The long non-coding RNA Fendrr links epigenetic control mechanisms to gene regulatory networks in mammalian embryogenesis

Por Grote, Phillip, Herrmann, Bernhard G
Publicado em 2013

Mechanisms of long noncoding RNA function in development and disease

Por Schmitz, Sandra U., Grote, Phillip, Herrmann, Bernhard G.
Publicado no Cell Mol Life Sci (2016)

The t-complex-encoded guanine nucleotide exchange factor Fgd2 reveals that two opposing signaling pathways promote transmission ratio distortion in the mouse

Por Bauer, Hermann, Véron, Nathalie, Willert, Jürgen, Herrmann, Bernhard G.
Publicado em 2007

The Nucleoside Diphosphate Kinase Gene Nme3 Acts as Quantitative Trait Locus Promoting Non-Mendelian Inheritance

Por Bauer, Hermann, Schindler, Sabrina, Charron, Yves, Willert, Jürgen, Kusecek, Barica, Herrmann, Bernhard G.
Publicado em 2012

Retention of gene products in syncytial spermatids promotes non-Mendelian inheritance as revealed by the t complex responder

Por Véron, Nathalie, Bauer, Hermann, Weiße, Andrea Y., Lüder, Gerhild, Werber, Martin, Herrmann, Bernhard G.
Publicado em 2009

WNT signaling, in synergy with T/TBX6, controls Notch signaling by regulating Dll1 expression in the presomitic mesoderm of mouse embryos

Por Hofmann, Michael, Schuster-Gossler, Karin, Watabe-Rudolph, Masami, Aulehla, Alexander, Herrmann, Bernhard G., Gossler, Achim
Publicado em 2004

An inducible RNA interference system for the functional dissection of mouse embryogenesis

Por Vidigal, Joana A., Morkel, Markus, Wittler, Lars, Brouwer-Lehmitz, Antje, Grote, Phillip, Macura, Karol, Herrmann, Bernhard G.
Publicado em 2010

Expression of Msgn1 in the presomitic mesoderm is controlled by synergism of WNT signalling and Tbx6

Por Wittler, Lars, Shin, Eun-ha, Grote, Phillip, Kispert, Andreas, Beckers, Anja, Gossler, Achim, Werber, Martin, Herrmann, Bernhard G
Publicado em 2007

Patterning and gastrulation defects caused by the t(w18) lethal are due to loss of Ppp2r1a

Por Lange, Lisette, Marks, Matthias, Liu, Jinhua, Wittler, Lars, Bauer, Hermann, Piehl, Sandra, Bläß, Gabriele, Timmermann, Bernd, Herrmann, Bernhard G.
Publicado no Biol Open (2017)

An RNA Interference Phenotypic Screen Identifies a Role for FGF Signals in Colon Cancer Progression

Por Leushacke, Marc, Spörle, Ralf, Bernemann, Christof, Brouwer-Lehmitz, Antje, Fritzmann, Johannes, Theis, Mirko, Buchholz, Frank, Herrmann, Bernhard G., Morkel, Markus
Publicado em 2011

Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium

Por Rudat, Carsten, Grieskamp, Thomas, Röhr, Christian, Airik, Rannar, Wrede, Christoph, Hegermann, Jan, Herrmann, Bernhard G., Schuster-Gossler, Karin, Kispert, Andreas
Publicado no PLoS One (2014)

Oncogenic β-catenin and PIK3CA instruct network states and cancer phenotypes in intestinal organoids

Por Riemer, Pamela, Rydenfelt, Mattias, Marks, Matthias, van Eunen, Karen, Thedieck, Kathrin, Herrmann, Bernhard G., Blüthgen, Nils, Sers, Christine, Morkel, Markus
Publicado no J Cell Biol (2017)

The tissue-specific lncRNA Fendrr is an essential regulator of heart and body wall development in the mouse

Por Grote, Phillip, Wittler, Lars, Währisch, Sandra, Hendrix, David, Beisaw, Arica, Macura, Karol, Bläss, Gaby, Kellis, Manolis, Werber, Martin, Herrmann, Bernhard G.
Publicado em 2013

The NH(2) Terminus of Titin Spans the Z-Disc: Its Interaction with a Novel 19-kD Ligand (T-cap) Is Required for Sarcomeric Integrity

Por Gregorio, Carol C., Trombitás, Karoly, Centner, Thomas, Kolmerer, Bernhard, Stier, Gunter, Kunke, Kathleen, Suzuki, Koichi, Obermayr, Franz, Herrmann, Bernhard, Granzier, Henk, Sorimachi, Hiroyuki, Labeit, Siegfried
Publicado em 1998

An Image-Based Genetic Assay Identifies Genes in T1D Susceptibility Loci Controlling Cellular Antiviral Immunity in Mouse

Por Liao, Juan, Jijon, Humberto B., Kim, Ira R., Goel, Gautam, Doan, Aivi, Sokol, Harry, Bauer, Hermann, Herrmann, Bernhard G., Lassen, Kara G., Xavier, Ramnik J.
Publicado em 2014

BRACHYURY directs histone acetylation to target loci during mesoderm development

Por Beisaw, Arica, Tsaytler, Pavel, Koch, Frederic, Schmitz, Sandra U, Melissari, Maria‐Theodora, Senft, Anna D, Wittler, Lars, Pennimpede, Tracie, Macura, Karol, Herrmann, Bernhard G, Grote, Phillip
Publicado no EMBO Rep (2017)

The mouse homeobox gene Not is required for caudal notochord development and affected by the truncate mutation

Por Ben Abdelkhalek, Hanaa, Beckers, Anja, Schuster-Gossler, Karin, Pavlova, Maria N., Burkhardt, Hannelore, Lickert, Heiko, Rossant, Janet, Reinhardt, Richard, Schalkwyk, Leonard C., Müller, Ines, Herrmann, Bernhard G., Ceolin, Marcelo, Rivera-Pomar, Rolando, Gossler, Achim
Publicado em 2004

DNA–Methylome Analysis of Mouse Intestinal Adenoma Identifies a Tumour-Specific Signature That Is Partly Conserved in Human Colon Cancer

Por Grimm, Christina, Chavez, Lukas, Vilardell, Mireia, Farrall, Alexandra L., Tierling, Sascha, Böhm, Julia W., Grote, Phillip, Lienhard, Matthias, Dietrich, Jörn, Timmermann, Bernd, Walter, Jörn, Schweiger, Michal R., Lehrach, Hans, Herwig, Ralf, Herrmann, Bernhard G., Morkel, Markus
Publicado em 2013

Somatic Mutation Profiles of MSI and MSS Colorectal Cancer Identified by Whole Exome Next Generation Sequencing and Bioinformatics Analysis

Por Timmermann, Bernd, Kerick, Martin, Roehr, Christina, Fischer, Axel, Isau, Melanie, Boerno, Stefan T., Wunderlich, Andrea, Barmeyer, Christian, Seemann, Petra, Koenig, Jana, Lappe, Michael, Kuss, Andreas W., Garshasbi, Masoud, Bertram, Lars, Trappe, Kathrin, Werber, Martin, Herrmann, Bernhard G., Zatloukal, Kurt, Lehrach, Hans, Schweiger, Michal R.
Publicado em 2010

Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy

Por Draaken, Markus, Knapp, Michael, Pennimpede, Tracie, Schmidt, Johanna M., Ebert, Anne-Karolin, Rösch, Wolfgang, Stein, Raimund, Utsch, Boris, Hirsch, Karin, Boemers, Thomas M., Mangold, Elisabeth, Heilmann, Stefanie, Ludwig, Kerstin U., Jenetzky, Ekkehart, Zwink, Nadine, Moebus, Susanne, Herrmann, Bernhard G., Mattheisen, Manuel, Nöthen, Markus M., Ludwig, Michael, Reutter, Heiko
Publicado no PLoS Genet (2015)