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Stephen D. Evans

Researcher at University of Leeds

Publications -  376
Citations -  12293

Stephen D. Evans is an academic researcher from University of Leeds. The author has contributed to research in topics: Monolayer & X-ray photoelectron spectroscopy. The author has an hindex of 55, co-authored 363 publications receiving 11281 citations. Previous affiliations of Stephen D. Evans include Aberystwyth University & University of Salford.

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The p7 protein of hepatitis C virus forms an ion channel that is blocked by the antiviral drug, Amantadine.

TL;DR: It is shown that p7 can be cross‐linked in vivo as hexamers, and this activity is abrogated by Amantadine, a compound that inhibits ion channels of influenza.
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Site-Directed Conjugation of “Clicked” Glycopolymers To Form Glycoprotein Mimics: Binding to Mammalian Lectin and Induction of Immunological Function

TL;DR: In addition, enzyme-linked immunosorbent assay (ELISA) revealed that the neoglycopolymer-protein materials described in this work possess significantly enhanced capacity to activate complement via the lectin pathway when compared with native unmodified BSA.
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Surface potential studies of alkyl-thiol monolayers adsorbed on gold

TL;DR: In this paper, the surface potential of monolayers of alkyl thiols adsorbed on gold have been measured using the Kelvin technique and the potential has been found to vary linearly with increasing chain length, n, for 6⩽ n ⩽22.
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Gold Nanoparticle Patterning of Silicon Wafers Using Chemical e-Beam Lithography

TL;DR: This strategy is to use direct-write electron beam patterning to convert nitro functionality in self-assembled monolayers of 3-(4-nitrophenoxy)-propyltrimethoxysilane to amino functionality, forming chemically well-defined surface architectures on the 100 nm scale.
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Vapour sensing using hybrid organic-inorganic nanostructured materials

TL;DR: In this article, small aromatic organothiol derivatives, with the structure HS-C6H4-X, have been used to stabilise gold nanoparticles and the electronic behavior indicates that conduction can be understood in terms of an activated electron tunnelling model.