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Clive J. Roberts

Researcher at University of Birmingham

Publications -  634
Citations -  22811

Clive J. Roberts is an academic researcher from University of Birmingham. The author has contributed to research in topics: Train & Energy consumption. The author has an hindex of 70, co-authored 614 publications receiving 20025 citations. Previous affiliations of Clive J. Roberts include Energy Institute & University of London.

Papers
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Polyethylenimine-graft-poly(ethylene glycol) copolymers: influence of copolymer block structure on DNA complexation and biological activities as gene delivery system.

TL;DR: The degree of PEGylation and the MW of P EG were found to strongly influence DNA condensation of PEI and therefore also affect the biological activity of the PEI-g-PEG/DNA complexes, providing a basis for the rational design of block copolymer gene delivery systems.
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Surface plasmon resonance analysis of dynamic biological interactions with biomaterials

TL;DR: A review of the diversity of SPR analysis shows the broad range of techniques that are routinely used alongside SPR analysis, and particular emphasis is given to the use of SPR as a complimentary tool.
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Comparison of calibration methods for atomic-force microscopy cantilevers

TL;DR: In this paper, the authors compared the experimentally determined values of stiffness for ten cantilever probes using four different methods, based on the acquisition and analysis of thermal distribution functions of the oscillator's amplitude fluctuations.
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Substrate stiffness affects early differentiation events in embryonic stem cells.

TL;DR: A fundamental role for mechanosensing in mammalian development is suggested and the mechanical environment should be taken into consideration when engineering implantable scaffolds or when producing therapeutically relevant cell populations in vitro is illustrated.
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3D printing of five-in-one dose combination polypill with defined immediate and sustained release profiles.

TL;DR: 3D extrusion printing was used to manufacture a multi-active solid dosage form that showed the intended immediate and sustained release profiles based upon the active/excipient ratio used and demonstrates that complex medication regimes can be combined in a single personalised tablet.