Zeitschriftenartikel (98)

  1. 11.
    Zeitschriftenartikel
    Fenouil, R.; Descostes, N.; Spinelli, .; Koch, F.; Maqbool, M. A.; Benoukraf, T.; Cauchy, P.; Innocenti , C.; Ferrier , P.; Andrau, J.-C.: Pasha: a versatile R package for piling chromatin HTS data. Bioinformatics 32 (16), S. 2528 - 2530 (2016)
  2. 12.
    Zeitschriftenartikel
    Schmitz, S. U.; Grote, P.; Herrmann, B. G.: Mechanisms of long noncoding RNA function in development and disease. Cellular and Molecular Life Sciences 73 (13), S. 2491 - 2509 (2016)
  3. 13.
    Zeitschriftenartikel
    Sudheer, S.; Liu, J.; Marks, M.; Koch, F.; Anurin, A.; Scholze, M.; Senft, A. D.; Wittler, L.; Macura, K.; Grote, P. et al.; Herrmann, B. G.: Different Concentrations of FGF Ligands, FGF2 or FGF8 Determine Distinct States of WNT-Induced Presomitic Mesoderm. Stem Cells 34 (7), S. 1790 - 800 (2016)
  4. 14.
    Zeitschriftenartikel
    Veenvliet, J. V.: Studying Mesodiencephalic Dopaminergic Neuron Development In Vivo to Improve Stem Cell Therapy in Parkinson’s Disease. The Journal of Neuroscience (2016)
  5. 15.
    Zeitschriftenartikel
    Spielmann, M.; Kakar, N.; Tayebi, N.; Leettola, C.; Nürnberg, G.; Sowada, N.; Lupiáñez, D. G.; Harabula, I.; Flöttmann, R.; Horn, D. et al.; Chan, W. L.; Wittler, L.; Yilmaz, R.; Altmüller, J.; Thiele, H.; van Bokhoven,, H.; Schwartz, C. E.; Nürnberg, P.; Bowie, J. U.; Ahmad, J.; Kubisch, C.; Mundlos, S.: Exome Sequencing and CRISPR/Cas Genome Editing Identify Mutations of ZAK as a Cause of Limb Defects in Humans and Mice. Genome Research 26 (2), S. 183 - 191 (2016)
  6. 16.
    Zeitschriftenartikel
    Marks, M.; Pennimpede, T.; Lange, L.; Grote, P.; Herrmann, B. G.; Wittler, L.: Analysis of the Fam181 gene family during mouse development reveals distinct strain-specific expression patterns, suggesting a role in nervous system development and function. Gene 575 (2 Pt 2), S. 438 - 451 (2016)
  7. 17.
    Zeitschriftenartikel
    Grote, P.; Herrmann, B. G.: Long noncoding RNAs in organogenesis: Making the difference. Trends in Genetics 31 (6), S. 329 - 335 (2015)
  8. 18.
    Zeitschriftenartikel
    Lupiáñez, D. G.; Kraft, K.; Heinrich, V.; Krawitz, P.; Brancati, F.; Klopocki, E.; Horn, D.; Kayserili, H.; Opitz, J. M.; Laxova, R. et al.; Santos-Simarro, F.; Gilbert-Dussardier, B.; Wittler, L.; Borschiwer, M.; Haas, S. A.; Osterwalder, M.; Franke, M.; Timmermann, B.; Hecht, J.; Spielmann, M.; Visel, A.; Mundlos, S.: Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions. Cell 161 (5), S. 1012 - 1025 (2015)
  9. 19.
    Zeitschriftenartikel
    Milenkovic, A.; Brandl, C.; Milenkovic, V. M.; Jendryke, T.; Sirianant, L.; Wanitchakool, P.; Zimmermann, S.; Reiff, C. M.; Horling, F.; Schrewe, H. et al.; Schreiber, R.; Kunzelmann, K.; Wetzel, C. H.; Weber, B. H. F.: Bestrophin 1 is indispensable for volume regulation in human retinal pigment epithelium cells. Proceedings of the National Academy of Sciences of the United States of America 112 (20), S. E2630 - E2639 (2015)
  10. 20.
    Zeitschriftenartikel
    Kraft, K.; Geuer, S.; Will, A. J.; Chan, W. L.; Paliou, C.; Borschiwer, M.; Harabula, I.; Wittler, L.; Franke, M.; Ibrahim, D. et al.; Kragesteen, B. K.; Spielmann, M.; Mundlos, S.; Lupianez, D. G.; Andrey, G.: Deletions, Inversions, Duplications: Engineering of Structural Variants using CRISPR/Cas in Mice. Cell Reports 10 (5), S. 833 - 839 (2015)
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