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<title>Generating specificity and diversity in the transcriptional response to hypoxia</title>
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<description>The sensing of oxygen levels and maintenance of oxygen homeostasis is crucial for cells. The hypoxic-sensitive regulation of gene expression allows information about the oxygen status to be converted into appropriate cellular responses. Although there is a core transcriptional pathway, the signalling cascade can be </description>
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<p>
<b>Generating specificity and diversity in the transcriptional response to hypoxia</b>
</p>
<p>Nature Reviews Genetics 10, 821 (2009). <a href="http://dx.doi.org/10.1038/nrg2665">doi:10.1038/nrg2665</a>
</p>
<p>Authors: Urban Lendahl, Kian Leong Lee, Henry Yang &amp; Lorenz Poellinger</p>
<p>The sensing of oxygen levels and maintenance of oxygen homeostasis is crucial for cells. The hypoxic-sensitive regulation of gene expression allows information about the oxygen status to be converted into appropriate cellular responses. Although there is a core transcriptional pathway, the signalling cascade can be </p>
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<dc:title>Generating specificity and diversity in the transcriptional response to hypoxia</dc:title>
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<dc:creator>Kian Leong Lee</dc:creator>
<dc:creator>Henry Yang</dc:creator>
<dc:creator>Lorenz Poellinger</dc:creator>
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<title>Common disorders are quantitative traits</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/o9ps23l-TyE/nrg2670</link>
<description>After drifting apart for 100 years, the two worlds of genetics — quantitative genetics and molecular genetics — are finally coming together in genome-wide association (GWA) research, which shows that the heritability of complex traits and common disorders is due to multiple genes of small </description>
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<p>
<b>Common disorders are quantitative traits</b>
</p>
<p>Nature Reviews Genetics 10, 872 (2009). <a href="http://dx.doi.org/10.1038/nrg2670">doi:10.1038/nrg2670</a>
</p>
<p>Authors: Robert Plomin, Claire M. A. Haworth &amp; Oliver S. P. Davis</p>
<p>After drifting apart for 100 years, the two worlds of genetics &#8212; quantitative genetics and molecular genetics &#8212; are finally coming together in genome-wide association (GWA) research, which shows that the heritability of complex traits and common disorders is due to multiple genes of small </p>
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<dc:title>Common disorders are quantitative traits</dc:title>
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<dc:creator>Claire M. A. Haworth</dc:creator>
<dc:creator>Oliver S. P. Davis</dc:creator>
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<title>Synthetic biology: understanding biological design from synthetic circuits</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/mcWGpDtwgAE/nrg2697</link>
<description>An important aim of synthetic biology is to uncover the design principles of natural biological systems through the rational design of gene and protein circuits. Here, we highlight how the process of engineering biological systems — from synthetic promoters to the control of cell–cell interactions </description>
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<p>
<b>Synthetic biology: understanding biological design from synthetic circuits</b>
</p>
<p>Nature Reviews Genetics 10, 859 (2009). <a href="http://dx.doi.org/10.1038/nrg2697">doi:10.1038/nrg2697</a>
</p>
<p>Authors: Shankar Mukherji &amp; Alexander van Oudenaarden</p>
<p>An important aim of synthetic biology is to uncover the design principles of natural biological systems through the rational design of gene and protein circuits. Here, we highlight how the process of engineering biological systems &#8212; from synthetic promoters to the control of cell&#8211;cell interactions </p>
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<dc:title>Synthetic biology: understanding biological design from synthetic circuits</dc:title>
<dc:creator>Shankar Mukherji</dc:creator>
<dc:creator>Alexander van Oudenaarden</dc:creator>
<dc:identifier>doi:10.1038/nrg2697</dc:identifier>
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<title>Induced pluripotent stem cells and reprogramming: seeing the science through the hype</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/0IzTmrfCU9c/nrg2700</link>
<description>No-one can have failed to notice the splash that induced pluripotent stem (iPS) cells have made in the few years since somatic cells were first reprogrammed to pluripotency. But what is their real promise, where should research efforts be focused, and are we at a </description>
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<p>
<b>Induced pluripotent stem cells and reprogramming: seeing the science through the hype</b>
</p>
<p>Nature Reviews Genetics 10, 878 (2009). <a href="http://dx.doi.org/10.1038/nrg2700">doi:10.1038/nrg2700</a>
</p>
<p>Authors: Juan Carlos Izpis&#250;a Belmonte, James Ellis, Konrad Hochedlinger &amp; Shinya Yamanaka</p>
<p>No-one can have failed to notice the splash that induced pluripotent stem (iPS) cells have made in the few years since somatic cells were first reprogrammed to pluripotency. But what is their real promise, where should research efforts be focused, and are we at a </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/0IzTmrfCU9c" height="1" width="1"/>]]></content:encoded>
<dc:title>Induced pluripotent stem cells and reprogramming: seeing the science through the hype</dc:title>
<dc:creator>Juan Carlos Izpisúa Belmonte</dc:creator>
<dc:creator>James Ellis</dc:creator>
<dc:creator>Konrad Hochedlinger</dc:creator>
<dc:creator>Shinya Yamanaka</dc:creator>
<dc:identifier>doi:10.1038/nrg2700</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 878 (2009)</dc:source>
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<title>Chromatin: Mapping genome-wide chromosome interactions</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/Nt-A4I6bc8s/nrg2701</link>
<description>Understanding chromosome folding is crucial for understanding the relationships between chromatin structure, gene activity and cellular function. Although recent technological developments, such as chromosome conformation capture (3C), have allowed the investigation of long-range interactions associated with specific loci, they do not allow unbiased genome-wide assessment </description>
<content:encoded><![CDATA[

<p>
<b>Chromatin: Mapping genome-wide chromosome interactions</b>
</p>
<p>Nature Reviews Genetics 10, 816 (2009). <a href="http://dx.doi.org/10.1038/nrg2701">doi:10.1038/nrg2701</a>
</p>
<p>Author: Meera Swami</p>
<p>Understanding chromosome folding is crucial for understanding the relationships between chromatin structure, gene activity and cellular function. Although recent technological developments, such as chromosome conformation capture (3C), have allowed the investigation of long-range interactions associated with specific loci, they do not allow unbiased genome-wide assessment </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/Nt-A4I6bc8s" height="1" width="1"/>]]></content:encoded>
<dc:title>Chromatin: Mapping genome-wide chromosome interactions</dc:title>
<dc:creator>Meera Swami</dc:creator>
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<dc:source>Nature Reviews Genetics 10, 816 (2009)</dc:source>
<dc:date>2009-10-27</dc:date>
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<title>Epigenetics: An expanding horizon for DNA methylation</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/c_qFcz-qFM4/nrg2702</link>
<description>The classical view of DNA methylation in mammals is that methylation of cytosine occurs in the context of CG dinucleotides, and that methylation patterns are established during embryogenesis and maintained in somatic cells, which enables the long-term stable silencing of transcription. Two recent papers shake </description>
<content:encoded><![CDATA[

<p>
<b>Epigenetics: An expanding horizon for DNA methylation</b>
</p>
<p>Nature Reviews Genetics 10, 818 (2009). <a href="http://dx.doi.org/10.1038/nrg2702">doi:10.1038/nrg2702</a>
</p>
<p>Author: Mary Muers</p>
<p>The classical view of DNA methylation in mammals is that methylation of cytosine occurs in the context of CG dinucleotides, and that methylation patterns are established during embryogenesis and maintained in somatic cells, which enables the long-term stable silencing of transcription. Two recent papers shake </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/c_qFcz-qFM4" height="1" width="1"/>]]></content:encoded>
<dc:title>Epigenetics: An expanding horizon for DNA methylation</dc:title>
<dc:creator>Mary Muers</dc:creator>
<dc:identifier>doi:10.1038/nrg2702</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 818 (2009)</dc:source>
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<title>Sex determination: The means to discriminate</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/tMNRhM6oK_k/nrg2704</link>
<description>Nature has a startling number of ways in which to establish differences between the sexes, and now a couple more can be added. In melons, an integrated model of sex determination — based on epigenetic repression mediated by a transposon — has been proposed to </description>
<content:encoded><![CDATA[

<p>
<b>Sex determination: The means to discriminate</b>
</p>
<p>Nature Reviews Genetics 10, 818 (2009). <a href="http://dx.doi.org/10.1038/nrg2704">doi:10.1038/nrg2704</a>
</p>
<p>Author: Tanita Casci</p>
<p>Nature has a startling number of ways in which to establish differences between the sexes, and now a couple more can be added. In melons, an integrated model of sex determination &#8212; based on epigenetic repression mediated by a transposon &#8212; has been proposed to </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/tMNRhM6oK_k" height="1" width="1"/>]]></content:encoded>
<dc:title>Sex determination: The means to discriminate</dc:title>
<dc:creator>Tanita Casci</dc:creator>
<dc:identifier>doi:10.1038/nrg2704</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 818 (2009)</dc:source>
<dc:date>2009-11-03</dc:date>
<prism:publicationName>Nature Reviews Genetics</prism:publicationName>
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<title>Speciation: New insights into hybrid sterility</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/C8lpMpBaXvQ/nrg2705</link>
<description>Speciation occurs when populations accumulate genetic differences that lead them to become reproductively isolated. Although many loci involved in reproductive incompatibility have been identified, the underlying biological mechanisms have remained elusive. Now, the first steps of a mechanism for hybrid sterility have been characterized in </description>
<content:encoded><![CDATA[

<p>
<b>Speciation: New insights into hybrid sterility</b>
</p>
<p>Nature Reviews Genetics 10, 820 (2009). <a href="http://dx.doi.org/10.1038/nrg2705">doi:10.1038/nrg2705</a>
</p>
<p>Author: Meera Swami</p>
<p>Speciation occurs when populations accumulate genetic differences that lead them to become reproductively isolated. Although many loci involved in reproductive incompatibility have been identified, the underlying biological mechanisms have remained elusive. Now, the first steps of a mechanism for hybrid sterility have been characterized in </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/C8lpMpBaXvQ" height="1" width="1"/>]]></content:encoded>
<dc:title>Speciation: New insights into hybrid sterility</dc:title>
<dc:creator>Meera Swami</dc:creator>
<dc:identifier>doi:10.1038/nrg2705</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 820 (2009)</dc:source>
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<title>Evolution: The routes of adaptation</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/zSCAediNZgM/nrg2706</link>
<description>Two studies that combine experimental evolution and genome resequencing have provided new insights into bacterial adaptation. One study reveals unexpected relationships between new mutations and their adaptive significance, whereas the other gives a mechanistic account of the evolution of rapid phenotype switching.Important questions about </description>
<content:encoded><![CDATA[

<p>
<b>Evolution: The routes of adaptation</b>
</p>
<p>Nature Reviews Genetics 10, 815 (2009). <a href="http://dx.doi.org/10.1038/nrg2706">doi:10.1038/nrg2706</a>
</p>
<p>Author: Tanita Casci</p>
<p>Two studies that combine experimental evolution and genome resequencing have provided new insights into bacterial adaptation. One study reveals unexpected relationships between new mutations and their adaptive significance, whereas the other gives a mechanistic account of the evolution of rapid phenotype switching.Important questions about </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/zSCAediNZgM" height="1" width="1"/>]]></content:encoded>
<dc:title>Evolution: The routes of adaptation</dc:title>
<dc:creator>Tanita Casci</dc:creator>
<dc:identifier>doi:10.1038/nrg2706</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 815 (2009)</dc:source>
<dc:date>2009-11-10</dc:date>
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<title>Gene expression: Regulators hidden in human proteome</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/SRvxvZHZVkY/nrg2708</link>
<description>A search for DNA–protein interactions has unexpectedly pulled out over 300 human proteins that are known for other biological roles. By highlighting the multitasking function of many human proteins, this work provides a new perspective on the molecular basis of organismal complexity.The study used </description>
<content:encoded><![CDATA[

<p>
<b>Gene expression: Regulators hidden in human proteome</b>
</p>
<p>Nature Reviews Genetics 10, 820 (2009). <a href="http://dx.doi.org/10.1038/nrg2708">doi:10.1038/nrg2708</a>
</p>
<p>Author: Tanita Casci</p>
<p>A search for DNA&#8211;protein interactions has unexpectedly pulled out over 300 human proteins that are known for other biological roles. By highlighting the multitasking function of many human proteins, this work provides a new perspective on the molecular basis of organismal complexity.The study used </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/SRvxvZHZVkY" height="1" width="1"/>]]></content:encoded>
<dc:title>Gene expression: Regulators hidden in human proteome</dc:title>
<dc:creator>Tanita Casci</dc:creator>
<dc:identifier>doi:10.1038/nrg2708</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 820 (2009)</dc:source>
<dc:date>2009-11-10</dc:date>
<prism:publicationName>Nature Reviews Genetics</prism:publicationName>
<prism:publicationDate>2009-11-10</prism:publicationDate>
<prism:doi>10.1038/nrg2708</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrg2708</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>820</prism:startingPage>
<prism:endingPage>820</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrg2709">
<title>Development: Size control by divide and rule</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/JPTuLc_FqeI/nrg2709</link>
<description>Size can be controlled at many levels, including the size a cell attains before it divides and the number of cells that form a complete organ. Therefore, as shown by two recent papers, lessons about growth regulation can be learnt both from studies of intrinsic </description>
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<p>
<b>Development: Size control by divide and rule</b>
</p>
<p>Nature Reviews Genetics 10, 816 (2009). <a href="http://dx.doi.org/10.1038/nrg2709">doi:10.1038/nrg2709</a>
</p>
<p>Author: Mary Muers</p>
<p>Size can be controlled at many levels, including the size a cell attains before it divides and the number of cells that form a complete organ. Therefore, as shown by two recent papers, lessons about growth regulation can be learnt both from studies of intrinsic </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/JPTuLc_FqeI" height="1" width="1"/>]]></content:encoded>
<dc:title>Development: Size control by divide and rule</dc:title>
<dc:creator>Mary Muers</dc:creator>
<dc:identifier>doi:10.1038/nrg2709</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 816 (2009)</dc:source>
<dc:date>2009-11-10</dc:date>
<prism:publicationName>Nature Reviews Genetics</prism:publicationName>
<prism:publicationDate>2009-11-10</prism:publicationDate>
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<prism:url>http://dx.doi.org/10.1038/nrg2709</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
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<item rdf:about="http://dx.doi.org/10.1038/nrg2715">
<title>Common disorders are quantitative traits</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/_pKz5ZJsLiU/nrg2715</link>
<description>Nature Rev. Genet.10, 872–878 (2009)An incorrect version of this article was previously published online (publication date 27 October 2009). In the second paragraph of the 'Identifying quantitative mechanisms' section on page 874 in this article, the </description>
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<p>
<b>Common disorders are quantitative traits</b>
</p>
<p>Nature Reviews Genetics 10, 883 (2009). <a href="http://dx.doi.org/10.1038/nrg2715">doi:10.1038/nrg2715</a>
</p>
<p>Author: Robert Plomin, Claire M. A. Haworth &amp; Oliver S. P. Davis</p>
<p>Nature Rev. Genet.10, 872&#8211;878 (2009)An incorrect version of this article was previously published online (publication date 27 October 2009). In the second paragraph of the 'Identifying quantitative mechanisms' section on page 874 in this article, the </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/_pKz5ZJsLiU" height="1" width="1"/>]]></content:encoded>
<dc:title>Common disorders are quantitative traits</dc:title>
<dc:creator>Robert Plomin</dc:creator>
<dc:creator>Claire M. A. Haworth</dc:creator>
<dc:creator>Oliver S. P. Davis</dc:creator>
<dc:identifier>doi:10.1038/nrg2715</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 883 (2009)</dc:source>
<dc:date>2009-11-09</dc:date>
<prism:publicationName>Nature Reviews Genetics</prism:publicationName>
<prism:publicationDate>2009-11-09</prism:publicationDate>
<prism:doi>10.1038/nrg2715</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrg2715</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Corrigendum</prism:section>
<prism:startingPage>883</prism:startingPage>
<prism:endingPage>883</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrg2715</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrg2681">
<title>Vertebrate limb bud development: moving towards integrative analysis of organogenesis</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/aosCco0IsIk/nrg2681</link>
<description>The limb bud is of paradigmatic value to understanding vertebrate organogenesis. Recent genetic analysis in mice has revealed the existence of a largely self-regulatory limb bud signalling system that involves many of the pathways that are known to regulate morphogenesis. These findings contrast with the </description>
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<p>
<b>Vertebrate limb bud development: moving towards integrative analysis of organogenesis</b>
</p>
<p>Nature Reviews Genetics 10, 845 (2009). <a href="http://dx.doi.org/10.1038/nrg2681">doi:10.1038/nrg2681</a>
</p>
<p>Authors: Rolf Zeller, Javier L&#243;pez-R&#237;os &amp; Aim&#233;e Zuniga</p>
<p>The limb bud is of paradigmatic value to understanding vertebrate organogenesis. Recent genetic analysis in mice has revealed the existence of a largely self-regulatory limb bud signalling system that involves many of the pathways that are known to regulate morphogenesis. These findings contrast with the </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/aosCco0IsIk" height="1" width="1"/>]]></content:encoded>
<dc:title>Vertebrate limb bud development: moving towards integrative analysis of organogenesis</dc:title>
<dc:creator>Rolf Zeller</dc:creator>
<dc:creator>Javier López-Ríos</dc:creator>
<dc:creator>Aimée Zuniga</dc:creator>
<dc:identifier>doi:10.1038/nrg2681</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 845 (2009)</dc:source>
<prism:publicationName>Nature Reviews Genetics</prism:publicationName>
<prism:doi>10.1038/nrg2681</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrg2681</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>845</prism:startingPage>
<prism:endingPage>858</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrg2681</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrg2683">
<title>The complex eukaryotic transcriptome: unexpected pervasive transcription and novel small RNAs</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/1rDJ7FwuTSE/nrg2683</link>
<description>Over the past few years, techniques have been developed that have allowed the study of transcriptomes without bias from previous genome annotations, which has led to the discovery of a plethora of unexpected RNAs that have no obvious coding capacities. There are many different kinds </description>
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<p>
<b>The complex eukaryotic transcriptome: unexpected pervasive transcription and novel small RNAs</b>
</p>
<p>Nature Reviews Genetics 10, 833 (2009). <a href="http://dx.doi.org/10.1038/nrg2683">doi:10.1038/nrg2683</a>
</p>
<p>Author: Alain Jacquier</p>
<p>Over the past few years, techniques have been developed that have allowed the study of transcriptomes without bias from previous genome annotations, which has led to the discovery of a plethora of unexpected RNAs that have no obvious coding capacities. There are many different kinds </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/1rDJ7FwuTSE" height="1" width="1"/>]]></content:encoded>
<dc:title>The complex eukaryotic transcriptome: unexpected pervasive transcription and novel small RNAs</dc:title>
<dc:creator>Alain Jacquier</dc:creator>
<dc:identifier>doi:10.1038/nrg2683</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 833 (2009)</dc:source>
<prism:publicationName>Nature Reviews Genetics</prism:publicationName>
<prism:doi>10.1038/nrg2683</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrg2683</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>833</prism:startingPage>
<prism:endingPage>844</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrg2683</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrg2710">
<title>Genetic and molecular insights into the development and evolution of sexual dimorphism</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/3EYZW0Lqkow/nrg2710</link>
<description>Nature Reviews Genetics10, 797–804 (2009)The image in Figure 1d of this article was incorrectly attributed to C. Lambert, whereas the source of the figure is actually unknown. The authors apologize for the error.</description>
<content:encoded><![CDATA[

<p>
<b>Genetic and molecular insights into the development and evolution of sexual dimorphism</b>
</p>
<p>Nature Reviews Genetics 10, 883 (2009). <a href="http://dx.doi.org/10.1038/nrg2710">doi:10.1038/nrg2710</a>
</p>
<p>Author: Thomas M. Williams &amp; Sean B. Carroll</p>
<p>Nature Reviews Genetics10, 797&#8211;804 (2009)The image in Figure 1d of this article was incorrectly attributed to C. Lambert, whereas the source of the figure is actually unknown. The authors apologize for the error.</p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/3EYZW0Lqkow" height="1" width="1"/>]]></content:encoded>
<dc:title>Genetic and molecular insights into the development and evolution of sexual dimorphism</dc:title>
<dc:creator>Thomas M. Williams</dc:creator>
<dc:creator>Sean B. Carroll</dc:creator>
<dc:identifier>doi:10.1038/nrg2710</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 883 (2009)</dc:source>
<prism:publicationName>Nature Reviews Genetics</prism:publicationName>
<prism:doi>10.1038/nrg2710</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrg2710</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Corrigendum</prism:section>
<prism:startingPage>883</prism:startingPage>
<prism:endingPage>883</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrg2710</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrg2711">
<title>Ageing: The impact of shrinking telomeres</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/B4LQpcucKtY/nrg2711</link>
<description>Shortening of telomeres to a critical length triggers a DNA-damage response that contributes to ageing. A new study using a mouse model of accelerated telomere shortening reveals specific transcriptomic and epigenetic changes that provide clues to how telomere shortening is linked to ageing.The Terc </description>
<content:encoded><![CDATA[

<p>
<b>Ageing: The impact of shrinking telomeres</b>
</p>
<p>Nature Reviews Genetics 10, 816 (2009). <a href="http://dx.doi.org/10.1038/nrg2711">doi:10.1038/nrg2711</a>
</p>
<p>Author: Louisa Flintoft</p>
<p>Shortening of telomeres to a critical length triggers a DNA-damage response that contributes to ageing. A new study using a mouse model of accelerated telomere shortening reveals specific transcriptomic and epigenetic changes that provide clues to how telomere shortening is linked to ageing.The Terc </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/B4LQpcucKtY" height="1" width="1"/>]]></content:encoded>
<dc:title>Ageing: The impact of shrinking telomeres</dc:title>
<dc:creator>Louisa Flintoft</dc:creator>
<dc:identifier>doi:10.1038/nrg2711</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 816 (2009)</dc:source>
<prism:publicationName>Nature Reviews Genetics</prism:publicationName>
<prism:doi>10.1038/nrg2711</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrg2711</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>816</prism:startingPage>
<prism:endingPage>816</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrg2711</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrg2713">
<title>In Brief</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/XdB84BxwBrU/nrg2713</link>
<description>Sequencing technologies</description>
<content:encoded><![CDATA[

<p>
<b>In Brief</b>
</p>
<p>Nature Reviews Genetics 10, 817 (2009). <a href="http://dx.doi.org/10.1038/nrg2713">doi:10.1038/nrg2713</a>
</p>
<p>Sequencing technologies</p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/XdB84BxwBrU" height="1" width="1"/>]]></content:encoded>
<dc:title>In Brief</dc:title>
<dc:identifier>doi:10.1038/nrg2713</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 817 (2009)</dc:source>
<prism:publicationName>Nature Reviews Genetics</prism:publicationName>
<prism:doi>10.1038/nrg2713</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrg2713</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>817</prism:startingPage>
<prism:endingPage>817</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrg2713</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrg2714">
<title>In Brief</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/-8cIjG-QZ0U/nrg2714</link>
<description>Human disease</description>
<content:encoded><![CDATA[

<p>
<b>In Brief</b>
</p>
<p>Nature Reviews Genetics 10, 819 (2009). <a href="http://dx.doi.org/10.1038/nrg2714">doi:10.1038/nrg2714</a>
</p>
<p>Human disease</p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/-8cIjG-QZ0U" height="1" width="1"/>]]></content:encoded>
<dc:title>In Brief</dc:title>
<dc:identifier>doi:10.1038/nrg2714</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 819 (2009)</dc:source>
<prism:publicationName>Nature Reviews Genetics</prism:publicationName>
<prism:doi>10.1038/nrg2714</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrg2714</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>819</prism:startingPage>
<prism:endingPage>819</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrg2716">
<title>From the editors</title>
<link>http://feeds.nature.com/~r/nrg/rss/current/~3/oP9RsTw6XhI/nrg2716</link>
<description>Certain technologies have changed the face of genetic research — notable examples being DNA cloning, Sanger sequencing and PCR. Now, next-generation sequencing is making waves that are being felt across genetics and genomics.As sequencing costs continue to fall, we will see a rapid increase </description>
<content:encoded><![CDATA[

<p>
<b>From the editors</b>
</p>
<p>Nature Reviews Genetics 10, 813 (2009). <a href="http://dx.doi.org/10.1038/nrg2716">doi:10.1038/nrg2716</a>
</p>
<p>Certain technologies have changed the face of genetic research &#8212; notable examples being DNA cloning, Sanger sequencing and PCR. Now, next-generation sequencing is making waves that are being felt across genetics and genomics.As sequencing costs continue to fall, we will see a rapid increase </p>
<img src="http://feeds.feedburner.com/~r/nrg/rss/current/~4/oP9RsTw6XhI" height="1" width="1"/>]]></content:encoded>
<dc:title>From the editors</dc:title>
<dc:identifier>doi:10.1038/nrg2716</dc:identifier>
<dc:source>Nature Reviews Genetics 10, 813 (2009)</dc:source>
<prism:publicationName>Nature Reviews Genetics</prism:publicationName>
<prism:doi>10.1038/nrg2716</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrg2716</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>From The Editors</prism:section>
<prism:startingPage>813</prism:startingPage>
<prism:endingPage>813</prism:endingPage>
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