Suchergebnisse

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)

Borodina, T. A.; Lehrach, H.; Soldatov, A. V.: DNA purification on homemade silica spin-columns. Analytical Biochemistry 321 (1), S. 135 - 137 (2003)

Gautschi, M.; Just, S.; Mun, A.; Ross, S.; Rücknagel, P.; Dubaquie, Y.; Ehrenhofer-Murray, A.; Rospert, S.: The yeast N-alpha-acetyltransferase NatA is quantitatively anchored to the ribosome and interacts with nascent polypeptides. Molecular and Cellular Biology 23 (20), S. 7403 - 7414 (2003)

Gunawan, B.; von Heydebreck, A.; Fritsch, T.; Huber, W.; Ringert, R.-H.; Jakse, G.; Fuezesi, L.: Cytogenetic and morphologic typing of 58 papillary renal cell carcinomas: Evidence for a cytogenetic evolution of type 2 from type 1 tumors. Cancer Research 63 (19), S. 6200 - 6205 (2003)

Haas, S. A.; Hild, M.; Wright, A. P. H.; Hain, T.; Talibi, D.; Vingron, M.: Genome-scale design of PCR primers and long oligomers for DNA microarrays. Nucleic Acids Research 31 (19), S. 5576 - 5581 (2003)

Heldt, C.; Listing, J.; Sozeri, O.; Blasing, F.; Frischbutter, S.; Mueller, B.: Differential expression of HLA class II genes associated with disease susceptibility and progression in rheumatoid arthritis. Arthritis and Rheumatism 48 (10), S. 2779 - 2787 (2003)