, and the possible role of bacterial lipopolysaccharides (LPS)

TL;DR: It is argued that bacterial cell wall components, such as the endotoxin lipopolysaccharide (LPS) of Gram-negative strains, might be the cause of the continuing and low-grade inflammation, characteristic of AD.
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Oscillatory, stochastic and chaotic growth rate fluctuations in permittistatically controlled yeast cultures

TL;DR: The identification of chaotic growth rates in cell cultures suggests that there may be novel methods for controlling the growth of such cultures.
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The simultaneous occurrence of both hypercoagulability and hypofibrinolysis in blood and serum during systemic inflammation, and the roles of iron and fibrin(ogen)

TL;DR: The analysis demonstrates the commonalities underpinning a variety of pathologies as seen in both hypercoagulability and hypofibrinolysis, and offers opportunities for both diagnostics and therapies.