Krauß, S.; So, J.; Hambrock, M.; Köhler, A.; Kunath, M.; Scharff, C.; Wessling, M.; Grzeschik, K.-H.; Schneider, R.; Schweiger, S.: Point mutations in GLI3 lead to misregulation of its subcellular localization. PLoS ONE 4, p. e7471 - e7471 (2009)

Gina, G.; Prinz, V.; Albrecht, M. W.; Harhausen, D.; Khojasteh, U.; Nacken, W.; Endrese, M.; Dirnagl, U.; Nietfeld, W.; Trendelenburg, G.: Endogenous TLR4 agonists Mrp-8 &-14 mediate CNS injury in focal cerebral ischemia. Mitochondrial Disease, pp. 1198 - 1204 (2009)

Adelfalk, C.; Janschek, J.; Revenkova, E.; Blei, C.; Liebe, B.; Göb, E.; Alsheimer, M.; Benavente, R.; de Boer, E.; Novak, I. et al.; Höög, C.; Scherthan, H.; Jessberger, R.: Cohesin SMC1β protects telomeres in meiocytes. Journal of Cell Biology 187 (2), pp. 185 - 199 (2009)

Brink, T. C.; Demetrius, L.; Lehrach, H.; Adjaye, J.: Activation of the immune response is a key feature of aging in mice. Biogerontology 10 (5), pp. 549 - 564 (2009)

Elefteriou, F.; Kolanczyk, M.; Schindeler, A.; Viskochil, D. H.; Hock, J. M.; Schorry, E. K.; Crawford, A. H.; Friedman, J. M.; Little, D.; Peltonen, J. et al.; Carey, J. C.; Feldman, D.; Yu, X.; Armstrong, L.; Birch, P.; Kendler, D. L.; Mundlos, S.; Yang, F.-C.; Agiostratidou, G.; Hunter-Schaedle, K.; Stevenson, D. A.: Skeletal abnormalities in neurofibromatosis type 1: approaches to therapeutic options. American Journal of Medical Genetics Part A 149A (10), pp. 2327 - 2338 (2009)

Geberta, C.; Wrenzyckia, C.; Herrmann, D.; Gröger, D.; Thiel, J.; Reinhardt, R.; Lehrach, H.; Hajkova, P.; Lucas-Hahn, A.; Carnwath, J. W. et al.; Niemann, H.: DNA methylation in the IGF2 intragenic DMR is re-established in a sex-specific manner in bovine blastocysts after somatic cloning. Genomics 94 (1), pp. 63 - 69 (2009)

Geberta, C.; Wrenzyckia, C.; Herrmann, D.; Gröger, D.; Thiel, J.; Reinhardt, R.; Lehrach, H.; Hajkova, P.; Lucas-Hahn, A.; Carnwath, J. W. et al.; Niemann, H.: DNA methylation in the IGF2 intragenic DMR is re-established in a sex-specific manner in bovine blastocysts after somatic cloning. Genomics 94 (1), pp. 63 - 69 (2009)

Haensel, J.; Kohlschmidt, N.; Pitz, S.; Keilmann, A.; Zenker, M.; Ullmann, R.; Haaf, T.; Bartsch, O.: Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder. American Journal of Medical Genetics Part A 149 (10), pp. 2236 - 2240 (2009)

Köhler, S.; Schulz, M. H.; Bauer, S.; Dölken, S.; Ott, C. E.; Mundlos, C.; Horn, D.; Mundlos, S.; Robinson, P. N.: Clinical Diagnostics with Semantic Similarity Searches in Ontologies. The American Journal of Human Genetics 85 (4), pp. 457 - 464 (2009)

Parkhomchuk, D.; Borodina, T.; Amstislavskiy, V.; Banaru, M.; Hallen, L.; Krobitsch, S.; Lehrach, H.; Soldatov, A.: Transcriptome analysis by strand-specific sequencing of complementary DNA. Nucleic Acids Research 37 (18), p. e123 - e123 (2009)

Parkhomchuk, D.; Borodina, T.; Amstislavskiy, V.; Banaru, M.; Hallen, L.; Krobitsch, S.; Lehrach, H.; Soldatov, A.: Transcriptome analysis by strand-specific sequencing of complementary DNA. Nucleic Acids Research 37 (18), p. e123 - e123 (2009)

Darii, E.; Lebeau, D.; Papin, N.; Rubina, A. Y.; Stomakhin, A.; Tost, J.; Sauer, S.; Savvateeva, E.; Dementieva, E.; Zasedatelev, A. et al.; Makarov, A. A.; Gut, I. G.: Quantification of target proteins using hydrogel antibody arrays and MALDI time-of-flight mass spectrometry (A2M2S). New Biotechnology 25 (6), pp. 404 - 416 (2009)

Wilson, D. N.; Gupta, R.; Mikolajka, A.; Nierhaus, K. H.: Ribosomal proteins: role in ribosomal functions. Encyclopedia of Life Sciences 2009, p. 10 - 10 (2009)

Wilson, D. N.; Starosta, A. L.; Yamamoto, H.; Nierhaus, K. H.: Inhibitors of the elongation cycle of protein synthesis. Encyclopedia of Life Sciences 2009, p. 13 - 13 (2009)

Erenpreisa, J.; Cragg, M. S.; Salmina, K.; Hausmann, M.; Scherthan, H.: The role of meiotic cohesin REC8 in chromosome segregation in γ irradiation-induced endopolyploid tumour cells. Experimental Cell Research 315 (15), pp. 2593 - 2603 (2009)

Stoeckius, M.; Maaskola, J.; Colombo, T.; Rahn, H.-P.; Friedländer, M. R.; Li, N.; Chen, W.; Piano, F.; Rajewsky, N.: Large-scale sorting of C. elegans embryos reveals the dynamics of small RNA expression. Nature Methods 6, pp. 745 - 751 (2009)

Hu, H. Y.; Yan, Z.; Xu, Y.; Hu, H.; Menzel, C.; Zhou, Y. H.; Chen, W.; Khaitovich, P.: Sequence features associated with microRNA strand selection in humans and flies. BMC Genomics 10, p. 413 - 413 (2009)

Guillard, M.; Dimopoulou, A.; Fischer, B.; Morava, E.; Lefeber, D. J.; Kornak, U.; Wevers, R. A.: Vacuolar H+-ATPase meets glycosylation in patients with cutis laxa. Biochimica et Biophysica Acta - Molecular Basis of Disease 1792, pp. 903 - 914 (2009)

Hilhorst-Hofstee, Y.; Tümer, Z.; Born, P.; Knijnenburg, J.; Hansson, K.; Yatawara, V.; Steensberg, J.; Ullmann, R.; Arkesteijn, G.; Tommerup, N. et al.; Larsen, L. A.: Molecular characterization of two patients with de novo interstitial deletions in 4q22-q24. American Journal of Medical Genetics Part A 149 (8), pp. 1830 - 1833 (2009)

Najm, J.; Horn, D.; Wimplinger, I.; Golden, J. A.; Chizhikov, V. V.; Sudi, J.; Christian, S. L.; Ullmann, R.; Kuechler, A.; Haas, C. A. et al.; Flubacher, A.; Charnas, L. R.; Uyanik, G.; Frank, U.; Klopocki, E.; Dobyns, W. B.; Kutsche, K.: Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum. Nature Genetics 40 (9), pp. 1065 - 1067 (2009)