Journal Article (230)

21.
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Azimzadeh, O.; Scherthan, H.; Sarioglu, H.; Barjaktarovic, Z.; Conrad, M.; Vogt, A.; Calzada-Wack, J.; Neff, F.; Aubele, M.; Buske, C. et al.; Atkinson, M. J.; Tapio, S.: Rapid proteomic remodeling of cardiac tissue caused by total body ionizing radiation. Proteomics 11 (16), pp. 3299 - 311 (2011)
22.
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Baasanjav, S.; Al-Gazali, L.; Hashiguchi, T.; Mizumoto, S.; Fischer, B.; Horn, D.; Seelow, D.; Ali, B. R.; Aziz, S. A.; Langer, R. et al.; Saleh, A. A.; Becker, C.; Nurnberg, G.; Cantagrel, V.; Gleeson, J. G.; Gomez, D.; Michel, J. B.; Stricker, S.; Lindner, T. H.; Nurnberg, P.; Sugahara, K.; Mundlos, S.; Hoffmann, K.: Faulty initiation of proteoglycan synthesis causes cardiac and joint defects. Am J Hum Genet 89 (1), pp. 15 - 27 (2011)
23.
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Bauer, S.; Robinson, P. N.; Gagneur, J.: Model-based gene set analysis for Bioconductor. Bioinformatics 27 (13), pp. 1882 - 3 (2011)
24.
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Becker, T.; Armache, J. P.; Jarasch, A.; Anger, A. M.; Villa, E.; Sieber, H.; Motaal, B. A.; Mielke, T.; Berninghausen, O.; Beckmann, R.: Structure of the no-go mRNA decay complex Dom34-Hbs1 bound to a stalled 80S ribosome. Nature Structural & Molecular Biology 18 (6), pp. 715 - 20 (2011)
25.
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Bertram, L.: Alzheimer's genetics in the GWAS era: a continuing story of 'replications and refutations'. Current Neurology and Neuroscience Reports 11 (3), pp. 246 - 53 (2011)
26.
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Bertram, L.; Hampel, H.: The role of genetics for biomarker development in neurodegeneration. Progress in Neurobiology 95 (4), pp. 501 - 4 (2011)
27.
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Bhushan, S.; Hoffmann, T.; Seidelt, B.; Frauenfeld, J.; Mielke, T.; Berninghausen, O.; Wilson, D. N.; Beckmann, R.: SecM-stalled ribosomes adopt an altered geometry at the peptidyl transferase center. PLoS Biology 9 (1), p. e1000581 (2011)
28.
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Blau, O.; Baldus, C. D.; Hofmann, W. K.; Thiel, G.; Nolte, F.; Burmeister, T.; Turkmen, S.; Benlasfer, O.; Schumann, E.; Sindram, A. et al.; Molkentin, M.; Mundlos, S.; Keilholz, U.; Thiel, E.; Blau, I. W.: Mesenchymal stromal cells of myelodysplastic syndrome and acute myeloid leukemia patients have distinct genetic abnormalities compared with leukemic blasts. Blood 118 (20), pp. 5583 - 92 (2011)
29.
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Bluemlein, K.; Gruning, N. M.; Feichtinger, R. G.; Lehrach, H.; Kofler, B.; Ralser, M.: No evidence for a shift in pyruvate kinase PKM1 to PKM2 expression during tumorigenesis. Oncotarget 2 (5), pp. 393 - 400 (2011)
30.
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Bluemlein, K.; Ralser, M.: Monitoring protein expression in whole-cell extracts by targeted label- and standard-free LC-MS/MS. Nature Protocols 6 (6), pp. 859 - 69 (2011)
31.
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Bordlein, A.; Scherthan, H.; Nelkenbrecher, C.; Molter, T.; Bosl, M. R.; Dippold, C.; Birke, K.; Kinkley, S.; Staege, H.; Will, H. et al.; Winterpacht, A.: SPOC1 (PHF13) is required for spermatogonial stem cell differentiation and sustained spermatogenesis. J Cell Sci 124 (Pt 18), pp. 3137 - 48 (2011)
32.
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Bormann, F.; Sers, C.; Seliger, B.; Handke, D.; Bergmann, T.; Seibt, S.; Lehrach, H.; Dahl, A.: Methylation-specific ligation detection reaction (msLDR): a new approach for multiplex evaluation of methylation patterns. Molecular Genetics and Genomics: MGG 286 (3-4), pp. 279 - 91 (2011)
33.
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Borodina, T.; Adjaye, J.; Sultan, M.: A strand-specific library preparation protocol for RNA sequencing. Methods in Enzymology 500, pp. 79 - 98 (2011)
34.
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Brameier, M.; Herwig, A.; Reinhardt, R.; Walter, L.; Gruber, J.: Human box C/D snoRNAs with miRNA like functions: expanding the range of regulatory RNAs. Nucleic Acids Research 39 (2), pp. 675 - 686 (2011)
35.
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Braunholz, D.; Hullings, M.; Gil-Rodriguez, M. C.; Fincher, C. T.; Mallozzi, M. B.; Loy, E.; Albrecht, M.; Kaur, M.; Limon, J.; Rampuria, A. et al.; Clark, D.; Kline, A.; Dalski, A.; Eckhold, J.; Tzschach, A.; Hennekam, R.; Gillessen-Kaesbach, G.; Wierzba, J.; Krantz, I. D.; Deardorff, M. A.; Kaiser, F. J.: Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction. Eur J Hum Genet (2011)
36.
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Brinkmeyer, J.; Mobascher, A.; Musso, F.; Schmitz, M.; Wagner, M.; Frommann, I.; Grunder, G.; Spreckelmeyer, K. N.; Wienker, T.; Diaz-Lacava, A. et al.; Holler, D.; Dahmen, N.; Thuerauf, N.; Clepce, M.; Kiefer, F.; de Millas, W.; Gallinat, J.; Winterer, G.: P50 sensory gating and smoking in the general population. Addict Biol 16 (3), pp. 485 - 98 (2011)
37.
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Budkevich, T.; Giesebrecht, J.; Altman, R. B.; Munro, J. B.; Mielke, T.; Nierhaus, K. H.; Blanchard, S. C.; Spahn, C. M.: Structure and dynamics of the mammalian ribosomal pretranslocation complex. Mol Cell 44 (2), pp. 214 - 24 (2011)
38.
Journal Article
Budkevich, T.; Giesebrecht, J.; Altman, R. B.; Munro, J. B.; Mielke, T.; Nierhaus, K. H.; Blanchard, S. C.; Spahn, C. M.: Structure and dynamics of the mammalian ribosomal pretranslocation complex. Molecular Cell 44 (2), pp. 214 - 24 (2011)
39.
Journal Article
Buonincontri, R.; Bache, I.; Silahtaroglu, A.; Elbro, C.; Nielsen, A. M.; Ullmann, R.; Arkesteijn, G.; Tommerup, N.: A cohort of balanced reciprocal translocations associated with dyslexia: identification of two putative candidate genes at DYX1. Behav Genet 41 (1), pp. 125 - 33 (2011)
40.
Journal Article
Busche, A.; Graul-Neumann, L. M.; Zweier, C.; Rauch, A.; Klopocki, E.; Horn, D.: Microdeletions of chromosome 7p21, including TWIST1, associated with significant microcephaly, facial dysmorphism, and short stature. Eur J Med Genet 54 (3), pp. 256 - 61 (2011)
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