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Search: WFRF:(Donnelly Liam)

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1.
  • Donnelly, Liam, et al. (author)
  • Inter-and intra-annual wood property variation in juvenile wood between six Sitka spruce clones
  • 2017
  • In: Silva Fennica. - : Finnish Society of Forest Science. - 0037-5330 .- 2242-4075. ; 51:4
  • Journal article (peer-reviewed)abstract
    • Increased growth rates have reduced rotation lengths, increasing the proportion of juvenile wood relative to mature wood, which may negatively affect mechanical performance of sawn timber. However, there is limited information available on the potential impact of breeding for vigour on juvenile wood in Sitka spruce (Picea sitchensis (Bong.) CarriÚre). In this study, the relationship between vigour (based on total height) and wood properties was investigated in six-year-old Sitka spruce clones grown in two replicated field trials in Ireland. Six clones were evaluated, two clones from each of three vigour (high, intermediate and low) classes. Discs were cut from the base of one ramet per replication for each clone to assess wood quality attributes. Radial tracheid width was significantly and positively correlated with ring width and height, and was negatively correlated with density. The wood of the most vigorous clone had significantly larger ring width with thinner cell walls and wider tracheids than all clones in the two other vigour classes, resulting in lower mean wood density. Latewood properties for all wood attributes measured differed significantly between the two sites. Wood property differences resulted primarily from variation in the proportions of early- and latewood in each annual ring. Additionally, the width of early- and latewood bands in each ring was found to be a more important determinant of juvenile wood quality than the characteristics of the cells within each band. Wood properties differed greatly between clones, suggesting that there is potential to improve juvenile wood properties through selective breeding.
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2.
  • Su, Zhan, et al. (author)
  • Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.
  • 2012
  • In: Nature Genetics. - : Springer Science and Business Media LLC. - 1061-4036 .- 1546-1718. ; 44:10
  • Journal article (peer-reviewed)abstract
    • Barrett's esophagus is an increasingly common disease that is strongly associated with reflux of stomach acid and usually a hiatus hernia, and it strongly predisposes to esophageal adenocarcinoma (EAC), a tumor with a very poor prognosis. We report the first genome-wide association study on Barrett's esophagus, comprising 1,852 UK cases and 5,172 UK controls in the discovery stage and 5,986 cases and 12,825 controls in the replication stage. Variants at two loci were associated with disease risk: chromosome 6p21, rs9257809 (Pcombined=4.09×10(-9); odds ratio (OR)=1.21, 95% confidence interval (CI)=1.13-1.28), within the major histocompatibility complex locus, and chromosome 16q24, rs9936833 (Pcombined=2.74×10(-10); OR=1.14, 95% CI=1.10-1.19), for which the closest protein-coding gene is FOXF1, which is implicated in esophageal development and structure. We found evidence that many common variants of small effect contribute to genetic susceptibility to Barrett's esophagus and that SNP alleles predisposing to obesity also increase risk for Barrett's esophagus.
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