407,733 research outputs found

    On fully nonlinear CR invariant equations on the Heisenberg group

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    AbstractIn this paper we provide a characterization of second order fully nonlinear CR invariant equations on the Heisenberg group, which is the analogue in the CR setting of the result proved in the Euclidean setting by A. Li and the first author in Li and Li (2003) [21]. We also prove a comparison principle for solutions of second order fully nonlinear CR invariant equations defined on bounded domains of the Heisenberg group and a comparison principle for solutions of a family of second order fully nonlinear equations on a punctured ball

    Corrigendum to “Reliability assessment of generic geared wind turbines by GTST-MLD model and Monte Carlo simulation” (Renewable Energy (2015) 83 (222–233), (S0960148115003158), (10.1016/j.renene.2015.04.035))

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    The authors regret that the Order of Authors in this article published in November 2015 is incorrect. Thus, the objective of this Corrigendum is to re-establish the originally agreed Order of Authors, as described below. Order of Authors from published Article: Yan-Fu Li, PhD; Sebastien Valla; Enrico Zio, PhD. Corrected Order of Authors to implement with this Corrigendum: Sebastien Valla, Yan-Fu Li, PhD; Enrico Zio, PhD. The Corresponding author to contact for these changes are the Primary Author, Sebastien Valla (email below). The authors would like to apologise for any inconvenience caused

    On the in-situ aqueous stability of an Mg-Li-(Al-Y-Zr) alloy: Role of Li

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    The aqueous stability of a corrosion resistant Mg-Li(-Al-Y-Zr)-alloy was investigated by combining in-situ confocal Raman Microscopy, Atomic Emission SpectroElectroChemistry, ex-situ Photoluminiscence Spectroscopy, Auger Electron Spectroscopy and Glow Discharge Optical Emission Spectroscopy. Li and Mg dissolved from visually intact anodic areas, leaving a Li-depleted metallic layer under approximately 100 nm thick Li-doped MgO. The transformation MgO→Mg(OH)2 was inhibited. Li2[Al2(OH)6]2·CO3·nH2O, LiAlO2, Y2O3 and Mg(OH)2 accumulated locally around active cathodic sites. New corrosion mechanism is proposed, which associates the improved corrosion resistance of Mg-Li alloys with an enhanced chemical stability and modified catalytic activity of MgO in presence of Li+

    Characterisation of Li in the surface film of a corrosion resistant Mg-Li(-Al-Y-Zr) alloy

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    Characterisation of Li in the surface film of a corrosion resistant Mg-Li(-Al-Y-Zr) allo

    Characterization of an alternatively spliced G(M2) activator protein, G(M2A) protein - An activator protein which stimulates the enzymatic hydrolysis of N-acetylneuraminic acid, but not N-acetylgalactosamine, from G(M2)

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    G(M2) activator protein is a protein cofactor which stimulates the enzymatic hydrolysis of both GalNAc and NeuAc from G(M2). We have previously isolated two cDNA clones, G(M2) activator cDNA and G(M2A) cDNA, for human G(M2) activator protein (Nagarajan, S., Chen, H.-C., Li, S.-C., Li, Y.-T., and Lockyer, J. M. (1992) Biochem. J. 282, 807-813). G(M2A) mRNA is an RNA alternative splicing product that contains exons 1, 2, 3, and intron 3 of the genomic DNA sequence of G(M2) activator protein (Klima, H., Tanaka, A., Schnabel, D., Nakano, T., Schroder, M., Suzuki, K., and Sandhoff, K. (1991) FEES Left. 289, 260-264). G(M2A) cDNA encodes a protein (G(M2A) protein) containing 1-109 of the 160 amino acids of human G(M2) activator protein, plus a tripeptide (VST) encoded by intron 3 at the COOH terminus. Thus, G(M2A) protein can be regarded as a form (truncated version) of G(M2) activator protein. We have expressed G(M2A) cDNA in Escherichia coli using pT7-7 as the vector. The recombinant G(M2A) protein was purified to an electrophoretically homogeneous form and was found to stimulate the hydrolysis of NeuAc from G(M2) by clostridial sialidase, but not the hydrolysis of GalNAc from G(M2) by beta-hexosaminidase A. Like G(M2) activator protein, G(M2A) protein also specifically recognized the terminal G(M2) epitope in GalNAc-GD1a and stimulated the hydrolysis of only the external NeuAc from this ganglioside by clostridial sialidase. These results enabled us to discern the enzymatic hydrolyses of GalNAc and NeuAc from the G(M2) epitope and established that the NeuAc recognition domain of G(M2) activator protein is located within amino acids 1-109. The presence of G(M2A) mRNA in human tissues and the selective stimulation of NeuAc hydrolysis by G(M2A) protein indicate that this activator protein may be involved in the catabolism of G(M2) through the asialo-G(M2) pathway

    TiF<sub>3</sub> catalyzed MgH<sub>2</sub> as a Li/Na ion battery anode

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    MgH2 has been considered as a potential anode material for Li ion batteries due to its low cost and high theoretical capacity. However, it suffers from low electronic conductivity and slow kinetics for hydrogen sorption at room temperature that results in poor reversibility, cycling stability and rate capability for Li ion storage. This work presents a MgH2–TiF3@CNT based Li ion battery anode manufactured via a conventional slurry based method. Working with a liquid electrolyte at room temperature, it achieves a high capacity retention of 543 mAh g−1 in 70 cycles at 0.2 C and an improved rate capability, thanks to the improved hydrogen sorption kinetics with the presence of catalytic TiF3. Meanwhile, the first realization of Na ion uptake in MgH2 has been evidenced in experiments.Accepted Author ManuscriptChemE/Materials for Energy Conversion and Storag

    SPECIFIC RECOGNITION OF N-ACETYLNEURAMINIC ACID IN THE G(M2) EPITOPE BY HUMAN G(M2) ACTIVATOR PROTEIN

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    G(M2) Activator is a low molecular weight protein cofactor that stimulates the enzymatic conversion of G(M2) into G(M3) by human beta-hexosaminidase A and also the conversion of G(M2) into G(A2) by clostridial sialidase (Wu, Y.-Y., Lockyer, J. M., Sugiyama, E., Pavlova, N. V., Li, Y.-T., and Li, S.- C. (1994) J. Biol. Chem. 269, 16276-16283). Among the five known activator proteins for the enzymatic hydrolysis of glycosphingolipids, only G(M2) activator is effective in stimulating the hydrolysis of G(M2). However, the mechanism of action of G(M2) activator is still not well understood, Using a unique disialosylganglioside, GalNAc-G(D1a), as the substrate, we were able to show that in the presence of G(M2) activator, GalNAc-G(D1a) was specifically converted into GalNAc-G(M1a) by clostridial sialidase, while in the presence of saposin B, a nonspecific activator protein, GalNAc-G(D1a) was converted into both GalNAc-G(M1a) and GalNAc-G(M1b). individual products generated from GalNAc-G(D1a) by clostridial sialidase were identified by thin layer chromatography, negative secondary ion mass spectrometry, and immunostaining with a monoclonal IgM that recognizes the G(M2) epitope. Our results clearly show that G(M2) activator recognizes the G(M2) epitope in GalNAc-G(D1a). Thus, G(M2) activator may interact with the trisaccharide structure of the G(M2) epitope and render the GalNAc and NeuAc residues accessible to beta-hexosaminidase A and sialidase, respectively

    On conformally invariant equations on Rn

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    Abstract. In this paper we provide a complete characterization of fully nonlinear conformally invariant differential operators of any integer order on Rn, which extends the result proved for operators of the second order by A. Li and the first named author in [38]. In particular we prove existence and uniqueness of a family of tensors (suitably invariant under Möbius transformations) which are the basic building blocks that appear in the definition of all conformally invariant differential operators on Rn. We also explicitly compute the tensors that are related to operators of order up to four. 1. Introduction an

    Characterisation of Li in the surface film of a corrosion resistant Mg-Li(-Al-Y-Zr) alloy

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    The surface film formed upon Mg-Li(-Al-Y-Zr) following aqueous immersion and air-exposure was investigated. This alloy (which contains 30.3 at. % Li) possesses a body-centred cubic (bcc) crystal structure and has been reported as being corrosion resistant. It was determined that the principal components of the surface film were Li2CO3 and Mg(OH)2 as characterised by grazing incidence X-ray diffraction (GIXRD). Hexagonal close-packed (hcp) grains near the alloy surface were detected by GIXRD and selected area electron diffraction (SAED). The spatial distribution of Li and Mg in the surface film was characterised by electron energy loss spectroscopy (EELS) and the distribution of other major elements in the alloy was characterised by scanning transmission electron microscopy (STEM) and energy dispersive X-ray spectroscopy (EDXS). It was observed that Li was distributed throughout the alloy surface film and with an elevated concentration in the so-called outer layer
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