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

Search: WFRF:(Graham S) > (2005-2009)

  • Result 1-10 of 62
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1.
  • Schael, S, et al. (author)
  • Precision electroweak measurements on the Z resonance
  • 2006
  • In: Physics Reports. - : Elsevier BV. - 0370-1573 .- 1873-6270. ; 427:5-6, s. 257-454
  • Research review (peer-reviewed)abstract
    • We report on the final electroweak measurements performed with data taken at the Z resonance by the experiments operating at the electron-positron colliders SLC and LEP. The data consist of 17 million Z decays accumulated by the ALEPH, DELPHI, L3 and OPAL experiments at LEP, and 600 thousand Z decays by the SLID experiment using a polarised beam at SLC. The measurements include cross-sections, forward-backward asymmetries and polarised asymmetries. The mass and width of the Z boson, m(Z) and Gamma(Z), and its couplings to fermions, for example the p parameter and the effective electroweak mixing angle for leptons, are precisely measured: m(Z) = 91.1875 +/- 0.0021 GeV, Gamma(Z) = 2.4952 +/- 0.0023 GeV, rho(l) = 1.0050 +/- 0.0010, sin(2)theta(eff)(lept) = 0.23153 +/- 0.00016. The number of light neutrino species is determined to be 2.9840 +/- 0.0082, in agreement with the three observed generations of fundamental fermions. The results are compared to the predictions of the Standard Model (SM). At the Z-pole, electroweak radiative corrections beyond the running of the QED and QCD coupling constants are observed with a significance of five standard deviations, and in agreement with the Standard Model. Of the many Z-pole measurements, the forward-backward asymmetry in b-quark production shows the largest difference with respect to its SM expectation, at the level of 2.8 standard deviations. Through radiative corrections evaluated in the framework of the Standard Model, the Z-pole data are also used to predict the mass of the top quark, m(t) = 173(+10)(+13) GeV, and the mass of the W boson, m(W) = 80.363 +/- 0.032 GeV. These indirect constraints are compared to the direct measurements, providing a stringent test of the SM. Using in addition the direct measurements of m(t) and m(W), the mass of the as yet unobserved SM Higgs boson is predicted with a relative uncertainty of about 50% and found to be less than 285 GeV at 95% confidence level. (c) 2006 Elsevier B.V. All rights reserved.
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2.
  • Abazov, V. M., et al. (author)
  • The upgraded DO detector
  • 2006
  • In: Nuclear Instruments and Methods in Physics Research Section A. - : Elsevier BV. - 0168-9002 .- 1872-9576. ; 565:2, s. 463-537
  • Journal article (peer-reviewed)abstract
    • The DO experiment enjoyed a very successful data-collection run at the Fermilab Tevatron collider between 1992 and 1996. Since then, the detector has been upgraded to take advantage of improvements to the Tevatron and to enhance its physics capabilities. We describe the new elements of the detector, including the silicon microstrip tracker, central fiber tracker, solenoidal magnet, preshower detectors, forward muon detector, and forward proton detector. The uranium/liquid -argon calorimeters and central muon detector, remaining from Run 1, are discussed briefly. We also present the associated electronics, triggering, and data acquisition systems, along with the design and implementation of software specific to DO.
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4.
  • Klionsky, Daniel J., et al. (author)
  • Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes
  • 2008
  • In: Autophagy. - : Landes Bioscience. - 1554-8627 .- 1554-8635. ; 4:2, s. 151-175
  • Research review (peer-reviewed)abstract
    • Research in autophagy continues to accelerate,1 and as a result many new scientists are entering the field. Accordingly, it is important to establish a standard set of criteria for monitoring macroautophagy in different organisms. Recent reviews have described the range of assays that have been used for this purpose.2,3 There are many useful and convenient methods that can be used to monitor macroautophagy in yeast, but relatively few in other model systems, and there is much confusion regarding acceptable methods to measure macroautophagy in higher eukaryotes. A key point that needs to be emphasized is that there is a difference between measurements that monitor the numbers of autophagosomes versus those that measure flux through the autophagy pathway; thus, a block in macroautophagy that results in autophagosome accumulation needs to be differentiated from fully functional autophagy that includes delivery to, and degradation within, lysosomes (in most higher eukaryotes) or the vacuole (in plants and fungi). Here, we present a set of guidelines for the selection and interpretation of the methods that can be used by investigators who are attempting to examine macroautophagy and related processes, as well as by reviewers who need to provide realistic and reasonable critiques of papers that investigate these processes. This set of guidelines is not meant to be a formulaic set of rules, because the appropriate assays depend in part on the question being asked and the system being used. In addition, we emphasize that no individual assay is guaranteed to be the most appropriate one in every situation, and we strongly recommend the use of multiple assays to verify an autophagic response.
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5.
  • Clark, Andrew G., et al. (author)
  • Evolution of genes and genomes on the Drosophila phylogeny
  • 2007
  • In: Nature. - : Springer Science and Business Media LLC. - 0028-0836 .- 1476-4687. ; 450:7167, s. 203-218
  • Journal article (peer-reviewed)abstract
    • Comparative analysis of multiple genomes in a phylogenetic framework dramatically improves the precision and sensitivity of evolutionary inference, producing more robust results than single-genome analyses can provide. The genomes of 12 Drosophila species, ten of which are presented here for the first time (sechellia, simulans, yakuba, erecta, ananassae, persimilis, willistoni, mojavensis, virilis and grimshawi), illustrate how rates and patterns of sequence divergence across taxa can illuminate evolutionary processes on a genomic scale. These genome sequences augment the formidable genetic tools that have made Drosophila melanogaster a pre-eminent model for animal genetics, and will further catalyse fundamental research on mechanisms of development, cell biology, genetics, disease, neurobiology, behaviour, physiology and evolution. Despite remarkable similarities among these Drosophila species, we identified many putatively non-neutral changes in protein-coding genes, non-coding RNA genes, and cis-regulatory regions. These may prove to underlie differences in the ecology and behaviour of these diverse species.
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6.
  • Zeggini, Eleftheria, et al. (author)
  • Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
  • 2008
  • In: Nature Genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 40:5, s. 638-645
  • Journal article (peer-reviewed)abstract
    • Genome-wide association (GWA) studies have identified multiple loci at which common variants modestly but reproducibly influence risk of type 2 diabetes (T2D)(1-11). Established associations to common and rare variants explain only a small proportion of the heritability of T2D. As previously published analyses had limited power to identify variants with modest effects, we carried out meta-analysis of three T2D GWA scans comprising 10,128 individuals of European descent and similar to 2.2 million SNPs (directly genotyped and imputed), followed by replication testing in an independent sample with an effective sample size of up to 53,975. We detected at least six previously unknown loci with robust evidence for association, including the JAZF1 (P=5.0 x 10(-14)), CDC123-CAMK1D (P=1.2 x 10(-10)), TSPAN8-LGR5 (P=1.1 x 10(-9)), THADA (P=1.1 x 10(-9)), ADAMTS9 (P=1.2 x 10(-8)) and NOTCH2 (P=4.1 x 10(-8)) gene regions. Our results illustrate the value of large discovery and follow-up samples for gaining further insights into the inherited basis of T2D.
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8.
  • Durakiewicz, T., et al. (author)
  • Observation of a kink in the dispersion of f-electrons
  • 2008
  • In: Europhysics letters. - : IOP Publishing. - 0295-5075 .- 1286-4854. ; 84:3, s. 37003-
  • Journal article (peer-reviewed)abstract
    • Strong interactions in correlated electron systems may result in the formation of heavy quasiparticles that exhibit kinks in their dispersion relation. Spectral weight is incoherently shifted away from the Fermi energy, but Luttinger's theorem requires the Fermi volume to remain constant. Our angle-resolved photoemission study of USb2 reveals a kink in a noncrossing 5f band, representing the first experimental observation of a kink structure in f-electron systems. The kink energy scale of 21 meV and the ultra-small peak width of 3 meV are observed. We propose the novel mechanism of renormalization of a point-like Fermi surface, and that Luttinger's theorem remains applicable.
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9.
  • Shin, J. H., et al. (author)
  • IA-2 autoantibodies in incident type I diabetes patients are associated with a polyadenylation signal polymorphism in GIMAP5
  • 2007
  • In: Genes Immun. - : Springer Science and Business Media LLC. - 1466-4879 .- 1476-5470. ; 8:6, s. 503-12
  • Journal article (peer-reviewed)abstract
    • In a large case-control study of Swedish incident type I diabetes patients and controls, 0-34 years of age, we tested the hypothesis that the GIMAP5 gene, a key genetic factor for lymphopenia in spontaneous BioBreeding rat diabetes, is associated with type I diabetes; with islet autoantibodies in incident type I diabetes patients or with age at clinical onset in incident type I diabetes patients. Initial scans of allelic association were followed by more detailed logistic regression modeling that adjusted for known type I diabetes risk factors and potential confounding variables. The single nucleotide polymorphism (SNP) rs6598, located in a polyadenylation signal of GIMAP5, was associated with the presence of significant levels of IA-2 autoantibodies in the type I diabetes patients. Patients with the minor allele A of rs6598 had an increased prevalence of IA-2 autoantibody levels compared to patients without the minor allele (OR=2.2; Bonferroni-corrected P=0.003), after adjusting for age at clinical onset (P=8.0 x 10(-13)) and the numbers of HLA-DQ A1*0501-B1*0201 haplotypes (P=2.4 x 10(-5)) and DQ A1*0301-B1*0302 haplotypes (P=0.002). GIMAP5 polymorphism was not associated with type I diabetes or with GAD65 or insulin autoantibodies, ICA, or age at clinical onset in patients. These data suggest that the GIMAP5 gene is associated with islet autoimmunity in type I diabetes and add to recent findings implicating the same SNP in another autoimmune disease.
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10.
  • Yang, X, et al. (author)
  • Unusual quasiparticle renormalizations from angle resolved photoemission on USb2
  • 2009
  • In: Philosophical Magazine. - : Informa UK Limited. - 1478-6435 .- 1478-6443. ; 89:22-24, s. 1893-1911
  • Journal article (peer-reviewed)abstract
    • Angle-resolved photoemission experiments have been performed on USb2, and very narrow quasiparticle peaks have been observed in a band, which local spin-density approximation (LSDA) predicts to osculate the Fermi energy. The observed band is found to be depressed by 17 meV below the Fermi energy. Furthermore, the inferred quasiparticle dispersion relation for this band exhibits a kink at an energy of about 23 meV below the Fermi energy. The kink is not found in LSDA calculations and, therefore, is attributable to a change in the quasiparticle mass renormalization by a factor of approximately 2. The existence of a kink in the quasiparticle dispersion relation of a band that does not cross the Fermi energy is unprecedented. The kink in the quasiparticle dispersion relation is attributed to the effect of the interband self-energy, involving transitions from the osculating band into a band that does cross the Fermi energy.
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  • Result 1-10 of 62
Type of publication
journal article (48)
conference paper (9)
research review (4)
book chapter (1)
Type of content
peer-reviewed (57)
other academic/artistic (5)
Author/Editor
Wolk, Alicja (6)
Goodwin, Graham C. (6)
Giovannucci, Edward (6)
Hunter, David J (6)
van den Brandt, Piet ... (6)
Rohan, Thomas E. (6)
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Spiegelman, Donna (6)
Freudenheim, Jo L. (6)
Miller, Anthony B. (6)
Schatzkin, Arthur (6)
Smith-Warner, Stepha ... (6)
McCullough, Marjorie ... (6)
Graham, J. (5)
Willett, Walter C. (5)
Buring, Julie E (5)
Zhang, Shumin M. (5)
Padyukov, L (4)
Giles, Graham G (4)
English, Dallas R. (4)
Bernstein, Leslie (4)
Horn-Ross, Pamela L. (4)
Rydén, L. (3)
Rojas, Cristian R., ... (3)
Kere, J (3)
Mannisto, Satu (3)
Adami, Hans Olov (3)
Jacobs, R. (3)
Vyse, TJ (3)
Albanes, Demetrius (3)
Dickstein, K (3)
Camm, J (3)
Rojas, Cristian R. (3)
Lindh, Christina (3)
Laakso, M. (3)
Leitzmann, Michael (3)
Plenge, RM (3)
Graham, RR (3)
Fuchs, Charles S (3)
Wood, D. (3)
Karlson, EW (3)
Pyorala, K (3)
Leitzmann, Michael F ... (3)
Dean, V (3)
Horner, K (3)
Schouten, Leo J. (3)
Graham, I (3)
Cho, Eunyoung (3)
Graham, Saxon (3)
Durakiewicz, T. (3)
Guziewicz, E. (3)
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University
Karolinska Institutet (22)
Uppsala University (20)
Royal Institute of Technology (12)
Lund University (9)
Umeå University (7)
University of Gothenburg (5)
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Malmö University (3)
Linköping University (2)
Luleå University of Technology (1)
Stockholm University (1)
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Language
English (62)
Research subject (UKÄ/SCB)
Medical and Health Sciences (19)
Natural sciences (9)
Engineering and Technology (6)
Social Sciences (1)

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