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Mefford, H. C.; Clauin, S.; Sharp, A. J.; Moller, R. S.; Ullmann, R.; Kapur, R.; Pinkel, D.; Cooper, G. M.; Ventura, M.; Ropers, H.-H. et al.; Tommerup, N.; Eichler, E. E.; Bellanne-Chantelot, C.: Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes and epilepsy. American Journal of Human Genetics: AJHG 81 (5), pp. 1057 - 1069 (2007)

Tenner, K.; Walther, D. J.; Bader, M.: Influence of human tryptophan hydroxylase 2 N- and Cterminus on enzymatic activity and oligomerization. Journal of Neurochemistry: Official Journal of the International Society for Neurochemistry 102 (6), pp. 1887 - 1894 (2007)

Zemojtel, T.; Penzkofer, T.; Schultz, J.; Dandekar, T.; Badge, R.; Vingron, M.: Exonization of active mouse L1s: a driver of transcriptome evolution? BMC Genomics 8, p. e392 - e392 (2007)

Varmark, H.; Llamazares, S.; Rebollo, E.; Lange, B.; Reina, J.; Schwarz, H.; Gonzalez, C.: Asterless is a centriolar protein required for centrosome function and embryo development in Drosophila. Current Biology 17 (20), pp. 1735 - 1745 (2007)

Adjaye, J.; Herwig, R.; Brink, T. C.; Herrmann, D.; Greber, B.; Sudheer, S.; Groth, D.; Carnwath, J. W.; Lehrach, H.; Niermann, H.: Conserved molecular portraits of bovine and human blastocysts as a consequence of the transition from maternal to embryonic control of gene expression. Physiological Genomics 31 (2), pp. 315 - 327 (2007)

Mendes, N.; Hanus, D.; Call, J.: Raising the level: Orangutans use water as a tool. Biology Letters 3 (5), pp. 453 - 455 (2007)

Beisel, C.; Buness, A.; Roustan-Espinosa, I. M.; Koch, B.; Schmitt, S.; Haas, S. A.; Hild, M.; Katsuyama, T.; Paro, R.: Comparing active and repressed expression states of genes controlled by the Polycomb/Trithorax group proteins. Proceedings of the National Academy of Sciences of the United States of America: PNAS 104 (42), pp. 16615 - 16620 (2007)

Abo-Dalo, B.; Kim, H.-G.; Roes, M.; Stefanova, M.; Higgins, A.; Shen, Y.; Mundlos, S.; Quade, B. J.; Gusella, J. F.; Kutsche, K.: Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome. American Journal of Medical Genetics / Part A 143 (22), pp. 2668 - 2674 (2007)

de la Chaux, N.; Messer, P. W.; Arndt, P.: DNA indels in coding regions reveal selective constraints on protein evolution in the human lineage. BMC Evolutionary Biology 7, pp. 191 - 102 (2007)

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Zi, Z.; Klipp, E.: Cellular signaling is potentially regulated by cell density in receptor trafficking networks. FEBS Letters 581 (24), pp. 4589 - 4595 (2007)

Friedel, S.; Saar, K.; Sauer, S.; Dempfle, A.; Walitza, S.; Renner, T.; Romanos, M.; Freitag, C.; Seitz, C.; Palmason, H. et al.; Scherag, A.; Windemuth-Kieselbach, C.; Schimmelmann, B. G.; Wewetzer, C.; Meyer, J.; Warnke, A.; Lesch, K. P.; Reinhardt, R.; Herpertz-Dahlmann, B.; Linder, M.; Hinney, A.; Remschmidt, H.; Schäfer, H.; Konrad, K.; Hübner, N.; Hebebrand, J.: Association and linkage of allelic variants of the dopamine transporter gene in ADHD. Molecular Psychiatry 12 (10), pp. 923 - 933 (2007)

Motazacker, M. M.; Rost, B. R.; Hucho, T.; Garshasb, M.; Kahriz, K.; Ullmann, R.; Abedini, S. S.; Nieh, S. E.; Amini, S. H.; Goswami, C. et al.; Tzschach, A.; Jensen, L. R.; Schmitz, D.; Ropers, H.-H.; Najmabadi, H.; Kuss, A. W.: A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation. The American Journal of Human Genetics: AJHG 81 (4), pp. 792 - 798 (2007)

Nierhaus, K. H.: Early steps of evolution and some ideas about a simplified translational machinery. Origins of Life and Evolution of Biospheres 37 (4-5), pp. 391 - 398 (2007)

Sclep, G.; Allemeersch, J.; Liechti, R.; De Meyer, B.; Beynon, J.; Bhalerao, R.; Moreau, Y.; Nietfeld, W.; Renou, J.-P.; Reymond, P. et al.; Kuiper, M. T. R. ..; Hilson, P.: CATMA, a comprehensive genome-scale resource for silencing and transcript profiling of Arabidopsis genes. BMC Bioinformatics 8, p. 400 - 400 (2007)

Seitz, V.; Stiege, A. C.; Mundlos, S.; Lenze, D.; Lammert, H.; Clermont, A.; Hirsch, B.; Von Der Wall, E.; Müller, H.; Kirsch, A. et al.; Diaz-Espada, F.; Uharek, L.; Anagnostopoulos, I.; Stein, H.; Hummel, M.: Immunoglobulin receptor evolution in follicular lymphoma and a review of literature. Leukemia & Lymphoma 48 (10), pp. 2063 - 2067 (2007)

Szaflarski, W.; Nierhaus, K. H.: Optimized energy consumption for protein synthesis. Origins of Life and Evolution of Biospheres 37 (4-5), pp. 423 - 428 (2007)

Uhrig, S.; Schlembach, D.; Waldispuehl-Geigl, J.; Schaffer, W.; Geigl, J.; Klopcki, E.; Mundlos, S.; Speicher, M. R.: Impact of array comparative genomic hybridization-derived information on genetic counseling demonstrated by prenatal diagnosis of the TAR (thrombocytopenia-absent-radius) syndrome-associated microdeletion 1q21.1. American Journal of Human Genetics: AJHG 81 (4), pp. 866 - 868 (2007)

Kousoulidou, L.; Parkel, S.; Zilina, O.; Palta, P.; Puusepp, H.; Remm, M.; Turner, G.; Boyle, J.; van Bokhoven, H.; de Brouwer, A. et al.; Van Esch, H.; Froyen, G.; Ropers, H.-H.; Chelly, J.; Moraine, C.; Gecz, J.; Kurg, A.; Patsalis, P. C.: Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH. European Journal of Medical Genetics 50 (6), pp. 399 - 410 (2007)