Effects of Freeze–Thawing and Intravenous Infusion on Mesenchymal Stromal Cell Gene Expression von Hoogduijn, Martin J., de Witte, Samantha F.H., Luk, Franka, van den Hout-van Vroonhoven, Mirjam C.G.N., Ignatowicz, Lech, Catar, Rusan, Strini, Tanja, Korevaar, Sander S., van IJcken, Wilfred F.J., Betjes, Michiel G.H., Franquesa, Marcella, Moll, Guido, Baan, Carla C.

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Inflammatory conditions affect gene expression and function of human adipose tissue‐derived mesenchymal stem cells von Crop, M.J, Baan, C.C, Korevaar, S.S, IJzermans, J.N.M, Pescatori, M, Stubbs, A.P, Van IJcken, W.F.J, Dahlke, M.H, Eggenhofer, E, Weimar, W, Hoogduijn, M.J

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PDGFRβ+ cells play a dual role as hematopoietic precursors and niche cells during mouse ontogeny von Sá da Bandeira, Diana, Kilpatrick, Alastair Morris, Marques, Madalena, Gomez-Salazar, Mario, Ventura, Telma, Gonzalez, Zaniah Nashira, Stefancova, Dorota, Rossi, Fiona, Vermeren, Matthieu, Vink, Chris Sebastiaan, Beltran, Mariana, Henderson, Neil Cowan, Jung, Bongnam, van der Linden, Reinier, van de Werken, Harmen Jan George, van Ijcken, Wilfred F.J., Betsholtz, Christer, Forbes, Stuart John, Cuervo, Henar, Crisan, Mihaela

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Regulated genes in psoriatic skin during treatment with fumaric acid esters von Onderdijk, A.J., Balak, D.M.W., Baerveldt, E.M., Florencia, E.F., Kant, M., Laman, J.D., van IJcken, W.F.J., Racz, E., de Ridder, D., Thio, H.B., Prens, E.P.

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Three Genome-wide Association Studies and a Linkage Analysis Identify HERC2 as a Human Iris Color Gene von Kayser, Manfred, Liu, Fan, Janssens, A. Cecile J.W., Rivadeneira, Fernando, Lao, Oscar, van Duijn, Kate, Vermeulen, Mark, Arp, Pascal, Jhamai, Mila M., van IJcken, Wilfred F.J., den Dunnen, Johan T., Heath, Simon, Zelenika, Diana, Despriet, Dominiek D.G., Klaver, Caroline C.W., Vingerling, Johannes R., de Jong, Paulus T.V.M., Hofman, Albert, Aulchenko, Yurii S., Uitterlinden, Andre G., Oostra, Ben A., van Duijn, Cornelia M.

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CITED2 and NCOR2 in anti-oestrogen resistance and progression of breast cancer von van Agthoven, T, Sieuwerts, A M, Veldscholte, J, Meijer-van Gelder, M E, Smid, M, Brinkman, A, den Dekker, A T, Leroy, I M, van IJcken, W F J, Sleijfer, S, Foekens, J A, Dorssers, L C J

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SF3B1 and EIF1AX mutations in uveal melanoma: a protective factor, or not? von KILIC, E, KOOPMANS, AE, YAVUZYIGITOGLU, S, VAARWATER, J, VAN IJCKEN, WFJ, PARIDAENS, D, DE KLEIN, JEMM

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Pandemic 2009 H1N1 Influenza Virus Causes Diffuse Alveolar Damage in Cynomolgus Macaques von Herfst, S., van den Brand, J. M. A., Schrauwen, E. J. A., de Wit, E., Munster, V. J., van Amerongen, G., Linster, M., Zaaraoui, F., van Ijcken, W. F. J., Rimmelzwaan, G. F., Osterhaus, A. D. M. E., Fouchier, R. A. M., Andeweg, A. C., Kuiken, T.

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12 DOC1-dependent recruitment of NURD reveals antagonism with SWI/SNF during epithelial-mesenchymal transition in oral cancer cells von Mohd-Sarip, A, Teeuwssen, M, Bot, A, Baatenburg de Jong, RJ, Looijenga, LHJ, Van Ijcken, WFJ, Van de Werken, HJG, Demmers, JA, Fodde, R, Verrijzer, CP

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Abstract P6-04-08: FOXA1 expression: regulated by EZH2 and associated with favorable outcome to tamoxifen in advanced breast cancer von Reijm, EA, Helmijr, JCA, Soler, CMJ, Beekman, R, Gerritse, FL, Prager-van, der Smissen WJC, Ruigrok-Ritstier, K, van IJcken, WFJ, Stevens, MG, Smid, M, Look, MP, Meijer, ME, Sieuwerts, AM, Sleijfer, S, Foekens, JA, Berns, EMJJ, Jansen, MPHM

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Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases von Perenthaler, E, Nikoncuk, A, Yousefi, S, Berdowski, WM, Alsagob, M, Capo, I, van der Linde, HC, van den Berg, P, Jacobs, EH, Putar, D, Ghazvini, M, Aronica, E, van IJcken, WFJ, de Valk, WG, Medici-van den Herik, E, van Slegtenhorst, M, Brick, L, Kozenko, M, Kohler, JN, Bernstein, JA, Monaghan, KG, Begtrup, A, Torene, R, Al Futaisi, A, Al Murshedi, F, Mani, R, Al Azri, F, Kamsteeg, E-J, Mojarrad, M, Eslahi, A, Khazaei, Z, Darmiyan, FM, Doosti, M, Karimiani, EG, Vandrovcova, J, Zafar, F, Rana, N, Kandaswamy, KK, Hertecant, J, Bauer, P, AlMuhaizea, MA, Salih, MA, Aldosary, M, Almass, R, Al-Quait, L, Qubbaj, W, Coskun, S, Alahmadi, KO, Hamad, MHA, Alwadaee, S, Awartani, K, Dababo, AM, Almohanna, F, Colak, D, Dehghani, M, Mehrjardi, MYV, Gunel, M, Ercan-Sencicek, AG, Passi, GR, Cheema, HA, Efthymiou, S, Houlden, H, Bertoli-Avella, AM, Brooks, AS, Retterer, K, Maroofian, R, Kaya, N, van Ham, TJ, Barakat, TS

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Zeb2 Regulates Cell Fate at the Exit from Epiblast State in Mouse Embryonic Stem Cells von Stryjewska, A, Dries, R, Pieters, T, Verstappen, G, Conidi, A, Coddens, K, Francis, A, Umans, L, van IJcken, WFJ, Berx, G, van Grunsven, LA, Grosveld, FG, Goossens, S, Haigh, JJ, Huylebroeck, D

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Loss of LMOD1 impairs smooth muscle cytocontractility and causes megacystis microcolon intestinal hypoperistalsis syndrome in humans and mice von Halim, D, Wilson, MP, Oliver, D, Brosens, E, Verheij, JBGM, Han, Y, Nanda, V, Lyu, Q, Doukas, M, Stoop, H, Brouwer, RWW, van IJcken, WFJ, Slivano, OJ, Burns, AJ, Christie, CK, de Mesy Bentley, KL, Brooks, AS, Tibboel, D, Xu, S, Jin, ZG, Djuwantono, T, Yan, W, Alves, MM, Hofstra, RMW, Miano, JM

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