20 research outputs found
Seroepidemiological aspects ofLeishmania spp. in dogs in the Itaguai micro-region, Rio de Janeiro, Brazil
Inhibition of placental mTOR signaling provides a link between placental malaria and reduced birthweight
PRODUCTION OF F-prime (1520) IN 8.25-GEV/C K- P INTERACTIONS
Presents results for the hypercharge exchange reaction K/sup -/p to f' Lambda from a high statistics experiment at 8.25 GeV/c using the CERN 2m HBC. The total and differential cross sections have been measured; the polarisation of the Lambda hyperon and the f' density matrix elements have been calculated as functions of momentum transfer. The authors also present detailed information on the relative strength of the natural and unnatural parity exchange contributions to the production mechanism. (9 refs)
Maternal nutrient restriction inhibits ureteric bud branching but does not affect the duration of nephrogenesis in rats
Scalable analysis of Big pathology image data cohorts using efficient methods and high-performance computing strategies
Assessment of immunity induced in mice by glycoproteins derived from different strains and species of Leishmania
A comparative study was undertaken on the immunogenic properties of 63kDa glycoproteins obtained from five different strains/species of Leishmania and assessed in C57BL/10 mice. The humoral immune response was assessed by ELISA against the five different antigens of the immunized animals. The cellular immune response was derived from Leishmania. The response was found to be species-specific in all of determined by means of the cytokine profiles secreted by the spleen cells of immunized animals. The presence of Âł-IFN and IL-2, and the absence of IL-4 in the supernatants of cells stimulated by L. amazonensis antigen established that the cellular response is of Th1 type. The five glycoproteins tested were equally effective in protecting C57BL/10 mice against challenge by L. amazonensis. About 50% of the immunized animals were protected for six months
Molecular dynamics simulations of ligand-induced backbone conformational changes in the binding site of the periplasmic lysine-, arginine-, ornithine-binding protein
The periplasmic lysine-, arginine-, ornithine-binding protein (LAOBP) traps its ligands by a large hinge bending movement between two globular domains. The overall geometry of the binding site remains largely unchanged between the open (unliganded) and closed (liganded) forms, with only a small number of residues exhibiting limited movement of their side chains. However, in the case of the ornithine-bound structure, the backbone peptide bond between Asp11 and Thr12 undergoes a large rotation. Molecular dynamics simulations have been used to investigate the origin and mechanism of this backbone movement. Simulations allowing flexibility of a limited region and of the whole binding site, with and without bound ligands, suggest that this conformational change is induced by the binding of ornithine, leading to the stabilisation of an energetically favourable alternative conformation