未登录 Routine CT Diagnostics Cause Dose-Dependent Gene Expression Changes in Peripheral Blood Cells 常规CT诊断会导致外周血细胞出现剂量依赖性的基因表达变化。 Kaatsch, Hanns Leonhard; Kubitscheck, Laura; Wagner, Simon; Hantke, Thomas; Preiss, Maximilian; Ostheim, Patrick; Nestler, Tim; Piechotka, Joel; Overhoff, Daniel; Brockmann, Marc A.; Waldeck, Stephan; Port, Matthias; Ullmann, Reinhard; Becker, Benjamin V. 分享 收藏
Gene expression changes and DNA damage after ex vivo exposure of peripheral blood cells to various CT photon spectra Kaatsch, Hanns Leonhard; Becker, Benjamin Valentin; Schule, Simone; Ostheim, Patrick; Nestler, Kai; Jakobi, Julia; Schaefer, Barbara; Hantke, Thomas; Brockmann, Marc A.; Abend, Michael; Waldeck, Stephan; Port, Matthias; Scherthan, Harry; Ullmann, Reinhard 分享 收藏
Genome-Wide Analysis of Interchromosomal Interaction Probabilities Reveals Chained Translocations and Overrepresentation of Translocation Breakpoints in Genes in a Cutaneous T-Cell Lymphoma Cell Line Steininger, Anne; Ebert, Grit; Becker, Benjamin V.; Assaf, Chalid; Moebs, Markus; Schmidt, Christian A.; Grabarczyk, Piotr; Jensen, Lars R.; Przybylski, Grzegorz K.; Port, Matthias; Kuss, Andreas W.; Ullmann, Reinhard 分享 收藏
SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorder Merker, Soeren; Reif, Andreas; Ziegler, Georg C.; Weber, Heike; Mayer, Ute; Ehlis, Ann-Christine; Conzelmann, Annette; Johansson, Stefan; Mueller-Reible, Clemens; Nanda, Indrajit; Haaf, Thomas; Ullmann, Reinhard; Romanos, Marcel; Fallgatter, Andreas J.; Pauli, Paul; Strekalova, Tatyana; Jansch, Charline; Vasquez, Alejandro Arias; Haavik, Jan; Ribases, Marta; Antoni Ramos-Quiroga, Josep; Buitelaar, Jan K.; Franke, Barbara; Lesch, Klaus-Peter 分享 收藏
A Flexible, GPU - Powered Fast Multipole Method for Realistic Biomolecular Simulations in Gromacs Kohnke, Bartosz; Ullmann, R. Thomas; Kutzner, Carsten; Beckmann, Andreas; Haensel, David; Kabadshow, Ivo; Dachsel, Holger; Hess, Berk; Grubmueller, Helmut 分享 收藏
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Inactivation of RUNX3/p46 Promotes Cutaneous T-Cell Lymphoma Haider, Ahmed; Steininger, Anne; Ullmann, Reinhard; Hummel, Michael; Dimitrova, Lora; Beyer, Marc; Vandersee, Staffan; Lenze, Dido; Sterry, Wolfram; Assaf, Chalid; Moebs, Markus 分享 收藏
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Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems Kumar, Raman; Corbett, Mark A.; Van Bon, Bregje W. M.; Gardner, Alison; Woenig, Joshua A.; Jolly, Lachlan A.; Douglas, Evelyn; Friend, Kathryn; Tan, Chuan; Van Esch, Hilde; Holvoet, Maureen; Raynaud, Martine; Field, Michael; Leffler, Melanie; Budny, Bartlomiej; Wisniewska, Marzena; Badura-Stronka, Magdalena; Latos-Bielenska, Anna; Batanian, Jacqueline; Rosenfeld, Jill A.; Basel-Vanagaite, Lina; Jensen, Corinna; Bienek, Melanie; Froyen, Guy; Ullmann, Reinhard; Hu, Hao; Love, Michael I.; Haas, Stefan A.; Stankiewicz, Pawel; Cheung, Sau Wai; Baxendale, Anne; Nicholl, Jillian; Thompson, Elizabeth M.; Haan, Eric; Kalscheuer, Vera M.; Gecz, Jozef 分享 收藏
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes Hu, H.; Haas, S. A.; Chelly, J.; Van Esch, H.; Raynaud, M.; de Brouwer, A. P. M.; Weinert, S.; Froyen, G.; Frints, S. G. M.; Laumonnier, F.; Zemojtel, T.; Love, M. I.; Richard, H.; Emde, A-K; Bienek, M.; Jensen, C.; Hambrock, M.; Fischer, U.; Langnick, C.; Feldkamp, M.; Wissink-Lindhout, W.; Lebrun, N.; Castelnau, L.; Rucci, J.; Montjean, R.; Dorseuil, O.; Billuart, P.; Stuhlmann, T.; Shaw, M.; Corbett, M. A.; Gardner, A.; Willis-Owen, S.; Tan, C.; Friend, K. L.; Belet, S.; van Roozendaal, K. E. P.; Jimenez-Pocquet, M.; Moizard, M-P; Ronce, N.; Sun, R.; O'Keeffe, S.; Chenna, R.; Van Boemmel, A.; Goeke, J.; Hackett, A.; Field, M.; Christie, L.; Boyle, J.; Haan, E.; Nelson, J.; Turner, G.; Baynam, G.; Gillessen-Kaesbach, G.; Mueller, U.; Steinberger, D.; Budny, B.; Badura-Stronka, M.; Latos-Bielenska, A.; Ousager, L. B.; Wieacker, P.; Criado, G. Rodriguez; Bondeson, M-L; Anneren, G.; Dufke, A.; Cohen, M.; Van Maldergem, L.; Vincent-Delorme, C.; Echenne, B.; Simon-Bouy, B.; Kleefstra, T.; Willemsen, M.; Fryns, J-P; Devriendt, K.; Ullmann, R.; Vingron, M.; Wrogemann, K.; Wienker, T. F.; Tzschach, A.; van Bokhoven, H.; Gecz, J.; Jentsch, T. J.; Chen, W.; Ropers, H-H; Kalscheuer, V. M. 分享 收藏
Familial 46,XY sex reversal without campomelic dysplasia caused by a deletion upstream of the SOX9 gene 由SOX9基因上游缺失引起的家族性46，XY性反转而无坎皮发育异常 Bhagavath, Bala; Layman, Lawrence C.; Ullmann, Reinhard; Shen, Yiping; Ha, Kyungsoo; Rehman, Khurram; Looney, Stephen; McDonough, Paul G.; Kim, Hyung-Goo; Carr, Bruce R. 分享 收藏
Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7 Ebert, Grit; Steininger, Anne; Weissmann, Robert; Boldt, Vivien; Lind-Thomsen, Allan; Grune, Jana; Badelt, Stefan; Hessler, Melanie; Peiser, Matthias; Hitzler, Manuel; Jensen, Lars R.; Mueller, Ines; Hu, Hao; Arndt, Peter F.; Kuss, Andreas W.; Tebel, Katrin; Ullmann, Reinhard 分享 收藏
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum Thorwarth, Anne; Schnittert-Huebener, Sarah; Schrumpf, Pamela; Mueller, Ines; Jyrch, Sabine; Dame, Christof; Biebermann, Heike; Kleinau, Gunnar; Katchanov, Juri; Schuelke, Markus; Ebert, Grit; Steininger, Anne; Boennemann, Carsten; Brockmann, Knut; Christen, Hans-Juergen; Crock, Patricia; deZegher, Francis; Griese, Matthias; Hewitt, Jacqueline; Ivarsson, Sten; Huebner, Christoph; Kapelari, Klaus; Plecko, Barbara; Rating, Dietz; Stoeva, Iva; Ropers, Hans-Hilger; Grueters, Annette; Ullmann, Reinhard; Krude, Heiko 分享 收藏
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome Moller, R. S.; Jensen, L. R.; Maas, S. M.; Filmus, J.; Capurro, M.; Hansen, C.; Marcelis, C. L. M.; Ravn, K.; Andrieux, J.; Mathieu, M.; Kirchhoff, M.; Rodningen, O. K.; de Leeuw, N.; Yntema, H. G.; Froyen, G.; Vandewalle, J.; Ballon, K.; Klopocki, E.; Joss, S.; Tolmie, J.; Knegt, A. C.; Lund, A. M.; Hjalgrim, H.; Kuss, A. W.; Tommerup, N.; Ullmann, R.; de Brouwer, A. P. M.; Stromme, P.; Kjaergaard, S.; Tuemer, Z.; Kleefstra, T. 分享 收藏
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Breakpoint characterization of the der(19)t(11;19)(q13;p13) in the ovarian cancer cell line SKOV-3 卵巢癌细胞系SKOV-3中der(19)t(11;19)(q13;p13) 的断点表征 Onkes, Wiebke; Fredrik, Regina; Micci, Francesca; Schoenbeck, Benjamin J.; Martin-Subero, Jose I.; Ullmann, Reinhard; Hilpert, Felix; Braeutigam, Karen; Janssen, Ottmar; Maass, Nicolai; Siebert, Reiner; Heim, Sverre; Arnold, Norbert; Weimer, Joerg 分享 收藏
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Translocations Disrupting PHF21A in the Potocki-Shaffer-Syndrome Region Are Associated with Intellectual Disability and Craniofacial Anomalies 在potocki-shaffer综合征区域中破坏PHF21A的易位与智力障碍和颅面异常有关 Kim, Hyung-Goo; Kim, Hyun-Taek; Leach, Natalia T.; Lan, Fei; Ullmann, Reinhard; Silahtaroglu, Asli; Kurth, Ingo; Nowka, Anja; Seong, Ihn Sik; Shen, Yiping; Talkowski, Michael E.; Ruderfer, Douglas; Lee, Ji-Hyun; Glotzbach, Caron; Ha, Kyungsoo; Kjaergaard, Susanne; Levin, Alex V.; Romeike, Bernd F.; Kleefstra, Tjitske; Bartsch, Oliver; Elsea, Sarah H.; Jabs, Ethylin Wang; MacDonald, Marcy E.; Harris, David J.; Quade, Bradley J.; Ropers, Hans-Hilger; Shaffer, Lisa G.; Kutsche, Kerstin; Layman, Lawrence C.; Tommerup, Niels; Kalscheuer, Vera M.; Shi, Yang; Morton, Cynthia C.; Kim, Cheol-Hee; Gusella, James F. 分享 收藏
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