Canonical Wnt Signaling Regulates Hematopoiesis in a Dosage-Dependent Fashion von Luis, Tiago C., Naber, Brigitta A.E., Roozen, Paul P.C., Brugman, Martijn H., de Haas, Edwin F.E., Ghazvini, Mehrnaz, Fibbe, Willem E., van Dongen, Jacques J.M., Fodde, Riccardo, Staal, Frank J.T.

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Orthogonal analysis of mitochondrial function in Parkinson’s disease patients von Barnhoorn, Sander, Milanese, Chiara, Li, Tracy, Dons, Lieke, Ghazvini, Mehrnaz, Sette, Martina, Farina, Stefania, Sproviero, Daisy, Payan-Gomez, Cesar, Mastroberardino, Pier G.

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The Trans-Activator RNF12 and Cis-Acting Elements Effectuate X Chromosome Inactivation Independent of X-Pairing von Barakat, Tahsin Stefan, Loos, Friedemann, van Staveren, Selma, Myronova, Elvira, Ghazvini, Mehrnaz, Grootegoed, J. Anton, Gribnau, Joost

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RNF12 activates Xist and is essential for X chromosome inactivation von Barakat, Tahsin Stefan, Gunhanlar, Nilhan, Pardo, Cristina Gontan, Achame, Eskeatnaf Mulugeta, Ghazvini, Mehrnaz, Boers, Ruben, Kenter, Annegien, Rentmeester, Eveline, Grootegoed, J Anton, Gribnau, Joost

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Modeling Rett Syndrome With Human Patient-Specific Forebrain Organoids von Gomes, Ana Rita, Fernandes, Tiago G, Vaz, Sandra H, Silva, Teresa P, Bekman, Evguenia P, Xapelli, Sara, Duarte, Sofia, Ghazvini, Mehrnaz, Gribnau, Joost, Muotri, Alysson R, Trujillo, Cleber A, Sebastião, Ana M, Cabral, Joaquim M S, Diogo, Maria Margarida

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The POU proteins Brn-2 and Oct-6 share important functions in Schwann cell development von Jaegle, Martine, Ghazvini, Mehrnaz, Mandemakers, Wim, Piirsoo, Marko, Driegen, Siska, Levavasseur, Francoise, Raghoenath, Smiriti, Grosveld, Frank, Meijer, Dies

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Cancer stemness in Apc- vs. Apc/KRAS-driven intestinal tumorigenesis von Ghazvini, Mehrnaz, Sonneveld, Petra, Kremer, Andreas, Franken, Patrick, Sacchetti, Andrea, Atlasi, Yaser, Roth, Sabrina, Joosten, Rosalie, Smits, Ron, Fodde, Riccardo

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Stable X Chromosome Reactivation in Female Human Induced Pluripotent Stem Cells von Barakat, Tahsin Stefan, Ghazvini, Mehrnaz, de Hoon, Bas, Li, Tracy, Eussen, Bert, Douben, Hannie, van der Linden, Reinier, van der Stap, Nathalie, Boter, Marjan, Laven, Joop S., Galjaard, Robert-Jan, Grootegoed, J. Anton, de Klein, Annelies, Gribnau, Joost

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Differential Contributions of Mammalian Rad54 Paralogs to Recombination, DNA Damage Repair, and Meiosis von Wesoly, Joanna, Agarwal, Sheba, Sigurdsson, Stefan, Bussen, Wendy, Van Komen, Stephen, Qin, Jian, van Steeg, Harry, van Benthem, Jan, Wassenaar, Evelyne, Baarends, Willy M., Ghazvini, Mehrnaz, Tafel, Agnieszka A., Heath, Helen, Galjart, Niels, Essers, Jeroen, Grootegoed, J. Anton, Arnheim, Norman, Bezzubova, Olga, Buerstedde, Jean-Marie, Sung, Patrick, Kanaar, Roland

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Epigenetic Characterization of the FMR1 Promoter in Induced Pluripotent Stem Cells from Human Fibroblasts Carrying an Unmethylated Full Mutation von de Esch, Celine E.F., Ghazvini, Mehrnaz, Loos, Friedemann, Schelling-Kazaryan, Nune, Widagdo, W., Munshi, Shashini T., van der Wal, Erik, Douben, Hannie, Gunhanlar, Nilhan, Kushner, Steven A., Pijnappel, W.W.M. Pim, de Vrij, Femke M.S., Geijsen, Niels, Gribnau, Joost, Willemsen, Rob

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Cystic renal‐epithelial derived induced pluripotent stem cells from polycystic kidney disease patients von Kenter, Annegien T., Rentmeester, Eveline, Riet, Job, Boers, Ruben, Boers, Joachim, Ghazvini, Mehrnaz, Xavier, Vanessa J., Leenders, Geert J.L.H., Verhagen, Paul C.M.S., Til, Marjan E., Eussen, Bert, Losekoot, Monique, Klein, Annelies, Peters, Dorien J.M., IJcken, Wilfred F.J., Werken, Harmen J.G., Zietse, Robert, Hoorn, Ewout J., Jansen, Gert, Gribnau, Joost H.

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Neural commitment of human pluripotent stem cells under defined conditions recapitulates neural development and generates patient-specific neural cells von Fernandes, Tiago G., Duarte, Sofia T., Ghazvini, Mehrnaz, Gaspar, Cláudia, Santos, Diana C., Porteira, Ana R., Rodrigues, Gonçalo M. C., Haupt, Simone, Rombo, Diogo M., Armstrong, Judith, Sebastião, Ana M., Gribnau, Joost, Garcia-Cazorla, Àngels, Brüstle, Oliver, Henrique, Domingos, Cabral, Joaquim M. S., Diogo, Maria Margarida

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Malignant Transformation Involving CXXC4 Mutations Identified in a Leukemic Progression Model of Severe Congenital Neutropenia von Olofsen, Patricia A., Fatrai, Szabolcs, van Strien, Paulina M.H., Obenauer, Julia C., de Looper, Hans W.J., Hoogenboezem, Remco M., Erpelinck-Verschueren, Claudia A.J., Vermeulen, Michael P.W.M., Roovers, Onno, Haferlach, Torsten, Jansen, Joop H., Ghazvini, Mehrnaz, Bindels, Eric M.J., Schneider, Rebekka K., de Pater, Emma M., Touw, Ivo P.

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Involvement of extracellular vesicle microRNA clusters in developing healthy and Rett syndrome brain organoids von Bahram Sangani, Nasim, Koetsier, Jarno, Gomes, Ana Rita, Diogo, Maria Margarida, Fernandes, Tiago G., Bouwman, Freek G., Mariman, Edwin C. M., Ghazvini, Mehrnaz, Gribnau, Joost, Curfs, Leopold M. G., Reutelingsperger, Chris P., Eijssen, Lars M. T.

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PML Plays a Key Role in Severe Congenital Neutropenia with Mutant ELANE Causing Neutrophil Elastase Protein Misfolding von Olofsen, Patricia, van Strien, Paulette, Roovers, Onno, De Looper, Hans, Hoogenboezem, Remco, Bosch, Dennis, Ghazvini, Mehrnaz, Bindels, Eric, De Pater, Emma, Touw, Ivo

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Trichothiodystrophy causative TFIIEβ mutation affects transcription in highly differentiated tissue von Theil, Arjan F, Mandemaker, Imke K, van den Akker, Emile, Swagemakers, Sigrid M A, Raams, Anja, Wüst, Tatjana, Marteijn, Jurgen A, Giltay, Jacques C, Colombijn, Richard M, Moog, Ute, Kotzaeridou, Urania, Ghazvini, Mehrnaz, von Lindern, Marieke, Hoeijmakers, Jan H J, Jaspers, Nicolaas G J, van der Spek, Peter J, Vermeulen, Wim

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A Simple Nonviral Method to Generate Human Induced Pluripotent Stem Cells Using SMAR DNA Vectors von Hartley, Anna, Burger, Luisa, Wincek, Cornelia L, Dons, Lieke, Li, Tracy, Grewenig, Annabel, Taşgın, Toros, Urban, Manuela, Roig-Merino, Alicia, Ghazvini, Mehrnaz, Harbottle, Richard P

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Functional dissection of the Oct6 Schwann cell enhancer reveals an essential role for dimeric Sox10 binding von Jagalur, Noorjahan B, Ghazvini, Mehrnaz, Mandemakers, Wim, Driegen, Siska, Maas, Alex, Jones, Erin A, Jaegle, Martine, Grosveld, Frank, Svaren, John, Meijer, Dies

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Patient-derived disease models of non-syndromic Craniosynostosis to unravel the role of the Fuzzy Planar Cell polarity (FUZ) in craniofacial development von Duarte, Filipa, van Neck, Johan, Gijsbertsen, Max, Swagemakers, Sigrid, Koedam, Marijke, Barrell, William, Ghazvini, Mehrnaz, van der Spek, Peter, Liu, Karen, Mathijssen, Irene, van de Peppel, Jeroen

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Trichothiodystrophy causative TFIIEβ mutation affects transcription in highly differentiated tissue von Theil, Arjan F, Mandemaker, Imke K, van den Akker, Emile, Swagemakers, Sigrid M.A, Raams, Anja, Wüst, Tatjana, Marteijn, Jurgen A, Giltay, Jacques C, Colombijn, Richard M, Moog, Ute, Kotzaeridou, Urania, Ghazvini, Mehrnaz, von Lindern, Marieke, Hoeijmakers, Jan H.J, Jaspers, Nicolaas G.J, van der Spek, Peter J, Vermeulen, Wim

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