Dreams Of Mother And Home

https://digitalcommons.library.umaine.edu/mmb-vp/5225/thumbnail.jp

A study of T cell receptor usage in allergic asthma and analysis of a humanised T cell receptor transgenic model of immunity to allergen

Imperial Users onl

Construction of exercises to extend and enrich word meanings at 2^1, 2^2, and 3^1 levels

Thesis (Ed.M.)--Boston Universit

Evaluation of the Induction of Immune Memory following Infant Immunisation with Serogroup C Neisseria meningitidis Conjugate Vaccines - Exploratory Analyses within a Randomised Controlled Trial

Aim: We measured meningococcal serogroup C (MenC)-specific memory B-cell responses in infants by Enzyme-Linked Immunospot (ELISpot) following different MenC conjugate vaccine schedules to investigate the impact of priming on immune memory. Methods: Infants aged 2 months were randomised to receive 1 or 2 doses of MenC-CRM197 at 3 or 3 and 4 months, 1 dose of MenC-TT at 3 months, or no primary MenC doses. All children received a Haemophilus influenzae type b (Hib)-MenC booster at 12 months. Blood was drawn at 5, 12, 12 months +6 days and 13 months of age. Results: Results were available for 110, 103, 76 and 44 children from each group respectively. Following primary immunisations, and prior to the 12-month booster, there were no significant differences between 1- or 2-dose primed children in the number of MenC memory B-cells detected. One month following the booster, children primed with 1 dose MenC-TT had more memory B-cells than children primed with either 1-dose (p = 0.001) or 2-dose (p<0.0001) MenC-CRM197. There were no differences in MenC memory B-cells detected in children who received 1 or 2 doses of MenC-CRM197 in infancy and un-primed children. Conclusions: MenC-specific memory B-cell production may be more dependent on the type of primary vaccine used than the number of doses administered. Although the mechanistic differences between MenC-CRM197 and MenC-TT priming are unclear, it is possible that structural differences, including the carrier proteins, may underlie differential interactions with B- and T-cell populations, and thus different effects on various memory B-cell subsets. A MenC-TT/Hib-MenC-TT combination for priming/boosting may offer an advantage in inducing more persistent antibody.peer-reviewe

Unconventional superconductivity in the nickel-chalcogenide superconductor, TlNi2_2Se2_2

We present the results of a study of the vortex lattice (VL) of the nickel chalcogenide superconductor TlNi2Se2, using small angle neutron scattering. This superconductor has the same crystal symmetry as the iron arsenide materials. Previous work points to it being a two-gap superconductor, with an unknown pairing mechanism. No structural transitions in the vortex lattice are seen in the phase diagram, arguing against d-wave gap symmetry. Empirical fits of the temperature-dependence of the form factor and penetration depth rule out a simple s-wave model, supporting the presence of nodes in the gap function. The variation of the VL opening angle with field is consistent with earlier reports of of multiple gaps

Will nature work with us? Erosion and flooding impacts on a UK barrier

‘Barrier island’ refers to a diverse collection of coastal landforms that often support substantial human populations, critical infrastructures, and ecosystems. Globally, many coastal barriers are experiencing climatically altered environmental forcing coupled with increasing anthropogenic pressures. This paper undertakes high resolution shoreline change analysis to reveal how Blakeney Point, a mixed sandy-gravel barrier located on the UK’s East Coast, has evolved over centennial, decadal and event timescales. We seek to establish the implications of barrier evolution, under contrasting management regimes, for present erosion and flooding hazards. Interrogating a series of alternative shoreline proxies reveals a series of interdependent behaviors. Over the 130-year period of study, Blakeney Point is shown to be rolling landward at a mean rate of 0.60 m a-1. Assuming continued landward retreat over the coming decades, future flood-generating storm events will encounter more landward shoreline positions than today. Superimposed on this trend, we observe the presence of alongshore migrating erosional hotspots which give rise to unpredictable morphologies at any given location on the spit. Finally, we find that instances of barrier setback are driven by individual storm events, which makes barrier retreat both highly variable and discontinuous in time and space. This is illustrated by the presence of overwash, particularly along stretches of the barrier that have experienced a recent shift in management regime towards a non-interventionist approach.This work was funded by the NERC/ESRC Data, Risk and Environmental Analytical Methods (DREAM) Centre, Grant/Award Number: NE/M009009/1. It is also a contribution to the NERC-funded project “Physical and Biological dynamic coastal processes and their role in coastal recovery” (BLUEcoast), Grant Award Number: NE/N015924/1

Conformational changes in Arp2/3 complex induced by ATP, WASp-VCA, and actin filaments

We used fluorescence spectroscopy and EM to determine how binding of ATP, nucleation-promoting factors, actin monomers, and actin filaments changes the conformation of Arp2/3 complex during the process that nucleates an actin filament branch. We mutated subunits of Schizosaccharomyces pombe Arp2/3 complex for labeling with fluorescent dyes at either the C termini of Arp2 and Arp3 or ArpC1 and ArpC3. We measured Förster resonance energy transfer (FRET) efficiency (ET_(eff)) between the dyes in the presence of the various ligands. We also computed class averages from electron micrographs of negatively stained specimens. ATP binding made small conformational changes of the nucleotide-binding cleft of the Arp2 subunit. WASp-VCA, WASp-CA, and WASp-actin-VCA changed the ET_(eff) between the dyes on the Arp2 and Arp3 subunits much more than between dyes on ArpC1 and ArpC3. Ensemble FRET detected an additional structural change that brought ArpC1 and ArpC3 closer together when Arp2/3 complex bound actin filaments. VCA binding to Arp2/3 complex causes a conformational change that favors binding to the side of an actin filament, which allows further changes required to nucleate a daughter filament

Keywords in the Cultures of Young People

DOI: 10.1353/jeu.2015.001