Search Results - Martin A. Rooimans

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  1. 1
    Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1

    Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1 by Petra van der Lelij, Krystyńa Chrzańowska, Barbara C. Godthelp, Martin A. Rooimans, Anneke B. Oostra, Markus Stümm, Małgorzata Z. Zdzienicka, Hans Joenje, Johan P. de Winter

    Published 2010
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  2. 2
    Localization of the Gene for Rapidly Progressive Autosomal Dominant Parkinsonism and Dementia with Pallido-Ponto-Nigral Degeneration to Chromosome 17q21

    Localization of the Gene for Rapidly Progressive Autosomal Dominant Parkinsonism and Dementia with Pallido-Ponto-Nigral Degeneration to Chromosome 17q21 by Mario Wijker, Zbigniew K. Wszołek, Eric C. Wolters, Martin A. Rooimans, Gerard Pals, Ronald F. Pfeiffer, Timothy Lynch, Robert L. Rodnitzky, Kirk C. Wilhelmsen, F. Arwert

    Published 1996
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  3. 3
    Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes

    Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes by Marieke Levitus, Martin A. Rooimans, Jûrgen Steltenpool, Nicolle F. C. Cool, Anneke B. Oostra, Christopher G. Mathew, Maureen E. Hoatlin, Quinten Waisfisz, Fré Arwert, Johan P. de Winter, Hans Joenje

    Published 2003
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  4. 4
    Evidence for at Least Eight Fanconi Anemia Genes

    Evidence for at Least Eight Fanconi Anemia Genes by Hans Joenje, Anneke B. Oostra, Mario Wijker, Franca M. di Summa, Carola G.M. van Berkel, Martin A. Rooimans, Wolfram Ebell, Margreet van Weel, Jan C. Pronk, Manuel Buchwald, Fré Arwert

    Published 1997
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  5. 5
    Complementation Analysis in Fanconi Anemia: Assignment of the Reference FA-H Patient to Group A

    Complementation Analysis in Fanconi Anemia: Assignment of the Reference FA-H Patient to Group A by Hans Joenje, Marieke Levitus, Quinten Waisfisz, Alan D. D’Andrea, Irene García-Higuera, Tommy Pearson, Carola G.M. van Berkel, Martin A. Rooimans, Neil V. Morgan, Christopher G. Mathew, Fré Arwert

    Published 2000
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  6. 6
    X-linked inheritance of Fanconi anemia complementation group B

    X-linked inheritance of Fanconi anemia complementation group B by Amom Ruhikanta Meetei, Marieke Levitus, Yutong Xue, Annette L. Medhurst, Michel Zwaan, Ling Chen, Martin A. Rooimans, Patrick Bier, Maureen E. Hoatlin, Gerard Pals, Johan P. de Winter, Weidong Wang, Hans Joenje

    Published 2004
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  7. 7
    Evidence for subcomplexes in the Fanconi anemia pathway

    Evidence for subcomplexes in the Fanconi anemia pathway by Annette L. Medhurst, El Houari Laghmani, Jûrgen Steltenpool, Miriam Ferrer, Chantal Fontaine, Jan de Groot, Martin A. Rooimans, Rik J. Scheper, Amom Ruhikanta Meetei, Weidong Wang, Hans Joenje, Johan P. de Winter

    Published 2006
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  8. 8
    Targeting the cell cycle in head and neck cancer by Chk1 inhibition: a novel concept of bimodal cell death

    Targeting the cell cycle in head and neck cancer by Chk1 inhibition: a novel concept of bimodal cell death by Anne M. van Harten, Marijke Buijze, Richard van der Mast, Martin A. Rooimans, Sanne R. Martens‐de Kemp, Costa Bachas, Arjen Brink, Marijke Stigter‐van Walsum, Rob M.F. Wolthuis, Ruud H. Brakenhoff

    Published 2019
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  9. 9
    Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M

    Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M by Sietske T. Bakker, Henri J. van de Vrugt, Martin A. Rooimans, Anneke B. Oostra, Jûrgen Steltenpool, Elly Delzenne‐Goette, Anja van der Wal, Martin van der Valk, Hans Joenje, Hein te Riele, Johan P. de Winter

    Published 2009
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  10. 10
    Identification of the Fanconi Anemia Complementation Group I Gene, <i>FANCI</i>

    Identification of the Fanconi Anemia Complementation Group I Gene, <i>FANCI</i> by Josephine C. Dorsman, Marieke Levitus, Davy Rockx, Martin A. Rooimans, Anneke B. Oostra, Anneke Haitjema, Sietske T. Bakker, Jûrgen Steltenpool, Dezső Schuler, Sheila Mohan, Detlev Schindler, Fré Arwert, Gerard Pals, Christopher G. Mathew, Quinten Waisfisz, Johan P. de Winter, Hans Joenje

    Published 2007
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  11. 11
    Defective sister chromatid cohesion is synthetically lethal with impaired APC/C function

    Defective sister chromatid cohesion is synthetically lethal with impaired APC/C function by Job de Lange, Atiq Faramarz, Anneke B. Oostra, Renée X. de Menezes, Ida H. van der Meulen, Martin A. Rooimans, Davy Rockx, Ruud H. Brakenhoff, Victor W. van Beusechem, Randall W. King, Johan P. de Winter, Rob M.F. Wolthuis

    Published 2015
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  12. 12
    Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M

    Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M by Thiyam Ramsing Singh, Sietske T. Bakker, Sheba Agarwal, Michael Jansen, Elke Grassman, Barbara C. Godthelp, Abdullah Mahmood Ali, Chang-hu Du, Martin A. Rooimans, Qiang Fan, Kebola Wahengbam, Jûrgen Steltenpool, Paul R. Andreassen, David A. Williams, Hans Joenje, Johan P. de Winter, Amom Ruhikanta Meetei

    Published 2009
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  13. 13
    Biallelic <i>BUB1</i> mutations cause microcephaly, developmental delay, and variable effects on cohesion and chromosome segregation

    Biallelic <i>BUB1</i> mutations cause microcephaly, developmental delay, and variable effects on cohesion and chromosome segregation by Sara Carvalhal, Ingrid Bader, Martin A. Rooimans, Anneke B. Oostra, Jesper A. Balk, René G. Feichtinger, Christine Beichler, Michael R. Speicher, Johanna M. van Hagen, Quinten Waisfisz, Mieke M. van Haelst, Martijn Bruijn, Alexandra Tavares, Johannes A. Mayr, Rob M.F. Wolthuis, Raquel A. Oliveira, Job de Lange

    Published 2022
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  14. 14
    Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene

    Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene by Johan P. de Winter, France Léveillé, Carola G.M. van Berkel, Martin A. Rooimans, Laura van der Weel, Jûrgen Steltenpool, Ilja Demuth, Neil V. Morgan, Noa Alon, Lucine Bosnoyan-Collins, Jeff Lightfoot, Peter A. J. Leegwater, Quinten Waisfisz, Kenshi Komatsu, Fré Arwert, Jan C. Pronk, Christopher G. Mathew, Martin Digweed, Manuel Buchwald, Hans Joenje

    Published 2000
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  15. 15
    Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion

    Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion by Janne J. M. van Schie, Atiq Faramarz, Jesper A. Balk, Grant S. Stewart, Erika Cantelli, Anneke B. Oostra, Martin A. Rooimans, Joanna L. Parish, Cynthia de Almeida Estéves, Katja Dumić, Ingeborg Barišić, Karin E. M. Diderich, Marjon A. van Slegtenhorst, Mohammad Mahtab, Francesca M. Pisani, Hein te Riele, Najim Ameziane, Rob M.F. Wolthuis, Job de Lange

    Published 2020
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  16. 16
    A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51

    A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51 by Najim Ameziane, Patrick May, Anneke Haitjema, Henri J. van de Vrugt, Sari E. van Rossum-Fikkert, Dejan Ristić, Gareth J. Williams, Jesper A. Balk, Davy Rockx, Hong Li, Martin A. Rooimans, Anneke B. Oostra, Eunike Velleuer, Ralf Dietrich, Onno B. Bleijerveld, Maarten Altelaar, Hanne Meijers‐Heijboer, Hans Joenje, Gustavo Glusman, Jared C. Roach, Leroy Hood, David J. Galas, Claire Wyman, Rudi Balling, Johan T. den Dunnen, Johan P. de Winter, Roland Kanaar, Richard Gelinas, Josephine C. Dorsman

    Published 2015
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  17. 17
    Genetic determinants of micronucleus formation in vivo

    Genetic determinants of micronucleus formation in vivo by David J. Adams, B. Barlas, R. E. McIntyre, Israel Salguero, Louise van der Weyden, Alberto Barros, José Roberto Vicente, Nadia Karimpour, Ali Haider, Marco Ranzani, Gemma Turner, Nancy A. Thompson, Victoria Harle, Rebeca Olvera-León, Carla Daniela Robles‐Espinoza, Anneliese O. Speak, Norbert Geisler, Wolfgang J. Weninger, Stefan H. Geyer, James Hewinson, Natasha A. Karp, Catherine Tudor, Angela L. Green, Cecilia Mazzeo, Emma Siragher, Charlotte Lillistone, Diane Gleeson, Debarati Sethi, Tanya Bayzetinova, Jonathan Burvill, Bishoy Habib, Lauren Weavers, Ryea Maswood, Evelina Miklejewska, Michael Woods, Evelyn Grau, Stuart Newman, Caroline Sinclair, Ellen Brown, Brendan Doe, Antonella Galli, Ramiro Ramírez‐Solis, Edward J. Ryder, Karen P. Steel, Allan Bradley, William C. Skarnes, David J. Adams, David Lafont, Valerie E. Vancollie, Robbie S. B. McLaren, Lena Hughes-Hallett, Christine Rowley, Emma Sanderson, Elizabeth Tuck, Monika Dąbrowska, Mark Griffiths, David Gannon, Nicola Cockle, Andrea Kirton, Joanna Bottomley, Catherine Ingle, Chris Lelliott, Jacqueline K. White, Beiyuan Fu, Fengtang Yang, Zuzanna Kozik, Jyoti S. Choudhary, Lu Yu, Marjon S. van Ruiten, Benjamin D. Rowland, Christopher J. Lelliott, Martin Del Castillo Velasco‐Herrera, Ruth Verstraten, Lotte Brückner, Anton G. Henssen, Martin A. Rooimans, Jeremy D. Lange, Timothy J. Mohun, Mark J. Arends, Katherine A. Kentistou, Paula A. Coelho, Yi Zhao, Heather Zecchini, John R. B. Perry, Stephen P. Jackson, Gabriel Balmus

    Published 2024
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