Suchergebnisse

Sperling, S.: Angeborene Herzfehler als molekulares Puzzle. Laborwelt 5 (5), S. 10 - 13 (2004)

Steinhoff, C.; Schulz, W. A.: Transcriptional regulation of the human LINE-1 retrotransposon L1.2B. Molecular Genetics and Genomics 270 (5), S. 394 - 402 (2004)

Timmermann, B.; Sauer, S.; Omran, H.; Sudbrak, R.; Reinhardt, R.: Vergleichende Sequenzierung von Kandidatengenen: die Resequencing-Plattform am MPI-MG. GenomXPress: Informationen aus der Deutschen Genomforschung 2004 (1), S. 17 - 19 (2004)

von Heydebreck, A.; Sperling, S.; Kaynak, B.; Lehrach, H.; Vingron, M.: Genexpressionsanalyse komplexer klinischer Phänotypen mittels cDNS-Arrays - Gene Expression Profiling of Complex Clinical Phenotypes using cDNA-Arrays. it - Information Technology 46 (1), S. 26 - 30 (2004)

Xue, Y. T.; Haas, S.; Brino, L.; Gusnanto, A.; Riemers, M.; Talibi, D.; Vingron, M.; Ekwall, K.; Wright, A. P. H.: A DNA microarray for fission yeast: minimal changes in global gene expression after temperature shift. Yeast 21 (1), S. 25 - 39 (2004)

Zhou, H.-M.; Weskamp, G.; Chesneau, V.; Sahin, U.; Vortkamp, A.; Horiuchi, K.; Chiusaroli, R.; Hahn, R.; Wilkes, D.; Fisher, P. et al.; Baron, R.; Manova, K.; Basson, C. T.; Hempstead, B.; Blobel, C. P.: Essential role for ADAM19 in cardiovascular morphogenesis. Molecular and Cellular Biology 24 (1), S. 96 - 104 (2004)

Walther, D. J.; Peter, J.-U.; Winter, S.; Holtje, M.; Paulmann, N.; Grohmann, M.; Vowinckel, J.; Alamo-Bethencourt, V.; Wilhelm, C. S.; Ahnert-Hilger, G. et al.; Bader, M.: Serotonylation of small GTPases is a signal transduction pathway that triggers platelet alpha-granule release. Cell 115 (7), S. 851 - 862 (2003)

Walther, D. J.; Peter, J.-U.; Winter, S.; Hötje, M.; Paulmann, N.; Grohmann, M.; Vowinckel, J.; Alamo-Bethencourt, V.; Wilhelm, C. S.; Ahnert-Hilger, G. et al.; Bader, M.: Serotonylation of small GTPases is a signal transduction pathway that triggers platelet -granule release. Cell 115 (7), S. 851 - 862 (2003)

Hild, M.; Beckmann, B.; Haas, S. A.; Koch, B.; Solovyev, V.; Busold, C.; Fellenberg, K.; Boutros, M.; Vingron, M.; Sauer, F. et al.; Hoheisel, J. D.; Paro, R.: An integrated gene annotation and transcriptional profiling approach towards the full gene content of the Drosophila genome. Genome Biology 5 (1), S. R3 - R3 (2003)

Krüger, M.; Meyerdierks, A.; Glöckner, F. O.; Amann, R.; Widdel, F.; Kube, M.; Reinhardt, R.; Kahnt, J.; Böcher, R.; Thauer, R. K. et al.; Shima, S.: A conspicuous nickel protein in microbial mats that oxidize methane anaerobically. Nature 426 (6968), S. 878 - 881 (2003)

Dostal, L.; Khare, D.; Bok, J.; Heinemann, U.; Lanka, E.; Welfle, H.: RP4 repressor protein KorB binds to the major groove of the operator DNA: A Raman study. Biochemistry 42 (49), S. 14476 - 14482 (2003)

Burgtorf, C.; Kepper, P.; Hoehe, M.; Schmitt, C.; Reinhardt, R.; Lehrach, H.; Sauer, S.: Clone-based systematic haplotyping (CSH): A procedure for physical haplotyping of whole genomes. Genome Research 13 (12), S. 2717 - 2724 (2003)

Connell, S. R.; Tracz, D. M.; Nierhaus, K. H.; Taylor, D. E.: Ribosomal protection proteins and their mechanism of tetracycline resistance. Antimicrobial Agents and Chemotherapy 47 (12), S. 3675 - 3681 (2003)

Gomot, M.; Gendrot, C.; Verloes, A.; Raynaud, M.; David, A.; Yntema, H. G.; Dessay, S.; Kalscheuer, V.; Frints, S.; Convert, P. et al.; Briault, S.; Blesson, S.; Toutain, A.; Chelly, J.; Desportes, V.; Moraine, C.: MECP2 gene mutations in non-syndromic X-linked mental retardation: Phenotype-genotype correlation. American Journal of Medical Genetics Part A 123A (2), S. 129 - 139 (2003)

Kalscheuer, V. M.; Freude, K.; Musante, L.; Jensen, L. R.; Yntema, H. G.; Gecz, J.; Sefiani, A.; Hoffmann, K.; Moser, B.; Haas, S. et al.; Gurok, U.; Haesler, S.; Aranda, B.; Nshedjan, A.; Tzschach, A.; Hartmann, N.; Roloff, T.-C.; Shoichet, S.; Hagens, O.; Tao, J.; van Bokhoven, H.; Turner, G.; Chelly, J.; Moraine, C.; Fryns, J.-P.; Nuber, U.; Hoeltzenbein, M.; Scharff, C.; Scherthan, H.; Lenzner, S.; Hamel, B. C. J.; Schweiger, S.; Ropers, H.-H.: Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation. Nature Genetics 35 (4), S. 313 - 315 (2003)

Lueking, A.; Possling, A.; Huber, O.; Beveridge, A.; Horn, M.; Eickhoff, H.; Schuchardt, J.; Lehrach, H.; Cahill, D. J.: A nonredundant human protein chip for antibody screening and serum profiling. Molecular & Cellular Proteomics 2 (12), S. 1342 - 1349 (2003)

Minguillon, C.; Jimenez-Delgado, S.; Panopoulou, G.; Garcia-Fernandez, J.: The amphioxus Hairy family: differential fate after duplication. Development 130 (24), S. 5903 - 5914 (2003)

Mueller, U.; Büssow, K.; Diehl, A.; Bartl, F. J.; Niesen, F. H.; Nyarsik, L.; Heinemann, U.: Rapid purification and crystal structure analysis of a small protein carrying two terminal affinity tags. Journal of Structural and Functional Genomics 4 (4), S. 217 - 225 (2003)

Poustka, A. J.; Groth, D.; Hennig, S.; Thamm, S.; Cameron, A.; Beck, A.; Reinhardt, R.; Herwig, R.; Panopoulou, G.; Lehrach, H.: Generation, annotation, evolutionary analysis, and database integration of 20,000 unique sea urchin EST clusters. Genome Research 13 (12), S. 2736 - 2746 (2003)

Salomonsen, J.; Marston, D.; Avila, D.; Bumstead, N.; Johansson, B.; Juul-Madsen, H.; Olesen, G. D.; Riegert, P.; Skjodt, K.; Vainio, O. et al.; Wiles, M. V.; Kaufman, J.: The properties of the single chicken MHC classical class II alpha chain (B-LA) gene indicate an ancient origin for the DR/E-like isotype of class II molecules. Immunogenetics 55 (9), S. 605 - 614 (2003)