Search results

Journal Article (15)

  1. 1.
    Journal Article
    Mutzel, V.; Okamoto, I.; Dunkel, I.; Saitou, M.; Giorgetti, L.; Heard, E.; Schulz, E. G.: A symmetric toggle switch explains the onset of random X inactivation in different mammals. Nature Structural and Molecular Biology 26 (5), pp. 350 - 360 (2019)
  2. 2.
    Journal Article
    Mutzel, V.; Okamoto, I.; Dunkel, I.; Saitou, M.; Giorgetti, L.; Heard, E.; Schulz, E. G.: Two coupled feedback loops explain random mono-allelic Xist upregulation at the onset of X-chromosome inactivation. bioRxive 2017 (2017)
  3. 3.
    Journal Article
    Chung, H.-R.; Xu, C.; Fuchs, A.; Mund, A.; Lange, M.; Staege, H.; Schubert, T.; Bian, C.; Dunkel, I.; Eberharter, A. et al.; Regnard, C.; Klinker, H.; Meierhofer, D.; Cozzuto, L.; Winterpracht, A.; Di Croce, L.; Min, J.; Will, H.; Kinkley, S.: PHF13 is a molecular reader and transcriptional co-regulator of H3K4me2/3. eLife 5 (2016)
  4. 4.
    Journal Article
    Cui, H.; Schlesinger, J.; Bansal, V.; Dunkel, I.; Meierhofer, D.; Rickert-Sperling, S.: 5Regulation of myogenesis via kinase driven activation of DPF3a, a BAF complex member and its interaction with transcription repressor HEY1. Cardiovascular Research 103 (Suppl 1) (2014)
  5. 5.
    Journal Article
    Grunert, M.; Dorn, C.; Schueler, M.; Dunkel, I.; Schlesinger, J.; Mebus, S.; Alexi-Meskishvili, V.; Perrot, A.; Wassilew, K.; Timmermann, B. et al.; Hetzer, R.; Berger, F.; Sperling, S. R.: Rare and Private Variations in Neural Crest, Apoptosis and Sarcomere Genes Define the Polygenic Background of Isolated Tetralogy of Fallot. Human Molecular Genetics 23 (12), pp. 3115 - 3128 (2014)
  6. 6.
    Journal Article
    Schlesinger, J.; Schueler, M.; Grunert, M.; Fischer, J. J.; Zhang, Q.; Krueger, T.; Lange, M.; Tönjes, M.; Dunkel, I.; Sperling, S.: The Cardiac Transcription Network Modulated by Gata4, Mef2a, Nkx2.5, Srf, Histone Modifications, and MircoRNAs. PLoS Genetics 7 (2) (2011)
  7. 7.
    Journal Article
    Chung, H.-R.; Dunkel, I.; Heise, F.; Linke, C.; Krobitsch, S.; Ehrenhofer-Murray, A. E.; Sperling, S. R.; Vingron, M.: The effect of MNase on nucleosome positioning data. PLoS ONE 5 (12), p. e15754 - e15754 (2010)
  8. 8.
    Journal Article
    Schlesinger, J.; Tönjes, M.; Schueler, M.; Zhang, Q.; Dunkel, I.; Sperling, S. R.: Evaluation of the LightCycler(R) 1536 Instrument for high-throughput quantitative real-time PCR. Methods 50 (4), pp. S19 - S22 (2010)
  9. 9.
    Journal Article
    Schlesinger, J.; Tönjes, M.; Schueler, M.; Zhang, Q.; Dunkel, I.; Sperling, S. R.: Evaluation of the LightCycler(R) 1536 Instrument for high-throughput quantitative real-time PCR. Methods 50 (4), pp. S19 - S22 (2010)
  10. 10.
    Journal Article
    Lange, M.; Kaynak, B.; Forster, U. B.; Tönjes, M.; Fischer, J. J.; Grimm, C.; Schlesinger, J.; Just, S.; Dunkel, I.; Krueger, T. et al.; Mebus, S.; Lehrach, H.; Lurz, R.; Gobom, J.; Rottbauer, W.; Abdelilah-Seyfried, S.; Sperling, S.: Regulation of muscle development by DPF3, a novel histone acetylation and methylation reader of the BAF chromatin remodeling complex. Genes and Development 22 (17), pp. 2370 - 2384 (2008)
  11. 11.
    Journal Article
    Lange, M.; Kaynak, B.; Forster, U. B.; Tönjes, M.; Fischer, J. J.; Grimm, C.; Schlesinger, J.; Just, S.; Dunkel, I.; Krueger, T. et al.; Mebus, S.; Lehrach, H.; Lurz, R.; Gobom, J.; Rottbauer, W.; Abdelilah-Seyfried, S.; Sperling, S.: Regulation of muscle development by DPF3, a novel histone acetylation and methylation reader of the BAF chromatin remodeling complex. Genes and Development 22 (17), pp. 2370 - 2384 (2008)
  12. 12.
    Journal Article
    Hammer, S.; Toenjes, M.; Lange, M.; Fischer, J. J.; Dunkel, I.; Mebus, S.; Grimm, C. H.; Hetzer, R.; Berger, F.; Sperling, S.: Characterization of TBX20 in human hearts and its regulation by TFAP2. Journal of Cellular Biochemistry 104 (3), pp. 1022 - 1033 (2008)
  13. 13.
    Journal Article
    Sperling, S.; Grimm, C. H.; Dunkel, I.; Mebus, S.; Sperling, H.-P.; Ebner, A.; Galli, R.; Lehrach, H.; Fusch, C.; Berger, F. et al.; Hammer, S.: Identification and functional analysis of CITED2 mutations in patients with congenital heart defects. Human Mutation 26 (6), pp. 575 - 582 (2005)
  14. 14.
    Journal Article
    Heiser, V.; Engernann, S.; Brocker, W.; Dunkel, I.; Boeddrich, A.; Waelter, S.; Nordhoff, E.; Lurz, R.; Schugardt, N.; Rautenberg, S. et al.; Herhaus, C.; Barnickel, G.; Boettcher, H.; Lehrach, H.; Wanker, E. E.: Identification of benzothiazoles as potential polyglutamine aggregation inhibitors of Huntington's disease by using an automated filter retardation assay. Proceedings of the National Academy of Sciences of the United States of America 99 (Suppl. 4), pp. 16400 - 16406 (2002)
  15. 15.
    Journal Article
    Heiser, V.; Engemann, S.; Bröcker, W.; Dunkel, I.; Boeddrich, A.; Waelter, S.; Nordhoff, E.; Lurz, R.; Schugardt, N.; Rautenberg, S. et al.; Herhaus, C.; Barnickel, G.; Böttcher, H.; Lehrach, H.; Wanker, E. E.: Identification of benzothiazoles as potential polyglutamine aggregation inhibitors of Huntington’s disease by using an automated filter retardation assay. Self-Perpetuating Structural States in Biology, Disease, and Genetics, pp. 16400 - 16406 (2002)
Go to Editor View