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Träfflista för sökning "WFRF:(Zheng Zheng) srt2:(2005-2009)"

Sökning: WFRF:(Zheng Zheng) > (2005-2009)

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1.
  • Ablikim, M., et al. (författare)
  • Measurements of (XcJ)-> K+K-K+K- decays
  • 2006
  • Ingår i: Physics Letters B. - : Elsevier BV. - 0370-2693 .- 1873-2445. ; 642:3, s. 197-202
  • Tidskriftsartikel (refereegranskat)abstract
    • Using 14M psi(2S) events taken with the BESII detector, chi(cJ) -> 2(K+K-) decays are studied. For the four-kaon final state, the branching fractions are B(chi(c0,1,2) ->.2(K+K-)) = (3.48 +/- 0.23 +/- 0.47) x 10(-3), (0.70 +/- 0.13 +/- 0.10) x 10(-3), and (2.17 +/- 0.20 +/- 0.31) x 10(-3). For the phi K+K- final state, the branching fractions, which are measured for the first time, are B(chi(c0,1,2) -> phi K+K-) = (1.03 +/- 0.22 +/- 0.15) x 10(-3), (0.46 +/- 0.16 +/- 0.06) x 10(-3), and (1.67 +/- 0.26 +/- 0.24) x 10(-4). For the phi phi final state, B(chi(c0,2) -> phi phi) = (0.94 +/- 0.21 +/- 0.13) x 10(-3) and (1.70 +/- 0.30 +/- 0.25) x 10(-3).
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2.
  • Zheng, L. R., et al. (författare)
  • Network Structured SnO2/ZnO Heterojunction Nanocatalyst with High Photocatalytic Activity
  • 2009
  • Ingår i: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 48:5, s. 1819-1825
  • Tidskriftsartikel (refereegranskat)abstract
    • A network-structured SnO2/ZnO heterojunction nanocatalyst with high photocatalytic activity was successfully synthesized through a simple two-step solvothermal method. The as-synthesized samples are characterized by X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, scanning electron microscopy, N-2 physical adsorption, and UV-vis spectroscopy. The results show that the SnO2/ZnO sample with a molar ratio of Sn/Zn = 1 is a mesoporous composite material composed of SnO2 and ZnO. The photocatalytic activity of SnO2/ZnO heterojunction nanocatalysts for the degradation of methyl orange is much higher than those of solvothermally synthesized SnO2 and ZnO samples, which can be attributed to the SnO2-ZnO heterojunction, the pore structure, and higher Brunauer-Emmeff-Teller (BET) surface area of the sample: (1) The SnO2-ZnO heterojunction improves the separation of photogenerated electron-hole pairs due to the potential energy differences between SnO2 and ZnO, thus enhancing the photocatalytic activity. (2) The SnO2/ZnO sample might possess more surface reaction sites and adsorb and transport more dye molecules due to the higher BET surface area and many pore channels, also leading to higher photocatalytic activity.
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3.
  • Birney, Ewan, et al. (författare)
  • Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
  • 2007
  • Ingår i: Nature. - : Springer Science and Business Media LLC. - 0028-0836 .- 1476-4687. ; 447:7146, s. 799-816
  • Tidskriftsartikel (refereegranskat)abstract
    • We report the generation and analysis of functional data from multiple, diverse experiments performed on a targeted 1% of the human genome as part of the pilot phase of the ENCODE Project. These data have been further integrated and augmented by a number of evolutionary and computational analyses. Together, our results advance the collective knowledge about human genome function in several major areas. First, our studies provide convincing evidence that the genome is pervasively transcribed, such that the majority of its bases can be found in primary transcripts, including non-protein-coding transcripts, and those that extensively overlap one another. Second, systematic examination of transcriptional regulation has yielded new understanding about transcription start sites, including their relationship to specific regulatory sequences and features of chromatin accessibility and histone modification. Third, a more sophisticated view of chromatin structure has emerged, including its inter-relationship with DNA replication and transcriptional regulation. Finally, integration of these new sources of information, in particular with respect to mammalian evolution based on inter- and intra-species sequence comparisons, has yielded new mechanistic and evolutionary insights concerning the functional landscape of the human genome. Together, these studies are defining a path for pursuit of a more comprehensive characterization of human genome function.
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4.
  • Emanuelsson, Olof, et al. (författare)
  • Assessing the performance of different high-density tiling microarray strategies for mapping transcribed regions of the human genome.
  • 2007
  • Ingår i: Genome Research. - : Cold Spring Harbor Laboratory. - 1088-9051 .- 1549-5469. ; 17:6, s. 886-897
  • Tidskriftsartikel (refereegranskat)abstract
    • Genomic tiling microarrays have become a popular tool for interrogating the transcriptional activity of large regions of the genome in an unbiased fashion. There are several key parameters associated with each tiling experiment (e.g., experimental protocols and genomic tiling density). Here, we assess the role of these parameters as they are manifest in different tiling-array platforms used for transcription mapping. First, we analyze how a number of published tiling-array experiments agree with established gene annotation on human chromosome 22. We observe that the transcription detected from high-density arrays correlates substantially better with annotation than that from other array types. Next, we analyze the transcription-mapping performance of the two main high-density oligonucleotide array platforms in the ENCODE regions of the human genome. We hybridize identical biological samples and develop several ways of scoring the arrays and segmenting the genome into transcribed and nontranscribed regions, with the aim of making the platforms most comparable to each other. Finally, we develop a platform comparison approach based on agreement with known annotation. Overall, we find that the performance improves with more data points per locus, coupled with statistical scoring approaches that properly take advantage of this, where this larger number of data points arises from higher genomic tiling density and the use of replicate arrays and mismatches. While we do find significant differences in the performance of the two high-density platforms, we also find that they complement each other to some extent. Finally, our experiments reveal a significant amount of novel transcription outside of known genes, and an appreciable sample of this was validated by independent experiments.
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5.
  • Hsu, Fang-Chi, et al. (författare)
  • A novel prostate cancer susceptibility locus at 19q13.
  • 2009
  • Ingår i: Cancer research. - 1538-7445. ; 69:7, s. 2720-3
  • Tidskriftsartikel (refereegranskat)abstract
    • A two-stage genome-wide association study (GWAS) of the Cancer Genetic Markers of Susceptibility (CGEMS) initiative identified single nucleotide polymorphisms (SNP) in 150 regions across the genome that may be associated with prostate cancer (PCa) risk. We filtered these results to identify 43 independent SNPs where the frequency of the risk allele was consistently higher in cases than in controls in each of the five CGEMS study populations. Genotype information for 22 of these 43 SNPs was obtained either directly by genotyping or indirectly by imputation in our PCa GWAS of 500 cases and 500 controls selected from a population-based case-control study in Sweden [Cancer of the Prostate in Sweden (CAPS)]. Two of these 22 SNPs were significantly associated with PCa risk (P<0.05). We then genotyped these two SNPs in the remaining cases (n=2,393) and controls (n=1,222) from CAPS and found that rs887391 at 19q13 was highly associated with PCa risk (P=9.4 x 10(-4)). A similar trend of association was found for this SNP in a case-control study from Johns Hopkins Hospital (JHH), albeit the result was not statistically significant. Altogether, the frequency of the risk allele of rs887391 was consistently higher in cases than controls among each of seven study populations examined, with an overall P=3.2 x 10(-7) from a combined allelic test. A fine-mapping study in a 110-kb region at 19q13 among CAPS and JHH study populations revealed that rs887391 was the most strongly associated SNP in the region. Additional confirmation studies of this region are warranted.
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6.
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7.
  • Sun, Jielin, et al. (författare)
  • Sequence variants at 22q13 are associated with prostate cancer risk.
  • 2009
  • Ingår i: Cancer research. - 1538-7445. ; 69:1, s. 10-5
  • Tidskriftsartikel (refereegranskat)abstract
    • To search for genetic variants that are associated with prostate cancer risk in the genome, we combined the data from our genome-wide association study (GWAS) in a population-based case-control study in Sweden with publicly available GWAS data from the Cancer Genetic Markers of Susceptibility (CGEMS) study. We limited the cases to those with aggressive disease in an attempt to identify risk variants that are associated with this most clinically relevant form of the disease. Among the most likely candidate single nucleotide polymorphisms (SNP) identified from the two GWAS, we sequentially confirmed one SNP at 22q13 in two independent study populations: the remaining subjects in Cancer of the Prostate in Sweden and a hospital-based case-control study at Johns Hopkins Hospital. Association of aggressive prostate cancer with the SNP at 22q13 was also observed in the publicly available data of four additional study populations from the second stage of the CGEMS study. In all seven study populations examined, the frequency of allele "C" of rs9623117 at 22q13 was consistently higher in aggressive cases than in controls. The combined allelic test was highly significant, with P = 5.0 x 10(-7). The odds ratio (OR) of allele C for aggressive prostate cancer was estimated to be 1.18 [95% confidence interval (95% CI), 1.11-1.26]. However, the SNP was also associated with nonaggressive prostate cancer, with an estimated OR of 1.11 (95% CI, 1.04-1.19; P = 0.004). The risk-associated variants are located within the genomic region of TNRC6B, a gene involved in miRNA-mediated mRNA degradation. Additional studies are warranted to further confirm the association.
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8.
  • Zhang, Fengling, et al. (författare)
  • Ordered mesoporous Ag-TiO2-KIT-6 heterostructure: synthesis, characterization and photocatalysis
  • 2009
  • Ingår i: Journal of Materials Chemistry. - : Royal Society of Chemistry (RSC). - 1364-5501 .- 0959-9428. ; 19:18, s. 2771-2777
  • Tidskriftsartikel (refereegranskat)abstract
    • Ordered mesoporous Ag-TiO2-KIT-6 heterostructured nanocrystals were successfully synthesized by a template-based method, where a layer of TiO2 and Ag2O nanoparticles were deposited on cubic (Ia3d) silica (KIT-6) in an orderly manner; at the same time, the formed Ag2O nanoparticles were photolyzed to metallic Ag nanoparticles. Our results show that Ag-TiO2-KIT-6 is an ordered mesoporous composite material, which is composed of Ag-TiO2 heterostructures and the amorphous KIT-6 template. In addition, Ag-TiO2-KIT-6 possesses the highest photocatalytic activity among the as-synthesized photocatalysts, which can be attributed to the Ag-TiO2 heterojunctions and the excellent texture: (1) Ag-TiO2 heterojunctions improve the separation of photogenerated electron-hole pairs due to the potential energy differences between Ag and TiO2 nanocrystals, thus enhancing the photocatalytic activity; (2) the Ag-TiO2-KIT-6 sample possesses a high BET surface area and a large number of ordered pore channels, which facilitate adsorption and transportation of dye molecules, also leading to higher photocatalytic activity. It was also found that the Ag-TiO2 heterostructure plays a more important role in enhancing the photocatalytic activity than high BET surface area.
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9.
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10.
  • Zheng, Linlin, et al. (författare)
  • Design and implementation of a fully reconfigurable chipless RFID tag using inkjet printing technology
  • 2008
  • Ingår i: Proceedings - IEEE International Symposium on Circuits and Systems. - 9781424420780 ; , s. 1524-1527
  • Konferensbidrag (refereegranskat)abstract
    • In this paper, a novel fully reconfigurable chipless RFID tag has been presented. 8-bit data are encoded by impedance mismatches along transmission line. Inkjet printing is used to reconfigure for special tag IDs. By integrating inkjet printing technology, printable tags are not only economically feasible but also technically efficient. The remarkable idea has been successfully validated both by simulation and experimental measurements.
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