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<title>Cell stimulation with optically manipulated microsources</title>
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<description>Microsources positioned with holographic optical tweezers can establish a highly localized, three-dimensional chemical gradient that allows the manipulation of polarization and migration in single cells.</description>
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<b>Cell stimulation with optically manipulated microsources</b>
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<p>Nature Methods. <a href="http://dx.doi.org/10.1038/nmeth.1400">doi:10.1038/nmeth.1400</a>
</p>
<p>Authors: Holger Kress, Jin-Gyu Park, Cecile O Mejean, Jason D Forster, Jason Park, Spencer S Walse, Yong Zhang, Dianqing Wu, Orion D Weiner, Tarek M Fahmy &amp; Eric R Dufresne</p>
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<dc:title>Cell stimulation with optically manipulated microsources</dc:title>
<dc:creator>Holger Kress</dc:creator>
<dc:creator>Jin-Gyu Park</dc:creator>
<dc:creator>Cecile O Mejean</dc:creator>
<dc:creator>Jason D Forster</dc:creator>
<dc:creator>Jason Park</dc:creator>
<dc:creator>Spencer S Walse</dc:creator>
<dc:creator>Yong Zhang</dc:creator>
<dc:creator>Dianqing Wu</dc:creator>
<dc:creator>Orion D Weiner</dc:creator>
<dc:creator>Tarek M Fahmy</dc:creator>
<dc:creator>Eric R Dufresne</dc:creator>
<dc:identifier>doi:10.1038/nmeth.1400</dc:identifier>
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<dc:date>2009-11-15</dc:date>
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<title>Transgenic microRNA inhibition with spatiotemporal specificity in intact organisms</title>
<link>http://feeds.nature.com/~r/nmeth/rss/aop/~3/-C3PqXqmJ9U/nmeth.1402</link>
<description>Tissue-specific expression of microRNA sponges allows precise regulation of microRNA activity in living flies. The authors investigate the role of miR-8 in the formation of neuromuscular junctions in detail.</description>
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<p>
<b>Transgenic microRNA inhibition with spatiotemporal specificity in intact organisms</b>
</p>
<p>Nature Methods. <a href="http://dx.doi.org/10.1038/nmeth.1402">doi:10.1038/nmeth.1402</a>
</p>
<p>Authors: Carlos M Loya, Cecilia S Lu, David Van Vactor &amp; Tudor A Fulga</p>
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<dc:title>Transgenic microRNA inhibition with spatiotemporal specificity in intact organisms</dc:title>
<dc:creator>Carlos M Loya</dc:creator>
<dc:creator>Cecilia S Lu</dc:creator>
<dc:creator>David Van Vactor</dc:creator>
<dc:creator>Tudor A Fulga</dc:creator>
<dc:identifier>doi:10.1038/nmeth.1402</dc:identifier>
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<title>An auxin-based degron system for the rapid depletion of proteins in nonplant cells</title>
<link>http://feeds.nature.com/~r/nmeth/rss/aop/~3/ua8lLmIFch0/nmeth.1401</link>
<description>A degradation pathway found in plants, dependent on the hormone auxin, can be transplanted and harnessed to induce rapid and reversible target protein degradation in both yeast and animal cells.</description>
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<p>
<b>An auxin-based degron system for the rapid depletion of proteins in nonplant cells</b>
</p>
<p>Nature Methods. <a href="http://dx.doi.org/10.1038/nmeth.1401">doi:10.1038/nmeth.1401</a>
</p>
<p>Authors: Kohei Nishimura, Tatsuo Fukagawa, Haruhiko Takisawa, Tatsuo Kakimoto &amp; Masato Kanemaki</p>
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<dc:title>An auxin-based degron system for the rapid depletion of proteins in nonplant cells</dc:title>
<dc:creator>Kohei Nishimura</dc:creator>
<dc:creator>Tatsuo Fukagawa</dc:creator>
<dc:creator>Haruhiko Takisawa</dc:creator>
<dc:creator>Tatsuo Kakimoto</dc:creator>
<dc:creator>Masato Kanemaki</dc:creator>
<dc:identifier>doi:10.1038/nmeth.1401</dc:identifier>
<dc:source>Nature Methods</dc:source>
<dc:date>2009-11-15</dc:date>
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<title>A genetically encoded reporter of synaptic activity in vivo</title>
<link>http://feeds.nature.com/~r/nmeth/rss/aop/~3/sPE4pQ63BGE/nmeth.1399</link>
<description>Fusion of the genetically-encoded calcium indicator GCaMP2 to synaptophysin localizes the sensor to neuron presynaptic terminals and conveys linear responsiveness over a wider range of spike frequencies. The sensor allowed measurement of synaptic activity caused by spiking as well as graded voltage signals during in vivo imaging in zebrafish.</description>
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<p>
<b>A genetically encoded reporter of synaptic activity in vivo</b>
</p>
<p>Nature Methods. <a href="http://dx.doi.org/10.1038/nmeth.1399">doi:10.1038/nmeth.1399</a>
</p>
<p>Authors: Elena Dreosti, Benjamin Odermatt, Mario M Dorostkar &amp; Leon Lagnado</p>
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<dc:title>A genetically encoded reporter of synaptic activity in vivo</dc:title>
<dc:creator>Elena Dreosti</dc:creator>
<dc:creator>Benjamin Odermatt</dc:creator>
<dc:creator>Mario M Dorostkar</dc:creator>
<dc:creator>Leon Lagnado</dc:creator>
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<dc:date>2009-11-08</dc:date>
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<title>Automated high-throughput mapping of promoter-enhancer interactions in zebrafish embryos</title>
<link>http://feeds.nature.com/~r/nmeth/rss/aop/~3/BFondmOeuaI/nmeth.1396</link>
<description>Methods for automated fluorescence imaging allow high-throughput examination of reporter expression patterns in zebrafish embryos. They are applied to mapping promoter-enhancer interactions in this organism.</description>
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<p>
<b>Automated high-throughput mapping of promoter-enhancer interactions in zebrafish embryos</b>
</p>
<p>Nature Methods. <a href="http://dx.doi.org/10.1038/nmeth.1396">doi:10.1038/nmeth.1396</a>
</p>
<p>Authors: Jochen Gehrig, Markus Reischl, &#201;va Kalm&#225;r, Marco Ferg, Yavor Hadzhiev, Andreas Zaucker, Chengyi Song, Simone Schindler, Urban Liebel &amp; Ferenc M&#252;ller</p>
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<dc:title>Automated high-throughput mapping of promoter-enhancer interactions in zebrafish embryos</dc:title>
<dc:creator>Jochen Gehrig</dc:creator>
<dc:creator>Markus Reischl</dc:creator>
<dc:creator>Éva Kalmár</dc:creator>
<dc:creator>Marco Ferg</dc:creator>
<dc:creator>Yavor Hadzhiev</dc:creator>
<dc:creator>Andreas Zaucker</dc:creator>
<dc:creator>Chengyi Song</dc:creator>
<dc:creator>Simone Schindler</dc:creator>
<dc:creator>Urban Liebel</dc:creator>
<dc:creator>Ferenc Müller</dc:creator>
<dc:identifier>doi:10.1038/nmeth.1396</dc:identifier>
<dc:source>Nature Methods</dc:source>
<dc:date>2009-11-08</dc:date>
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<title>Optical interrogation of neural circuits in Caenorhabditis elegans</title>
<link>http://feeds.nature.com/~r/nmeth/rss/aop/~3/EkWt5xM_JdU/nmeth.1397</link>
<description>Neuronal stimulation with channelrhodopsin-2 is combined with calcium fluorescence imaging to study neural connections in intact Caenorhabditis elegans.</description>
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<p>
<b>Optical interrogation of neural circuits in Caenorhabditis elegans</b>
</p>
<p>Nature Methods. <a href="http://dx.doi.org/10.1038/nmeth.1397">doi:10.1038/nmeth.1397</a>
</p>
<p>Authors: Zengcai V Guo, Anne C Hart &amp; Sharad Ramanathan</p>
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<dc:title>Optical interrogation of neural circuits in Caenorhabditis elegans</dc:title>
<dc:creator>Zengcai V Guo</dc:creator>
<dc:creator>Anne C Hart</dc:creator>
<dc:creator>Sharad Ramanathan</dc:creator>
<dc:identifier>doi:10.1038/nmeth.1397</dc:identifier>
<dc:source>Nature Methods</dc:source>
<dc:date>2009-11-08</dc:date>
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<title>Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators</title>
<link>http://feeds.nature.com/~r/nmeth/rss/aop/~3/ENrhj3PwEm0/nmeth.1398</link>
<description>An improved version of the GCaMP genetically encoded calcium indicator, called GCaMP3, has higher calcium affinity and increased baseline fluorescence, dynamic range and stability. GCaMP3 performs better than existing genetically encoded calcium indicators in several assays and organisms, including in vivo imaging of neuronal signaling in worms, flies and mice.</description>
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<p>
<b>Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators</b>
</p>
<p>Nature Methods. <a href="http://dx.doi.org/10.1038/nmeth.1398">doi:10.1038/nmeth.1398</a>
</p>
<p>Authors: Lin Tian, S Andrew Hires, Tianyi Mao, Daniel Huber, M Eugenia Chiappe, Sreekanth H Chalasani, Leopoldo Petreanu, Jasper Akerboom, Sean A McKinney, Eric R Schreiter, Cornelia I Bargmann, Vivek Jayaraman, Karel Svoboda &amp; Loren L Looger</p>
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<dc:title>Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators</dc:title>
<dc:creator>Lin Tian</dc:creator>
<dc:creator>S Andrew Hires</dc:creator>
<dc:creator>Tianyi Mao</dc:creator>
<dc:creator>Daniel Huber</dc:creator>
<dc:creator>M Eugenia Chiappe</dc:creator>
<dc:creator>Sreekanth H Chalasani</dc:creator>
<dc:creator>Leopoldo Petreanu</dc:creator>
<dc:creator>Jasper Akerboom</dc:creator>
<dc:creator>Sean A McKinney</dc:creator>
<dc:creator>Eric R Schreiter</dc:creator>
<dc:creator>Cornelia I Bargmann</dc:creator>
<dc:creator>Vivek Jayaraman</dc:creator>
<dc:creator>Karel Svoboda</dc:creator>
<dc:creator>Loren L Looger</dc:creator>
<dc:identifier>doi:10.1038/nmeth.1398</dc:identifier>
<dc:source>Nature Methods</dc:source>
<dc:date>2009-11-08</dc:date>
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<title>High-speed nanoscopic tracking of the position and orientation of a single virus</title>
<link>http://feeds.nature.com/~r/nmeth/rss/aop/~3/XhQMJdVtKdI/nmeth.1395</link>
<description>A combination of scattering interferometry and single-molecule fluorescence microscopy allows visualization of both the position and orientation of single Simian virus 40 particles on lipid bilayers and provides evidence of viral interaction with receptors in membrane nanodomains.</description>
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<p>
<b>High-speed nanoscopic tracking of the position and orientation of a single virus</b>
</p>
<p>Nature Methods. <a href="http://dx.doi.org/10.1038/nmeth.1395">doi:10.1038/nmeth.1395</a>
</p>
<p>Authors: Philipp Kukura, Helge Ewers, Christian M&#252;ller, Alois Renn, Ari Helenius &amp; Vahid Sandoghdar</p>
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<dc:title>High-speed nanoscopic tracking of the position and orientation of a single virus</dc:title>
<dc:creator>Philipp Kukura</dc:creator>
<dc:creator>Helge Ewers</dc:creator>
<dc:creator>Christian Müller</dc:creator>
<dc:creator>Alois Renn</dc:creator>
<dc:creator>Ari Helenius</dc:creator>
<dc:creator>Vahid Sandoghdar</dc:creator>
<dc:identifier>doi:10.1038/nmeth.1395</dc:identifier>
<dc:source>Nature Methods</dc:source>
<dc:date>2009-11-01</dc:date>
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