The ATOM-Seq sequence capture panel can accurately predict microsatellite instability status in formalin-fixed tumour samples, alongside routine gene mutation testing von Srihar, Kanishta, Gusnanto, Arief, Richman, Susan D., West, Nicholas P., Galvin, Leanne, Bottomley, Daniel, Hemmings, Gemma, Glover, Amy, Natarajan, Subaashini, Miller, Rebecca, Arif, Sameira, Rossington, Hannah, Dunwell, Thomas L., Dailey, Simon C., Fontarum, Gracielle, George, Agnes, Wu, Winnie, Quirke, Phil, Wood, Henry M.

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The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 von Abdelhamed, Zakia A., Abdelmottaleb, Dina I., El-Asrag, Mohammed E., Natarajan, Subaashini, Wheway, Gabrielle, Inglehearn, Chris F., Toomes, Carmel, Johnson, Colin A.

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The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway von Abdelhamed, Zakia A, Natarajan, Subaashini, Wheway, Gabrielle, Inglehearn, Christopher F, Toomes, Carmel, Johnson, Colin A, Jagger, Daniel J

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Tyrosine phosphorylation profiling in FGF-2 stimulated human embryonic stem cells von Ding, Vanessa M Y, Boersema, Paul J, Foong, Leong Yan, Preisinger, Christian, Koh, Geoffrey, Natarajan, Subaashini, Lee, Dong-Yup, Boekhorst, Jos, Snel, Berend, Lemeer, Simone, Heck, Albert J R, Choo, Andre

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HEXIM1 induces differentiation of human pluripotent stem cells von Ding, Vanessa, Lew, Qiao Jing, Chu, Kai Ling, Natarajan, Subaashini, Rajasegaran, Vikneswari, Gurumurthy, Meera, Choo, Andre B H, Chao, Sheng-Hao

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An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes von Wheway, Gabrielle, Schmidts, Miriam, Mans, Dorus A., Szymanska, Katarzyna, Nguyen, Thanh-Minh T., Racher, Hilary, Phelps, Ian G., Toedt, Grischa, Kennedy, Julie, Wunderlich, Kirsten A., Sorusch, Nasrin, Abdelhamed, Zakia A., Natarajan, Subaashini, Herridge, Warren, van Reeuwijk, Jeroen, Horn, Nicola, Boldt, Karsten, Parry, David A., Letteboer, Stef J. F., Roosing, Susanne, Adams, Matthew, Bell, Sandra M., Bond, Jacquelyn, Higgins, Julie, Morrison, Ewan E., Tomlinson, Darren C., Slaats, Gisela G., van Dam, Teunis J. P., Huang, Lijia, Kessler, Kristin, Giessl, Andreas, Logan, Clare V., Boyle, Evan A., Shendure, Jay, Anazi, Shamsa, Aldahmesh, Mohammed, Al Hazzaa, Selwa, Hegele, Robert A., Ober, Carole, Frosk, Patrick, Mhanni, Aizeddin A., Chodirker, Bernard N., Chudley, Albert E., Lamont, Ryan, Bernier, Francois P., Beaulieu, Chandree L., Gordon, Paul, Pon, Richard T., Donahue, Clem, Barkovich, A. James, Wolf, Louis, Toomes, Carmel, Thiel, Christian T., Boycott, Kym M., McKibbin, Martin, Inglehearn, Chris F., Stewart, Fiona, Omran, Heymut, Huynen, Martijn A., Sergouniotis, Panagiotis I., Alkuraya, Fowzan S., Parboosingh, Jillian S., Innes, A. Micheil, Willoughby, Colin E., Giles, Rachel H., Webster, Andrew R., Ueffing, Marius, Blacque, Oliver, Gleeson, Joseph G., Wolfrum, Uwe, Beales, Philip L., Gibson, Toby, Doherty, Dan, Mitchison, Hannah M., Roepman, Ronald, Johnson, Colin A.

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Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel-Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt s... von Abdelhamed, Zakia A, Wheway, Gabrielle, Szymanska, Katarzyna, Natarajan, Subaashini, Toomes, Carmel, Inglehearn, Chris, Johnson, Colin A

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Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling von Logan, Clare V, Szabadkai, György, Sharpe, Jenny A, Parry, David A, Torelli, Silvia, Childs, Anne-Marie, Kriek, Marjolein, Phadke, Rahul, Johnson, Colin A, Roberts, Nicola Y, Bonthron, David T, Pysden, Karen A, Whyte, Tamieka, Munteanu, Iulia, Foley, A Reghan, Wheway, Gabrielle, Szymanska, Katarzyna, Natarajan, Subaashini, Abdelhamed, Zakia A, Morgan, Joanne E, Roper, Helen, Santen, Gijs W E, Niks, Erik H, van der Pol, W Ludo, Lindhout, Dick, Raffaello, Anna, De Stefani, Diego, den Dunnen, Johan T, Sun, Yu, Ginjaar, Ieke, Sewry, Caroline A, Hurles, Matthew, Rizzuto, Rosario, Duchen, Michael R, Muntoni, Francesco, Sheridan, Eamonn

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Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel–Gruber syndrome von Wheway, Gabrielle, Abdelhamed, Zakia, Natarajan, Subaashini, Toomes, Carmel, Inglehearn, Chris, Johnson, Colin A.

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FGF-2 modulates Wnt signaling in undifferentiated hESC and iPS cells through activated PI3-K/GSK3β signaling von Ding, Vanessa M.Y., Ling, Ling, Natarajan, Subaashini, Yap, Miranda G.S., Cool, Simon M., Choo, Andre B.H.

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HEXIM1 Induces Differentiation of Human Pluripotent Stem Cells. e72823 von Ding, Vanessa, Lew, Qiao Jing, Chu, Kai Ling, Natarajan, Subaashini, Rajasegaran, Vikneswari, Gurumurthy, Meera, Choo, Andre BH, Chao, Sheng-Hao

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FGF-2 modulates Wnt signaling in undifferentiated hESC and iPS cells through activated PI3-K/GSK3beta signaling von Ding, Vanessa M Y, Ling, Ling, Natarajan, Subaashini, Yap, Miranda G S, Cool, Simon M, Choo, Andre B H

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