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<title>Nature Biotechnology</title>
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<title>Protein microarrays with carbon nanotubes as multicolor Raman labels</title>
<link>http://dx.doi.org/10.1038/nbt.1501</link>
<description>The picomolar sensitivity of fluorescence-based protein detection limits the use of protein arrays in research and clinical diagnosis. Chen et al. use antibody-tagged single-walled carbon nanotubes as multicolor Raman labels to detect femtomolar levels of serum analytes over a wide dynamic range.</description>
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<p>
<b>Protein microarrays with carbon nanotubes as multicolor Raman labels</b>
</p>
<p>Nature Biotechnology. <a href="http://dx.doi.org/10.1038/nbt.1501">doi:10.1038/nbt.1501</a>
</p>
<p>Authors: Zhuo Chen, Scott M Tabakman, Andrew P Goodwin, Michael G Kattah, Dan Daranciang, Xinran Wang, Guangyu Zhang, Xiaolin Li, Zhuang Liu, Paul J Utz, Kaili Jiang, Shoushan Fan
&amp; Hongjie Dai</p>
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<dc:title>Protein microarrays with carbon nanotubes as multicolor Raman labels</dc:title>
<dc:creator>Zhuo Chen</dc:creator>
<dc:creator>Scott M Tabakman</dc:creator>
<dc:creator>Andrew P Goodwin</dc:creator>
<dc:creator>Michael G Kattah</dc:creator>
<dc:creator>Dan Daranciang</dc:creator>
<dc:creator>Xinran Wang</dc:creator>
<dc:creator>Guangyu Zhang</dc:creator>
<dc:creator>Xiaolin Li</dc:creator>
<dc:creator>Zhuang Liu</dc:creator>
<dc:creator>Paul J Utz</dc:creator>
<dc:creator>Kaili Jiang</dc:creator>
<dc:creator>Shoushan Fan</dc:creator>
<dc:creator>Hongjie Dai</dc:creator>
<dc:identifier>doi:10.1038/nbt.1501</dc:identifier>
<dc:source>Nature Biotechnology</dc:source>
<dc:date>2008-10-26</dc:date>
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<title>Efficient and rapid generation of induced pluripotent stem cells from human keratinocytes</title>
<link>http://dx.doi.org/10.1038/nbt.1503</link>
<description>Aasen et al. boost the efficiency of human induced pluripotent stem (iPS) cell generation 100-fold by starting with keratinocytes rather than fibroblasts. They also produce iPS cells from plucked adult hair, an easily accessible source of cells that avoids the need for a biopsy.</description>
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<p>
<b>Efficient and rapid generation of induced pluripotent stem cells from human keratinocytes</b>
</p>
<p>Nature Biotechnology. <a href="http://dx.doi.org/10.1038/nbt.1503">doi:10.1038/nbt.1503</a>
</p>
<p>Authors: Trond Aasen, Angel Raya, Maria J Barrero, Elena Garreta, Antonella Consiglio, Federico Gonzalez, Rita Vassena, Josipa Bili&#263;, Vladimir Pekarik, Gustavo Tiscornia, Michael Edel, St&#233;phanie Bou&#233;
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<dc:title>Efficient and rapid generation of induced pluripotent stem cells from human keratinocytes</dc:title>
<dc:creator>Trond Aasen</dc:creator>
<dc:creator>Angel Raya</dc:creator>
<dc:creator>Maria J Barrero</dc:creator>
<dc:creator>Elena Garreta</dc:creator>
<dc:creator>Antonella Consiglio</dc:creator>
<dc:creator>Federico Gonzalez</dc:creator>
<dc:creator>Rita Vassena</dc:creator>
<dc:creator>Josipa Bili&#263;</dc:creator>
<dc:creator>Vladimir Pekarik</dc:creator>
<dc:creator>Gustavo Tiscornia</dc:creator>
<dc:creator>Michael Edel</dc:creator>
<dc:creator>St&#233;phanie Bou&#233;</dc:creator>
<dc:creator>Juan Carlos Izpis&#250; Belmonte</dc:creator>
<dc:identifier>doi:10.1038/nbt.1503</dc:identifier>
<dc:source>Nature Biotechnology</dc:source>
<dc:date>2008-10-17</dc:date>
<prism:publicationName>Nature Biotechnology</prism:publicationName>
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<title>Induction of pluripotent stem cells from primary human fibroblasts with only Oct4 and Sox2</title>
<link>http://dx.doi.org/10.1038/nbt.1502</link>
<description>One strategy for advancing induced pluripotent stem (iPS) cell technology toward the clinic is to replace the reprogramming genes with small molecules. Huangfu et al. show that the HDAC inhibitor valproic acid can substitute for the reprogramming gene Klf4, allowing human iPS cells to be generated with only two transgenes, Oct4 and Sox2.</description>
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<p>
<b>Induction of pluripotent stem cells from primary human fibroblasts with only Oct4 and Sox2</b>
</p>
<p>Nature Biotechnology. <a href="http://dx.doi.org/10.1038/nbt.1502">doi:10.1038/nbt.1502</a>
</p>
<p>Authors: Danwei Huangfu, Kenji Osafune, Ren&#233; Maehr, Wenjun Guo, Astrid Eijkelenboom, Shuibing Chen, Whitney Muhlestein
&amp; Douglas A Melton</p>
]]></content:encoded>
<dc:title>Induction of pluripotent stem cells from primary human fibroblasts with only Oct4 and Sox2</dc:title>
<dc:creator>Danwei Huangfu</dc:creator>
<dc:creator>Kenji Osafune</dc:creator>
<dc:creator>Ren&#233; Maehr</dc:creator>
<dc:creator>Wenjun Guo</dc:creator>
<dc:creator>Astrid Eijkelenboom</dc:creator>
<dc:creator>Shuibing Chen</dc:creator>
<dc:creator>Whitney Muhlestein</dc:creator>
<dc:creator>Douglas A Melton</dc:creator>
<dc:identifier>doi:10.1038/nbt.1502</dc:identifier>
<dc:source>Nature Biotechnology</dc:source>
<dc:date>2008-10-12</dc:date>
<prism:publicationName>Nature Biotechnology</prism:publicationName>
<prism:publicationDate>2008-10-12</prism:publicationDate>
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<title>An integrated software system for analyzing ChIP-chip and ChIP-seq data</title>
<link>http://dx.doi.org/10.1038/nbt.1505</link>
<description>Analyzing the massive and heterogenous datasets from genome-wide chromatin immunoprecipitation (ChIP) datasets presents several computational and statistical challenges. Ji et al. present a software suite that integrates all steps in ChIP-chip and ChIP-seq data analyses and illustrate the use of these tools by comparing the ability of the two platforms to identify transcription factor binding sites.</description>
<content:encoded><![CDATA[

<p>
<b>An integrated software system for analyzing ChIP-chip and ChIP-seq data</b>
</p>
<p>Nature Biotechnology. <a href="http://dx.doi.org/10.1038/nbt.1505">doi:10.1038/nbt.1505</a>
</p>
<p>Authors: Hongkai Ji, Hui Jiang, Wenxiu Ma, David S Johnson, Richard M Myers
&amp; Wing H Wong</p>
]]></content:encoded>
<dc:title>An integrated software system for analyzing ChIP-chip and ChIP-seq data</dc:title>
<dc:creator>Hongkai Ji</dc:creator>
<dc:creator>Hui Jiang</dc:creator>
<dc:creator>Wenxiu Ma</dc:creator>
<dc:creator>David S Johnson</dc:creator>
<dc:creator>Richard M Myers</dc:creator>
<dc:creator>Wing H Wong</dc:creator>
<dc:identifier>doi:10.1038/nbt.1505</dc:identifier>
<dc:source>Nature Biotechnology</dc:source>
<dc:date>2008-11-02</dc:date>
<prism:publicationName>Nature Biotechnology</prism:publicationName>
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<title>Enrichment of tomato fruit with health-promoting anthocyanins by expression of select transcription factors</title>
<link>http://dx.doi.org/10.1038/nbt.1506</link>
<description>Fruit-specific overexpression of a pair of snapdragon transcription factors produces tomatoes that uniformly accumulate anthocyanins at levels unprecedented for metabolic engineering.  When included as a dietary supplement, the purple tomatoes increase the life spans of tumorigenic p53 knockout mice.</description>
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<p>
<b>Enrichment of tomato fruit with health-promoting anthocyanins by expression of select transcription factors</b>
</p>
<p>Nature Biotechnology. <a href="http://dx.doi.org/10.1038/nbt.1506">doi:10.1038/nbt.1506</a>
</p>
<p>Authors: Eugenio Butelli, Lucilla Titta, Marco Giorgio, Hans-Peter Mock, Andrea Matros, Silke Peterek, Elio G W M Schijlen, Robert D Hall, Arnaud G Bovy, Jie Luo
&amp; Cathie Martin</p>
<p>Dietary consumption of anthocyanins, a class of pigments produced by higher plants, has been associated with protection against a broad range of human diseases. However, anthocyanin levels in the most commonly eaten fruits and vegetables may be inadequate to confer optimal benefits. When we expressed two transcription factors from snapdragon in tomato, the fruit of the plants accumulated anthocyanins at levels substantially higher than previously reported for efforts to engineer anthocyanin accumulation in tomato and at concentrations comparable to the anthocyanin levels found in blackberries and blueberries. Expression of the two transgenes enhanced the hydrophilic antioxidant capacity of tomato fruit threefold and resulted in fruit with intense purple coloration in both peel and flesh. In a pilot test, cancer-susceptible Trp53&#8722;/&#8722; mice fed a diet supplemented with the high-anthocyanin tomatoes showed a significant extension of life span.</p>
]]></content:encoded>
<dc:title>Enrichment of tomato fruit with health-promoting anthocyanins by expression of select transcription factors</dc:title>
<dc:creator>Eugenio Butelli</dc:creator>
<dc:creator>Lucilla Titta</dc:creator>
<dc:creator>Marco Giorgio</dc:creator>
<dc:creator>Hans-Peter Mock</dc:creator>
<dc:creator>Andrea Matros</dc:creator>
<dc:creator>Silke Peterek</dc:creator>
<dc:creator>Elio G W M Schijlen</dc:creator>
<dc:creator>Robert D Hall</dc:creator>
<dc:creator>Arnaud G Bovy</dc:creator>
<dc:creator>Jie Luo</dc:creator>
<dc:creator>Cathie Martin</dc:creator>
<dc:identifier>doi:10.1038/nbt.1506</dc:identifier>
<dc:source>Nature Biotechnology</dc:source>
<dc:date>2008-10-26</dc:date>
<prism:publicationName>Nature Biotechnology</prism:publicationName>
<prism:publicationDate>2008-10-26</prism:publicationDate>
<prism:section>Letter</prism:section>
</item>
<item rdf:about="http://dx.doi.org/10.1038/nbt.1499">
<title>Activity motifs reveal principles of timing in transcriptional control of the yeast metabolic network</title>
<link>http://dx.doi.org/10.1038/nbt.1499</link>
<description>Chechik et al. define activity motifs, which extend the concept of a network motif from the static to the dynamic realm. Mapping functional data onto network structure enables them to reveal new systems-level principles describing how yeast cells integrate exogenous signals and use transcriptional regulation to optimize metabolic responses to environmental perturbations.</description>
<content:encoded><![CDATA[

<p>
<b>Activity motifs reveal principles of timing in transcriptional control of the yeast metabolic network</b>
</p>
<p>Nature Biotechnology. <a href="http://dx.doi.org/10.1038/nbt.1499">doi:10.1038/nbt.1499</a>
</p>
<p>Authors: Gal Chechik, Eugene Oh, Oliver Rando, Jonathan Weissman, Aviv Regev
&amp; Daphne Koller</p>
]]></content:encoded>
<dc:title>Activity motifs reveal principles of timing in transcriptional control of the yeast metabolic network</dc:title>
<dc:creator>Gal Chechik</dc:creator>
<dc:creator>Eugene Oh</dc:creator>
<dc:creator>Oliver Rando</dc:creator>
<dc:creator>Jonathan Weissman</dc:creator>
<dc:creator>Aviv Regev</dc:creator>
<dc:creator>Daphne Koller</dc:creator>
<dc:identifier>doi:10.1038/nbt.1499</dc:identifier>
<dc:source>Nature Biotechnology</dc:source>
<dc:date>2008-10-26</dc:date>
<prism:publicationName>Nature Biotechnology</prism:publicationName>
<prism:publicationDate>2008-10-26</prism:publicationDate>
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