Pennimpede, T.; Proske, J.; Koenig, A.; Vidigal, J. A.; Morkel, M.; Bramsen, J. B.; Herrmann, B. G.; Wittler, L.: In vivo knockdown of Brachyury results in skeletal defects and urorectal malformations resembling caudal regression syndrome. Developmental Biology 372 (1), S. 55 - 67 (2012)

Farrall, A.; Riemer, P.; Leushacke, M.; Sreekumar, A.; Grimm, C.; Hermann, B. G.; Morkel, M.: Wnt and BMP signals control intestinal adenoma cell fates. International Journal of Cancer 131 (10), S. 2242 - 2252 (2012)

Sudheer, S.; Bhushan, R.; Fauler, B.; Lehrach, H.; Adjaye, J.: FGF inhibition directs BMP4-mediated differentiation of human embryonic stem cells to syncytiotrophoblast. Stem Cells and Development 21 (16), S. 2987 - 3000 (2012)

Geffers, L.; Herrmann, B. G.; Eichele, G.: Web-based digital gene expression atlases for the mouse. Mammalian Genome 23, S. 525 - 538 (2012)

Kämpjärvi, K.; Mäkinen, N.; Kilpivaara, O.; Arola, J.; Heinonen, H.-R.; Böhm, J.; Abdel-Wahab, O.; Lehtonen, H. J.; Pelttari, L. M.; Mehine, M. et al.; Schrewe, H.; Nevanlinna, H.; Levine, R. L.; Hokland, P.; Böhling, T.; Mecklin, J.-P.; Bützow, R.; Aaltonen, L. A.; Vahteristo, P.: Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer. British Journal of Cancer 107, S. 1761 - 1765 (2012)

Wittler, L.; Hilger, A.; Proske, J.; Pennimpede, T.; Draaken, M.; Ebert, A.-K.; Rösch, W.; Stein, R.; Nöthen, M. M.; Reutter, H. et al.; Ludwig, M.: Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadias. Gene 506 (2), S. 392 - 395 (2012)

Krautzberger, M. K.; Kosiol, B.; Scholze, M.; Schrewe, H.: Expression of vasorin (Vasn) during embryonic development of the mouse. Gene Expression Patterns 12 (5-6), S. 167 - 171 (2012)

Kammerer, R.; Rüttiger, L.; Riesenberg, R.; Schäuble, C.; Krupar, R.; Kamp, A.; Sunami, K.; Eisenried, A.; Hennenberg, M.; Grunert, F. et al.; Breß, A.; Battaglia, S.; Schrewe, H.; Knipper, M.; Schneider, M. R.: Loss of the mammal-specific tectorial membrane component CEA cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies. Journal of Biological Chemistry 287, S. 21584 - 21598 (2012)

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

Schwaerzer, G. K.; Hiepen, C.; Schrewe, H.; Nickel, J.; Ploeger, F.; Sebald, W.; Mueller, T.; Knaus, P.: New insights into the molecular mechanism of multiple synostoses syndrome (SYNS): mutation within the GDF5 knuckle epitope causes noggin-resistance. Journal of Bone and Mineral Research 27 (2), S. 429 - 442 (2012)