784 research outputs found

    Design-for-test structure to facilitate test vector application with low performance loss in non-test mode.

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    A switching based circuit is described which allows application of voltage test vectors to internal nodes of a chip without the problem of backdriving. The new circuit has low impact on the performance of an analogue circuit in terms of loss of bandwidth and allows simple application of analogue test voltages into internal nodes. The circuit described facilitates implementation of the forthcoming IEEE 1149.4 DfT philosophy [1]

    Self-assembling nanoparticles containing dexamethasone as a novel therapy in allergic airways inflammation.

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    Nanocarriers can deliver a wide variety of drugs, target them to sites of interest, and protect them from degradation and inactivation by the body. They have the capacity to improve drug action and decrease undesirable systemic effects. We have previously developed a well-defined non-toxic PEG-dendritic block telodendrimer for successful delivery of chemotherapeutics agents and, in these studies, we apply this technology for therapeutic development in asthma. In these proof-of-concept experiments, we hypothesized that dexamethasone contained in self-assembling nanoparticles (Dex-NP) and delivered systemically would target the lung and decrease allergic lung inflammation and airways hyper-responsiveness to a greater degree than equivalent doses of dexamethasone (Dex) alone. We found that ovalbumin (Ova)-exposed mice treated with Dex-NP had significantly fewer total cells (2.78 ± 0.44 × 10(5) (n = 18) vs. 5.98 ± 1.3 × 10(5) (n = 13), P<0.05) and eosinophils (1.09 ± 0.28 × 10(5) (n = 18) vs. 2.94 ± 0.6 × 10(5) (n = 12), p<0.05) in the lung lavage than Ova-exposed mice alone. Also, lower levels of the inflammatory cytokines IL-4 (3.43 ± 1.2 (n = 11) vs. 8.56 ± 2.1 (n = 8) pg/ml, p<0.05) and MCP-1 (13.1 ± 3.6 (n = 8) vs. 28.8 ± 8.7 (n = 10) pg/ml, p<0.05) were found in lungs of the Dex-NP compared to control, and they were not lower in the Dex alone group. In addition, respiratory system resistance was lower in the Dex-NP compared to the other Ova-exposed groups suggesting a better therapeutic effect on airways hyperresponsiveness. Taken together, these findings from early-stage drug development studies suggest that the encapsulation and protection of anti-inflammatory agents such as corticosteroids in nanoparticle formulations can improve efficacy. Further development of novel drugs in nanoparticles is warranted to explore potential treatments for chronic inflammatory diseases such as asthma

    Nucleon Electromagnetic Form Factors from Lattice QCD using 2+1 Flavor Domain Wall Fermions on Fine Lattices and Chiral Perturbation Theory

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    We present a high-statistics calculation of nucleon electromagnetic form factors in Nf=2+1N_f=2+1 lattice QCD using domain wall quarks on fine lattices, to attain a new level of precision in systematic and statistical errors. Our calculations use 323×6432^3 \times 64 lattices with lattice spacing a=0.084 fm for pion masses of 297, 355, and 403 MeV, and we perform an overdetermined analysis using on the order of 3600 to 7000 measurements to calculate nucleon electric and magnetic form factors up to Q2≈Q^2 \approx 1.05 GeV2^2. Results are shown to be consistent with those obtained using valence domain wall quarks with improved staggered sea quarks, and using coarse domain wall lattices. We determine the isovector Dirac radius r1vr_1^v, Pauli radius r2vr_2^v and anomalous magnetic moment Îșv\kappa_v. We also determine connected contributions to the corresponding isoscalar observables. We extrapolate these observables to the physical pion mass using two different formulations of two-flavor chiral effective field theory at one loop: the heavy baryon Small Scale Expansion (SSE) and covariant baryon chiral perturbation theory. The isovector results and the connected contributions to the isoscalar results are compared with experiment, and the need for calculations at smaller pion masses is discussed.Comment: 44 pages, 40 figure

    Nucleon structure from mixed action calculations using 2+1 flavors of asqtad sea and domain wall valence fermions

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    We present high statistics results for the structure of the nucleon from a mixed-action calculation using 2+1 flavors of asqtad sea and domain wall valence fermions. We perform extrapolations of our data based on different chiral effective field theory schemes and compare our results with available information from phenomenology. We discuss vector and axial form factors of the nucleon, moments of generalized parton distributions, including moments of forward parton distributions, and implications for the decomposition of the nucleon spin.Comment: 68 pages, 47 figures. Main revision points: improved discussion of chiral fits and systematic uncertainties, several minor refinements. Accepted for publication in Phys.Rev.

    Quantitative basic residue requirements in the cleavage-activation site of the fusion glycoprotein as a determinant of virulence for Newcastle disease virus

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    Newcastle disease virus exhibits a wide range of pathogenicity and virulence which, as with all paramyxoviruses, is directly related to the cleavability of a precursor (F0) of the fusion glycoprotein by cellular proteases. Sequence analyses of the cleavage site of several virulent and avirulent isolates of the Newcastle disease virus serotype reveal a correlation between virulence or pathogenicity and a high content of basic amino acid residues at the cleavage site. A similar correlation has been seen for other paramyxoviruses

    Nucleon Generalized Parton Distributions from Full Lattice QCD

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    We present a comprehensive study of the lowest moments of nucleon generalized parton distributions in N_f=2+1 lattice QCD using domain wall valence quarks and improved staggered sea quarks. Our investigation includes helicity dependent and independent generalized parton distributions for pion masses as low as 350 MeV and volumes as large as (3.5 fm)^3, for a lattice spacing of 0.124 fm. We use perturbative renormalization at one-loop level with an improvement based on the non-perturbative renormalization factor for the axial vector current, and only connected diagrams are included in the isosinglet channel.Comment: 40 pages, 49 figures; Revised chiral extrapolations in sections A-K, main conclusions unchange

    Brane universes tested by supernovae

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    We discuss observational constrains coming from supernovae Ia \cite{Perlmutter99} imposed on the behaviour of the Randall-Sundrum models. In the case of dust matter on the brane, the difference between the best-fit general relativistic model with a Λ\Lambda-term \cite{Perlmutter99} and the best-fit brane models becomes detectable for redshifts z>0.6z > 0.6. It is interesting that brane models predict brighter galaxies for such redshifts which is in agreement with the measurement of the z=1.7z = 1.7 supernova \cite{Riess01} and with the New Data from the High Z Supernovae Search Team \cite{schmit02}. We also demonstrate that the fit to supernovae data can also be obtained, if we admit the "super-negative" dark energy p=−(4/3)ϱp = - (4/3) \varrho on the brane, where the dark energy in a way mimics the influence of the cosmological constant. It also appears that the dark energy enlarges the age of the universe which is demanded in cosmology. Finally, we propose to check for dark radiation and brane tension by the application of the angular diameter of galaxies minimum value test.Comment: 4 pages, 5 figures, REVTEX4, amended versio
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