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    <dc:date>2011-08-09T00:00:00Z</dc:date>
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    <title>Genomic biomarkers in predictive medicine. An interim analysis</title>
    <link>http://www.embomolmed.org/details/journalArticle/1311357/Genomic_biomarkers_in_predictive_medicine__An_interim_analysis.html</link>
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    <dc:date>2011-07-11T00:00:00Z</dc:date>
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    <title>Scientists contemplate unexplained death in Austrian Alps</title>
    <link>http://www.embomolmed.org/details/journalArticle/1239787/Scientists_contemplate_unexplained_death_in_Austrian_Alps.html</link>
    <description>Abstract
      
         The recent EMBO Molecular Medicine Workshop on Cell Death and Disease was held this past March in the picturesque Alpen ski‐town
            of Obergurgl, Austria. Scientists working on diverse mechanisms and pathways of cell death convened to present and discuss
            their current research. Topics included not only cell death signalling pathways, their etiology in human disease, and potential
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    <dc:date>2011-06-14T00:00:00Z</dc:date>
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    <title>Return of the Trojan horse: intracellular phenotype switching and immune evasion by &lt;i &gt;Staphylococcus aureus&lt;/i&gt;</title>
    <link>http://www.embomolmed.org/details/journalArticle/1026795/Return_of_the_Trojan_horse_intracellular_phenotype_switching_and_immune_evasion_.html</link>
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         Staphylococcus aureus small colony variants (SCVs), which are characterized by slow growth and a range of morphological and metabolic changes including
            altered antibiotic resistance profiles, have been studied for several decades. This Closeup highlights findings described
            in this issue of EMBO Molecular Medicine by Tuchscherr et al (2011), who present strong evidence that SCVs can arise in chronic infection models when S. aureus is...</description>
    <dc:date>2011-02-25T00:00:00Z</dc:date>
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         Copy number variations (CNV) within the genome are extremely abundant. In this closeup, Canales and Walz discuss how CNV are
            associated with normal variation, genomic disorders, genome evolution, adaptive traits and how the use of a novel screen described
            by Ermakova et al in this issue that is designed to identify human disease‐relevant phenotypes associated with CNV in the
            mouse can help elucidating susceptibility or...</description>
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