487 research outputs found
Slow flows of yield stress fluids: complex spatio-temporal behaviour within a simple elasto-plastic model
A minimal athermal model for the flow of dense disordered materials is
proposed, based on two generic ingredients: local plastic events occuring above
a microscopic yield stress, and the non-local elastic release of the stress
these events induce in the material. A complex spatio-temporal rheological
behaviour results, with features in line with recent experimental observations.
At low shear rates, macroscopic flow actually originates from collective
correlated bursts of plastic events, taking place in dynamically generated
fragile zones. The related correlation length diverges algebraically at small
shear rates. In confined geometries bursts occur preferentially close to the
walls yielding an intermittent form of flow localization.Comment: 4 pages, 4 figure
Cloning, Expression, and Purification of a Nitric Oxide Synthase-Like Protein from Bacillus cereus
The nitric oxide synthase-like protein from Bacillus cereus (bcNOS) has been cloned, expressed, and characterized. This small hemeprotein (356 amino acids in length) has a mass of 43 kDa and forms a dimer. The recombinant protein showed similar spectral shifts to the mammalian NOS proteins and could bind the substrates L-arginine and NG-hydroxy-L-arginine as well as the ligand imidazole. Low levels of activity were recorded for the hydrogen peroxide-dependent oxidation of NG-hydroxy-L-arginine and L-arginine by bcNOS, while a reconstituted system with the rat neuronal NOS reductase domain showed no activity. The recombinant bcNOS protein adds to the complement of bacterial NOS-like proteins that are used for the investigation of the mechanism and function of NO in microorganisms
2-[18F]fluoro-2-deoxy-D-glucose positron emission tomography (FDG-PET) can identify chronic lymphocytic leukaemia (CLL) stage A et stage B patients
Purpose: There is no data in the literature concerning the utility of 2-[18F]fluoro-2-deoxy-d-glucose positron emission tomography (FDG-PET) in chronic lymphocytic leukaemia (CLL), except for the diagnosis of Richter\u27s transformations. The purpose of this study was to assess the potential role of FDG-PET in CLL stages A and B. Materials and methods: Thirty-five patients (61 ñ 9 years; 11 women, 24 men; 8B and 27A) have benefited of a FDG-PET scan at baseline, for example, before an eventual treatment. FDG-PET scans were analyzed visually and the maximum values of the Standardised Uptake Value (SUVmax) were measured in the main lymph nodes areas. The ability of FDG-PET to differentiate stages A and B patients was evaluated by Student\u27s tests and Receiver Operating Characteristics (ROC) analysis. Results: All patients with a normal FDG-PET (n = 18) were stages A. The remaining 17 patients (9A and 8B) showed hypermetabolisms in nodal areas above (n = 17) and below (n = 9) the diaphragm, and no visceral involvement. The lymph nodes hypermetabolisms were always bilateral, and of low intensity (†mediastinum; 9A), or of higher intensity (â„ liver, 8B). The SUVmax of stage B (n = 8) were significantly higher than those of the 27 stages A, in all lymph nodes areas except in mediastinum. The highest intensity of FDG uptake was observed in axillary area in stages B patients (SUVmax = 2.74 ñ 1.03). An axillary SUVmax of 1.33 is the most suitable value for the discrimination between stages A and B patients (ROC; AUC = 0.968; sensitivity 1.00; specificity 0.91). Conclusion: Lymph nodes hypermetabolisms are constant in the B stage, and more intense than in stage A. These anomalies are always bilateral, unlike what is observed in Richter\u27s transformation. The intensity of axillary lymph nodes FDG uptake can distinguish CLL stages A and B
Large magnetoresistance by Pauli blockade in hydrogenated graphene
We report the observation of a giant positive magnetoresistance in millimetre
scale hydrogenated graphene with magnetic field oriented in the plane of the
graphene sheet. A positive magnetoresistance in excess of 200\% at a
temperature of 300 mK was observed in this configuration, reverting to negative
magnetoresistance with the magnetic field oriented normal to the graphene
plane. We attribute the observed positive, in-plane, magnetoresistance to
Pauli-blockade of hopping conduction induced by spin polarization. Our work
shows that spin polarization in concert with electron-electron interaction can
play a dominant role in magnetotransport within an atomic monolayer.Comment: 6 pages, 3 figures, and supplemental informatio
UDP-glucuronosyltransferase UGT1A7 genetic polymorphisms in hepatocellular carcinoma: a differential impact according to seropositivity of HBV or HCV markers?
<p>Abstract</p> <p>Background:</p> <p>We conducted a case-control study to evaluate the role of UDP-glucuronosyltransferase 1A7 (UGT1A7) polymorphisms in the onset of hepatocellular carcinoma (HCC).</p> <p>Methods:</p> <p>The study included 165 patients with HCC, 134 with cirrhosis and 142 controls without liver disease, matched for age and hospital. All were men younger than 75 years. HCC and cirrhosis patients were stratified according to time since cirrhosis diagnosis.</p> <p>Results:</p> <p>We found a positive association between the UGT1A7*3/*3 genotype and HCC when the comparison was restricted to patients whose disease was of viral origin [OR = 3.4 (0.3â45)] but a negative association when it included only alcoholic patients [OR = 0.1 (0.02â0.6), p = 0.01].</p> <p>Conclusion:</p> <p>Our study shows that UGT1A7 may play a role in hepatocellular carcinogenesis and that this role may differ according to the primary cause of the cirrhosis.</p
Limited oxidative stress favors resistance to skeletal muscle atrophy in hibernating brown bears (Ursus Arctos)
publishedVersio
Lipidomics reveals seasonal shifts in a large-bodied hibernator, the brown bear
publishedVersio
Association between circulating levels of sex steroid hormones and esophageal adenocarcinoma in the FINBAR Study
Funding: The study was supported by NIH Intramural Research Program, National Cancer Institute; Cancer Focus Northern Ireland (formerly the Ulster Cancer Foundation); the Northern Ireland R&D office; and the Health Research Board, Ireland. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Peer reviewedPublisher PD
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