Zeitschriftenartikel (970)

921.
Zeitschriftenartikel
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)
922.
Zeitschriftenartikel
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), S. 840 - 853 (2010)
923.
Zeitschriftenartikel
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, S. 2723 - 2731 (2010)
924.
Zeitschriftenartikel
Herrmann, B. G.: Embryology meets cancer research. Public Service Review: Science and Technology 7, S. 242 - 243 (2010)
925.
Zeitschriftenartikel
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)
926.
Zeitschriftenartikel
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), S. 1021 - 6 (2010)
927.
Zeitschriftenartikel
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), S. 626 - 632 (2010)
928.
Zeitschriftenartikel
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), S. 157 - 60 (2010)
929.
Zeitschriftenartikel
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), S. 291 - 5 (2010)
930.
Zeitschriftenartikel
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), S. 673 - 683 (2009)
931.
Zeitschriftenartikel
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), S. 41 - 9 (2009)
932.
Zeitschriftenartikel
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), S. 4566 - 4576 (2008)
933.
Zeitschriftenartikel
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), S. 2270 - 2275 (2008)
934.
Zeitschriftenartikel
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, S. 305 - 312 (2008)
935.
Zeitschriftenartikel
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), S. 2501 - 11 (2008)
936.
Zeitschriftenartikel
Mayr, J. A.; Zimmermann, F.; Meierhofer, D.; Schmeller, N.; Sperl, W.; Kofler, B.: Biochemical consequences of a pathogenic A3243G mtDNA mutation. Mitochondrion 6 (5), S. 268 - 269 (2006)
937.
Zeitschriftenartikel
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), S. 3864 - 2868 (2006)
938.
Zeitschriftenartikel
Dale, J. K.; Malapert, P.; Chal, J.; Vilhais-Neto, G.; Maroto, M.; Johnson , T.; Jayasinghe, S.; Paul, T.; Herrmann, B. G.; Pourquié, O.: Oscillations of the Snail Genes in the Presomitic Mesoderm Coordinate Segmental Patterning and Morphogenesis in Vertebrate Somitogenesis. Developmental Cell 10 (3), S. 355 - 366 (2006)
939.
Zeitschriftenartikel
Meierhofer, D.; Ebner, S.; Mayr, J. A.; Jones, N. D.; Kofler, B.; Sperl, W.: Platelet transfusion can mimic somatic mtDNA mutations. Leukemia: the Journal of Normal and Malignant Hemopoiese ; Official Journal of the Leukemia Research Fund U.K. 20 (2), S. 362 - 363 (2006)
940.
Zeitschriftenartikel
Meierhofer, D.; Mayr, J. A.; Fink, K.; Schmeller, N.; Kofler, B.; Sperl, W.: Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolism. British Journal of Cancer 94 (2), S. 268 - 274 (2006)
Zur Redakteursansicht