Torthaí cuardaigh - Martin Digweed

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  1. 1
    Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia

    Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia de réir Martin Digweed

    Foilsithe / Cruthaithe 2002
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    Artigo
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  2. 2
    Nijmegen breakage syndrome (NBS)

    Nijmegen breakage syndrome (NBS) de réir Krystyńa Chrzańowska, Hanna Gregorek, Bożenna Dembowska‐Bagińska, Maria Kalina, Martin Digweed

    Foilsithe / Cruthaithe 2012
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    Revisão
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  3. 3
    Cancer Risk of Heterozygotes With the NBN Founder Mutation

    Cancer Risk of Heterozygotes With the NBN Founder Mutation de réir E Seemanová, Petr Jarolı́m, Pavel Seeman, Raymonda Varon, Martin Digweed, M Swift, Karl Sperling

    Foilsithe / Cruthaithe 2007
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    Artigo
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  4. 4
    Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita

    Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita de réir Tom Vulliamy, Richard Beswick, Michael Kirwan, Anna Marrone, Martin Digweed, Amanda J. Walne, Inderjeet Dokal

    Foilsithe / Cruthaithe 2008
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    Artigo
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  5. 5
    Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair

    Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair de réir Koji Nakanishi, Yun‐Gui Yang, Andrew J. Pierce, Toshiyasu Taniguchi, Martin Digweed, Alan D. D’Andrea, Zhao‐Qi Wang, Maria Jasin

    Foilsithe / Cruthaithe 2005
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  6. 6
    Nibrin functions in Ig class-switch recombination

    Nibrin functions in Ig class-switch recombination de réir Sven Kracker, Yvonne Bergmann, Ilja Demuth, Pierre‐Olivier Frappart, Gabriele Hildebrand, Rainer Christine, Zhao‐Qi Wang, Karl Sperling, Martin Digweed, Andreas Radbruch

    Foilsithe / Cruthaithe 2005
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  7. 7
    The Fanconi anemia group A protein modulates homologous repair of DNA double-strand breaks in mammalian cells

    The Fanconi anemia group A protein modulates homologous repair of DNA double-strand breaks in mammalian cells de réir Yun‐Gui Yang, Zdenko Herceg, Koji Nakanishi, Ilja Demuth, C. Piccoli, Jocelyne Michelon, Gabriele Hildebrand, Maria Jasin, Martin Digweed, Zhao‐Qi Wang

    Foilsithe / Cruthaithe 2005
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  8. 8
    Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

    Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome de réir Raymonda Varon, Christine Vissinga, Matthias Platzer, Karen Cerosaletti, Krystyńa Chrzańowska, Kathrin Saar, Georg Beckmann, E Seemanová, Paul R. Cooper, Norma J. Nowak, Markus Stümm, Corry M.R. Weemaes, Richard A. Gatti, Richard K. Wilson, Martin Digweed, André Rosenthal, Karl Sperling, Patrick Concannon, André Reis

    Foilsithe / Cruthaithe 1998
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    Artigo
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  9. 9
    Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene

    Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene de réir 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

    Foilsithe / Cruthaithe 2000
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  10. 10
    Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans

    Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans de réir Federica Buonocore, Peter Kühnen, Jenifer P. Suntharalingham, Ignacio del Valle, Martin Digweed, Harald Stachelscheid, Noushafarin Khajavi, Mohammed Didi, Angela F. Brady, Oliver Blankenstein, Annie Procter, Paul Dimitri, J K Wales, Paolo Ghirri, Dieter Knöbl, Brigitte Strahm, Miriam Erlacher, Marcin W. Włodarski, Wei Chen, George Kokai, Glenn Anderson, Deborah Morrogh, Dale Moulding, Shane McKee, Charlotte M. Niemeyer, Annette Grüters, John C. Achermann

    Foilsithe / Cruthaithe 2017
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