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), pp. 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), pp. 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), pp. 858 - 865 (2003)

Walther, D. J.; Bader, M.: A unique central tryptophan hydroxylase isoform. Biochemical Pharmacology 66 (9), pp. 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), pp. 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), pp. 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), pp. 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), pp. 12277 - 12282 (2003)

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

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

Borodina, T. A.; Lehrach, H.; Soldatov, A. V.: DNA purification on homemade silica spin-columns. Analytical Biochemistry 321 (1), pp. 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), pp. 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), pp. 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), pp. 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), pp. 2779 - 2787 (2003)

Kaynak, B.; von Heydebreck, A.; Mebas, S.; Seelow, D.; Vogel, J.; Sperling, H.-P.; Pregla, R.; Alexi-Meskishvili, V.; Hetzer, R.; Lange, P. E. et al.; Vingron, M.; Lehrach, H.; Sperling, S.: A genome-wide transcriptional fingerprint of normal and malformed human hearts. Circulation 107, pp. 2467 - 2474 (2003)

Kehrer-Sawatzki, H.; Tinschert, S.; Jenne, D. E.: Heterogeneity of breakpoints in non-LCR-mediated large constitutional deletions of the 17q11.2 NF1 tumour suppressor region. Journal of Medical Genetics 40 (10), p. e116 - e116 (2003)

Kontou, M.; Adelfalk, C.; Hirsch-Kauffmann, M.; Schweiger, M.: Suboptimal action of NF-kappa B in Fanconi anemia cells results from low levels of thioredoxin. Biological Chemistry 384 (10-11), pp. 1501 - 1507 (2003)

Rhyner, C.; Konthur, Z.; Blaser, K.; Crameri, R.: High-throughput isolation of recombinant antibodies against recombinant allergens. BioTechniques 35 (4), pp. 672 - 674 (2003)

Rivals, E.; Rahmann, S.: Combinatorics of periods in strings. Journal of Combinatorial Theory Series A 104 (1), pp. 95 - 113 (2003)