Journal Article (833)

781.
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)
782.
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)
783.
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)
784.
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)
785.
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)
786.
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)
787.
Journal Article
Herrmann, B. G.: Embryology meets cancer research. Public Service Review: Science and Technology 7, pp. 242 - 243 (2010)
788.
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)
789.
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)
790.
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)
791.
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)
792.
Journal Article
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)
793.
Journal Article
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)
794.
Journal Article
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)
795.
Journal Article
Meierhofer, D.; Wang, X.; Huang, L.; Kaiser, P.: Quantitative analysis of global ubiquitination in HeLa cells by mass spectrometry. Journal of Proteome Research 7 (10), pp. 4566 - 4576 (2008)
796.
Journal Article
Mayr, J. A.; Meierhofer, D.; Zimmermann, F.; Feichtinger, R.; Kögler, C.; Ratschek, M.; Schmeller, N.; Sperl, W.; Kofler, B.: Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma. Clinical Cancer Research 14 (8), pp. 2270 - 2275 (2008)
797.
Journal Article
Deutsch, E. W.; Ball, C. A.; Berman, J. J.; Bova, G. S.; Brazma, A.; Bumgarner, R. E.; Campbell, D.; Causton, H. C.; Christiansen, J. H.; Daian, F. et al.; Dauga, D.; Davidson, D. R.; Gimenez, G.; Goo, Y. A.; Grimmond, S.; Henrich, T.; Herrmann, B. G.; Johnson, M. H.; Korb, M.; Mills, J. C.; Oudes, A. J.; Parkinson, H. E.; Pascal, L. E.; Pollet, N.; Quackenbush, J.; Ramialison, M.; Ringwald, M.; Salgado, D.; Sansone, S.-A.; Sherlock, G.; Stoeckert, Jr, C. J.; Swedlow, J.; Taylor, R. C.; Walashek, L.; Warford, A.; Wilkinson, D. G.; Zhou, Y.; Zon, L. I.; Liu, A. Y.; True, L. D.: Minimum Information Specification For In Situ Hybridization and Immunohistochemistry Experiments (MISFISHIE). Nature biotechnology 26, pp. 305 - 312 (2008)
798.
Journal Article
Schell-Apacik, C. C.; Wagner, K.; Bihler, M.; Ertl-Wagner, B.; Heinrich, U.; Klopocki, E.; Kalscheuer, V. M.; Muenke, M.; von Voss, H.: Agenesis and dysgenesis of the corpus callosum: clinical, genetic and neuroimaging findings in a series of 41 patients. Am J Med Genet A 146A (19), pp. 2501 - 11 (2008)
799.
Journal Article
Mayr, J. A.; Zimmermann, F.; Meierhofer, D.; Schmeller, N.; Sperl, W.; Kofler, B.: Biochemical consequences of a pathogenic A3243G mtDNA mutation. Mitochondrion 6 (5), pp. 268 - 269 (2006)
800.
Journal Article
Wiesbauer, M.; Meierhofer, D.; Mayr, J. A.; Sperl, W.; Paulweber, B.; Kofler, B.: Multiplex primer extension analysis for rapid detection of major European mitochondrial haplogroups. Electrophoresis 27 (19), pp. 3864 - 2868 (2006)
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