Publications of Ilona Dunkel

Gjaltema, R.; Schwämmle, T.; Kautz, P.; Robson, M.; Schöpflin, R.; Lustig, L. R.; Brandenburg, L.; Dunkel, I.; Vechiatto, C.; Ntini, E. et al.; Mutzel, V.; Schmiedel, V.; Marsico, A.; Mundlos, S.; Schulz, E. G.: Distal and proximal cis-regulatory elements sense X chromosome dosage and developmental state at the Xist locus. Molecular Cell 82 (1), pp. 190 - 208 (2022)

Pacini, G.; Dunkel, I.; Mages, N.; Mutzel, V.; Timmermann, B.; Marsico, A.; Schulz, E. G.: Integrated analysis of Xist upregulation and gene silencing at the onset of random X-chromosome inactivation at high temporal and allelic resolution. bioRxiv (The Preprintserver for biology) 2020 (2020)

Sahu, A.; Li, N.; Dunkel, I.; Chung, H.: EPIGENE: genome-wide transcription unit annotation using a multivariate probabilistic model of histone modifications. Epigenetics & Chromatin 13, 13:20 (2020)

Grunert, M.; Appelt, S.; Dunkel, I.; Berger, F.; Sperling, S. R.: Altered microRNA and target gene expression related to Tetralogy of Fallot. Scientific Reports 9, 19063 (2019) (2019)

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), pp. 1087 - 1099 (2019)

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)

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, pp. 1 - 54 (2017)

Kinkley, S.; Helmuth, J.; Polansky, J. K.; Dunkel, I.; Gasparoni, G.; Fröhler, S.; Chen, W.; Walter, J.; Hamann, A.; Chung, H.-R.: reChIP-seq reveals widespread bivalency of H3K4me3 and H3K27me3 in CD4+ memory T-Cells. Nature Communications 7, 7:12514 (2016)

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, 5:e10607 (2016)

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), S 1 (2014)

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)

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), e1001313 (2011)

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)

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)

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)

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)

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)

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)

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)

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)