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  <channel rdf:about="http://hdl.handle.net/2328/4796">
    <title>DSpace Community: Flinders' staff research collected for reporting or funder mandate purposes.</title>
    <link>http://hdl.handle.net/2328/4796</link>
    <description>Flinders' staff research collected for reporting or funder mandate purposes.</description>
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://hdl.handle.net/2328/26700" />
        <rdf:li rdf:resource="http://hdl.handle.net/2328/26699" />
        <rdf:li rdf:resource="http://hdl.handle.net/2328/26688" />
        <rdf:li rdf:resource="http://hdl.handle.net/2328/26686" />
      </rdf:Seq>
    </items>
    <dc:date>2013-05-22T18:09:11Z</dc:date>
  </channel>
  <item rdf:about="http://hdl.handle.net/2328/26700">
    <title>Myb-binding protein 1A (MYBBP1A) is essential for early embryonic development, controls cell cycle and mitosis, and acts as a tumor suppressor</title>
    <link>http://hdl.handle.net/2328/26700</link>
    <description>Title: Myb-binding protein 1A (MYBBP1A) is essential for early embryonic development, controls cell cycle and mitosis, and acts as a tumor suppressor
Authors: Mori, Silvia; Bernardi, Rosa; Laurent, Audrey; Resnati, Massimo; Crippa, Ambra; Gabrieli, Arianna; Keough, Rebecca Anne; Gonda, Thomas J; Blasi, Francesco
Abstract: MYBBP1A is a predominantly nucleolar transcriptional regulator involved in rDNA synthesis and p53 activation via&#xD;
acetylation. However little further information is available as to its function. Here we report that MYBBP1A is&#xD;
developmentally essential in the mouse prior to blastocyst formation. In cell culture, down-regulation of MYBBP1A&#xD;
decreases the growth rate of wild type mouse embryonic stem cells, mouse embryo fibroblasts (MEFs) and of human HeLa&#xD;
cells, where it also promotes apoptosis. HeLa cells either arrest at G2/M or undergo delayed and anomalous mitosis. At&#xD;
mitosis, MYBBP1A is localized to a parachromosomal region and gene-expression profiling shows that its down-regulation&#xD;
affects genes controlling chromosomal segregation and cell cycle. However, MYBBP1A down-regulation increases the&#xD;
growth rate of the immortalized NIH3T3 cells. Such Mybbp1a down-regulated NIH3T3 cells are more susceptible to Ras-induced&#xD;
transformation and cause more potent Ras-driven tumors. We conclude that MYBBP1A is an essential gene with&#xD;
novel roles at the pre-mitotic level and potential tumor suppressor activity.</description>
    <dc:date>2012-10-08T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/2328/26699">
    <title>The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in Caucasians with primary open angle glaucoma</title>
    <link>http://hdl.handle.net/2328/26699</link>
    <description>Title: The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in Caucasians with primary open angle glaucoma
Authors: Wiggs, Janey L; Hewitt, Alex W; Fan, Bao Jian; Wang, Dan Yi; O'Brien, Colm; Realini, Anthony; Craig, Jamie E; Dimasi, David Paul; Mackey, David A; Haines, Jonathan L; Pasquale, Louis R; Figueiredo Sena, Dayse R
Abstract: Background: Loss of vision in glaucoma is due to apoptotic retinal ganglion cell loss. While p53 modulates apoptosis, gene&#xD;
association studies between p53 variants and glaucoma have been inconsistent. In this study we evaluate the association&#xD;
between a p53 variant functionally known to influence apoptosis (codon 72 Pro/Arg) and the subset of primary open angle&#xD;
glaucoma (POAG) patients with early loss of central visual field.&#xD;
Methods: Genotypes for the p53 codon 72 polymorphism (Pro/Arg) were obtained for 264 POAG patients and 400 controls&#xD;
from the U.S. and in replication studies for 308 POAG patients and 178 controls from Australia (GIST). The glaucoma patients&#xD;
were divided into two groups according to location of initial visual field defect (either paracentral or peripheral). All cases&#xD;
and controls were Caucasian with European ancestry.&#xD;
Results: The p53-PRO/PRO genotype was more frequent in the U.S. POAG patients with early visual field defects in the&#xD;
paracentral regions compared with those in the peripheral regions or control group (p = 2.761025). We replicated this&#xD;
finding in the GIST cohort (p = 7.361023, and in the pooled sample (p = 6.661027) and in a meta-analysis of both the US&#xD;
and GIST datasets (1.361026, OR 2.17 (1.58–2.98 for the PRO allele).&#xD;
Conclusions: These results suggest that the p53 codon 72 PRO/PRO genotype is potentially associated with early&#xD;
paracentral visual field defects in primary open-angle glaucoma patients.</description>
    <dc:date>2012-09-26T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/2328/26688">
    <title>Combination of selenium and green tea improves the efficacy of chemoprevention in a rat colorectal cancer model by modulating genetic and epigenetic biomarkers</title>
    <link>http://hdl.handle.net/2328/26688</link>
    <description>Title: Combination of selenium and green tea improves the efficacy of chemoprevention in a rat colorectal cancer model by modulating genetic and epigenetic biomarkers
Authors: Hu, Ying; Young, Graeme Paul; Margison, Geoffrey; Le Leu, Richard Kevin
Abstract: Defining biomarkers of colorectal cancer prevention by dietary or chemopreventive agents and translation to human intervention studies</description>
    <dc:date>2013-04-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/2328/26686">
    <title>Impact of ethnicity and socio-economic status on Staphylococcus aureus bacteremia incidence and mortality: a heavy burden in Indigenous Australians</title>
    <link>http://hdl.handle.net/2328/26686</link>
    <description>Title: Impact of ethnicity and socio-economic status on Staphylococcus aureus bacteremia incidence and mortality: a heavy burden in Indigenous Australians
Authors: Tong, Steven Y C; van Hal, Sebastian J; Einsiedel, Lloyd John; Currie, Bart John; Turnidge, John D
Abstract: This prospective study identified more than 7500 Staphylococcus aureus bacteremia (SAB) episodes&#xD;
occurring in population of 16,453,420 resulting in a&#xD;
crude annual incidence of 11. 2 episodes per 100,000 population.&#xD;
Overall Indigenous Australians were 5 .9 times more&#xD;
likely to have a SAB, especially community-associated&#xD;
MRSA episodes (29.2 times) compared to non-Indigenous&#xD;
Australians. Populations in the lowest SES quintile had&#xD;
an increased SAB incidence compared to higher quintiles.&#xD;
However, there remained a disparity between Indigenous&#xD;
and non-Indigenous populations across all SES&#xD;
quintiles. Thus our study provides robust evidence that&#xD;
Indigenous populations and lower SES populations are at&#xD;
increased risk of SAB. Furthermore, standard measures&#xD;
of SES do not explain the disparity in rates between Indigenous&#xD;
and non-Indigenous populations.</description>
    <dc:date>2012-10-09T00:00:00Z</dc:date>
  </item>
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