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DeKelver, R. C.; Choi, V. M.; Moehle, E. A.; Paschon, D. E.; Hockemeyer, D.; Meijsing, S. H.; Sancak, Y.; Cui, X.; Steine, E. J.; Miller, J. C. et al.; Tam, P.; Bartsevich, V. V.; Meng, X.; Rupniewski, I.; Gopalan, S. M.; Sun, H. C.; Pitz, K. J.; Rock, J. M.; Zhang, L.; Davis, G. D.; Rebar, E. J.; Cheeseman, I. M.; Yamamoto, K. R.; Sabatini, D. M.; Jaenisch, R.; Gregory, P. D.; Urnov, F. D.: Functional genomics, proteomics, and regulatory DNA analysis in isogenic settings using zinc finger nuclease-driven transgenesis into a safe harbor locus in the human genome. Genome Research 20 (8), pp. 1133 - 1142 (2010)

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, pp. 2723 - 2731 (2010)

Szczurek, E.; Biecek, P.; Tiuryn, J.; Vingron, M.: Introducing knowledge into differential expression analysis. Journal of Computational Biology 17 (8), pp. 953 - 967 (2010)

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), pp. 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), pp. 1535 - 1539 (2010)

Kantaputra, P. N.; Klopocki, E.; Hennig, B. P.; Praphanphoj, V.; Le Caignec, C.; Isidor, B.; Kwee, M. L.; Shears, D. J.; Mundlos, S.: Mesomelic dysplasia Kantaputra type is associated with duplications of the HOXD locus on chromosome 2q. European Journal of Human Genetics 18 (12), pp. 1310 - 1314 (2010)

Löhr, U.; Chung, H. R.; Beller, M.; Jäckle, H.: Bicoid: Morphogen function revisited. Fly (Austin) 4 (3), pp. 236 - 240 (2010)

Storlazzi, C. T.; Lonoce, A.; Guastadisegni, M. C.; Trombetta, D.; D'Addabbo, P.; Daniele, G.; L'Abbate, A.; Macchia, G.; Surace, C.; Kok, K. et al.; Ullmann, R.; Purgato, S.; Palumbo, O.; Carella, M.; Ambros, P. F.; Rocchi, M.: Gene amplification as double minutes or homogeneously staining regions in solid tumors: Origin and structure. Genome Research 20 (9), pp. 1198 - 1206 (2010)

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), pp. 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), pp. 71 - 83 (2010)

Bourbeillon, J.; Orchard, S.; Benhar, I.; Borrebaeck, C.; de Daruvar, A.; Dubel, S.; Frank, R.; Gibson, F.; Gloriam, D.; Haslam, N. et al.; Hiltker, T.; Humphrey-Smith, I.; Hust, M.; Juncker, D.; Koegl, M.; Konthur, Z.; Korn, B.; Krobitsch, S.; Muyldermans, S.; Nygren, P.-Å.; Palcy, S.; Polic, B.; Rodriguez, H.; Sawyer, A.; Schlapshy, M.; Snyder, M.; Stoevesandt, O.; Taussig, M. J.; Templin, M.; Uhlen, M.; van der Maarel, S.; Wingren, C.; Hermjakob, H.; Sherman, D.: Minimum information about a protein affinity reagent (MIAPAR). Nature biotechnology 28 (7), pp. 650 - 653 (2010)

Dutrannoy, V.; Demuth, I.; Baumann, U.; Schindler, D.; Konrat, K.; Neitzel, H.; Gillessen-Kaesbach, G.; Radszewski, J.; Rothe, S.; Schellenberger, M. T. et al.; Nurnberg, G.; Nurnberg, P.; Teik, K. W.; Nallusamy, R.; Reis, A.; Sperling, K.; Digweed, M.; Varon, R.: Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotype. Human Mutation 31 (9), pp. 1059 - 1068 (2010)

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

Kielbasa, S. M.; Bluthgen, N.; Fahling, M.; Mrowka, R.: Targetfinder.org: a resource for systematic discovery of transcription factor target genes. Nucleic Acids Research 38 Suppl, pp. W233 - W238 (2010)

Kielbasa, S. M.; Klein, H.; Roider, H. G.; Vingron, M.; Blüthgen, N.: TransFind--predicting transcriptional regulators for gene sets. Nucleic Acids Research 38 Suppl, pp. W275 - W280 (2010)

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), pp. 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, p. 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, pp. 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), pp. 949 - 956 (2010)