528 research outputs found

    Graph Processing on GPUs:A Survey

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    Vremenski razlučeni fotoluminescentni spektri legure (AlxGa1−x)0.51In0.49P (x = 0.29)

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    Measurements of time-resolved photoluminescence (TRPL) spectra were made in a study of the optical properties of partially ordered quaternary (AlxGa1-x)0.51In0.49P (x=0.29) alloy. Both excitation-wavelength dependence of lifetime and excitation-intensity dependence of lifetime show a wide distribution of carriers. In TRPL spectra measured at 300 K, a blue-shift of photoluminescence (PL) peaks in (AlxGa1-x)0.51In0.49P is observed. The phenomenon is in agreement with the Z-shaped temperature dependence of the PL peak. Possible origins of the blue-shift and Z-shaped behaviour of PL peak are presented.Načinili smo vremenski-razlučena (VR) mjerenja fotoluminescentnih (FL) spektara radi istraživanja optičkih svojstava djelomično sređene četverokomponentne legure (AlxGa1−x)0.51In0.49P (x = 0.29). Obje ovisnosti vremena života, uzbuda – valna duljina i uzbuda – intenzitet pokazuju široku raspodjelu nositelja. VR FL spektri (AlxGa1−x)0.51In0.49P na 300 K pokazuju plavi pomak fotoluminescentnih linija. Ta je pojava u skladu s temperaturnom ovisnošću FL vrha u vidu slova Z. Raspravljaju se mogući uzroci plavog pomaka i Z-ovisnosti FL vrha

    5-Carb­oxy-2-isopropyl-1H-imidazol-3-ium-4-carboxyl­ate monohydrate

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    In the title compound, C8H10N2O4·H2O, the imidazole N atom is protonated and one of the carboxyl­ate groups is deprotoned, forming a zwitterion. An intra­molecular O—H⋯O hydrogen bond occurs. The crystal structure is stabilized by inter­molecular N—H⋯O and O—H⋯O hydrogen bonds. In addition, inter­molecular N—H⋯O and O—H⋯O hydrogen bonds link the mol­ecules into two-dimensional networks parallel to (10)

    Haplotype of gene Nedd4 binding protein 2 associated with sporadic nasopharyngeal carcinoma in the Southern Chinese population

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    <p>Abstract</p> <p>Background</p> <p>Bcl-3 as an oncoprotein is overexpressed in nasopharyngeal carcinoma (NPC). Nedd4 binding protein 2 (N4BP2), which is located in the NPC susceptibility locus, is a Bcl-3 binding protein. This study is aimed to explore the association between N4BP2 genetic polymorphism and the risk of NPC.</p> <p>Methods</p> <p>We performed a hospital-based case-control study, including 531 sporadic NPC and 480 cancer-free control subjects from southern China. PCR-sequencing was carried out on Exons, promoter region and nearby introns of the N4BP2 gene. The expression pattern of N4BP2 and Bcl-3 was also analyzed.</p> <p>Results</p> <p>We observed a statistically significant difference in haplotype blocks ATTA and GTTG between cases and controls. In addition, three novel SNPs were identified, two of which were in exons (loc123-e3l-snp2, position 39868005, A/G, Met171Val; RS17511668-SNP2, position 39926432, G/A, Glu118Lys), and one was in the intron6 (RS794001-SNP1, position 39944127, T/G). Moreover, N4BP2 was at higher levels in a majority of tumor tissues examined, relative to paired normal tissues.</p> <p>Conclusion</p> <p>These data suggest that haplotype blocks ATTA and GTTG of N4BP2 is correlation with the risk of sporadic nasopharyngeal carcinoma in the Southern Chinese population and N4BP2 has a potential role in the development of NPC.</p

    The Online Data Quality Monitoring System at BESIII

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    The online Data Quality Monitoring (DQM) plays an important role in the data taking process of HEP experiments. BESIII DQM samples data from online data flow, reconstructs them with offline reconstruction software, and automatically analyzes the reconstructed data with user-defined algorithms. The DQM software is a scalable distributed system. The monitored results are gathered and displayed in various formats, which provides the shifter with current run information that can be used to find problems early. This paper gives an overview of DQM system at BESIII.Comment: Already submit to Chinese Physics

    catena-Poly[[(5-carb­oxy-2H-1,2,3-triazole-4-carboxyl­ato-κ2 N 3,O 4)sodium]-di-μ-aqua-κ4 O:O]

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    In the title coordination polymer, [Na(C4H2N3O4)(H2O)2]n, the NaI atom is six-coordinated by one O atom and one N atom from a 2H-1,2,3-triazole-4-carb­oxy-5-carboxyl­ate ligand and four O atoms from four water mol­ecules, forming a distorted octa­hedal geometry. The NaI atoms are bridged by water mol­ecules into a chain structure along [100]. Inter­molecular N—H⋯O, O—H⋯N and O—H⋯O hydrogen bonds connect the chains. An intra­molecular O—H⋯O hydrogen bond between the carboxyl­ate groups is observed

    The molecular basis of the genesis of basal tone in internal anal sphincter

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    Smooth muscle sphincters exhibit basal tone and control passage of contents through organs such as the gastrointestinal tract; loss of this tone leads to disorders such as faecal incontinence. However, the molecular mechanisms underlying this tone remain unknown. Here, we show that deletion of myosin light-chain kinases (MLCK) in the smooth muscle cells from internal anal sphincter (IAS-SMCs) abolishes basal tone, impairing defecation. Pharmacological regulation of ryanodine receptors (RyRs), L-type voltage-dependent Ca(2+) channels (VDCCs) or TMEM16A Ca(2+)-activated Cl(-) channels significantly changes global cytosolic Ca(2+) concentration ([Ca(2+)]i) and the tone. TMEM16A deletion in IAS-SMCs abolishes the effects of modulators for TMEM16A or VDCCs on a RyR-mediated rise in global [Ca(2+)]i and impairs the tone and defecation. Hence, MLCK activation in IAS-SMCs caused by a global rise in [Ca(2+)]i via a RyR-TMEM16A-VDCC signalling module sets the basal tone. Targeting this module may lead to new treatments for diseases like faecal incontinence
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