Journal Article (799)

741.
Journal Article
Schütze, T.; Wilhelm, B.; Greiner, N.; Braun, H.; Peter, F.; Mörl, M.; Erdmann, V. A.; Lehrach, H.; Konthur, Z.; Menger, M. et al.; Arndt, P. F.; Glökler, J.: Probing the SELEX Process with Next-Generation Sequencing. PLoS ONE 6 (12), e29604 (2011)
742.
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Mayr, J. A.; Zimmermann, F. A.; Fauth, C.; Bergheim, C.; Meierhofer, D.; Radmayr, D.; Zschocke, J.; Koch, J.; Sperl, W.: Lipoic acid synthetase deficiency causes neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevation. The American Journal of Human Genetics 89 (6), pp. 792 - 797 (2011)
743.
Journal Article
Adrover, M. À.; Zi, Z.; Duch, A.; Schaber, J.; González-Novo, A.; Jimenez, J.; Nadal-Ribelles, M.; Clotet, J.; Klipp, E.; Posas, F.: Time-dependent quantitative multicomponent control of the G1-S network by the stress-activated protein kinase Hog1 upon osmostress. Science Signaling 4 (192), p. ra63 (2011)
744.
Journal Article
Zi, Z.; Feng, Z.; Chapnick, D. A.; Dahl, M.; Deng, D.; Klipp, E.; Moustakas, A.; Liu, X.: Quantitative analysis of transient and sustained transforming growth factor-β signaling dynamics. Molecular Systems Biology 2011 (7), 7: 492 (2011)
745.
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Zi, Z.: Sensitivity analysis approaches applied to systems biology models. IET Systems Biology 5 (6), pp. 336 - 346 (2011)
746.
Journal Article
Zi, Z.: SBML-PET-MPI: a parallel parameter estimation tool for Systems Biology Markup Language based models. Bioinformatics 27 (7), pp. 1028 - 1029 (2011)
747.
Journal Article
Schlesinger, J.; Schueler, M.; Grunert, M.; Fischer, J. J.; Zhang, Q.; Krueger, T.; Lange, M.; Tönjes, M.; Dunkel, I.; Sperling, S.: The Cardiac Transcription Network Modulated by Gata4, Mef2a, Nkx2.5, Srf, Histone Modifications, and MircoRNAs. PLoS Genetics 7 (2), e1001313 (2011)
748.
Journal Article
Schulz, E. G.; Elphège , P. N.; Heard, E.: Rnf12 – A Jack of All Trades in X Inactivation. PLoS Genetics 7 (1), e1002002 (2011)
749.
Journal Article
Schulz, E. G.; Nora, E. P.; Heard, E.: Rnf12--a jack of all trades in X inactivation? PLoS Genetics 7 (1), e1002002 (2011)
750.
Journal Article
Love, M. I.; Mysickova, A.; Sun, R.; Kalscheuer, V. M.; Vingron, M.; Haas, S. A.: Modeling read counts for CNV detection in exome sequencing data. Statistical Applications in Genetics and Molecular Biology 10 (1) (2011)
751.
Journal Article
Althoff, G. E. M.; Wolfer, D. P.; Timmesfeld, N.; Kanzler, B.; Schrewe, H.; Axel, P.: Long-Term Expression of Tissue-Inhibitor of Matrix Metalloproteinase-1 in the Murine Central Nervous System Does Not Alter the Morphological and Behavioral Phenotype but Alleviates the Course of Experimental Allergic Encephalomyelitis. The American Journal of Pathology 177 (2), pp. 840 - 853 (2010)
752.
Journal Article
Rocha, P. P.; Scholze, M.; Bleiß, W.; Schrewe, H.: Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling. Development 137, pp. 2723 - 2731 (2010)
753.
Journal Article
Herrmann, B. G.: Embryology meets cancer research. Public Service Review: Science and Technology 7, pp. 242 - 243 (2010)
754.
Journal Article
Zi, Z.; Liebermeister, W.; Klipp, E.: A quantitative study of the Hog1 MAPK response to fluctuating osmotic stress in Saccharomyces cerevisiae. A Quantitative Study of the Hog1 MAPK Response to Fluctuating Osmotic Stress in Saccharomyces cerevisiae 5 (3), e9522 (2010)
755.
Journal Article
Endele, S.; Rosenberger, G.; Geider, K.; Popp, B.; Tamer, C.; Stefanova, I.; Milh, M.; Kortum, F.; Fritsch, A.; Pientka, F. K. et al.; Hellenbroich, Y.; Kalscheuer, V. M.; Kohlhase, J.; Moog, U.; Rappold, G.; Rauch, A.; Ropers, H. H.; von Spiczak, S.; Tonnies, H.; Villeneuve, N.; Villard, L.; Zabel, B.; Zenker, M.; Laube, B.; Reis, A.; Wieczorek, D.; Van Maldergem, L.; Kutsche, K.: Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Nat Genet 42 (11), pp. 1021 - 6 (2010)
756.
Journal Article
Rocha, P. P.; Bleiss, W.; Schrewe, H.: Mosaic Expression of Med12 in Female Mice Leads to Exencephaly, Spina Bifida, and Craniorachischisis. Birth Defects Research Part A: Clinical and Molecular Teratology 88 (8), pp. 626 - 632 (2010)
757.
Journal Article
Slezak, R.; Luczak, K.; Kalscheuer, V.; Neumann, T. E.; Sasiadek, M. M.: Noonan-like/multiple giant cell lesion syndrome in two adult patients with SOS1 gene mutations. Clin Dysmorphol 19 (3), pp. 157 - 60 (2010)
758.
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Tzschach, A.; Bisgaard, A. M.; Kirchhoff, M.; Graul-Neumann, L. M.; Neitzel, H.; Page, S.; Ahmed, A.; Muller, I.; Erdogan, F.; Ropers, H. H. et al.; Kalscheuer, V. M.; Ullmann, R.: Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11. Eur J Hum Genet 18 (3), pp. 291 - 5 (2010)
759.
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Schulz, E. G.; Mariani, L.; Radbruch, A.; Höfer, T.: Sequential polarization and imprinting of type 1 T-helper lymphocytes by interferon-γ and interleukin-12. Immunity 30 (5), pp. 673 - 683 (2009)
760.
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Hu, H.; Wrogemann, K.; Kalscheuer, V.; Tzschach, A.; Richard, H.; Haas, S. A.; Menzel, C.; Bienek, M.; Froyen, G.; Raynaud, M. et al.; Van Bokhoven, H.; Chelly, J.; Ropers, H.; Chen, W.: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing. Hugo J 3 (1-4), pp. 41 - 9 (2009)
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