Zeitschriftenartikel (161)

61.
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Drews, K.; Jozefczuk, J.; Prigione, A.; Adjaye, J.: Human induced pluripotent stem cells--from mechanisms to clinical applications. Journal of Molecular Medicine-JMM 90 (7), S. 735 - 745 (2012)
62.
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Kamburov, A.; Stelzl, U.; Herwig, R.: IntScore: a web tool for confidence scoring of biological interactions. Nucleic Acids Research (London) 40 (Web Server issue), S. W140 - W146 (2012)
63.
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Ott, C. E.; Hein, H.; Lohan, S.; Hoogeboom, J.; Foulds, N.; Grunhagen, J.; Stricker, S.; Villavicencio-Lorini, P.; Klopocki, E.; Mundlos, S.: Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia. Journal of Medical Genetics (London) 49 (7), S. 437 - 441 (2012)
64.
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Ropers, H.-H.: On the future of genetic risk assessment. Journal of Community Genetics 3 (3), S. 229 - 236 (2012)
65.
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Rosenfeld, J. A.; Traylor, R. N.; Schaefer, G. B.; McPherson, E. W.; Ballif, B. C.; Klopocki, E.; Mundlos, S.; Shaffer, L. G.; Aylsworth, A. S.: Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes. European journal og human genetics: EJHG ; the official journal of the European Society of Human Genetics 20 (7), S. 754 - 761 (2012)
66.
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Schimek, M. G.; Mysickova, A.; Budinská, E.: An Inference and Integration Approach for the Consolidation of Ranked Lists. Communications in Statistics - Simulation and Computation 41 (7), S. 1152 - 1166 (2012)
67.
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Wallace, B. C.; Small, K.; Brodley, C. E.; Lau, J.; Schmid, C. H.; Bertram, L.; Lill, C. M.; Cohen, J. T.; Trikalinos, T. A.: Toward modernizing the systematic review pipeline in genetics: efficient updating via data mining. GENETICS IN MEDICINE 14 (7), S. 663 - 669 (2012)
68.
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Abu Dawud, R.; Schreiber, K.; Schomburg, D.; Adjaye, J.: Human embryonic stem cells and embryonal carcinoma cells have overlapping and distinct metabolic signatures. PLoS One 7 (6), S. e39896 - e39896 (2012)
69.
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Pin, P. A.; Zhang, W.; Vogt, S. H.; Dally, N.; Büttner, B.; Schulze-Buxloh, G.; Jelly, N. S.; Chia, T. Y.P.; Mutasa-Gottgens, E. S.; Dohm, J. C. et al.; Himmelbauer, H.; Weisshaar, B.; Kraus, J.; Gielen, J. J.L.; Lommel, M.; Weyens, G.; Wahl, B.; Schechert, A.; Nilsson, O.; Jung, C.; Kraft, T.; Müller, A. E.: The role of a pseudo-response regulator gene in life cycle adaptation and domestication of beet. Current Biology 22 (12), S. 1095 - 1101 (2012)
70.
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Sultan, M.; Dokel, S.; Amstislavskiy, V.; Wuttig, D.; Sultmann, H.; Lehrach, H.; Yaspo, M. L.: A simple strand-specific RNA-Seq library preparation protocol combining the Illumina TruSeq RNA and the dUTP methods. Biochemical and Biophysical Research Communications 422 (4), S. 643 - 646 (2012)
71.
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Ni, S.; Vingron, M.: R2KS: a novel measure for comparing gene expression based on ranked gene lists. Journal of Computational Biology 19 (6), S. 766 - 775 (2012)
72.
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Drews, K.; Tavernier, G.; Demeester, J.; Lehrach, H.; de Smedt, S. C.; Rejman, J.; Adjaye, J.: The cytotoxic and immunogenic hurdles associated with non-viral mRNA-mediated reprogramming of human fibroblasts. Biomaterials 33 (16), S. 4059 - 4068 (2012)
73.
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Kliem, M.; Sauer, S.: The essence on mass spectrometry based microbial diagnostics. Current Opinion in Microbiology 15 (3), S. 397 - 402 (2012)
74.
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Klopocki, E.; Kaehler, C.; Foulds, N.; Shah, H.; Joseph, B.; Vogel, H.; Luttgen, S.; Bald, R.; Besoke, R.; Held, K. et al.; Mundlos, S.; Kurth, I.: Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly. European journal og human genetics: EJHG ; the official journal of the European Society of Human Genetics 20 (6), S. 705 - 708 (2012)
75.
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Lill, C. M.; Zipp, F.: [The genetic profile of multiple sclerosis: risk genes and the "dark matter"]. Der Nervenarzt 83 (6), S. 705 - 713 (2012)
76.
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Querfurth, R.; Fischer, A.; Schweiger, M. R.; Lehrach, H.; Mertes, F.: Creation and application of immortalized bait libraries for targeted enrichment and next-generation sequencing. Biotechniques 52 (6), S. 375 - 380 (2012)
77.
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Welzel, F.; Kaehler, C.; Isau, M.; Hallen, L.; Lehrach, H.; Krobitsch, S.: FOX-2 dependent splicing of ataxin-2 transcript is affected by ataxin-1 overexpression. PLoS One 7 (5), S. e37985 - e37985 (2012)
78.
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Ziv, L.; Muto, A.; Schoonheim, P. J.; Meijsing, S. H.; Strasser, D.; Ingraham, H. A.; Schaaf, M. J.; Yamamoto, K. R.; Baier, H.: An affective disorder in zebrafish with mutation of the glucocorticoid receptor. Molecular Psychiatry 18 (6), S. 681 - 91 (2012)
79.
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Nora, E. P.; Lajoie, B. R.; Schulz, E. G.; Giorgetti, L.; Okamoto, I.; Servant, N.; Piolot, T.; van Berkum, N. L.; Meisig, J.; Sedat, J. et al.; Gribnau, J.; Barillot, E.; Blüthgen, N.; Dekker, J.; Heard, E.: Spatial partitioning of the regulatory landscape of the X-inactivation centre. Nature 485 (7398), S. 381 - 385 (2012)
80.
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Dreher, F.; Kreitler, T.; Hardt, C.; Kamburov, A.; Yildirimman, R.; Schellander, K.; Lehrach, H.; Lange, B. M. H.; Herwig, R.: DIPSBC--data integration platform for systems biology collaborations. BMC Bioinformatics 13, 13:85 (2012)
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