1,658 research outputs found

    Speculations on Isolated Lepton Events at HERA

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    Speculations on mechanisms which might be responsible for events with an isolated high p_T lepton, a hadron jet and missing energy, as observed in the H1 experiment at HERA, are discussed.Comment: LaTeX, 6 pages, 2 figures, presented at the XXXI Conference of Theoretical Physics "Matter to the Deepest", Ustron, Poland, September 5-11, 200

    Reconstruction of Fundamental SUSY Parameters

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    We summarize methods and expected accuracies in determining the basic low-energy SUSY parameters from experiments at future e+^+e−^- linear colliders in the TeV energy range, combined with results from LHC. In a second step we demonstrate how, based on this set of parameters, the fundamental supersymmetric theory can be reconstructed at high scales near the grand unification or Planck scale. These analyses have been carried out for minimal supergravity [confronted with GMSB for comparison], and for a string effective theory.Comment: 8 pages, latex, 7 figures, expanded version of contributions to the proceedings of ICHEP.2002 (Amstersdam) and LCWS.2002 (Jeju Island

    Stau-catalyzed 6^6Li Production in Big-Bang Nucleosynthesis

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    If the gravitino mass is in the region from a few GeV to a few 10's GeV, the scalar lepton X such as stau is most likely the next lightest supersymmetry particle. The negatively charged and long-lived X^- may form a Coulomb bound state (A X) with a nucleus A and may affect the big-bang nucleosynthesis through catalyzed fusion process. We calculate a production cross section of Li6 from the catalyzed fusion (He4 X^-) + d \to Li6 + X^- by solving the Schr\"{o}dinger equation exactly for three-body system of He4, d, and X. We utilize the state-of-the-art coupled-channel method, which is known to be very accurate to describe other three-body systems in nuclear and atomic reactions. The importance of the use of appropriate nuclear potential and the exact treatment of the quantum tunneling in the fusion process are emphasized. We find that the astrophysical S-factor at the Gamow peak corresponding to T=10 keV is 0.038 MeV barn. This leads to the Li6 abundance from the catalyzed process as Li6|_{CBBN}\simeq 4.3\times 10^{-11} (D/2.8\times 10^{-5}) ([n_{X^-}/s]/10^{-16}) in the limit of long lifetime of X. Particle physics implication of this result is also discussed.Comment: 16 pages, 7 figure

    LHC/ILC Interplay in SUSY Searches

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    Combined analyses at the Large Hadron Collider and at the International Linear Collider are important to reveal precisely the new physics model as, for instance, supersymmetry. Examples are presented where ILC results as input for LHC analyses could be crucial for the identification of signals as well as of the underlying model. The synergy of both colliders leads also to rather accurate SUSY parameter determination and powerful mass constraints even if the scalar particles have masses in the multi-TeV range.Comment: 5 pages, contribution to the proceedings of EPS0

    Experimental Zika Virus Infection in the Pregnant Common Marmoset Induces Spontaneous Fetal Loss and Neurodevelopmental Abnormalities.

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    During its most recent outbreak across the Americas, Zika virus (ZIKV) was surprisingly shown to cause fetal loss and congenital malformations in acutely and chronically infected pregnant women. However, understanding the underlying pathogenesis of ZIKV congenital disease has been hampered by a lack of relevant in vivo experimental models. Here we present a candidate New World monkey model of ZIKV infection in pregnant marmosets that faithfully recapitulates human disease. ZIKV inoculation at the human-equivalent of early gestation caused an asymptomatic seroconversion, induction of type I/II interferon-associated genes and proinflammatory cytokines, and persistent viremia and viruria. Spontaneous pregnancy loss was observed 16-18 days post-infection, with extensive active placental viral replication and fetal neurocellular disorganization similar to that seen in humans. These findings underscore the key role of the placenta as a conduit for fetal infection, and demonstrate the utility of marmosets as a highly relevant model for studying congenital ZIKV disease and pregnancy loss

    Identification and validation of oncologic miRNA biomarkers for Luminal A-like breast cancer

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    Introduction: Breast cancer is a common disease with distinct tumor subtypes phenotypically characterized by ER and HER2/neu receptor status. MiRNAs play regulatory roles in tumor initiation and progression, and altered miRNA expression has been demonstrated in a variety of cancer states presenting the potential for exploitation as cancer biomarkers. Blood provides an excellent medium for biomarker discovery. This study investigated systemic miRNAs differentially expressed in Luminal A-like (ER+PR+HER2/neu-) breast cancer and their effectiveness as oncologic biomarkers in the clinical setting. Methods: Blood samples were prospectively collected from patients with Luminal A-like breast cancer (n=54) and controls (n=56). RNA was extracted, reverse transcribed and subjected to microarray analysis (n=10 Luminal A-like; n=10 Control). Differentially expressed miRNAs were identified by artificial neural network (ANN) data-mining algorithms. Expression of specific miRNAs was validated by RQ-PCR (n=44 Luminal A; n=46 Control) and potential relationships between circulating miRNA levels and clinicopathological features of breast cancer were investigated. Results: Microarray analysis identified 76 differentially expressed miRNAs. ANN revealed 10 miRNAs for further analysis ( miR-19b, miR-29a, miR-93, miR-181a, miR-182, miR-223, miR-301a, miR-423-5p, miR-486-5 and miR-652 ). The biomarker potential of 4 miRNAs ( miR-29a, miR-181a , miR-223 and miR-652 ) was confirmed by RQ-PCR, with significantly reduced expression in blood of women with Luminal A-like breast tumors compared to healthy controls (p=0.001, 0.004, 0.009 and 0.004 respectively). Binary logistic regression confirmed that combination of 3 of these miRNAs ( miR-29a, miR-181a and miR-652 ) could reliably differentiate between cancers and controls with an AUC of 0.80. Conclusion: This study provides insight into the underlying molecular portrait of Luminal A-like breast cancer subtype. From an initial 76 miRNAs, 4 were validated with altered expression in the blood of women with Luminal A-like breast cancer. The expression profiles of these 3 miRNAs, in combination with mammography, has potential to facilitate accurate subtype- specific breast tumor detection
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