Søgeresultater - Digweed, Martin
- Showing 1 - 15 results of 15
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Endogenous hSNM1B/Apollo interacts with TRF2 and stimulates ATM in response to ionizing radiation af Demuth, Ilja, Bradshaw, Paul S., Lindner, Anika, Anders, Marco, Heinrich, Stefanie, Kallenbach, Julia, Schmelz, Karin, Digweed, Martin, Meyn, M. Stephen, Concannon, Patrick
Udgivet 2008Text -
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Yeast XRS2 and human NBN gene: Experimental evidence for homology using codon optimized cDNA af Demuth, Ilja, Krebs, Simon K., Dutrannoy, Véronique, Linke, Christian, Krobitsch, Sylvia, Varon, Raymonda, Lang, Christine, Raab, Andreas, Sperling, Karl, Digweed, Martin
Udgivet 2018Text -
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Telomere attrition and dysfunction: a potential trigger of the progeroid phenotype in nijmegen breakage syndrome af Habib, Raneem, Kim, Ryong, Neitzel, Heidemarie, Demuth, Ilja, Chrzanowska, Krystyna, Seemanova, Eva, Faber, Renaldo, Digweed, Martin, Voss, Reinhard, Jäger, Kathrin, Sperling, Karl, Walter, Michael
Udgivet 2020Text -
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A Systematic Proteomic Study of Irradiated DNA Repair Deficient Nbn-Mice af 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
Udgivet 2009Text -
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Correction: A Systematic Proteomic Study of Irradiated DNA Repair Deficient Nbn-Mice af 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
Udgivet 2009Text -
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The Slavic NBN Founder Mutation: A Role for Reproductive Fitness? af 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
Udgivet 2016Text -
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Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene af 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
Udgivet 2000Text -
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Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans af 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.
Udgivet 2017Text