Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR von Sempou, Emily, Kostiuk, Valentyna, Zhu, Jie, Cecilia Guerra, M., Tyan, Leonid, Hwang, Woong, Camacho-Aguilar, Elena, Caplan, Michael J., Zenisek, David, Warmflash, Aryeh, Owens, Nick D. L., Khokha, Mustafa K.

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Activation of the Aryl Hydrocarbon Receptor Dampens the Severity of Inflammatory Skin Conditions von Di Meglio, Paola, Duarte, João H., Ahlfors, Helena, Owens, Nick D.L., Li, Ying, Villanova, Federica, Tosi, Isabella, Hirota, Keiji, Nestle, Frank O., Mrowietz, Ulrich, Gilchrist, Michael J., Stockinger, Brigitta

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Developmentally dynamic changes in DNA methylation in the human pancreas von MacCalman, Ailsa, De Franco, Elisa, Franklin, Alice, Flaxman, Christine S, Richardson, Sarah J, Murrall, Kathryn, Burrage, Joe, Walker, Emma M, Morgan, Noel G, Hattersley, Andrew T, Dempster, Emma L, Hannon, Eilis, Jeffries, Aaron R, Owens, Nick D L, Mill, Jonathan

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Author Correction: Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR von Sempou, Emily, Kostiuk, Valentyna, Zhu, Jie, Cecilia Guerra, M., Tyan, Leonid, Hwang, Woong, Camacho-Aguilar, Elena, Caplan, Michael J., Zenisek, David, Warmflash, Aryeh, Owens, Nick D. L., Khokha, Mustafa K.

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Maternal pluripotency factors initiate extensive chromatin remodelling to predefine first response to inductive signals von Gentsch, George E., Spruce, Thomas, Owens, Nick D. L., Smith, James C.

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High-resolution analysis of gene activity during the Xenopus mid-blastula transition von Collart, Clara, Owens, Nick D L, Bhaw-Rosun, Leena, Cooper, Brook, De Domenico, Elena, Patrushev, Ilya, Sesay, Abdul K, Smith, James N, Smith, James C, Gilchrist, Michael J

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Efficient high-throughput sequencing of a laser microdissected chromosome arm von Seifertova, Eva, Zimmerman, Lyle B, Gilchrist, Michael J, Macha, Jaroslav, Kubickova, Svatava, Cernohorska, Halina, Zarsky, Vojtech, Owens, Nick D L, Sesay, Abdul K, Tlapakova, Tereza, Krylov, Vladimir

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Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements von Laver, Thomas W, Wakeling, Matthew N, Caswell, Richard C, Bunce, Benjamin, Yau, Daphne, Männistö, Jonna M E, Houghton, Jayne A L, Hopkins, Jasmin J, Weedon, Michael N, Saraff, Vrinda, Kershaw, Melanie, Honey, Engela M, Murphy, Nuala, Giri, Dinesh, Nath, Stuart, Tangari Saredo, Ana, Banerjee, Indraneel, Hussain, Khalid, Owens, Nick D L, Flanagan, Sarah E

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Chemical Detection Using the Receptor Density Algorithm von Hilder, J. A., Owens, N. D. L., Neal, M. J., Hickey, P. J., Cairns, S. N., Kilgour, D. P. A., Timmis, J., Tyrrell, A. M.

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Expression of ribosomopathy genes during Xenopus tropicalis embryogenesis von Robson, Andrew, Owens, Nick D L, Baserga, Susan J, Khokha, Mustafa K, Griffin, John N

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Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development von Owens, Nick D.L., Blitz, Ira L., Lane, Maura A., Patrushev, Ilya, Overton, John D., Gilchrist, Michael J., Cho, Ken W.Y., Khokha, Mustafa K.

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Disrupted β-cell-specific gene silencing causes congenital hyperinsulinism von Owens, Nick D L, Flanagan, Sarah E

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Nup107 contributes to the maternal to zygotic transition by preventing the premature nuclear export of pri-miRNA 427 von Kostiuk, Valentyna, Kabir, Rakib, Levangie, Kaitlin, Empke, Stefany, Morgan, Kimberly, Owens, Nick D L, Lusk, C Patrick, Khokha, Mustafa K

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Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinism von Wakeling, Matthew N., Owens, Nick D. L., Hopkinson, Jessica R., Johnson, Matthew B., Houghton, Jayne A. L., Dastamani, Antonia, Flaxman, Christine S., Wyatt, Rebecca C., Hewat, Thomas I., Hopkins, Jasmin J., Laver, Thomas W., van Heugten, Rachel, Weedon, Michael N., De Franco, Elisa, Patel, Kashyap A., Ellard, Sian, Morgan, Noel G., Cheesman, Edmund, Banerjee, Indraneel, Hattersley, Andrew T., Dunne, Mark J., Richardson, Sarah J., Flanagan, Sarah E.

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Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus von Gentsch, George E., Spruce, Thomas, Monteiro, Rita S., Owens, Nick D.L., Martin, Stephen R., Smith, James C.

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Expression of an engineered cecropin gene cassette in transgenic tobacco plants confers disease resistance to Pseudomonas syringae pv. tabaci von Huang, Y. (University of Alaska, Fairbanks.), Nordeen, R.O, Di, M, Owens, L.D, McBeath, J.H

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Primate-specific ZNF808 is essential for pancreatic development in humans von De Franco, Elisa, Owens, Nick D. L., Montaser, Hossam, Wakeling, Matthew N., Saarimäki-Vire, Jonna, Triantou, Athina, Ibrahim, Hazem, Balboa, Diego, Caswell, Richard C., Jennings, Rachel E., Kvist, Jouni A., Johnson, Matthew B., Muralidharan, Sachin, Ellard, Sian, Wright, Caroline F., Maddirevula, Sateesh, Alkuraya, Fowzan S., Hanley, Neil A., Flanagan, Sarah E., Otonkoski, Timo, Hattersley, Andrew T., Imbeault, Michael

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Genetic links between ovarian ageing, cancer risk and de novo mutation rates von Stankovic, Stasa, Shekari, Saleh, Huang, Qin Qin, Gardner, Eugene J., Ivarsdottir, Erna V., Owens, Nick D. L., Mavaddat, Nasim, Azad, Ajuna, Hawkes, Gareth, Kentistou, Katherine A., Beaumont, Robin N., Day, Felix R., Zhao, Yajie, Jonsson, Hakon, Rafnar, Thorunn, Tragante, Vinicius, Sveinbjornsson, Gardar, Oddsson, Asmundur, Styrkarsdottir, Unnur, Gudmundsson, Julius, Stacey, Simon N., Gudbjartsson, Daniel F., Kennedy, Kitale, Wood, Andrew R., Weedon, Michael N., Ong, Ken K., Wright, Caroline F., Hoffmann, Eva R., Sulem, Patrick, Hurles, Matthew E., Ruth, Katherine S., Martin, Hilary C., Stefansson, Kari, Perry, John R. B., Murray, Anna

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A large pseudoautosomal region on the sex chromosomes of the frog Silurana tropicalis von Bewick, Adam J, Chain, Frédéric J J, Zimmerman, Lyle B, Sesay, Abdul, Gilchrist, Michael J, Owens, Nick D L, Seifertova, Eva, Krylov, Vladimir, Macha, Jaroslav, Tlapakova, Tereza, Kubickova, Svatava, Cernohorska, Halina, Zarsky, Vojtech, Evans, Ben J

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Molecular asymmetry in the 8-cell stage Xenopus tropicalis embryo described by single blastomere transcript sequencing von De Domenico, Elena, Owens, Nick D.L., Grant, Ian M., Gomes-Faria, Rosa, Gilchrist, Michael J.

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