Suchergebnisse

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), S. 3115 - 3128 (2014)

Dorn, C.; Grunert, M.; Sperling, S.: Application of high-throughput sequencing for studying genomic variations in congenital heart disease. Briefings in Functional Genomics 13 (1), S. 51 - 65 (2014)

Meyer, T.; Ruppert, V.; Ackermann, S.; Richter, A.; Perrot, A.; Sperling, S.; Posch, M. G.; Maisch, B.; Pankuweit, S.: Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy. European journal of human genetics: EJHG ; the official journal of the European Society of Human Genetics 21 (3), S. 294 - 300 (2013)

van Engelen, K.; Postma, A. V.; van de Meerakker, J. B. A.; Roos-Hesselink, J. W.; Helderman-van den Enden, A. T. J. M.; Vliegen, H. W.; Rahman, T.; Baars, M. J. H.; Sels, J.-W.; Bauer, U. et al.; Pickardt, T.; Sperling, S.; Moorman, A. F. M.; Keavney, B.; Goodship, J.; Klaassen, S.; Mulder, B. J. M.: Ebstein´s anomaly may be caused by mutations in the sarcomere protein gene MYH7. Netherlands Heart Journal 21 (3), S. 113 - 117 (2013)

van Engelen, K.; Postma, A. V.; van de Meerakker, J. B. A.; Roos-Hesselink, J. W.; Helderman-van den Enden, A. T. J. M.; Vliegen, H. W.; Rahman, T.; Baars, M. J. H.; Sels, J. W.; Bauer, U. et al.; Pickardt, T.; Sperling, S.; Moorman, A. F. M.; Keavney, B.; Goodship, J.; Klaassen, S.; Mulder, B. J. M.: Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7. Netherlands Heart Journal 21 (3), S. 113 - 117 (2013)

Schueler, M.; Zhang, Q.; Schlesinger, J.; Tönjes, M.; Sperling, S.: Dynamics of Srf, p300 and histone modifications during cardiac maturation in mouse. Molecular BioSystems 8 (2), S. 495 - 503 (2012)

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)

Jürchott, K.; Kuban, R.-J.; Krech, T.; Blüthgen, N.; Stein, U.; Walther, W.; Friese, C.; iełbasa, S. M.; Ungethüm, U.; Lund, P. et al.; Knösel, T.; Kemmner, W.; Morkel, M.; Fritzmann, J.; Schlag, P. M.; Birchmeier, W.; Krueger, T.; Sperling, S.; Sers, C.; Royer, H.-D.; Herzel, H.; Schäfer, R.: Identification of Y-box binding protein 1 as a core regulator of MEK/ERK pathway dependent gene signatures in colorectal cancer cells. PLoS Genetics 6 (12), S. e1001231 - e1001231 (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), S. 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), S. 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), S. 1022 - 1033 (2008)

Toenjes, M.; Schueler, M.; Hammer, S.; Pape, U. J.; Fischer, J. J.; Felix Berger, F.; Vingron, M.; Sperling, S.: Prediction of cardiac transcription networks based on molecular data and complex clinical phenotypes. Molecular BioSystems: A New High Quality Chemical Biology Journal with A Particular Focus on the Interface between Chemistry and the -Omic Sciences and Systems Biology 4 (6), S. 589 - 598 (2008)

Fischer, J. J.; Toedling, J.; Krueger, T.; Schueler, M.; Huber, W.; Sperling, S.: Combinatorial effects of four histone modifications in transcription and differentiation. Genomics 91 (1), S. 41 - 51 (2008)

Toedling, J.; Skylar, O.; Krueger, T.; Fischer, J. J.; Sperling, S.; Huber, W.: Ringo – an R/Bioconductor package for analyzing ChIP-chip readouts. BMC Bioinformatics 8, S. 443 - 443 (2007)

Sperling, S.: Transcriptional regulation at a glance. BMC Bioinformatics 8 (Suppl. 6), S. S2 - S2 (2007)

Purmann, A.; Toedling, J.; Schueler, M.; Carninci, P.; Lehrach, H.; Hayashizaki, Y.; Huber, W.; Sperling, S.: Genomic organization of transcriptomes in mammals: coregulation and cofunctionality. Genomics 89 (5), S. 580 - 587 (2007)

Liu, H.; Wang, H.; Shi, Z.; Wang, H.; Yang, C.; Sperling, S.; Tan, W.; Lu, Z.: TaqMan probe array for quantitative detection of DNA targets. Nucleic Acids Research (London) 34, S. e4 - e4 (2006)

Pape, U. J.; Grossmann, S.; Hammer, S.; Sperling, S.; Vingron, M.: A new statistical model to select target sequences bound by transcription factors. Genome Informatics 17 (1), S. 134 - 140 (2006)

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), S. 575 - 582 (2005)

Vogel, J. H.; von Heydebreck, A.; Purmann, A.; Sperling, S.: Chromosomal clustering of a human transcriptome reveals regulatory background. BMC Bioinformatics 6, S. 230 - 230 (2005)