Suchergebnisse

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)

Glokler, J.; Angenendt, P.: Protein and antibody microarray technology. Interactions in Biological Systems, S. 229 - 240 (2003)

Hejnar, J. r. Ä.; Elleder, D.; Hajkova, P.; Walter, J.; Blazkova, J.; Svoboda, J.: Demethylation of host-cell DNA at the site of avian retrovirus integration. Biochemical and Biophysical Research Communications 311 (3), S. 641 - 648 (2003)

Adelfalk, C.; Kontou, M.; Hirsch-Kauffmann, M.; Schweiger, M.: Physical and functional interaction of the Werner syndrome protein with poly-ADP ribosyl transferase. FEBS Letters 554 (1-2), S. 55 - 58 (2003)

Arndt, P. F.; Petrov, D. A.; Hwa, T.: Distinct changes of genomic biases in nucleotide substitution at the time of mammalian radiation. Molecular Biology and Evolution 20 (11), S. 1887 - 1896 (2003)

Hoefele, J.; Sudbrak, R.; Otto, E.; Imm, A.; O'Toole, J.; Hildebrandt, F.: Mutational analysis in nephronophthisis type 4. Journal of the American Society of Nephrology 14 (Suppl. S), S. 359A - 359A (2003)

Hoehe, M. R.; Timmermann, B.; Lehrach, H.: Human inter-individual DNA sequence variation in candidate genes, drug targets, the importance of haplotypes and pharmacogenomics. Current Pharmaceutical Biotechnology 4 (6), S. 351 - 378 (2003)

Riebeling, P.; Polz, S.; Tost, F.; Weiss, J. S.; Kuivaniemi, H.; Hoeltzenbein, M.: Schnyder's crystalline corneal dystrophy. Further narrowing of the linkage interval at chromosome 1p34.1-p36? Ophthalmologe 100 (11), S. 979 - 983 (2003)

Shoichet, S. A.; Hoffmann, K.; Menzel, C.; Trautmann, U.; Moser, B.; Hoeltzenbein, M.; Echenne, B.; van Bokhoven, H.; Moraine, C.; Fryns, J.-P. et al.; Chelly, J.; Rott, H.-D.; Ropers, H.-H.; Kalscheuer, V. M.: Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation. American Journal of Human Genetics 73 (6), S. 1341 - 1354 (2003)

Tuerkmen, S.; Gillessen-Kaesbach, G.; Meinecke, P.; Albrecht, B.; Neumann, L. M.; Hesse, V.; Palanduz, S.; Balg, S.; Majewski, F.; Fuchs, S. et al.; Zschieschang, P.; Greiwe, M.; Mennicke, K.; Kreuz, F. R.; Dehmel, H. J.; Rodeck, B.; Kunze, J.; Tinschert, S.; Mundlos, S.; Horn, D.: Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes. European Journal of Human Genetics 11 (11), S. 858 - 865 (2003)

Walther, D. J.; Bader, M.: A unique central tryptophan hydroxylase isoform. Biochemical Pharmacology 66 (9), S. 1673 - 1680 (2003)

Busch, A.; Engemann, S.; Lurz, R.; Okazawa, H.; Lehrach, H.; Wanker, E. E.: Mutant huntingtin promotes the fibrillogenesis of wild-type huntingtin - A potential mechanism for loss of huntingtin function in Huntington's disease. Journal of Biological Chemistry 278 (42), S. 41452 - 41461 (2003)

Busch, A.; Engemann, S.; Lurz, R.; Okazawa, H.; Lehrach, H.; Wanker, E. E.: Mutant huntingtin promotes the fibrillogenesis of wild-type huntingtin - A potential mechanism for loss of huntingtin function in Huntington's disease. Journal of Biological Chemistry 278 (42), S. 41452 - 41461 (2003)

Ziegelin, G.; Niedenzu, T.; Lurz, R.; Saenger, W.; Lanka, E.: Hexameric RSF1010 helicase RepA: the structural and functional importance of single amino acid residues. Nucleic Acids Research 31 (20), S. 5917 - 5929 (2003)

Lehmann, K.; Seemann, P.; Stricker, S.; Sammar, M.; Meyer, B.; Suering, K.; Majewski, F.; Tinschert, S.; Grzeschik, K.-H. H.; Mueller, D. et al.; Knaus, P.; Nurnberg, P.; Mundlos, S.: Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2. Proceedings of the National Academy of Sciences of the United States of America 100 (21), S. 12277 - 12282 (2003)

Fernandez-Capetillo, O.; Liebe, B.; Scherthan, H.; Nussenzweig, A.: H2AX regulates meiotic telomere clustering. Journal of Cell Biology 163 (1), S. 15 - 20 (2003)

Manke, T.; Bringas, R.; Vingron, M.: Correlating protein-DNA and protein-protein interaction networks. Journal of Molecular Biology 333 (1), S. 75 - 85 (2003)