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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.
Papers
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Journal ArticleDOI
The roles of dormant microbes in the development of pre-eclampsia
Douglas B. Kell,Louise C. Kenny +1 more
Book ChapterDOI
SpeedyGenesXL: an Automated, High-Throughput Platform for the Preparation of Bespoke Ultralarge Variant Libraries for Directed Evolution.
TL;DR: SpeedyGenesXL, an automated, high-throughput platform for the production of wild-type genes, Boolean OR, combinatorial, or combinatorially-OR-type libraries based on the Speedy Genes methodology, offers a flexible platform for library synthesis, capable of generating many different bespoke, diverse libraries simultaneously.
Book ChapterDOI
Is the Transmembrane Electrochemical Potential a Competent Intermediate in Membrane Associated ATP Synthesis
Bruno Andrea Melandri,Giovanni Venturoli,Rita Casadio,Giovanni Felice Azzone,Douglas B. Kell,Hans V. Westerhoff +5 more
TL;DR: The chemiosmotic hypothesis for oxidative and photosynthetic phosphorylation has given a powerful impulse to the study and the understanding of membrane associated electron transfer and its coupling to ATP formation.
Book ChapterDOI
Control Analysis of Metabolic Channeling
Pedro Mendes,Douglas B. Kell +1 more
TL;DR: A growing body of experimental evidence supports the view that many consecutive enzymes in metabolic pathways form aggregates which transfer their common intermediate metabolite(s) directly, without its escape into a bulk phase.
Journal ArticleDOI
Polarographic investigation of some cytokinins
Malcolm R. Smyth,Douglas B. Kell +1 more
TL;DR: The cytokinins constitute one of the five groups of plant hormones, and are characterised by their ability to promote cell division in cultured plant callus tissue under appropriate conditions as discussed by the authors.