3,117 research outputs found
Oxygen Moment Formation and Canting in Li2CuO2
The possibilities of oxygen moment formation and canting in the quasi-1D
cuprate Li2CuO2 are investigated using single crystal neutron diffraction at 2
K. The observed magnetic intensities could not be explained without the
inclusion of a large ordered oxygen moment of 0.11(1) Bohr magnetons.
Least-squares refinement of the magnetic structure of Li2CuO2 in combination
with a spin-density Patterson analysis shows that the magnetization densities
of the Cu and O atoms are highly aspherical, forming quasi-1D ribbons of
localised Cu and O moments. Magnetic structure refinements and low-field
magnetization measurements both suggest that the magnetic structure of Li2CuO2
at 2 K may be canted. A possible model for the canted configuration is
proposed.Comment: 10 pages, 8 figures (screen resolution
Equity Must Accompany Economic Growth for Good Health
K. Srinath Reddy discusses a new research study by S. V. Subramanian and colleagues that found no strong evidence of recent economic growth in India being associated with a reduction in child undernutrition
Blood ethanol concentrations during and following constant‐rate intravenous infusion of alcohol
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/117025/1/cpt1976192213.pd
Thin film interference in the optomechanical response of micromechanical silicon cantilevers
The mechanical response of uncoated silicon microcantilevers is shown to modulate as a function of incident wavelength. Cantilever motion is measured interferometrically, using phase sensitive detection in response to a mechanically chopped excitation source. Thin film interference modeling shows that the fraction of absorbed light within the cantilever varies periodically over the range of 450-1000 nm, in excellent agreement with the measurements. The results show that the optomechanical responsivity of these cantilevers can be tuned due to the effect via an appropriate selection of incident wavelength, incidence angle, lever thickness, and optical constants of the lever. (c) 2006 American Institute of Physics
Timing and documentation of key events in neonatal resuscitation
Only a minority of babies require extended resuscitation at birth. Resuscitations concerning babies who die or who survive with adverse outcomes are increasingly subject to medicolegal scrutiny. Our aim was to describe real-life timings of key resuscitation events observed in a historical series of newborns who required full resuscitation at birth. Twenty-seven babies born in our centre over a 10-year period had an Apgar score of 0 at 1 min and required full resuscitation. The median (95% confidence interval) postnatal age at achieving key events were commencing cardiac compressions, 2.0 (1.5–4.0) min; endotracheal intubation, 3.8 (2.0–6.0) min; umbilical venous catheterisation 9.0 (7.5–12.0) min; and administration of first adrenaline dose 10.0 (8.0–14.0) min. Conclusion: The wide range of timings presented from real-life cases may prove useful to clinicians involved in medical negligence claims and provide a baseline for quality improvements in resuscitation training
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Modeling Progressive Fibrosis with Pluripotent Stem Cells Identifies an Anti-fibrotic Small Molecule.
Progressive organ fibrosis accounts for one-third of all deaths worldwide, yet preclinical models that mimic the complex, progressive nature of the disease are lacking, and hence, there are no curative therapies. Progressive fibrosis across organs shares common cellular and molecular pathways involving chronic injury, inflammation, and aberrant repair resulting in deposition of extracellular matrix, organ remodeling, and ultimately organ failure. We describe the generation and characterization of an in vitro progressive fibrosis model that uses cell types derived from induced pluripotent stem cells. Our model produces endogenous activated transforming growth factor β (TGF-β) and contains activated fibroblastic aggregates that progressively increase in size and stiffness with activation of known fibrotic molecular and cellular changes. We used this model as a phenotypic drug discovery platform for modulators of fibrosis. We validated this platform by identifying a compound that promotes resolution of fibrosis in in vivo and ex vivo models of ocular and lung fibrosis
Are language production problems apparent in adults who no longer meet diagnostic criteria for attention-deficit/hyperactivity disorder?
In this study, we examined sentence production in a sample of adults (N = 21) who had had attention-deficit/hyperactivity disorder (ADHD) as children, but as adults no longer met DSM-IV diagnostic criteria (APA, 2000). This “remitted” group was assessed on a sentence production task. On each trial, participants saw two objects and a verb. Their task was to construct a sentence using the objects as arguments of the verb. Results showed more ungrammatical and disfluent utterances with one particular type of verb (i.e., participle). In a second set of analyses, we compared the remitted group to both control participants and a “persistent” group, who had ADHD as children and as adults. Results showed that remitters were more likely to produce ungrammatical utterances and to make repair disfluencies compared to controls, and they patterned more similarly to ADHD participants. Conclusions focus on language output in remitted ADHD, and the role of executive functions in language production
Anti-PD-1 immunotherapy leads to tuberculosis reactivation via dysregulation of TNF-alpha
Previously, we developed a 3-dimensional cell culture model of human tuberculosis (TB) and demonstrated its potential to interrogate the host-pathogen interaction (Tezera et al., 2017a). Here, we use the model to investigate mechanisms whereby immune checkpoint therapy for cancer paradoxically activates TB infection. In patients, PD-1 is expressed in Mycobacterium tuberculosis (Mtb)-infected lung tissue but is absent in areas of immunopathology. In the microsphere model, PD-1 ligands are up-regulated by infection, and the PD-1/PD-L1 axis is further induced by hypoxia. Inhibition of PD-1 signalling increases Mtb growth, and augments cytokine secretion. TNF-a is responsible for accelerated Mtb growth, and TNF-a neutralisation reverses augmented Mtb growth caused by anti-PD-1 treatment. In human TB, pulmonary TNF-a immunoreactivity is increased and circulating PD-1 expression negatively correlates with sputum TNF-a concentrations. Together, our findings demonstrate that PD-1 regulates the immune response in TB, and inhibition of PD-1 accelerates Mtb growth via excessive TNF-a secretion.</p
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