2,402 research outputs found

    Discovery of a second SALMFamide gene in the sea urchin Strongylocentrotus purpuratus reveals that L-type and F-type SALMFamide neuropeptides coexist in an echinoderm species

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    NOTICE: this is the author’s version of a work that was accepted for publication in MARINE GENOMICS. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in MARINE GENOMICS, [VOL 3, ISSUE 2, (2010)] DOI: 10.1016/j.margen.2010.08.00

    miRNA_targets : a database for miRNA target predictions in coding and non-coding regions of mRNAs

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    AbstractMicroRNAs (miRNAs) are small non-coding RNAs that play a role in post-transcriptional regulation of gene expression in most eukaryotes. They help in fine-tuning gene expression by targeting messenger RNAs (mRNA). The interactions of miRNAs and mRNAs are sequence specific and computational tools have been developed to predict miRNA target sites on mRNAs, but miRNA research has been mainly focused on target sites within 3′ untranslated regions (UTRs) of genes. There is a need for an easily accessible repository of genome wide full length mRNA — miRNA target predictions with versatile search capabilities and visualization tools. We have created a web accessible database of miRNA target predictions for human, mouse, cow, chicken, Zebra fish, fruit fly and Caenorhabditis elegans using two different target prediction algorithms, The database has target predictions for miRNA's on 5′ UTRs, coding region and 3′ UTRs of all mRNAs. This database can be freely accessed at http://mamsap.it.deakin.edu.au/mirna_targets/

    A Measurement of the Ds+ Lifetime

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    A high statistics measurement of the Ds+ lifetime from the Fermilab fixed-target FOCUS photoproduction experiment is presented. We describe the analysis of the two decay modes, Ds+ -> phi(1020)pi+ and Ds+ -> \bar{K}*(892)0K+, used for the measurement. The measured lifetime is 507.4 +/- 5.5 (stat.) +/- 5.1 (syst.) fs using 8961 +/- 105 Ds+ -> phi(1020)pi+ and 4680 +/- 90 Ds+ -> \bar{K}*(892)0K+ decays. This is a significant improvement over the present world average.Comment: 5 pages, 3 figures, 2 tables, submitted to PR

    A Non-parametric Approach to the D+ to K*0bar mu+ nu Form Factors

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    Using a large sample of D+ -> K- pi+ mu+ nu decays collected by the FOCUS photoproduction experiment at Fermilab, we present the first measurements of the helicity basis form factors free from the assumption of spectroscopic pole dominance. We also present the first information on the form factor that controls the s-wave interference discussed in a previous paper by the FOCUS collaboration. We find reasonable agreement with the usual assumption of spectroscopic pole dominance and measured form factor ratios.Comment: 14 pages, 5 figures, and 2 tables. We updated the previous version by changing some words, removing one plot, and adding two tables. These changes are mostly stylisti

    Search for Λc+pK+π\Lambda_c^+ \to p K^+ \pi^- and Ds+K+K+πD_s^+ \to K^+ K^+ \pi^- Using Genetic Programming Event Selection

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    We apply a genetic programming technique to search for the double Cabibbo suppressed decays Λc+pK+π\Lambda_c^+ \to p K^+ \pi^- and Ds+K+K+πD_s^+ \to K^+ K^+ \pi^-. We normalize these decays to their Cabibbo favored partners and find BR(\text{BR}(\Lambda_c^+ \to p K^+ \pi^-)/BR()/\text{BR}(\Lambda_c^+ \to p K^- \pi^+)=(0.05±0.26±0.02)) = (0.05 \pm 0.26 \pm 0.02)% and BR(\text{BR}(D_s^+ \to K^+ K^+ \pi^-)/BR()/\text{BR}(D_s^+ \to K^+ K^- \pi^+)=(0.52±0.17±0.11)) = (0.52\pm 0.17\pm 0.11)% where the first errors are statistical and the second are systematic. Expressed as 90% confidence levels (CL), we find <0.46< 0.46 % and <0.78 < 0.78% respectively. This is the first successful use of genetic programming in a high energy physics data analysis.Comment: 10 page

    Study of the D^0 \to pi^-pi^+pi^-pi^+ decay

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    Using data from the FOCUS (E831) experiment at Fermilab, we present new measurements for the Cabibbo-suppressed decay mode D0ππ+ππ+D^0 \to \pi^-\pi^+\pi^-\pi^+. We measure the branching ratio Γ(D0π+ππ+π)/Γ(D0Kπ+ππ+)=0.0914±0.0018±0.0022\Gamma(D^0 \to\pi^+\pi^- \pi^+\pi^-)/\Gamma(D^0 \to K^-\pi^+\pi^-\pi^+) = 0.0914 \pm 0.0018 \pm 0.0022. An amplitude analysis has been performed, a first for this channel, in order to determine the resonant substructure of this decay mode. The dominant component is the decay D0a1(1260)+πD^0 \to a_1(1260)^+ \pi^-, accounting for 60% of the decay rate. The second most dominant contribution comes from the decay D0ρ(770)0ρ(770)0D^0 \to \rho(770)^0\rho(770)^0, with a fraction of 25%. We also study the a1(1260)a_1(1260) line shape and resonant substructure. Using the helicity formalism for the angular distribution of the decay D0ρ(770)0ρ(770)0D^0 \to \rho(770)^0\rho(770)^0, we measure a longitudinal polarization of PL=(71±4±2)P_L = (71 \pm 4\pm 2)%.Comment: 38 pages, 8 figures. accepted for publication in Physical Review

    Measurement of the branching ratio of the decay D^0 -> \pi^-\mu^+\nu relative to D^0 -> K^-\mu^+\nu

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    We present a new measurement of the branching ratio of the Cabibbo suppressed decay D^0\to \pi^-\mu^+\nu relative to the Cabibbo favored decay D^0\to K^-\mu^+\nu and an improved measurement of the ratio |\frac{f_+^{\pi}(0)}{f_+^{K}(0)}|. Our results are 0.074 \pm 0.008 \pm 0.007 for the branching ratio and 0.85 \pm 0.04 \pm 0.04 \pm 0.01 for the form factor ratio, respectively.Comment: 13pages, 3 figure

    Study of the decay asymmetry parameter and CP violation parameter in the Lambdac+ --> Lambda pi+ decay

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    Using data from the FOCUS (E831) experiment at Fermilab, we present a new measurement of the weak decay-asymmetry parameter alpha(Lambdac) in Lambdac --> Lambda pi decay. Comparing particle with antiparticle decays, we obtain the first measurement of the CP violation parameter : A = [alpha(Lambdac)+alpha(antiLambda_c)]/[alpha(Lambdac)-alpha(antiLambda_c)]. We obtain alpha(Lambdac)=-0.78+-0.16+-0.13 and A = -0.07+-0.19+-0.12 where errors are statistical and systematic.Comment: 18 pages, to be submitted to Phys. Lett. B For a list of the FOCUS collaboration, see http://www-focus.fnal.gov/authors.htm

    Application of Genetic Programming to High Energy Physics Event Selection

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    We review genetic programming principles, their application to FOCUS data samples, and use the method to study the doubly Cabibbo suppressed decay D+ -> K+ pi+ pi- relative to its Cabibbo favored counterpart, D+ -> K- pi+ pi+. We find that this technique is able to improve upon more traditional analysis methods. To our knowledge, this is the first application of the genetic programming technique to High Energy Physics data.Comment: 39 page
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