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Schwarzbraun, T.; Ullmann, R.; Schubert, M.; Ledinegg, M.; Ofner, L.; Windpassinger, C.; Wagner, K.; Kroisel, P. M.; Petek, E.: Characterisation of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development. Cytogenetics and Genome Research 115 (1), pp. 84 - 89 (2006)

Tzschach, A.; Hoeltzenbein, M.; Hoffmann, K.; Menzel, C.; Beyer, A.; Ocker, V.; Wurster, G.; Raynaud, M.; Ropers, H.-H.; Kalscheuer, V. M.: Heterotaxy and cardiac defect in a girl with chromosome translocation t(X;1)(q26;p13.1) and involvement of ZIC3. European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 14 (12), pp. 1317 - 1320 (2006)

Ayerdi-Izquierdo, A.; Stavrides, G.; Sellés-Martínez, J.J.; Larrea, L.; Bovo, G.; López de Munain, A.; Bisulli, F.; Martí-Massó, J. F.; Michelucci, R.; Poza, J. J. et al.; Tinuper, P.; Stephani, U.; Striano, P.; Striano, S.; Staub, E.; Sarafidou, T.; Hinzmann, B.; Moschonas, N.; Siebert, R.; Deloukas, P.; Nobile, C.; Pérez-Tur, J.: Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy. Epilepsy Research 70 (2-3), pp. 118 - 126 (2006)

Gebert, C.; Wrenzycki, C.; Herrmann, D.; Gröger, D.; Reinhardt, R.; Hajkova, P.; Lucas-Hahn, A.; Carnwath, J.; Lehrach, H.; Niemann, H.: The bovine IGF2 gene is differentially methylated in oocyte and sperm DNA. Genomics: Internat. Journal of Gene Mapping and Nucleotide Sequencing ; Emphasizing Analyses of the Human and other Complex Genomes 88 (2), pp. 222 - 229 (2006)

Gebert, C.; Wrenzycki, C.; Herrmann, D.; Gröger, D.; Reinhardt, R.; Hajkova, P.; Lucas-Hahn, A.; Carnwath, J.; Lehrach, H.; Niemann, H.: The bovine IGF2 gene is differentially methylated in oocyte and sperm DNA. Genomics: Internat. Journal of Gene Mapping and Nucleotide Sequencing ; Emphasizing Analyses of the Human and other Complex Genomes 88 (2), pp. 222 - 229 (2006)

Hoffmann, K.; Müller, J. S.; Stricker, S.; Megarbane, A.; Rajab, A.; Lindner, T. H.; Cohen, M.; Chouery, E.; Adaimy, L.; Ghanem, I. et al.; Delague, V.; Boltshauser, E.; Talim, B.; Horvath, R.; Robinson, P. N.; Lochmüller, H.; Hübner, C.; Mundlos, S.: Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit. American Journal of Human Genetics (Chicago, IL) 79 (2), pp. 303 - 312 (2006)

Makrantonaki, E.; Adjaye, J.; Herwig, R.; Brink, T. C.; Groth, D.; Hultschig, C.; Lehrach, H.; Zouboulis, C. C.: Age-specific hormonal decline is accompanied by transcriptional changes in human sebocytes in vitro. Aging Cell 5 (4), pp. 331 - 344 (2006)

Nierhaus, K.: Decoding errors and the involvement of the E-site. Biochimie 88 (8), pp. 1013 - 1019 (2006)

Schaber, J.; Kofahl, B.; Kowald, A.; Klipp, E.: A modelling approach to quantify dynamic crosstalk between the pheromone and the starvation pathway in baker's yeast. FEBS Journal 273 (15), pp. 3520 - 3533 (2006)

Woods, C. G.; Stricker, S.; Seemann, P.; Stern, R.; Cox, J.; Sherridan, E.; Roberts, E.; Springell, K.; Scott, S.; Karbani, G. et al.; Sharif, S. M.; Toomes, C.; Bond, J.; Kumar, D.; Al-Gazali, L.; Mundlos, S.: Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome. American Journal of Human Genetics (Chicago, IL) 79 (2), pp. 402 - 408 (2006)

Koch, M.; Veit, G.; Stricker, S.; Bhatt, P.; Kutsch, S.; Zhou, P.; Reinders, E.; Hahn, R. A.; Song, R.; Burgeson, R. E. et al.; Gerecke, D. R.; Mundlos, S.; Gordon, M. K.: Expression of Type XXIII Collagen mRNA and Protein. Journal of Biological Chemistry 281 (30), pp. 21546 - 21557 (2006)

Erkel, C.; Kube, M.; Reinhard, R.; Liesack, W.: Genome of Rice Cluster I Archaea—the Key Methane Producers in the Rice Rhizosphere. Science 313 (5785), pp. 370 - 372 (2006)

Hornef, N.; Olbrich, H.; Horvath, J.; Zariwala, M. A.; Fliegauf, M.; Loges, N. T.; Wildhaber, J.; Noone, P. G.; Kennedy, M.; Antonarakis, S. E. et al.; Blouin, J.-L.; Bartoloni, L.; Nüsslein, T.; Ahrens, P.; Griese, M.; Kuhl, H.; Sudbrak, R.; Knowles, M. R.; Reinhardt, R.; Omran, H.: DNAH5 Mutations are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects. American Journal of Respiratory and Critical Care Medicine: an Official Journal of the American Thoracic Society, Medical Section of the Lung Association 174 (2), pp. 120 - 126 (2006)

Hornef, N.; Olbrich, H.; Horvath, J.; Zariwala, M. A.; Fliegauf, M.; Loges, N. T.; Wildhaber, J.; Noone, P. G.; Kennedy, M.; Antonarakis, S. E. et al.; Blouin, J.-L.; Bartoloni, L.; Nüsslein, T.; Ahrens, P.; Griese, M.; Kuhl, H.; Sudbrak, R.; Knowles, M. R.; Reinhardt, R.; Omran, H.: DNAH5 Mutations are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects. American Journal of Respiratory and Critical Care Medicine: an Official Journal of the American Thoracic Society, Medical Section of the Lung Association 174 (2), pp. 120 - 126 (2006)

Traut, W.; Weichenhan, D.; Himmelbauer, H.; Winking, H.: New members of the neurexin superfamily: multiple rodent homologues of the human CASPR5 gene. Mammalian Genome 17 (7), pp. 723 - 731 (2006)

Mohamed, S. A.; Aherrahrou, Z.; Liptau, H.; Erasmi, A. W.; Hagemann, C.; Wrobel, S.; Borzym, K.; Schunkert, H.; Sievers, H. H.; Erdmann, J.: Novel missense mutations (p.T596M and p.P1797H) in NOTCH1 in patients with bicuspid aortic valve. Biochemical and Biophysical Research Communications 354 (4), pp. 1460 - 1465 (2006)

Angenendt, P.; Kreutzberger, J.; Glökler, J.; Hoheisel, J. D.: Generation of high density protein microarrays by cell-free in situ expression of unpurified PCR products. Molecular & Cellular Proteomics 5, pp. 1658 - 1666 (2006)

Hecht, J.; Kuhl, H.; Haas, S. A. ..; Bauer, S.; Poustka, A. J.; Lienau, J.; Schell, H.; Stiege, A. C.; Seitz, V.; Reinhardt, R. et al.; Duda, G. N.; Mundlos, S.; Robinson, P. N.: Gene identification and analysis of transcripts differentially regulated in fracture healing by EST sequencing in the domestic sheep. BMC Genomics 7, pp. 172 - 192 (2006)

Yeang, C.-H.; Vingron, M.: A joint model of regulatory and metabolic networks. BMC Bioinformatics 7, p. 332 - 332 (2006)