Publikationen von Bernhard G. Herrmann

Matthias Marks, Tracie Pennimpede, Lisette Lange, Phillip Grote, Bernhard G. Herrmann, and Lars Wittler, "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), 438-451 (2016).

Phillip Grote and Bernhard G. Herrmann, "Long noncoding RNAs in organogenesis: Making the difference," Trends in Genetics 31 (6), 329-335 (2015).

Carsten Rudat, Thomas Grieskamp, Christian Röhr, Rannar Airik, Christoph Wrede, Jan Hegermann, Bernhard G. Herrmann, Karin Schuster-Gossler, and Andreas Kispert, "Upk3b is dispensable for development and integrity of urothelium and mesothelium," PLoS One 9 (11), e112112 (2014).

H. Reutter, M. Draaken, T. Pennimpede, L. Wittler, F. F. Brockschmidt, A. K. Ebert, E. Bartels, W. Rösch, T. M. Boemers, K. Hirsch, E. Schmiedeke, C. Meesters, T. Becker, R. Stein, B. Utsch, E. Mangold, A. Nordenskjöld, G. Barker, C. C. Kockum, N. Zwink, G. Homdahl, G. Läckgren, E. Jenetzky, W. F. Feitz, C. Marcelis, C. H. Wijers, I. A. Van Rooij, J. P. Gearhart, B. G. Herrmann, M. Ludwig, S. A. Boyadjiev, M. M. Nöthen, and M. Mattheisen, "Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder," Human Molecular Genetics 23 (20), 5536-5544 (2014).

Juan Liao, Humberto B. Jijon, Ira R. Kim, Gautam Goel, Aivi Doan, Harry Sokol, Hermann Bauer, Bernhard G. Herrmann, Kara G. Lassen, and Ramnik J. Xavier, "An Image-Based Genetic Assay Identifies Genes in T1D Susceptibility Loci Controlling Cellular Antiviral Immunity in Mouse.," PLoS One 9 (9), e108777 (2014).

Vinod Kumar, Shih-Chin Cheng, Melissa D. Johnson, Sanne Smeekens, Agnieszka Wojtowicz, Evangelos Giamarellos-Bourboulis, Juha Karjalainen, Lude Franke, Sebo Withoff, Theo S. Plantinga, Frank van de Veerdonk, Jos van der Meer, Leo A. B. Joosten, Harry Sokol, Hermann Bauer, Bernhard G. Herrmann, Pierre-Yves Bochud, Oscar Marchetti, John R. Perfect, Ramnik Xavier, Bart Jan Kullberg, Cisca Wijmenga, and Mihai Netea, "Immunochip SNP array identifies novel genetic variants conferring susceptibility to candidaemia," Nature Communications 5, 5:4675 (2014).

Pamela Riemer, Amulya Sreekumar, Sören Reinke, Roland Rad, Reinhold Schäfer, Christine Sers, Hendrik Bläker, Bernhard G. Herrmann, and Markus Morkel, "Transgenic expression of oncogenic BRAF induces loss of stem cells in the mouse intestine, which is antagonized by β-Catenin activity," Oncogene 2014, 1-12 (2014).

Benedikt Schwartz, Matthias Marks, Lars Wittler, Martin Werber, Sandra Währisch, Alfred Nordheim, Bernhard G. Herrmann, and Phillip Grote, "SRF is essential for mesodermal cell migration during elongation of the embryonic body axis," Mechanisms of Development 133, 23-35 (2014).

M. Draaken, F. Baudisch, B. Timmermann, H. Kuhl, M. Kerick, J. Proske, L. Wittler, T. Pennimpede, A. K. Ebert, W. Rösch, R. Stein, E. Bartels, C. von Lowtzow, T. M. Boemers, S. Herms, J. P. Gearhart, Y. Lakshmanan, C. C. Kockum, G. Holmdahl, G. Läckgren, A. Nordenskjöld, S. A. Boyadjiev, B. G. Herrmann, M. M. Nöthen, M. Ludwig, and H. Reutter, "Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region," Birth Defects Research Part A: Clinical and Molecular Teratology 100 (6), 512-517 (2014).

Pawaree Saisawat, Stefan Kohl, Alina C. Hilger, Daw-Yang Hwang, Heon Yung Gee, Gabriel C. Dworschak, Velibor Tasic, Tracie Pennimpede, Sivakumar Natarajan, Ethan Sperry, Danilo S. Matassa, Natasa Stajic, Radovan Bogdanovic, Ivo de Blaauw, Carlo L. M. Marcelis, Charlotte H. W. Wijers, Enrika Bartels, Eberhard Schmiedeke, Dominik Schmidt, Stefanie Märzheuser, Sabine Grasshoff-Derr, Stefan Holland-Cunz, Michael Ludwig, Markus M. Nöthen, Markus Draaken, Erwin Brosens, Hugo Heij, Dick Tibboel, Bernhard G. Hermann, Benjamin D. Solomon, Annelies de Klein, Iris A. L. M. van Rooij, Franca Esposito, Heiko M. Reutter, and Friedhelm Hildebrandt, "Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association," Kidney International 85 (6), 1310-1317 (2014).

Martin Werber, Lars Wittler, Bernd Timmermann, Phillip Grote, and Bernhard G. Herrmann, "The tissue-specific transcriptomic landscape of the mid-gestational mouse embryo," Development 141 (11), 2325-2330 (2014).

A. Hilger, C. Schramm, T. Pennimpede, L. Wittler, G. C. Dworschak, E. Bartels, H. Engels, A. M. Zink, F. Degenhardt, A. M. Müller, E. Schmiedeke, S. Grasshoff-Derr , S. Märzheuser, S. Hosie, S. Holland-Cunz , C. H. Wijers, C. L. Marcelis, I. A. van Rooij , F. Hildebrandt, B. G. Hermann, M. M. Nöthen, M. Ludwig, H. Reutter, and M. Draaken, "De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association," European journal of human genetics: EJHG ; the official journal of the European Society of Human Genetics 21 (12), 1377-1382 (2013).

Phillip Grote and Bernhard G. Herrmann, "The long non-coding RNA Fendrr links epigenetic control mechanisms to gene regulatory networks in mammalian embryogenesis," RNA Biology 10 (10), 1579-1585 (2013).

Markus Draaken, Sadaf S. Mughal, Tracie Pennimpede, Stefanie Wolter, Lars Wittler, Anne-Karoline Ebert, Wolfgang Rösch, Raimund Stein, Enrika Bartels, Dominik Schmidt, Thomas M. Boemers, Eberhard Schmiedeke, Per Hoffmann, Susanne Moebus, Bernhard G. Herrmann, Markus M. Nöthen, Heiko Reutter, and Michael Ludwig, "Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12.," Birth Defects Research, Part A: Clinical and Molecular Teratology 97 (3), 133-139 (2013).

Christina Grimm, Lukas Chavez, Mireia Vilardell, Alexandra Farrall, Sascha Tierling, Julia W. Böhm, Phillip Grote, Matthias Lienhard, Jörn Dietrich, Bernd Timmermann, Jörn Walter, Michal R. Schweiger, Hans Lehrach, Ralf Herwig, Bernhard G. Herrmann, and Markus Morkel, "DNA–Methylome Analysis of Mouse Intestinal Adenoma Identifies a Tumour-Specific Signature That Is Partly Conserved in Human Colon Cancer," PLoS Genetics 9 (2), e1003250-e1003250 (2013).

Phillip Grote, Lars Wittler, David Hendrix, Sandra Währisch, Arica Beisaw, Karol Macura, Gabi Bläss, Manolis Kellis, Martin Werber, and Bernhard G. Herrmann, "The tissue-specific IncRNA Fendrr is an essential regulator of heart and body wall development in the mouse.," Developmental Cell 24 (2), 206-214 (2013).

Tracie Pennimpede, Judith Proske, Andrea Koenig, Joana A. Vidigal, Markus Morkel, Jesper B. Bramsen, Bernhard G. Herrmann, and Lars Wittler, "In vivo knockdown of Brachyury results in skeletal defects and urorectal malformations resembling caudal regression syndrome," Developmental Biology 372 (1), 55-67 (2012).

Alexandra Farrall, Pamela Riemer, Marc Leushacke, Amulya Sreekumar, Christina Grimm, Bernhard G. Hermann, and Markus Morkel, "Wnt and BMP signals control intestinal adenoma cell fates," International Journal of Cancer 131 (10), 2242-2252 (2012).

Lars Geffers, Bernhard G. Herrmann, and Gregor Eichele, "Web-based digital gene expression atlases for the mouse," Mammalian Genome 23, 525-538 (2012).

Hermann Bauer, Sabrina Schindler, Yves Charon, Jürgen Willert, Barica Kusecek, and Bernhard G. Herrmann, "The nucleoside diphosphate kinase gene Nme3 acts as quantitative trait locus promoting non-Mendelian inheritance," PLoS Genetics 8 (3), e1002567-e1002567 (2012).