Our publications listed in the Puplication Repository of the Max Planck Society (PuRe)

Journal Article (147)

81.
Journal Article
Klipp, E.; Liebermeister, W.; Helbig, A.; Kowald, A.; Schaber, J.: Systems biology standards—the community speaks. Nature Biotechnology 25 (4), pp. 390 - 391 (2007)
82.
Journal Article
Meyer, S.; Fergusson, W. D.; Whetton, A. D.; Moreira-Leite, F.; Pepper, S. D.; Miller, C.; Saunders, E. K.; White, D. J.; Will, A. M.; Eden, T. et al.; Ikeda, H.; Ullmann, R.; Tuerkmen, S.; Gerlach, A.; Klopocki, E.; Tönnies, H.: Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption. Genes, Chromosomes and Cancer 46 (4), pp. 359 - 372 (2007)
83.
Journal Article
Nonhoff, U.; Ralser, M.; Welzel, F.; Piccini, I.; Balzereit, D.; Yaspo, M.-L.; Lehrach, H.; Krobitsch, S.: Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules. Molecular Biology of the Cell 18 (4), pp. 1385 - 1396 (2007)
84.
Journal Article
Belloso, J. M.; Bache, I.; Guitart, M.; Caballin, M. R.; Halgren, C.; Kirchhoff, M.; Ropers, H.-H.; Tommerup, N.; Tümer, Z.: Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome. European Journal og Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 15 (6), pp. 711 - 713 (2007)
85.
Journal Article
Gerisch, B.; Rottiers, V.; Li, D.; Motola, D. L.; Cummins, C. L.; Lehrach, H.; Mangelsdorf, D. J.; Antebi, A.: A bile acid-like steroid modulates Caenorhabditis elegans lifespan through nuclear receptor signaling. Proceedings of the National Academy of Sciences of the United States of America 104 (12), pp. 5014 - 5019 (2007)
86.
Journal Article
Sauer, S.: The essence of DNA sample preparation for MALDI mass spectrometry. Journal of Biochemical and Biophysical Methods 70 (2), pp. 311 - 318 (2007)
87.
Journal Article
Connell, S. R.; Takemoto, C.; Wilson, D. N.; Wang, H.; Murayama, K.; Terada, T.; Shirouzu, M.; Rost, M.; Schüler, M.; Giesebrecht, J. et al.; Dabrowski, M.; Mielke, T.; Fucini, P.; Yokoyama, S.; Spahn, C. M. T.: Structural basis for interaction of the ribosome with the switch regions of GTP-bound elongation factors. Molecular Cell 25 (5), pp. 751 - 764 (2007)
88.
Journal Article
Estrugo, D.; Fischer, A.; Hess, F.; Scherthan, H.; Belka, C.; Nils Cordes, N.: Ligand bound beta1 integrins inhibit procaspase-8 for mediating cell adhesion-mediated drug and radiation resistance in human leukemia cells. PLoS One 2 (3), p. e269 - e269 (2007)
89.
Journal Article
Chen, W.; Jensen, L. R.; Gecz, J.; Fryns, J.-P.; Moraine, C.; de Brouwer, A.; Chelly, J.; Moser, B.; Ropers, H.-H.; Kuss, A. W.: Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation. European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 15 (3), pp. 375 - 378 (2007)
90.
Journal Article
Chen, W.; Jensen, L. R.; Gecz, J.; Fryns, J.-P.; Moraine, C.; de Brouwer, A.; Chelly, J.; Moser, B.; Ropers, H.-H.; Kuss, A. W.: Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation. European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 15 (3), pp. 375 - 378 (2007)
91.
Journal Article
Najmabadi, H.; Motazacker, M. M.; Garshasbi, M.; Kahrizi, K.; Tzschach, A.; Chen, W.; Behjati, F.; Hadavi, V.; Nieh, S. E.; Abedini, S. S. et al.; Vazifehmand, R.; Firouzabadi, S. G.; Jamali, P.; Falah, M.; Seifati, S. M.; Grüters, A.; Lenzner, S.; Jensen, L. R.; Rüschendorf, F.; Kuss, A. W.; Ropers, H.-H.: Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci. Human Genetics 121 (1), pp. 43 - 48 (2007)
92.
Journal Article
Scheich, C.; Kümmel, D.; Soumailakakis, D.; Heinemann, U.; Büssow, K.: Vectors for co-expression of an unrestricted number of proteins. Nucleic Acids Research (London) 35 (6), p. e43 - e43 (2007)
93.
Journal Article
Trepczi, B.; Lienau, J.; Schell, H.; Epari, D. R.; Thompson, M. S.; Hoffmann, J.-E.; Kadow-Romacker, A.; Mundlos, S.; Duda, G. N.: Endochondral ossification in vitro is influenced by mechanical bending. Bone 40 (3), pp. 597 - 603 (2007)
94.
Journal Article
Trivedi, C. M.; Luo, Y.; Yin, Z.; Zhang, M.; Zhu, W.; Wang, T.; Floss, T.; Goettlicher, M.; Ruiz Noppinger, P.; Wurst, W. et al.; Ferrari, V. A.; Abrams, C. S.; Gruber, P. J.; Epstein, J. A.: Hdac2 regulates the cardiac hypertrophic response by modulating Gsk3 beta activity. Nature Medicine 13 (3), pp. 324 - 331 (2007)
95.
Journal Article
Trivedi, C. M.; Luo, Y.; Yin, Z.; Zhang, M.; Zhu, W.; Wang, T.; Floss, T.; Goettlicher, M.; Ruiz Noppinger, P.; Wurst, W. et al.; Ferrari, V. A.; Abrams, C. S.; Gruber, P. J.; Epstein, J. A.: Hdac2 regulates the cardiac hypertrophic response by modulating Gsk3bold beta activity. Nature Medicine 13 (3), pp. 324 - 331 (2007)
96.
Journal Article
Kolanczyk, M.; Kossler, N.; Kühnisch, J.; Lavitas, L.; Stricker, S.; Wilkening, U.; Manjubala, I.; Fratzl, P.; Spörle, R.; Herrmann, B. G. et al.; Parada, L. F.; Kornak, U.; Mundlos, S.: Multiple roles for neurofibromin in skeletal development and growth. Human Molecular Genetics 16 (8), pp. 232 - 240 (2007)
97.
Journal Article
Goswami, C.; Hucho, T.; Hucho, F.: Identification and characterisation of novel tubulin-binding motifs located within the C-terminus of TRPV1. Journal of Neurochemistry: Official Journal of the International Society for Neurochemistry 101 (1), pp. 250 - 262 (2007)
98.
Journal Article
Bais, A. S.; Grossmann, S.; Vingron, M.: Simultaneous alignment and annotation of cis-regulatory regions. Bioinformatics 23 (2), pp. e44 - e49 (2007)
99.
Journal Article
Castori, M.; Brancati, F.; Mingarelli, R.; Mundlos, S.; Dallapiccola, B.: A novel patient with Cooks syndrome supports splitting from "classic" brachydactyly type B. American Journal of Medical Genetics/ Part A 143 (2), pp. 195 - 199 (2007)
100.
Journal Article
Erdogan, F.; Ullmann, R.; Chen, W.; Schubert, M.; Adolph, S.; Hultschig, C.; Kalscheuer, V. M.; Ropers, H.-H.; Spaich, C.; Tzschach, A.: Characterization of a 5.3 Mb deletion in 15q14 by Comparative Genomic Hybridization using a whole genome ”tiling path” BAC array in a girl with heart defect, cleft palate and developmental delay. American Journal of Medical Genetics Part A 143 (2), pp. 172 - 178 (2007)
Go to Editor View