38 research outputs found

    A Panchromatic Study of Massive Stars in the Extremely Metal-poor Local Group Dwarf Galaxy Leo A*

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    We characterize massive stars (M > 8 M⊙) in the nearby (D ∼ 0.8 Mpc) extremely metal-poor (Z ∼ 5% Z⊙) galaxy Leo A using Hubble Space Telescope ultraviolet (UV), optical, and near-infrared (NIR) imaging along with Keck/Low-Resolution Imaging Spectrograph and MMT/Binospec optical spectroscopy for 18 main-sequence OB stars. We find that: (a) 12 of our 18 stars show emission lines, despite not being associated with an H ii region, suggestive of stellar activity (e.g., mass loss, accretion, binary star interaction), which is consistent with previous predictions of enhanced activity at low metallicity; (b) six are Be stars, which are the first to be spectroscopically studied at such low metallicity—these Be stars have unusual panchromatic SEDs; (c) for stars well fit by the TLUSTY nonlocal thermodynamic equilibrium models, the photometric and spectroscopic values of log(Teff)\mathrm{log}({T}_{\mathrm{eff}}) and log(g)\mathrm{log}(g) agree to within ∼0.01 dex and ∼0.18 dex, respectively, indicating that near-UV/optical/NIR imaging can be used to reliably characterize massive (M ∼ 8–30 M⊙) main-sequence star properties relative to optical spectroscopy; (d) the properties of the most-massive stars in H II regions are consistent with constraints from previous nebular emission line studies; and (e) 13 stars with M > 8M⊙ are >40 pc from a known star cluster or H II region. Our sample comprises ∼50% of all known massive stars at Z ≲ 10% Z⊙with derived stellar parameters, high-quality optical spectra, and panchromatic photometry

    Genes to Diseases (G2D) Computational Method to Identify Asthma Candidate Genes

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    Asthma is a complex trait for which different strategies have been used to identify its environmental and genetic predisposing factors. Here, we describe a novel methodological approach to select candidate genes for asthma genetic association studies. In this regard, the Genes to Diseases (G2D) computational tool has been used in combination with a genome-wide scan performed in a sub-sample of the Saguenay−Lac-St-Jean (SLSJ) asthmatic familial collection (n = 609) to identify candidate genes located in two suggestive loci shown to be linked with asthma (6q26) and atopy (10q26.3), and presenting differential parent-of-origin effects. This approach combined gene selection based on the G2D data mining analysis of the bibliographic and protein public databases, or according to the genes already known to be associated with the same or a similar phenotype. Ten genes (LPA, NOX3, SNX9, VIL2, VIP, ADAM8, DOCK1, FANK1, GPR123 and PTPRE) were selected for a subsequent association study performed in a large SLSJ sample (n = 1167) of individuals tested for asthma and atopy related phenotypes. Single nucleotide polymorphisms (n = 91) within the candidate genes were genotyped and analysed using a family-based association test. The results suggest a protective association to allergic asthma for PTPRE rs7081735 in the SLSJ sample (p = 0.000463; corrected p = 0.0478). This association has not been replicated in the Childhood Asthma Management Program (CAMP) cohort. Sequencing of the regions around rs7081735 revealed additional polymorphisms, but additional genotyping did not yield new associations. These results demonstrate that the G2D tool can be useful in the selection of candidate genes located in chromosomal regions linked to a complex trait

    Rank among surgeons based on percentage mortality for study replicates 1–8.

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    Mean and overall rank scores are also listed; a lower ranking corresponds with higher mortality. (DOCX)</p
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