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Tomimatsu, Kosuke, Bihary, Dora, Olan, Ioana, Parry, Aled J, Schoenfelder, Stefan, Chan, Adelyne SL, Slater, Guy St C, Ito, Yoko, Rugg-Gunn, Peter J, Kirschner, Kristina et al (show 10 more authors) , Bermejo-Rodriguez, Camino ORCID: 0000-0002-7554-1640, Seko, Tomomi, Kugoh, Hiroyuki, Shiraishi, Ken, Sayama, Koji, Kimura, Hiroshi, Fraser, Peter, Narita, Masako, Samarajiwa, Shamith A and Narita, Masashi (2022) Locus-specific induction of gene expression from heterochromatin loci during cellular senescence. NATURE AGING, 2 (1). 31-+.

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Kirschner, Kristina, Samarajiwa, Shamith A, Cairns, Jonathan M, Menon, Suraj, Perez-Mancera, Pedro A, Tomimatsu, Kosuke, Bermejo-Rodriguez, Camino ORCID: 0000-0002-7554-1640, Ito, Yoko, Chandra, Tamir, Narita, Masako et al (show 6 more authors) , Lyons, Scott K, Lynch, Andy G, Kimura, Hiroshi, Ohbayashi, Tetsuya, Tavare, Simon and Narita, Masashi (2015) Phenotype Specific Analyses Reveal Distinct Regulatory Mechanism for Chronically Activated p53. PLOS GENETICS, 11 (3). e1005053-.

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Ito, Yoko, Carss, Keren J, Duarte, Sofia T, Hartley, Taila, Keren, Boris, Kurian, Manju A, Marey, Isabelle, Charles, Perinne, Mendonca, Carla, Nava, Caroline et al (show 9 more authors) , Pfundt, Rolph, Sanchis-Juan, Alba, van Bokhoven, Hans, van Essen, Anthony, van Ravenswaaij-Arts, Conny, Boycott, Kym M, Kernohan, Kristin D, Dyack, Sarah and Raymond, F Lucy (2018) <i>De Novo</i> Truncating Mutations in <i>WASF1</i> Cause Intellectual Disability with Seizures. AMERICAN JOURNAL OF HUMAN GENETICS, 103 (1). pp. 144-153.