Max Planck Publications of Lastname Lab

Manke, T.; Demetrius, L.; Vingron, M.: An entropic characterization of protein interaction networks and cellular robustness. Interface: Journal of the Royal Society 11 (3), pp. 843 - 850 (2006)

Liebermeister, W.; Klipp, E.: Bringing metabolic networks to life: integration of kinetic, metabolic, and proteomic data. Theoretical Biology & Medical Modelling 3, p. 42 - 42 (2006)

Liebermeister, W.; Klipp, E.: Bringing metabolic networks to life: convenience rate law and thermodynamic constraints. Theoretical Biology & Medical Modelling 3, p. 41 - 41 (2006)

Schefe, J. H.; Menk, M.; Reinemund, J.; Effertz, K.; Hobbs, R. M.; Pandolfi, P. P.; Ruiz, P.; Unger, T.; Funke-Kaiser, H.: A Novel Signal Transduction Cascade Involving Direct Physical Interaction of the Renin/Prorenin Receptor With the Transcription Factor Promyelocytic Zinc Finger Protein. Circulation Research 99 (12), pp. 1355 - 1366 (2006)

Bauer, M.; Kube, M.; Teeling, H.; Richter,, M.; Lombardot, T.; Allers, E.; Wuerdemann, C. A.; Quast, C.; Kuhl, H.; Knaus, F. et al.; Woebken, D.; Kerstin Bischof, K.; Mussmann, M.; Choudhur, J. V.; Meyer, F.; Reinhardt, R.; Amann, R. I.; Gloeckner, F. O.: Whole genome analysis of the marine Bacteroidetes 'Gramella forsetii' reveals adaptations to degradation of polymeric organic matter. Environmental Microbiology 8 (12), pp. 2201 - 2213 (2006)

Grad, I.; McKee, T. A.; Ludwig, S. M.; Hoyle, G. W.; Ruiz, P.; Wurst, W.; Floss, T.; Miller, C. A.; Picard, D.: The Hsp90 cochaperone p23 is essential for perinatal survival (triangledown). Molecular and Cellular Biology (Washington, DC) 26 (23), pp. 8976 - 8983 (2006)

Klopocki, E.; Neumann, L. M.; Tönnies, H.; Ropers, H.-H.; Mundlos, S.; Ullmann, R.: Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene. European Journal of Human Genetics: the Official Journal of the European Society of Human Genetics. 14 (121), pp. 1274 - 1279 (2006)

Klopocki, E.; Neumann, L. M.; Tönnies, H.; Ropers, H.-H.; Mundlos, S.; Ullmann, R.: Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene. European Journal of Human Genetics: the Official Journal of the European Society of Human Genetics. 14 (121), pp. 1274 - 1279 (2006)

Lapraz, F.; Röttinger, E.; Duboc, V.; Range, R.; Duloquin, L.; Walton, K.; Wu, S.-Y.; Bradham, C.; Loza, M. A.; Hibino, T. et al.; Wilson, K.; Poustka, A.; McClay, D.; Angerer, L.; Gache, C.; Lepage, T.: RTK and TGF-β signaling pathways genes in the sea urchin genome. Developmental Biology 300 (1), pp. 132 - 152 (2006)

Lehmann, K.; Seemann, P.; Boergermann, J.; Morin, G.; Reif, S.; Knaus, P.; Mundlos, S.: A novel R486Q mutation in BMPR1B resulting in either a brachydactyly type C/symphalangism-like phenotype or brachydactyly type A2. European Journal of Human Genetics 14 (12), pp. 1248 - 1254 (2006)

Schüler, M.; Connell, S. R.; Lescoute, A.; Giesebrecht, J.; Dabrowski, M.; Schroeer, B.; Mielke, T.; Penczek, P. A.; Westhof, E.; Spahn, C. M. T.: Structure of the ribosome-bound cricket paralysis virus IRES RNA. Nature Structural & Molecular Biology 13 (12), pp. 1092 - 1096 (2006)

Stricker, S.; Van Wijk, N. V.; Witte, F.; Brieske, N.; Seidel, K.; Mundlos, S.: Cloning and expression pattern of chicken Ror2 and functional characterization of truncating mutations in Brachydactyly type B and Robinow syndrome. Developmental Dynamics 235 (12), pp. 3456 - 3465 (2006)

Wilson, D. N.; Nierhaus, K.: The E-site story: the importance of maintaining two tRNAs on the ribosome during protein synthesis. Cellular and Molecular Life Sciences 63 (23), pp. 2725 - 2737 (2006)

Zahn, C.; Hommel, A.; Lu,, L.; Hong, W.; Walther, D. J.; Florian, S.; Joost, H.-G.; Schürmann, A.: Knockout of Arfrp1 leads to disruption of ARF-like1 (ARL1) targeting to the trans-Golgi in mouse embryos and HeLa cells. Molecular Membrane Biology 23, pp. 475 - 485 (2006)

Halic, M.; Blau, M.; Becker, T.; Mielke, T.; Pool, M. R.; Wild, K.; Sinning, I.; Beckmann, R.: Following the signal sequence from ribosomal tunnel exit to signal recognition particle. Nature 444 (7118), pp. 507 - 511 (2006)

So, J.; Suckow, V.; Kijas, Z.; Kalscheuer, V.; Moser, B.; Winter, J.; Baars, M.; Firth, H.; Lunt, P.; Hamel, B. et al.; Meinecke, P.; Moraine, C.; Odent, S.; Schinzel, A.; van der Smagt, J.J.; Devriendt, K.; Albrecht, B.; Gillessen-Kaesbach, G.; van der Burgt, I.; Petrij, F.; Faivre, L.; McGaughran, J.; McKenzie, F.; Opitz, J. M.; Cox, T.; Schweiger, S.: Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. American Journal of Medical Genetics Part A 132A (1), pp. 1 - 7 (2006)

So, J.; Suckow, V.; Kijas, Z.; Kalscheuer, V.; Moser, B.; Winter, J.; Baars, M.; Firth, H.; Lunt, P.; Hamel, B. et al.; Meinecke, P.; Moraine, C.; Odent, S.; Schinzel, A.; van der Smagt, J.J.; Devriendt, K.; Albrecht, B.; Gillessen-Kaesbach, G.; van der Burgt, I.; Petrij, F.; Faivre, L.; McGaughran, J.; McKenzie, F.; Opitz, J. M.; Cox, T.; Schweiger, S.: Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. American Journal of Medical Genetics Part A 132A (1), pp. 1 - 7 (2006)

Haesler, S.: Also sprach der Zebrafink. Gehirn & Geist: das Magazin für Psychologie und Hirnforschung 2006 (12), pp. 52 - 57 (2006)

Qin, Y.; Polacek, N.; Vesper, O.; Staub, E.; Einfeldt, E.; Wilson, D. N.; Nierhaus, K.: The Highly Conserved LepA Is a Ribosomal Elongation Factor that Back-Translocates the Ribosome. Cell 127 (4), pp. 721 - 733 (2006)

Liebe, B.; Petukhova, G.; Barchi, M.; Bellani, M.; Braselmann, H.; Nakano, T.; Pandita, T. K.; Jasin, M.; Fornace, A.; Meistrich, M. L. et al.; Baarends, W. M.; Schimenti, J.; de Lange, T.; Keeney, S.; Camerini-Otero, R. D.; Scherthan, H.: Mutations that affect meiosis in male mice influence the dynamics of the mid-preleptotene and bouquet stages. Experimental Cell Research 312 (19), pp. 3768 - 3781 (2006)