نتائج البحث - Digweed, Martin
- يعرض 1 - 15 نتائج من 15
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DNA Damage in Nijmegen Breakage Syndrome Cells Leads to PARP Hyperactivation and Increased Oxidative Stress حسب Krenzlin, Harald, Demuth, Ilja, Salewsky, Bastian, Wessendorf, Petra, Weidele, Kathrin, Bürkle, Alexander, Digweed, Martin
منشور في 2012نص -
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Endogenous hSNM1B/Apollo interacts with TRF2 and stimulates ATM in response to ionizing radiation حسب Demuth, Ilja, Bradshaw, Paul S., Lindner, Anika, Anders, Marco, Heinrich, Stefanie, Kallenbach, Julia, Schmelz, Karin, Digweed, Martin, Meyn, M. Stephen, Concannon, Patrick
منشور في 2008نص -
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Yeast XRS2 and human NBN gene: Experimental evidence for homology using codon optimized cDNA حسب Demuth, Ilja, Krebs, Simon K., Dutrannoy, Véronique, Linke, Christian, Krobitsch, Sylvia, Varon, Raymonda, Lang, Christine, Raab, Andreas, Sperling, Karl, Digweed, Martin
منشور في 2018نص -
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Nibrin functions in Ig class-switch recombination حسب Kracker, Sven, Bergmann, Yvonne, Demuth, Ilja, Frappart, Pierre-Olivier, Hildebrand, Gabriele, Christine, Rainer, Wang, Zhao-Qi, Sperling, Karl, Digweed, Martin, Radbruch, Andreas
منشور في 2005نص -
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Telomere attrition and dysfunction: a potential trigger of the progeroid phenotype in nijmegen breakage syndrome حسب Habib, Raneem, Kim, Ryong, Neitzel, Heidemarie, Demuth, Ilja, Chrzanowska, Krystyna, Seemanova, Eva, Faber, Renaldo, Digweed, Martin, Voss, Reinhard, Jäger, Kathrin, Sperling, Karl, Walter, Michael
منشور في 2020نص -
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A Systematic Proteomic Study of Irradiated DNA Repair Deficient Nbn-Mice حسب Melchers, Anna, Stöckl, Lars, Radszewski, Janina, Anders, Marco, Krenzlin, Harald, Kalischke, Candy, Scholz, Regina, Jordan, Andreas, Nebrich, Grit, Klose, Joachim, Sperling, Karl, Digweed, Martin, Demuth, Ilja
منشور في 2009نص -
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Correction: A Systematic Proteomic Study of Irradiated DNA Repair Deficient Nbn-Mice حسب Melchers, Anna, Stöckl, Lars, Radszewski, Janina, Anders, Marco, Krenzlin, Harald, Kalischke, Candy, Scholz, Regina, Jordan, Andreas, Nebrich, Grit, Klose, Joachim, Sperling, Karl, Digweed, Martin, Demuth, Ilja
منشور في 2009نص -
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The Slavic NBN Founder Mutation: A Role for Reproductive Fitness? حسب Seemanova, Eva, Varon, Raymonda, Vejvalka, Jan, Jarolim, Petr, Seeman, Pavel, Chrzanowska, Krystyna H., Digweed, Martin, Resnick, Igor, Kremensky, Ivo, Saar, Kathrin, Hoffmann, Katrin, Dutrannoy, Véronique, Karbasiyan, Mohsen, Ghani, Mehdi, Barić, Ivo, Tekin, Mustafa, Kovacs, Peter, Krawczak, Michael, Reis, André, Sperling, Karl, Nothnagel, Michael
منشور في 2016نص -
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Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene حسب de Winter, Johan P., Léveillé, France, van Berkel, Carola G. M., Rooimans, Martin A., van der Weel, Laura, Steltenpool, Jurgen, Demuth, Ilja, Morgan, Neil V., Alon, Noa, Bosnoyan-Collins, Lucine, Lightfoot, Jeff, Leegwater, Peter A., Waisfisz, Quinten, Komatsu, Kenshi, Arwert, Fré, Pronk, Jan C., Mathew, Christopher G., Digweed, Martin, Buchwald, Manuel, Joenje, Hans
منشور في 2000نص -
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Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans حسب Buonocore, Federica, Kühnen, Peter, Suntharalingham, Jenifer P., Del Valle, Ignacio, Digweed, Martin, Stachelscheid, Harald, Khajavi, Noushafarin, Didi, Mohammed, Brady, Angela F., Blankenstein, Oliver, Procter, Annie M., Dimitri, Paul, Wales, Jerry K.H., Ghirri, Paolo, Knöbl, Dieter, Strahm, Brigitte, Erlacher, Miriam, Wlodarski, Marcin W., Chen, Wei, Kokai, George K., Anderson, Glenn, Morrogh, Deborah, Moulding, Dale A., McKee, Shane A., Niemeyer, Charlotte M., Grüters, Annette, Achermann, John C.
منشور في 2017نص