Zeitschriftenartikel (223)

121.
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Denekamp, N. Y.; Reinhardt, R.; Kube, M.; Lubzens, E.: Presence of late embryogenesis abundant (LEA) proteins in a nondesiccated, diapausing invertebrate embryo (Rotifers). Biology of Reproduction 82 (4), S. 714 - 724 (2010)
122.
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Glökler, J.; Schütze, T.; Konthur, Z.: Automation in the high-throughput selection of random combinatorial libraries-different approaches for select applications. Molecules 15 (4), S. 2478 - 2490 (2010)
123.
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Lill, C. M.; Schjeide, B. M.; Roehr, J. T.; Zauft, U.; Allen, N. C.; Zipp, F.; McQueen, M. B.; Kavvoura, F. K.; Ioannidis, J. P.; Khoury, M. J. et al.; Tanzi, R. E.; Bertram, L.: Correspondence to Sand et al. “Critical Reappraisal of a Catechol-O-Methyltransferase Transversion Variant in Schizophrenia”. Biological Psychiatry 67 (7), S. e45 - e48 (2010)
124.
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Manke, T.; Heinig, M.; Vingron, M.: Quantifying the effect of sequence variation on regulatory interactions. Hum Mutation 31 (4), S. 477 - 483 (2010)
125.
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Pearson, G. A.; Hoarau, G.; Lago-Leston, A.; Coyer, J. A.; Kube, M.; Reinhardt, R.; Henckel, K.; Serrão, E. T. A.; Corre, E.; Olsen, J. L.: An Expressed Sequence Tag Analysis of the Intertidal Brown Seaweeds Fucus serratus (L.) and F. vesiculosus (L.) (Heterokontophyta, Phaeophyceae) in Response to Abiotic Stressors. Marine Biotechnology (New York, N.Y.) 12 (2), S. 195 - 213 (2010)
126.
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Phadke, S. R.; Fischer, B.; Gupta, N.; Ranganath, P.; Kabra, M.; Kornak, U.: Novel mutations in Indian patients with autosomal recessive infantile malignant osteopetrosis. Indian J Med Res 131, S. 508 - 514 (2010)
127.
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Warren, W. C.; Clayton, D. F.; Ellegren, H.; Arnold, A. P.; Hillier, L. W.; Kunstner, A.; Searle, S.; White, S.; Vilella, A. J.; Fairley, S. et al.; Heger, A.; Kong, L.; Ponting, C. P.; Jarvis, E. D.; Mello, C. V.; Minx, P.; Lovell, P.; Velho, T. A.; Ferris, M.; Balakrishnan, C. N.; Sinha, S.; Blatti, C.; London, S. E.; Li, Y.; Lin, Y. C.; George, J.; Sweedler, J.; Southey, B.; Gunaratne, P.; Watson, M.; Nam, K.; Backstrom, N.; Smeds, L.; Nabholz, B.; Itoh, Y.; Whitney, O.; Pfenning, A. R.; Howard, J.; Volker, M.; Skinner, B. M.; Griffin, D. K.; Ye, L.; McLaren, W. M.; Flicek, P.; Quesada, V.; Velasco, G.; Lopez-Otin, C.; Puente, X. S.; Olender, T.; Lancet, D.; Smit, A. F.; Hubley, R.; Konkel, M. K.; Walker, J. A.; Batzer, M. A.; Gu, W.; Pollock, D. D.; Chen, L.; Cheng, Z.; Eichler, E. E.; Stapley, J.; Slate, J.; Ekblom, R.; Birkhead, T.; Burke, T.; Burt, D.; Scharff, C.; Adam, I.; Richard, H.; Sultan, M.; Soldatov, A.; Lehrach, H.; Edwards, S. V.; Yang, S. P.; Li, X.; Graves, T.; Fulton, L.; Nelson, J.; Chinwalla, A.; Hou, S.; Mardis, E. R.; Wilson, R. K.: The genome of a songbird. Nature 464 (7289), S. 757 - 762 (2010)
128.
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Vidigal, J. A.; Morkel, M.; Wittler, L.; Brouwer-Lehmitz, A.; Grote, P.; Macura, K.; Herrmann, B. G.: An inducible RNA interference system for the functional dissection of mouse embryogenesis. Nucleic Acids Research 38 (11), S. e122 - e122 (2010)
129.
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Kornak, U.; Brancati, F.; Le Merrer, M.; Lichtenbelt, K.; Höhne, W.; Tinschert, S.; Garaci, F. G.; Dallapiccola, B.; Nürnberg, P.: Three novel mutations in the ANK membrane protein cause craniometaphyseal dysplasia with variable conductive hearing loss. American Journal of Medical Genetics Part A 152A (4), S. 870 - 874 (2010)
130.
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Tzschach, A.; Menzel, C.; Erdogan, F.; Istifli, E. S.; Rieger, M.; Ovens-Raeder, A.; Macke, A.; Ropers, H.-H.; Ullmann, R.; Kalscheuer, V. M.: Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangement. American Journal of Medical Genetics. Part A. 152A (4), S. 1008 - 1012 (2010)
131.
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Wang, Y.; Mah, N.; Prigione, A.; Wolfrum, K.; Andrade-Navarro, M. A.; Adjaye, J.: A transcriptional roadmap to the induction of pluripotency in somatic cells. (2010)
132.
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Lesch, K.-P.; Selch, S.; Renner, T. J.; Jacob, C.; Nguyen, T. T.; Hahn, T.; Romanos, M.; Walitza, S.; Shoichet, S.; Dempfle, A. et al.; Heine, M.; Boreatti-Hümmer, A.; Romanos, J.; Gross-Lesch, S.; Zerlaut, H.; Wultsch, T.; Heinzel, S.; Fassnacht, M.; Fallgatter, A.; Allolio, B.; Schäfer, H.; A Warnke, A.; Reif, A. ..; Ropers, H.-H.; Ullmann, R.: Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree1. Molecular Psychiatry, S. 1 - 13 (2010)
133.
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Santigosa, E.; Geay, F.; Tonon, T.; Le Delliou, H.; Kuhl, H.; Reinhardt, R.; Corcos, L.; Cahu, C.; Zambonino-Infante, J. L.; Mazurais, D.: Cloning, tissue expression analysis, and functional characterization of two Δ6-desaturase variants of sea bass (Dicentrarchus labrax L.). Marine Biotechnology 2010, S. epub - epub (2010)
134.
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Budny, B.; Badura-Stronka, M.; Materna-Kiryluk, A.; Tzschach, A.; Raynaud, M.; Latos-Bielenska, A.; Ropers, H.-H.: Novel missense mutations in the ubiquitination-related gene UBE2A cause a recognizable X-linked mental retardation syndrome. Clinical Genetics: an International Journal of Genetics in Medicine 77 (6), S. 541 - 551 (2010)
135.
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Krawitz, P.; Rödelsperger, C.; Jäger, M.; Jostins, L.; Bauer, S.; Robinson, P. N.: Microindel detection in short-read sequence data. Bioinformatics 26 (6), S. 722 - 729 (2010)
136.
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Klopocki, E.; Hennig, B. P.; Dathe, K.; Koll, R.; de Ravel, T.; Baten, E.; Blom, E.; Gillerot, Y.; Weigel, J. F.; Krüger, G. et al.; Hiort, O.; Seemann, P.; Mundlos, S.: Deletion and point mutations of PTHLH cause brachydactyly type E. The American Journal of Human Genetics 86 (3), S. 434 - 439 (2010)
137.
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Qiu, W.; Hu, Y.; Andersen, T. E.; Jafari, A.; Li, N.; Wei Chen, W. C.; Kassem, M.: Tumor necrosis factor receptor superfamily member 19 (TNFRSF19) regulates differentiation fate of human mesenchymal (stromal) stem cells through canonical Wnt signalling and C/EBP. The Journal of Biological Chemistry 285 (19), S. 14438 - 14449 (2010)
138.
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Sharma, C. M.; Hoffmann, S.; Darfeuille, F.; Reignier, J.; Findeiß, S.; Sittka, A.; Chabas, S.; Reiche, K.; Hackermüller, J.; Reinhardt, R. et al.; Stadler, P. F.; Vogel, J.: The primary transcriptome of the major human pathogen Helicobacter pylori. Nature 464 (7286), S. 250 - 255 (2010)
139.
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Zhang, Y.; Jurkowska, R.; Soeroes, S.; Rajavelu, A.; Dhayalan, A.; Bock, I.; Rathert, P.; Brandt, O.; Reinhardt, R.; Fischle, W. et al.; Jeltsch, A.: Chromatin methylation activity of Dnmt3a and Dnmt3a/3L is guided by interaction of the ADD domain with the histone H3 tail. Nucleic Acids Research 38 (13), S. 4246 - 4253 (2010)
140.
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Schlesinger, J.; Tönjes, M.; Schueler, M.; Zhang, Q.; Dunkel, I.; Sperling, S. R.: Evaluation of the LightCycler(R) 1536 Instrument for high-throughput quantitative real-time PCR. Methods 50 (4), S. S19 - S22 (2010)
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