<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0">
  <channel>
    <title>PuSH - HMGU Publikationen</title>
    <link>https://push-zb.helmholtz-munich.de</link>
    <description>
    PuSH - Publikationen-Server des Helmholtz Zentrums München
    </description>
    <language>de-de</language>

    <item>
      <title><![CDATA[Christophersen, I.E.* et al. Fifteen genetic loci associated with the electrocardiographic P wave. Circ. Cardiovasc. Genet. 10:e001667 (2017)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52032&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52032&amp;la=de</guid>
      <pubDate>Thu, 05 Oct 2017 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Mayosi, B.M.* et al. Identification of cadherin 2 (CDH2) mutations in arrhythmogenic right ventricular cardiomyopathy. Circ. Cardiovasc. Genet. 10:e001605 (2017)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50992&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50992&amp;la=de</guid>
      <pubDate>Thu, 22 Jun 2017 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Crotti, L.* et al. Genetic modifiers for the long-QT syndrome: How important Is the role of variants in the 3&#039; untranslated region of KCNQ1? Circ. Cardiovasc. Genet. 9, 330-339 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49279&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49279&amp;la=de</guid>
      <pubDate>Thu, 25 Aug 2016 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Crotti, L.* et al. Response by Crotti et al to letter regarding article, &quot;Genetic modifiers for the long-QT syndrome: How important is the role of variants in the 3 &#039; untranslated region of KCNQ1?&quot; Circ. Cardiovasc. Genet. 9, 581-582 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50584&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50584&amp;la=de</guid>
      <pubDate>Tue, 14 Mar 2017 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Golbus, J.R.* et al. Common and rare genetic variation in CCR2, CCR5, or CX3CR1 and risk of atherosclerotic coronary heart disease and glucometabolic traits. Circ. Cardiovasc. Genet. 9, 250-258 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50590&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50590&amp;la=de</guid>
      <pubDate>Sat, 31 Dec 2016 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Joehanes, R.* et al. Epigenetic signatures of cigarette smoking. Circ. Cardiovasc. Genet. 9, 436-447 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49757&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49757&amp;la=de</guid>
      <pubDate>Wed, 19 Oct 2016 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Lacruz, M.E.* et al. Cardiovascular risk factors associated with blood metabolite concentrations and their alterations over a 4-year period in a population-based cohort. Circ. Cardiovasc. Genet. 9, 487-494 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49834&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49834&amp;la=de</guid>
      <pubDate>Mon, 31 Oct 2016 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Milano, A.* et al. Sudden cardiac arrest and rare genetic variants in the community. Circ. Cardiovasc. Genet. 9, 147-153 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47742&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=47742&amp;la=de</guid>
      <pubDate>Wed, 03 Feb 2016 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Parmar, P.G.* et al. International genome-wide association study consortium identifies novel loci associated with blood pressure in children and adolescents. Circ. Cardiovasc. Genet. 9, 266-278 (2016)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48093&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48093&amp;la=de</guid>
      <pubDate>Mon, 14 Mar 2016 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Asl, H.F.* et al. Expression quantitative trait loci acting across multiple tissues are enriched in inherited risk for coronary artery disease. Circ. Cardiovasc. Genet. 8, 305-315 (2015)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44845&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44845&amp;la=de</guid>
      <pubDate>Fri, 15 May 2015 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Kolder, I.C.* et al. Analysis for genetic modifiers of disease severity in patients with long QT syndrome type 2. Circ. Cardiovasc. Genet. 8, 447-456 (2015)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=43612&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=43612&amp;la=de</guid>
      <pubDate>Fri, 06 Mar 2015 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Lieb, W.* et al. Genome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genes. Circ. Cardiovasc. Genet. 8, 131-140 (2015)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42906&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42906&amp;la=de</guid>
      <pubDate>Sun, 07 Dec 2014 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Pfeifer, L. et al. DNA methylation of lipid-related genes affects blood lipid levels. Circ. Cardiovasc. Genet. 8, 334-342 (2015)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44846&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44846&amp;la=de</guid>
      <pubDate>Fri, 15 May 2015 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Ross, S.* et al. Effect of bile acid sequestrants on the risk of cardiovascular events: A mendelian randomization analysis. Circ. Cardiovasc. Genet. 8, 618-627 (2015)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46920&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46920&amp;la=de</guid>
      <pubDate>Wed, 07 Oct 2015 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Schäfer, A.S.* et al. Genetic evidence for PLASMINOGEN as a shared genetic risk factor of coronary artery disease and periodontitis. Circ. Cardiovasc. Genet. 8, 159-167 (2015)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42900&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42900&amp;la=de</guid>
      <pubDate>Fri, 05 Dec 2014 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Zeller, T.* et al. Molecular characterization of the NLRC4 expression in relation to interleukin-18 levels. Circ. Cardiovasc. Genet. 8, 717-726 (2015)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46794&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46794&amp;la=de</guid>
      <pubDate>Mon, 14 Sep 2015 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[de Villiers, C.P.* et al. AKAP9 is a genetic modifier of congenital long-QT syndrome type 1. Circ. Cardiovasc. Genet. 7, 599-606 (2014)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31877&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31877&amp;la=de</guid>
      <pubDate>Wed, 06 Aug 2014 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Holmes, M.V.* et al. Novel genetic approach to investigate the role of plasma secretory phospholipase A2 (sPLA(2))-V isoenzyme in coronary heart disease modified mendelian randomization analysis using PLA2G5 expression levels. Circ. Cardiovasc. Genet. 7, 144-150 (2014)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31380&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31380&amp;la=de</guid>
      <pubDate>Mon, 26 May 2014 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Kronenberg, F.* et al. Plasma concentrations of afamin are associated with the prevalence and development of metabolic syndrome. Circ. Cardiovasc. Genet. 7, 822-829 (2014)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=32064&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=32064&amp;la=de</guid>
      <pubDate>Wed, 03 Sep 2014 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Lüneburg, N.* et al. Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine. Circ. Cardiovasc. Genet. 7, 864-872 (2014)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=32360&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=32360&amp;la=de</guid>
      <pubDate>Thu, 25 Sep 2014 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Makita, N.* et al. Novel calmodulin (CALM2) mutations associated with congenital arrhythmia susceptibility. Circ. Cardiovasc. Genet. 7, 466-474 (2014)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31599&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31599&amp;la=de</guid>
      <pubDate>Fri, 13 Jun 2014 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Duchatelet, S.* et al. Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome. Circ. Cardiovasc. Genet. 6, 354-361 (2013)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=27317&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=27317&amp;la=de</guid>
      <pubDate>Fri, 20 Sep 2013 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Mäkelä, K.M.* et al. Genome-wide association study pinpoints a new functional apolipoprotein B variant influencing oxidized low-density lipoprotein levels but not cardiovascular events: AtheroRemo Consortium. Circ. Cardiovasc. Genet. 6, 73-81 (2013)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23530&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23530&amp;la=de</guid>
      <pubDate>Thu, 21 Mar 2013 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Chu, A.Y.* et al. Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy. Circ. Cardiovasc. Genet. 5, 676-685 (2012)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=11873&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=11873&amp;la=de</guid>
      <pubDate>Mon, 31 Dec 2012 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Davies, R.W.* et al. A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex. Circ. Cardiovasc. Genet. 5, 217-225 (2012)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=10545&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=10545&amp;la=de</guid>
      <pubDate>Wed, 24 Oct 2012 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Kääb, S.* et al. A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes. Circ. Cardiovasc. Genet. 5, 91-99 (2012)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8157&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8157&amp;la=de</guid>
      <pubDate>Tue, 24 Jul 2012 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Murabito, J.M.* et al. Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies. Circ. Cardiovasc. Genet. 5, 100-112 (2012)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8161&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8161&amp;la=de</guid>
      <pubDate>Tue, 24 Jul 2012 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Edmondson, A.C.* et al. Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol. Circ. Cardiovasc. Genet. 4, 145-155 (2011)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6753&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6753&amp;la=de</guid>
      <pubDate>Fri, 02 Dec 2011 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Lucas, G.* et al. Post-genomic update on a classical candidate gene for coronary artery disease: ESR1. Circ. Cardiovasc. Genet. 4, 647-654 (2011)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7315&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7315&amp;la=de</guid>
      <pubDate>Mon, 23 Apr 2012 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Meder, B.* et al. Targeted next-generation sequencing for the molecular genetic diagnostics of cardiomyopathies. Circ. Cardiovasc. Genet. 4, 110-122 (2011)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4062&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4062&amp;la=de</guid>
      <pubDate>Thu, 30 Jun 2011 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Schnabel, R.B.* et al. Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: The National Heart, Lung, and Blood Institute&#039;s Candidate Gene Association Resource (CARe) project. Circ. Cardiovasc. Genet. 4, 557-564 (2011)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6809&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6809&amp;la=de</guid>
      <pubDate>Wed, 21 Dec 2011 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Wild, P.S.* et al. A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. Circ. Cardiovasc. Genet. 4, 403-412 (2011)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6754&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6754&amp;la=de</guid>
      <pubDate>Fri, 02 Dec 2011 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Teupser, D.* et al. Genetic regulation of serum phytosterol levels and risk of coronary artery disease. Circ. Cardiovasc. Genet. 3, 331-339 (2010)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5579&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5579&amp;la=de</guid>
      <pubDate>Mon, 25 Oct 2010 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Body, S.C.* et al. Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgery. Circ. Cardiovasc. Genet. 2, 499-506 (2009)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=294&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=294&amp;la=de</guid>
      <pubDate>Thu, 31 Dec 2009 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Dehghan, A.* et al. Association of novel genetic Loci with circulating fibrinogen levels: A genome-wide association study in 6 population-based cohorts. Circ. Cardiovasc. Genet. 2, 125-133 (2009)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1033&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1033&amp;la=de</guid>
      <pubDate>Mon, 14 Sep 2009 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Marroni, F.* et al. A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: The EUROSPAN project. Circ. Cardiovasc. Genet. 2, 322-328 (2009)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=753&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=753&amp;la=de</guid>
      <pubDate>Thu, 31 Dec 2009 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Heid, I.M. et al. Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions. Circ. Cardiovasc. Genet. 1, 10-20 (2008)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5600&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5600&amp;la=de</guid>
      <pubDate>Wed, 31 Dec 2008 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Rutsch, F.* et al. Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy. Circ. Cardiovasc. Genet. 1, 133-40 (2008)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2618&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2618&amp;la=de</guid>
      <pubDate>Thu, 31 Dec 2009 00:00:00 +0000</pubDate>
    </item>
    
    <item>
      <title><![CDATA[Sedlacek, K.* et al. Common genetic variants in ANK2 modulate QT interval: Results from the KORA study. Circ. Cardiovasc. Genet. 1, 93-99 (2008)]]></title>
      <description><![CDATA[]]></description>
      <link>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4023&amp;la=de</link>
      <guid>https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4023&amp;la=de</guid>
      <pubDate>Wed, 31 Dec 2008 00:00:00 +0000</pubDate>
    </item>
    </channel>
</rss>