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Rocha, P. P.; Scholze, M.; Bleiß, W.; Schrewe, H.: Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling. Development 137, S. 2723 - 2731 (2010)

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Scholz, A.-K.; Klebl, B. M.; Morkel, M.; Lehrach, H.; Dahl, A.; Lange, B. M.H.: A Flexible Multiwell Format for Immunofluorescence Screening Microscopy of Small-Molecule Inhibitors. Assay and Drug Development Technologies. 8 (5), S. 571 - 580 (2010)

Shafeghati, Y.; Kahrizi, K.; Najmabadi, H.; Kuss, A. W.; Ropers, H.-H.; Tzschach, A.: Brachyphalangy, polydactyly and tibial aplasia/hypoplasia syndrome (OMIM 609945): case report and review of the literature. European Journal of Pediatrics 169 (12), S. 1535 - 1539 (2010)

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Mao, L.; Römer, I.; Nebrich, G.; Klein, O.; Koppelstatter, A.; Hin, S. C.; Hartl, D.; Zabel, C.: Aging in mouse brain is a cell/tissue-level phenomenon exacerbated by proteasome loss. Journal of Proteome Research 9 (7), S. 3551 - 3560 (2010)

Balbach, S. T.; Esteves, T. C.; Brink, T.; Gentile, L.; McLaughlin, K. J.; Adjaye, J. A.; Boiani, M.: Governing cell lineage formation in cloned mouse embryos. Developmental Biology 343 (1-2), S. 71 - 83 (2010)

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Herrmann, B. G.: Embryology meets cancer research. Public Service Review: Science and Technology 7, S. 242 - 243 (2010)

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Thorwarth, A.; Mueller, I.; Biebermann, H.; Ropers, H.-H.; Grueters, A.; Krude, H.; Ullmann, R.: Screening chromosomal aberrations by array comparative genomic hybridization in 80 patients with congenital hypothyroidism and thyroid dysgenesis. The Journal of Clinical Endocrinology & Metabolism 95 (7), S. 3446 - 3452 (2010)

Kube, M.; Migdoll, A. M.; Gehring, I.; Heitmann, K.; Mayer, Y.; Kuhl, H.; Knaust, F.; Geider, K.; Reinhardt, R.: Genome comparison of the epiphytic bacteria Erwinia billingiae and E. tasmaniensis with the pear pathogen E. pyrifoliae. BMC Genomics 11, S. 11:393 - 11:393 (2010)

Mann, K.; Wilt, F. H.; Poustka, A. J.: Proteomic analysis of sea urchin (Strongylocentrotus purpuratus) spicule matrix. Proteome Science 8, S. 33 - 45 (2010)

Walczak-Sztulpa, J.; Eggenschwiler, J.; Osborn, D.; Brown, D. A.; Emma, F.; Klingenberg, C.; Hennekam, R. C.; Torre, G.; Garshasbi, M.; Tzschach, A. et al.; Szczepanska, M.; Krawczynski, M.; Zachwieja, J.; Zwolinska, D.; Beales, P. L.; Ropers, H.-H.; Latos-Bielenska, A.; Kuss, A. W.: Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene. American Journal of Human Genetics 86 (6), S. 949 - 956 (2010)