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Lesurtel, M.; Graf, R.; Aleil, B.; Walther, D. J.; Tian, Y.; Jochum, W.; Gachet, C.; Bader, M.; Clavien, P.-A.: Platelet-derived serotonin mediates liver regeneration. Science 312 (5770), S. 104 - 107 (2006)

Dawson, K.; Seemann, P.; Sebald, E.; King, L.; Edwards, M.; Williams III, J.; Mundlos, S.; Krakow, D.: GDF5 Is a Second Locus for Multiple-Synostosis Syndrome. American Journal of Human Genetics (Chicago, IL) 78 (4), S. 708 - 712 (2006)

Klopocki, E.; Fiebig, B.; Robinson, P. N.; Tönnies, H.; Erdogan, F.; Ropers, H.-H.; Mundlos, S.; Ullmann, R.: A novel 8 Mb interstitial deletion of chromosome 8p12-p21.2. American Journal of Medical Genetics Part A 140A (8), S. 873 - 877 (2006)

Kreutzberger, J.: Protein microarrays: a chance to study microorganisms? Applied Microbiology and Biotechnology 70 (4), S. 383 - 390 (2006)

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Rottiers, V.; Motola, D. L.; Gerisch, B.; Cummins, C. L.; Nishiwaki, K.; Mangelsdorf, D. J.; Antebi, A.: Hormonal Control of C. elegans Dauer Formation and Life Span by a Rieske-like Oxygenase. Developmental Cell 10 (4), S. 473 - 482 (2006)

Messer, P. W.; Arndt, P. F.: CorGen-measuring and generating long-range correlations for DNA sequence analysis. Nucleic Acids Research 34, S. W692 - W695 (2006)

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Gilling, M.; Dullinger, J. S.; Gesk, S.; Metzke-Heidemann, S.; Siebert, R.; Meyer, T.; Brondum-Nielsen, K.; Tommerup, N.; Ropers, H.-H.; Tümer, Z. et al.; Kalscheuer, V. M.; Thomas, N. S.: Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)(p11.2q21.2) mutation among Northern Europeans. American Journal of Human Genetics: AJHG / American Society of Human Genetics 78 (5), S. 878 - 883 (2006)

Paszkiewicz, K. H.; Sternberg, M. J. E.; Lappe, M.: Prediction of viable circular permutants using a graph theoretic approach. Bioinformatics 22 (1), S. 1353 - 1358 (2006)

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Steinhoff, C.; Vingron, M.: Review: Normalization and Quantification of Differential Expression. Briefings in Bioinformatics 7 (2), S. 166 - 177 (2006)

Dale, J. K.; Malapert, P.; Chal, J.; Vilhais-Neto, G.; Herrmann, B.; Maroto, M.; Johnson, T.; Jayasinghe, S.; 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)

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Guerasimova, A.; Nyarsik, L.; Liu, J.-P.; Schwartz, R.; Lange, M.; Lehrach, H.; Janitz, M.: Liquid-based hybridization assay with real-time detection in miniaturized array platforms. Biomolecular Engineering 23 (1), S. 35 - 40 (2006)

Kjaer, K. W.; Eiberg, H.; Hansen, L.; van der Hagen, C. B.; Rosendahl, K.; Tommerup, N.; Mundlos, S.: A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2. Journal of Medical Genetics (London) 43 (3), S. 225 - 231 (2006)

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