F Frank et al. Nature 000 , 1-5 (2010) doi:10.1038/nature09039

Oct 21, 2014

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Crystal structures of hAGO2 MID domain in complex with UMP, AMP, CMP and GMP. F Frank et al. Nature 000 , 1-5 (2010) doi:10.1038/nature09039.

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F Frank et al. Nature 000 , 1-5 (2010) doi:10.1038/nature09039

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Crystal structures of hAGO2 MID domain in complex with UMP, AMP, CMP and GMP. F Frank et al.Nature000, 1-5 (2010) doi:10.1038/nature09039

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Phasic dopamine signalling in response to CS and US presentation during the acquisition of Pavlovian conditional approach behaviour in bHR and bLR rats. SB Flagel et al. Nature 000 , 1-5 (2010) doi:10.1038/nature09588.

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Disruption of IPN or MHb signalling increases nicotine intake in rats. CD Fowler et al. Nature 000 , 1-5 (2010) doi:10.1038/nature09797.

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The BK intracellular subunit contains two RCK domains. YK Wu et al. Nature 000 , 1-5 (2010) doi:10.1038/nature09252.

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Nfkbiz  /  mice are resistant to EAE owing to a CD4  T-cell-intrinsic defect in T H 17 development. K Okamoto et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08922.

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J Chandrashekar et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08783

ENaC is necessary for high sensitivity taste responses to sodium salts. J Chandrashekar et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08783.

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J Chandrashekar et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08783

ENaC function in TRCs is required for behavioural attraction to salt. J Chandrashekar et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08783.

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F Wang et al. Nature 000 , 1 - 5 (2011) doi:10.1038/nature09780

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F Wang et al. Nature 000 , 1 - 5 (2011) doi:10.1038/nature09780

Structure of the hexameric complex between MecA121 and ClpC - D2. F Wang et al. Nature 000 , 1 - 5 (2011) doi:10.1038/nature09780.

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M Boudsocq et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08794

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F-A Bava et al. Nature 000 , 1 - 5 (2013) doi:10.1038/nature 11901

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T Matsui et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08858

Derepression of exogenous retrovirus expression on Eset depletion is accompanied by reduced levels of proviral H3K9me3 and DNA methylation. T Matsui et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08858.

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T Matsui et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08858

Intrinsic KMTase activity is crucial for ESET-mediated ERV silencing. T Matsui et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08858.

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J-F Flot et al. Nature 000 , 1-5 (2013) doi:10.1038/nature 12326

A genome structure incompatible with conventional meiosis. J-F Flot et al. Nature 000 , 1-5 (2013) doi:10.1038/nature 12326.

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N Muraki et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08950

Common architecture of DPOR and nitrogenase. N Muraki et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08950.

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ZJ Duan et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08973

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T Matsui et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08858

ESET is required for silencing, H3K9me3 and H4K20me3 of class I and II ERVs in ES cells. T Matsui et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08858.

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T Matsui et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08858

Deletion of ESET does not lead to global DNA demethylation of ERVs. T Matsui et al. Nature 000 , 1-5 (2010) doi:10.1038/nature08858.

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F Wang et al. Nature 000 , 1 - 5 (2011) doi:10.1038/nature09780

Architecture of the MecA–ClpC molecular machine. F Wang et al. Nature 000 , 1 - 5 (2011) doi:10.1038/nature09780.

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I Itzhaki et al. Nature 000 , 1-5 (2010) doi:10.1038/nature09747

Drug screening using LQTS human iPSC-CMs. I Itzhaki et al. Nature 000 , 1-5 (2010) doi:10.1038/nature09747.

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