Zeitschriftenartikel (83)

21.
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Segal, J.; Mülleder, M.; Krüger, A.; Adler, T.; Scholze-Wittler, M.; Becker, L.; Calzada-Wack, J.; Garrett, L.; Hölter, S. M.; Rathkolb, B. et al.; Rozman, J.; Racz, I.; Fischer, R.; Busch, D. H.; Neff, F.; Klingenspor, M.; Klopstock, T.; Grüning, N.-M.; Michel, S.; Lukaszewska-McGreal, B.; Voigt, I.; Hartmann, L.; Timmermann, B.; Lehrach, H.; Wolf, E.; Wurst, W.; Gailus-Durner, V.; Fuchs, H.; de Angelis, M. H.; Schrewe, H.; Yuneva, M.; Ralser, M.: Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase (TPI) deficiency. Journal of Inherited Metabolic Disease 22 (5), S. 839 - 849 (2019)
22.
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Schade, S.; Ogilvie, L. A.; Kessler, T.; Schütte, M.; Wierling, C.; Lange, B. M.; Lehrach, H.; Yaspo, M.-L.: A data- and model-drivenapproach for cancer treatment. Der Onkologe 25 (Suppl. 2), S. S132 - S137 (2019)
23.
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Guo, J.; Bertalan, G.; Meierhofer, D.; Klein, C.; Schreyer, S.; Steiner, B.; Wang, S.; Vieira da Silva, R.; Infante-Duarte, C.; Koch, S. et al.; Boehm-Sturm, P.; Braun, J.; Sack, I.: Brain maturation is associated with increasing tissue stiffness and decreasing tissue fluidity. Acta Biomaterialia, pii: S1742-7061(19)30592-6 (2019)
24.
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Bose, D.; Neumann, A.; Timmermann, B.; Meinke, S.; Heyd, F.: Differential Interleukin-2 Transcription Kinetics Render Mouse but Not Human T Cells Vulnerable to Splicing Inhibition Early after Activation. Molecular and Cellular Biology (Washington, DC) 39 (16), e00035-19 (2019)
25.
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Meierhofer, D.: Acylcarnitine profiling by low-resolution LC-MS. PLoS One 14 (8), e0221342 (2019)
26.
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Kopp, W.; Vingron, M.: DNA Motif Match Statistics Without Poisson Approximation. Journal of Computational Biology 26 (8), S. 846 - 865 (2019)
27.
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Schade, S.; Ogilvie, L. A.; Kessler, T.; Schütte, M.; Wierling, C.; Lange, B. M.; Lehrach, H.; Yaspo, M.-L.: Ein daten- und modellgesteuerter Ansatz zur Behandlung maligner Tumoren. Der Onkologe 25 (Suppl. 1), S. S109 - S115 (2019)
28.
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Malik, V.; Glaser, L. V.; Zimmer, D.; Velychko, S.; Weng, M.; Holzner, M.; Arend, M.; Chen, Y.; Srivastava, Y.; Veerapandian, V. et al.; Shah, Z.; Esteban, M. A.; Wang, H.; Chen, J.; Scholer, H. R.; Hutchins, A. P.; Meijsing, S. H.; Pott, S.; Jauch, R.: Pluripotency reprogramming by competent and incompetent POU factors uncovers temporal dependency for Oct4 and Sox2. Nature Communications 10 (1), 3477 (2019)
29.
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Despang, A.; Schöpflin, R.; Franke, M.; Ali, S.; Jerković, I.; Paliou, C.; Chan, W.-L.; Timmermann, B.; Wittler, L.; Vingron, M. et al.; Mundlos, S.; Ibrahim, D. M.: Functional dissection of the Sox9-Kcnj2 locus identifies nonessential and instructive roles of TAD architecture. Nature Genetics 51 (8), S. 1263 - 1271 (2019)
30.
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Nazaryan-Petersen, L.; Oliveira, I. R.; Mehrjouy, M. M.; Mendez, J. M. M.; Bak, M.; Bugge, M.; Kalscheuer, V. M.; Bache, I.; Hancks, D. C.; Tommerup, N.: Multigenic truncation of the semaphorin-plexin pathway by a germline chromothriptic rearrangement associated with Moebius syndrome. Human Mutation 40 (8), S. 1057 - 1062 (2019)
31.
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Xiao, Y.; Meierhofer, D.: Are hydroethidine-based probes reliable for ROS detection? ANTIOXIDANTS & REDOX SIGNALING 31 (4), S. 359 - 367 (2019)
32.
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Sen, N.-E.; Canet-Pons, J.; Halbach, M. V.; Arsovic, A.; Pilatus, U.; Chae, W.-H.; Kaya, Z.-E.; Seidel, K.; Rollmann, E.; Mittelbronn, M. et al.; Meierhofer, D.; De Zeeuw, C. I.; Bosman, L. W. J.; Gispert, S.; Auburger, G.: Generation of an Atxn2-CAG100 knock-in mouse reveals N-acetylaspartate production deficit due to early Nat8l dysregulation. Neurobiology of Disease 132, 104559 (2019)
33.
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Xiao, Y.; Meierhofer, D.: Glutathione Metabolism in Renal Cell Carcinoma Progression and Implications for Therapies. International Journal of Molecular Sciences 20 (15), E3672 (2019)
34.
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Fattahi, Z.; Beheshtian, M.; Mohseni, M.; Poustchi, H.; Sellars, E.; Nezhadi, S. H.; Amini, A.; Arzhangi, S.; Jalalvand, K.; Jamali, P. et al.; Mohammadi, Z.; Davarnia, B.; Nikuei, P.; Oladnabi, M.; Mohammadzadeh, A.; Zohrehvand, E.; Nejatizadeh, A.; Shekari, M.; Bagherzadeh, M.; Shamsi‐Gooshki, E.; Börno, S.; Timmermann, B.; Haghdoost, A.; Najafipour, R.; Khorram Khorshid, H. R.; Kahrizi, K.; Malekzadeh, R.; Akbari, M. R.; Najmabadi, H.: Iranome: A catalogue of genomic variations in the Iranian population. Human Mutation 2019, S. 1 - 17 (2019)
35.
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Gudmundsson, S.; Wilbe, M.; Filipek-Górniok, B.; Molin, A.-M.; Ekvall, S.; Johansson, J.; Allalou, A.; Gylje, H.; Kalscheuer, V. M.; Ledin, J. et al.; Annerén, G.; Bondeson, M.-L.: TAF1, associated with intellectual disability in humans, is essential for embryogenesis and regulates neurodevelopmental processes in zebrafish. Scientific Reports 9, 10730 (2019)
36.
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Seiler, E.; Trappe, K.; Renard, B. Y.: Where did you come from, where did you go: Refining metagenomic analysis tools for horizontal gene transfer characterisation. PLOS Computational Biology 15 (7), e1007208 (2019)
37.
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Zi, Z.: Molecular Engineering of the TGF-β Signaling Pathway. Journal of Molecular Biology (London) 431 (15), S. 2644 - 2654 (2019)
38.
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Brandt, R.; Sell, T.; Lüthen, M.; Uhlitz, F.; Klinger, B.; Riemer, P.; Giesecke-Thiel, C.; Schulze, S.; El-Shimy, I. A.; Kunkel, D. et al.; Fauler, B.; Mielke, T.; Mages, N.; Herrmann, B. G.; Sers, C.; Blüthgen, N.; Morkel, M.: Cell type-dependent differential activation of ERK by oncogenic KRAS in colon cancer and intestinal epithelium. Nature Communications 10 (1), 2919 (2019)
39.
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Barros de Andrade e Sousa, L.; Jonkers, I.; Syx, L.; Dunkel, I.; Chaumeil, J.; Picard, C.; Foret, B.; Chen, C.-J.; Lis, J. T.; Heard, E. et al.; Schulz, E. G.; Marsico, A.: Kinetics of Xist-induced gene silencing can be predicted from combinations of epigenetic and genomic features. Genome Research 29 (7), S. 1087 - 1099 (2019)
40.
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Hu, H.; Kahrizi, K.; Musante, L.; Fattahi, Z.; Herwig, R.; Hosseini, M.; Oppitz, C.; Abedini, S. S.; Suckow, V.; Farzaneh, L. et al.; Beheshtian, M.; Lipkowitz, B.; Akhtarkhavari, T.; Mehvari, S.; Otto, S.; Mohseni, M.; Arzhangi, S.; Jamali, P.; Mojahedi, F.; Taghdiri, M.; Papari, E.; Soltani Banavandi, M. J.; Akbari, S.; Tonekaboni, S. H.; Dehghani, H.; Ebrahimpou, M. R.; Bader, I.; Davarnia, B.; Cohen, M.; Khodaei, H.; Albrecht, B.; Azimi, S.; Zirn, B.; Bastami, M.; Wieczorek, D.; Bahrami, G.; Keleman, K.; Vahid, L. N.; Timmermann, B.; Pourfatemi, F.; Jankhah, A.; Chen, W.; Nikuei, P.; Kalscheuer, V. M.; Oladnabi, M.; Wienker, T. F.; Ropers, H.-H.; Najmabadi, H.: Genetics of intellectual disability in consanguineous families. Molecular Psychiatry 24 (7), S. 1027 - 1039 (2019)
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