228 research outputs found
Imaging apparatus and controller for photographing products
The invention provides an all-in-one imaging apparatus for photographing products, particularly suitable for photographing fashion related products such as apparel products, fashion accessories or other life style products. The imaging apparatus comprising a table part, a portable controller for user interaction with the table part, and a storage for storing images. The table part comprises a substantially horizontal table surface for supporting the product, lights, a fixture for fixing a camera, a backlighting system below the table surface, and an embedded system comprising an embedded computer and a wireless communication controller. The embedded computer controls the camera, switches the backlighting system, wirelessly transmits a live stream from the camera to the portable controller, and wirelessly receives instructions from the portable controller
Electrical transport properties of bulk NiFe alloys and related spin-valve systems
Within the Kubo-Greenwood formalism we use the fully relativistic,
spin-polarized, screened Korringa-Kohn-Rostoker method together with the
coherent-potential approximation for layered systems to calculate the
resistivity for the permalloy series NiFe. We are able to
reproduce the variation of the resistivity across the entire series; notably
the discontinuous behavior in the vicinity of the structural phase transition
from bcc to fcc. The absolute values for the resistivity are within a factor of
two of the experimental data. Also the giant magnetoresistance of a series of
permalloy-based spin-valve structures is estimated; we are able to reproduce
the trends and values observed on prototypical spin-valve structures.Comment: 6 pages, ReVTeX + 4 figures (Encapsulated Postscript), submitted to
PR
Data for development reloaded: visual matrix techniques for the exploration and analysis of massive mobile phone data
Adaptive changes in sexual signalling in response to urbanization
Urbanization can cause species to adjust their sexual displays, because the effectiveness of mating signals is influenced by environmental conditions. Despite many examples that show that mating signals in urban conditions differ from those in rural conditions, we do not know whether these differences provide a combined reproductive and survival benefit to the urban phenotype. Here we show that male túngara frogs have increased the conspicuousness of their calls, which is under strong sexual and natural selection by signal receivers, as an adaptive response to city life. The urban phenotype consequently attracts more females than the forest phenotype, while avoiding the costs that are imposed by eavesdropping bats and midges, which we show are rare in urban areas. Finally, we show in a translocation experiment that urban frogs can reduce risk of predation and parasitism when moved to the forest, but that forest frogs do not increase their sexual attractiveness when moved to the city. Our findings thus reveal that urbanization can rapidly drive adaptive signal change via changes in both natural and sexual selection pressures
Whole-genome sequencing reveals two prolonged simultaneous outbreaks involving Pseudomonas aeruginosa high-risk strains ST111 and ST235 with resistance to quaternary ammonium compounds
Objective
Water-bearing systems are known as frequent Pseudomonas aeruginosa (PA) outbreak sources. However, many older buildings continue to have sanitary facilities in high-risk departments such as the ICU. We present two simultaneous prolonged multi-drug-resistant (MDR) PA outbreaks detected at the ICU of a pulmonology hospital, which were resolved by whole-genome sequencing (WGS).
Methods
Outbreak management and investigations were initiated in August 2019 after detecting two patients with nosocomial VIM-2-positive MDR PA. The investigations involved weekly patient screenings for four months and extensive environmental sampling for 15 months. All patient and environmental isolates were collected and analysed by WGS.
Results
From April to September 2019, we identified 10 patients with nosocomial MDR PA, including five VIM-2-positive strains. VIM-2-positive strains were also detected in nine sink drains, two toilets, and a cleaning bucket. WGS revealed that of 16 VIM-2-positive isolates, 14 were ST111 that carried qacE, or qacEΔ1 genes, whereas 13 isolates clustered (difference of ≤11 alleles by cgMLST). OXA-2 (two toilets), and OXA-2, OXA-74, PER-1 (two patients, three toilets) qacEΔ1-positive ST235 isolates dominated among VIM-2-negative isolates. The remaining seven PA strains were ST17, ST233, ST273, ST309 and ST446. Outbreak containment was achieved by replacing U-bends, and cleaning buckets, and switching from quaternary ammonium compounds (QUATs) to oxygen-releasing disinfectant products.
Conclusion
Comprehension and management of two simultaneous MDR PA outbreaks involving the high-risk strains ST111 and ST235 were facilitated by precise control due to identification of different outbreak sources per strain, and by the in-silico detection of high-level QUATs resistance in all isolates
Stromal Hedgehog signalling is downregulated in colon cancer and its restoration restrains tumour growth
A role for Hedgehog (Hh) signalling in the development of colorectal cancer
(CRC) has been proposed. In CRC and other solid tumours, Hh ligands are
upregulated; however, a specific Hh antagonist provided no benefit in a
clinical trial. Here we use Hh reporter mice to show that downstream Hh
activity is unexpectedly diminished in a mouse model of colitis-associated
colon cancer, and that downstream Hh signalling is restricted to the stroma.
Functionally, stroma-specific Hh activation in mice markedly reduces the
tumour load and blocks progression of advanced neoplasms, partly via the
modulation of BMP signalling and restriction of the colonic stem cell
signature. By contrast, attenuated Hh signalling accelerates colonic
tumourigenesis. In human CRC, downstream Hh activity is similarly reduced and
canonical Hh signalling remains predominantly paracrine. Our results suggest
that diminished downstream Hh signalling enhances CRC development, and that
stromal Hh activation can act as a colonic tumour suppressor
Fetal volume measurements with three dimensional ultrasound in the first trimester of pregnancy, related to pregnancy outcome, a prospective cohort study
Mutational Analyses of the Influenza A Virus Polymerase Subunit PA Reveal Distinct Functions Related and Unrelated to RNA Polymerase Activity
Influenza A viral polymerase is a heterotrimeric complex that consists of PA, PB1, and PB2 subunits. We previously reported that a di-codon substitution mutation (G507A-R508A), denoted J10, in the C-terminal half of PA had no apparent effect on viral RNA synthesis but prevented infectious virus production, indicating that PA may have a novel role independent of its polymerase activity. To further examine the roles of PA in the viral life cycle, we have now generated and characterized additional mutations in regions flanking the J10 site from residues 497 to 518. All tested di-codon mutations completely abolished or significantly reduced viral infectivity, but they did so through disparate mechanisms. Several showed effects resembling those of J10, in that the mutant polymerase supported normal levels of viral RNA synthesis but nonetheless failed to generate infectious viral particles. Others eliminated polymerase activity, in most cases by perturbing the normal nuclear localization of PA protein in cells. We also engineered single-codon mutations that were predicted to pack near the J10 site in the crystal structure of PA, and found that altering residues K378 or D478 each produced a J10-like phenotype. In further studies of J10 itself, we found that this mutation does not affect the formation and release of virion-like particles per se, but instead impairs the ability of those particles to incorporate each of the eight essential RNA segments (vRNAs) that make up the viral genome. Taken together, our analysis identifies mutations in the C-terminal region of PA that differentially affect at least three distinct activities: protein nuclear localization, viral RNA synthesis, and a trans-acting function that is required for efficient packaging of all eight vRNAs
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