Selected Publications

Selected Publications 2002 - 2015

2015

Grote P & Herrmann BG (2015). Long noncoding RNAs in organogenesis: Making the difference. Trends in Genetics, doi: 10.1016/j.tig.2015.02.002

2014

Riemer P, Sreekumar A, Reinke S, Rad R, Schäfer R, Sers C, Bläker H, Herrmann BG & Morkel M (2014). Transgenic expression of oncogenic BRAF induces loss of stem cells in the mouse intestine, which is antagonized by β-Catenin activity. Oncogene, doi 10.1038/onc. 2014.247

Schwartz B, Marks M, Wittler L, Werber M, Währisch S, Nordheim A, Herrmann BG & Grote P (2014). SRF is essential for mesodermal cell migration during elongation of the embryonic body axis. Mechanisms of Development, doi: 10.1016/j.mod.2014.07.001

Werber M, Wittler L, Timmermann B, Grote P & Herrmann BG (2014) The tissue-specific transcriptomic landscape of the mid-gestational mouse embryo. Development, 141, 1-6

2013

Grimm C, Chavez L, Vilardell M, Farrall AL, Tierling S, Böhm JW, Grote P, Lienhard M, Timmermann B, Walter J, Schweiger MR, Lehrach H, Herwig R, Herrmann BG, Morkel M. (2013) DNA-methylome analysis of mouse intestinal adenoma identifies a tumor-specific signature that is partly conserved in human colon cancer. PLoS Genetics, 9, e1003250

Grote P & Herrmann BG (2013). The long non-coding RNA Fendrr links epigenetic control mechanisms to gene regulatory networks in mammalian embryogenesis. RNA Biology, 10, 1–7

Grote P, Wittler L, Hendrix D, Koch F, Währisch S, Macura K, Bläss G, Kellis M, Werber M, Herrmann BG. (2013) The tissue-specific IncRNA Fendrr is an essential regulator of heart and body wall development in the mouse. Dev Cell, Vol. 24, 206-214; doi:10.1016/j.devcel.2012.12.012

2012

Bauer H, Schindler S, Charron Y, Willert J, Kusecek B, Herrmann BG. (2012) The nucleoside diphosphate kinase gene Nme3 acts as quantitative trait locus promoting non-Mendelian inheritance. PLoS Genetics, Vol. 8 (3), e1002567. Doi:10.1371

Farrall AL, Riemer P, Leushacke M, Sreekumar A, Grimm C, Herrmann BG, Morkel M. (2012) Wnt and BMP signals control intestinal adenoma cell fates. Int J Cancer, No. 3663, DOI: 10.1002/ijc.27500

Geffers L, Herrmann BG,  Eichele G. (2012)  Web-based Digital Gene Expression Atlases for the Mouse. Mammalian Genome, Vol. 23, 525-538

Herrmann BG, Bauer H. (2012) The mouse t-haplotype: a selfish chromosome – genetics molecular mechanism and evolution. In Evolution of the House Mouse (ed. Macholan, Baird, Munclinger), Cambridge University Press

Pennimpede T, Proske J, König A, Vidigal JA, Morkel M, Bramsen JB, Herrmann BG, Wittler  L (2012). In vivo knockdown of Brachyury results in skeletal defects and urorectal malformations resembling caudal regression syndrome. Dev Biol 372, 55–67

2011

Leushacke M, Spörle R, Bernemann C, Brouwer-Lehmitz A, Fritzmann J, Theis M, Buchholz F, Herrmann BG, Morkel M (2011). An RNA interference phenotypic screen identifies a role for FGF signals in colon cancer progression. PLoS ONE, Vol. 6, e23381

2010

Rocha PP, Bleiss W, Schrewe H (2010). Mosaic Expression of Med12 in Female Mice Leads to Exencephaly, Spina Bifida, and Craniorachischisis. Birth Defects Research (Part A) 88:626-632

Rocha PP, Scholze M, Bleiß W, Schrewe H (2010). Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling. Development 137, 2723-2731, doi:10.1242/dev.053660. Published by The Company of Biologists Ltd.

Scholz AK, Klebl BM, Morkel M, Lehrach H, Dahl A, Lange BM (2010). A Flexible Multiwell Format for Immunofluorescence Screening Microscopy of Small-Molecule Inhibitors. Assay Drug Dev Technol 8, 571–580

Timmermann B, Kerick M, Roehr C, Fischer A, Isau M, Boerno ST, Wunderlich A, Barmeyer C, Seemann P, Koenig J, Lappe M, Kuss AW, Garshasb M, Bertram L, Trappe K, Werber M, Herrmann BG, Zatloukal K, Lehrach H, Schweiger MR (2010). Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis. PLoS ONE, Vol. 5 (12) pp. e15661

Vidigal JA, Morkel M, Wittler L, Brouwer-Lehmitz A, Grote P, Macura K, Herrmann BG (2010). An inducible RNA interference system fort he functional dissection of mouse embryogenesis. Nucleic Acids Res 38, e122 (doi:10.1093/nar/gkq199)

2009

Verón N, Bauer H, Weisse A, Lüder G, Werber M, Herrmann BG (2009). Retention of gene products in syncytial spermatids promotes non-Mendelian inheritance as revealed by the t-complex-responder. Genes Dev 23, 2705-2710

2008

Deutsch EW, Ball CA, Berman JJ, Bova JS, Brazma A, Bumgarner RE, Campbell D, Causton HC, Christiansen J, Daian F, Dauga D, Davidson DR, Gimenez G, Goo YA, Grimmond S, Henrich T,  Herrmann BG, Johnson MH, Korb M, Mills JC, Oudes AJ, Parkinson HE, Pascal LE, Pollet N, Quackenbush J, Ramialison M, Ringwald M, Salgado D, Sansone SA, Sherlock G, Stoeckert CJ Jr., Swedlow J, Taylor RC, Walashek L, Warford A, Wilkinson DG, Zhou Y, Zon LI, Liu AY, True LD (2008).  Minimum Information Specification For In Situ Hybridization and Immunohistochemistry Experiments (MISFISHIE). Nature Biotechnology 26, 305-312

2007

Bauer H, Véron N, Willert J, Herrmann BG (2007). The t-complex-encoded guanine nucleotide exchange factor Fgd2 reveals that two opposing signaling pathways promote transmission ratio distortion in the mouse. Genes Dev 21 (1), 143-147

Wittler L, Shin Eh, Grote P, Kispert A, Beckers A, Gossler A, Werber M, Herrmann BG (2007). Expression of Msgn1 in the presomitic mesoderm is controlled by synergism of WNT signalling and Tbx6. EMBO Rep 8 (8), 784-789

2006

Dale JK, Malapert P, Chal J, Vilhais-Neto G, Maroto M, Johnson T, Jayasinghe S, Trainor P, Herrmann BG, Pourquié O (2006). Oscillations of the Snail Genes in the Presomitic Mesoderm Coordinate Segmental Patterning and Morphogenesis in Vertebrate Somitogenesis. Dev Cell 10, 355–366

Grote P & Conradt B (2006). The PLZF-like protein TRA-4 cooperates with the Gli-like transcription factor TRA-1 to promote female development in C. elegans. Dev Cell 11, 561-573.

2005

Bauer H, Willert J, Koschorz B & Herrmann BG (2005). The t complex−encoded GTPase-activating protein Tagap1 acts as a transmission ratio distorter in mice. Nature Genetics 37 (9), 969-973

2004

Abdelkhalek HB, Becker A, Schuster-Gossler K, Pavlova MN, Burkhardt H, Lickert H, Rossant J, Reinhardt R, Schalkwyk LC, Müller I, Hermann BG, Ceolin M, Rivera-Pomar R & Gossler A (2004). The mouse homeobox gene Not is required for caudal notochord development and affected by the truncate mutation. Genes Dev 18 (14), 1725-1736

Aulehla A & Herrmann BG (2004). Segmentation in vertebrates: clock and gradient finally joined. Genes Dev 18 (17), 2060-2067

Hofmann M, Schuster-Gossler K, Watabe-Rudolph M, Aulehla A, Herrmann BG & Gossler A (2004). WNT signaling, in synergy with T/TBX6, controls Notch signaling by regulating Dll1 expression in the presomitic mesoderm of mouse embryos. Genes Dev 18 (22), 2712-2717

2003

Aulehla A, Wehrle C, Brand-Saberi B, Kemler R, Gossler A, Kanzler B, Herrmann BG (2003). Wnt3a plays a major role in the segmentation clock controlling somitogenesis. Dev Cell 4 (3), 395-406

2002

Gitton Y, Dahmane N, Baik S, iAltaba AR, Neidhardt L, Scholze M, Herrmann BG, Kahlem P, Benkhala A, Schrinner S, Yildirimman R, Herwig R, Lehrach H & Yaspo ML (2002). A gene expression map of human chromosome 21 orthologues in the mouse. Nature 420 (6917), 586-590 (2002)

 
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