The battle for hearts and minds: the media relations of the antiwar movement in the UK

This dissertation examines the relations between the local base of the anti-Iraq War movement and the local press in the UK. It is, as such, a study of the interactions between local newsworkers and local activists, as well as a Content Analysis study of how the Iraq crisis, and particularly opposition to military action, was reported on in the pages of the local press. Key questions to be addressed include how local journalists assessed the legitimacy of the antiwar movement; how, and the reasons why, opponents of the war sought local press coverage, and with what consequences (if any) their interactions with the media may have had for the movement; and how the local press handled the almost uniquely controversial nature of the Iraq crisis in its reporting. Most previous research on the Iraq crisis has focused on the national media local media has hitherto been absent from the research agenda. Likewise, the majority of research on social movements has usually focused on the national leaderships of those movements again the local dimension of social movements has rarely been studied. In these ways it is hoped that the study makes a unique contribution to research into both the reporting of the Iraq crisis, and to the study of the interactions between social movements and the media

Exp 2 reflectance profiles clay models

Body reflectance of clay model fish held in tanks with black or white horizontal background

Exp 2 change in light and horiz background

Changes in body reflectance in fish held in tanks with varying light intensity and horizontal background reflectanc

Exp 1 reflectance profiles clay models

Body reflectance of clay model fish photographed in tanks with black or white substrate

Exp 1 change in light and substrate

Changes in body reflectance of fish held in tanks with varying light intensity and substrate reflectanc

What does local food mean to you? Report of findings

This report sets out the findings of ‘What does local food mean to you?’, a research project conducted in 2012/13 by the University of Leicester’s Cultural Production and Consumption Research Group

MOESM4 of HIV-1 capsid is involved in post-nuclear entry steps

Additional file 4: Fig. S4. Conditions for the CsA washout assay. (A) H126Q cells were infected with WT HIV-1GFP vector by spinoculation in the presence of CsA (1 μM) or C-A1 (3 μM). The drug was washed out at the indicated time points (time of washout) and cells were analysed by FACS 48 h later to determine the percentage of infected (GFP+) cells. (B) Same as (A) but T5Cyp cells expressing functional human TRIMCyp were used. (C) A prolonged time of uncoating assay, in which CsA was washed out at the indicated time points. Rescue of infection reaches a plateau after 10 h. Average ± SD of three independent experiments are shown in (A-C)

MOESM4 of HIV-1 capsid is involved in post-nuclear entry steps

Additional file 4: Fig. S4. Conditions for the CsA washout assay. (A) H126Q cells were infected with WT HIV-1GFP vector by spinoculation in the presence of CsA (1 μM) or C-A1 (3 μM). The drug was washed out at the indicated time points (time of washout) and cells were analysed by FACS 48 h later to determine the percentage of infected (GFP+) cells. (B) Same as (A) but T5Cyp cells expressing functional human TRIMCyp were used. (C) A prolonged time of uncoating assay, in which CsA was washed out at the indicated time points. Rescue of infection reaches a plateau after 10 h. Average ± SD of three independent experiments are shown in (A-C)

MOESM5 of HIV-1 capsid is involved in post-nuclear entry steps

Additional file 5: Fig. S5. CsA washout assays in cells depleted of Nup153 or control DsRed cells. T5Cyp cells expressing an shRNA against Nup153 or DsRed (control) were infected at an MOI of 0.01–0.05 with an HIV-1GFP vector (WT) in the presence of CsA (1 μM). The drug was washed out at the indicated time points (time of washout) and cells were analysed by FACS 48 h later to determine the percentage of infected (GFP+) cells. To control for specificity, cells were infected in the same way using the N74D mutant virus. Raw data of three independent experiments are shown. The data have been used to compile fold rescue levels shown in Figure 6