Suchergebnisse

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, S. 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), S. 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), S. 1501 - 1507 (2003)

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

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

Schubbe, S.; Kube, M.; Scheffel, A.; Wawer, C.; Heyen, U.; Meyerdierks, A.; Madkour, M. H.; Mayer, F.; Reinhardt, R.; Schuler, D.: Characterization of a spontaneous nonmagnetic mutant of Magnetospirillum gryphiswaldense reveals a large deletion comprising a putative magnetosome island. Journal of Bacteriology 185 (19), S. 5779 - 5790 (2003)

Strauch, E.; Goelz, G.; Knabner, D.; Konietzny, A.; Lanka, E.; Appel, B.: A cryptic plasmid of Yersinia enterocolitica encodes a conjugative transfer system related to the regions of CloDF13 Mob and IncX Pil. Microbiology-SGM 149 (10), S. 2829 - 2845 (2003)

Volleth, M.; Stumm, M.; Kaischeuer, V. M.; Reschke, K.; Liehr, T.; Wieacker, P.: Premature ovarian failure in a woman with an unusual pseudoisodicentric X chromosome. Geburtshilfe und Frauenheilkunde 63 (10), S. 1054 - 1057 (2003)

Zeitz, C.; Scherthan, H.; Freier, S.; Feil, S.; Suckow, V.; Schweiger, S.; Berger, W.: NYX (Nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein. Investigative Ophthalmology & Visual Science 44 (10), S. 4184 - 4191 (2003)

Beißbarth, T.; Borisevich, I.; Hörlein, A.; Kenzelmann, M.; Hergenhahn, M.; Klewe-Nebenius, A.; Klären, R.; Korn, B.; Schmid, W.; Vingron, M. et al.; Schütz, G.: Analysis of CREM-dependent gene expression during mouse spermatogenesis. Molecular and Cellular Endocrinology 212 (1-2), S. 29 - 39 (2003)

Fahrig, R.; Heinrich, J. C.; Nickel, B.; Wilfert, F.; Leisser, C.; Krupitza, G.; Praha, C.; Sonntag, D.; Fiedler, B.; Scherthan, H. et al.; Ernst, H.: Inhibition of induced chemoresistance by cotreatment with (E)-5-(2-bromovinyl)-2'-deoxyuridine (RP101). Cancer Research 63 (18), S. 5745 - 5753 (2003)

Most, P.; Remppis, A.; Pleger, S. T.; Loffler, E.; Ehlermann, P.; Bernotat, J.; Kleuss, C.; Heierhorst, J.; Ruiz, P.; Witt, H. et al.; Karczewski, P.; Mao, L.; Rockman, H. A.; Duncan, S. J.; Katus, H. A.; Koch, W. J.: Transgenic overexpression of the Ca2+-binding protein S100A1 in the heart leads to increased in vivo myocardial contractile performance. Journal of Biological Chemistry 278 (36), S. 33809 - 33817 (2003)

Angenendt, P.; Glokler, J.; Konthur, Z.; Lehrach, H.; Cahill, D. J.: 3D protein microarrays: Performing multiplex immunoassays on a single chip. Analytical Chemistry 75 (17), S. 4368 - 4372 (2003)

Bonne, A.; Gosele, C.; den Bieman, M.; Gillissen, G.; Kreitler, T.; Pravenec, M.; Kren, V.; van Lith, H.; van Zutphen, B.: Sequencing and chromosomal localization of Fabp6 and an intronless Fabp6 segment in the rat. Molecular Biology Reports 30 (3), S. 173 - 176 (2003)

Engeli, S.; Baranov, S.; Soldatov, A.; Lehrach, H.; Luft, F. C.; Sharma, A. M.: Differential expression of human adipose-tissue genes in obesity-hypertension. Hypertension 42 (3), S. 422 - 422 (2003)

Engels, H.; Ehrbrecht, A.; Zahn, S.; Bosse, K.; Vrolijk, H.; White, S.; Kalscheuer, V.; Hoovers, J. M. N.; Schwanitz, G.; Propping, P. et al.; Tanke, H. J.; Wiegant, J.; Raap, A. K.: Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation. European Journal of Human Genetics 11 (9), S. 643 - 651 (2003)

Hoehe, M. R.: Haplotypes and the systematic analysis of genetic variation in genes and genomes. Pharmacogenomics 4 (5), S. 571 - 582 (2003)

Kornak, U.; Mundlos, S.: Genetic disorders of the skeleton: a developmental approach. American Journal of Human Genetics 73 (3), S. 447 - 474 (2003)

Lottaz, C.; Iseli, C.; Jongeneel, C. V.; Bucher, P.: Modeling sequencing errors by combining Hidden Markov models. Proceedings of the European Conference on Computational Biology (ECCB 2003), S. ii103 - ii112 (2003)

Meunier, D.; Peters, T.; Lüttges, A.; Curfs, J.; Fundele, R.: Preferential expression of the G90 gene in post-mitotic cells during mouse embryonic development. Anatomy and Embryology 207 (2), S. 109 - 117 (2003)