Zeitschriftenartikel (247)

121.
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Kerschnitzki, M.; Wagermaier, W.; Roschger, P.; Seto, J.; Shahar, R.; Duda, G. N.; Mundlos, S.; Fratzl, P.: The organization of the osteocyte network mirrors the extracellular matrix orientation in bone. J Struct Biol 173 (2), S. 303 - 11 (2011)
122.
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Kielbasa, S. M.; Wan, R.; Sato, K.; Horton, P.; Frith, M. C.: Adaptive seeds tame genomic sequence comparison. Genome Res 21 (3), S. 487 - 93 (2011)
123.
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Klopocki, E.; Lohan, S.; Brancati, F.; Koll, R.; Brehm, A.; Seemann, P.; Dathe, K.; Stricker, S.; Hecht, J.; Bosse, K. et al.; Betz, R. C.; Garaci, F. G.; Dallapiccola, B.; Jain, M.; Muenke, M.; Ng, V. C.; Chan, W.; Chan, D.; Mundlos, S.: Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis. Am J Hum Genet 88 (1), S. 70 - 5 (2011)
124.
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Kohler, S.; Bauer, S.; Mungall, C. J.; Carletti, G.; Smith, C. L.; Schofield, P.; Gkoutos, G. V.; Robinson, P. N.: Improving ontologies by automatic reasoning and evaluation of logical definitions. BMC Bioinformatics 12, S. 418 (2011)
125.
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Kohlmann, A.; Klein, H. U.; Weissmann, S.; Bresolin, S.; Chaplin, T.; Cuppens, H.; Haschke-Becher, E.; Garicochea, B.; Grossmann, V.; Hanczaruk, B. et al.; Hebestreit, K.; Gabriel, C.; Iacobucci, I.; Jansen, J. H.; te Kronnie, G.; van de Locht, L.; Martinelli, G.; McGowan, K.; Schweiger, M. R.; Timmermann, B.; Vandenberghe, P.; Young, B. D.; Dugas, M.; Haferlach, T.: The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratories. Leukemia: Official Journal of the Leukemia Society of America, Leukemia Research Fund, U.K 25 (12), S. 1840 - 8 (2011)
126.
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Kolanczyk, M.; Mautner, V.; Kossler, N.; Nguyen, R.; Kuhnisch, J.; Zemojtel, T.; Jamsheer, A.; Wegener, E.; Thurisch, B.; Tinschert, S. et al.; Holtkamp, N.; Park, S. J.; Birch, P.; Kendler, D.; Harder, A.; Mundlos, S.; Kluwe, L.: MIA is a potential biomarker for tumour load in neurofibromatosis type 1. BMC Med 9, S. 82 (2011)
127.
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Kolanczyk, M.; Pech, M.; Zemojte, T.; Yamamoto, H.; Mikula, I.; Calvaruso, M.-A.; van den Brand, M.; Richter, R.; Fischer, B.; Ritz, A. et al.; Kossler, N.; Thurisch, B.; Spoerle, R.; Smeitink, J.; Kornak, U.; Chan, D.; Vingron, M.; Martasek, P.; Lightowlers, R. N.; Nijtmans, L.; Schuelke, M.; Nierhaus, K. H.; Mundlos, S.: NOA1 is an essential GTPase required for mitochondrial protein synthesis. Molecular Biology of the Cell 22 (1), S. 1 - 11 (2011)
128.
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Koopmann, A.; Dinter, C.; Grosshans, M.; von der Goltz, C.; Hentschel, R.; Dahmen, N.; Gallinat, J.; Wagner, M.; Grunder, G.; Thurauf, N. et al.; Wienker, T.; Brinkmeyer, J.; Mobascher, A.; Spreckelmeyer, K. N.; Clepce, M.; de Millas, W.; Wiedemann, K.; Winterer, G.; Kiefer, F.: Psychological and hormonal features of smokers at risk to gain weight after smoking cessation--results of a multicenter study. Horm Behav 60 (1), S. 58 - 64 (2011)
129.
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Kornak, U.: Animal models with pathological mineralization phenotypes. Joint Bone Spine 78 (6), S. 561 - 7 (2011)
130.
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Kortum, F.; Das, S.; Flindt, M.; Morris-Rosendahl, D. J.; Stefanova, I.; Goldstein, A.; Horn, D.; Klopocki, E.; Kluger, G.; Martin, P. et al.; Rauch, A.; Roumer, A.; Saitta, S.; Walsh, L. E.; Wieczorek, D.; Uyanik, G.; Kutsche, K.; Dobyns, W. B.: The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. J Med Genet 48 (6), S. 396 - 406 (2011)
131.
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Kossler, N.; Stricker, S.; Rodelsperger, C.; Robinson, P. N.; Kim, J.; Dietrich, C.; Osswald, M.; Kuhnisch, J.; Stevenson, D. A.; Braun, T. et al.; Mundlos, S.; Kolanczyk, M.: Neurofibromin (Nf1) is required for skeletal muscle development. Hum Mol Genet 20 (14), S. 2697 - 709 (2011)
132.
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Koster, D. M.; Haselbach, D.; Lehrach, H.; Seitz, H.: A DNAzyme based label-free detection system for miniaturized assays. Molecular BioSystems 7 (10), S. 2882 - 9 (2011)
133.
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Kowald, A.; Wierling, C.: Standards, tools, and databases for the analysis of yeast 'omics data. Methods in Molecular Biology 759, S. 345 - 65 (2011)
134.
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Krobitsch, S.; Kazantsev, A. G.: Huntington's Disease: from Molecular Basis to Therapeutic Advances. The International Journal of Biochemistry & Cell Biology. 43 (1), S. 20 - 24 (2011)
135.
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Krobitsch, S.; Kazantsev, A. G.: Huntington's disease: From molecular basis to therapeutic advances. Int J Biochem Cell Biol 43 (1), S. 20 - 4 (2011)
136.
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Kruger, A.; Gruning, N. M.; Wamelink, M. M.; Kerick, M.; Kirpy, A.; Parkhomchuk, D.; Bluemlein, K.; Schweiger, M. R.; Soldatov, A.; Lehrach, H. et al.; Jakobs, C.; Ralser, M.: The pentose phosphate pathway is a metabolic redox sensor and regulates transcription during the antioxidant response. Antioxidants & Redox Signaling 15 (2), S. 311 - 24 (2011)
137.
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Kruger, A.; Ralser, M.: ATM is a redox sensor linking genome stability and carbon metabolism. Science Signaling 4 (167), S. pe17 (2011)
138.
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Kühn, A.: The "Virtual Patient" system: modeling cancer using deep sequencing technologies for personalized cancer treatment. Journal of Consumer Protection and Food Safety, S. 8 (2011)
139.
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Kühn, A.; Wierling, C.: Der virtuelle Patient - neue Wege in der Krebsforschung. Laborwelt 12 (6), S. 19 - 20 (2011)
140.
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Kunde, S. A.; Musante, L.; Grimme, A.; Fischer, U.; Muller, E.; Wanker, E. E.; Kalscheuer, V. M.: The X-chromosome-linked intellectual disability protein PQBP1 is a component of neuronal RNA granules and regulates the appearance of stress granules. Hum Mol Genet 20 (24), S. 4916 - 31 (2011)
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