Frints, S. G. M.; Jun, L.; Fryns, J.-P.; Devriendt, K.; Teulingkx, R.; Van den Berghe, L.; De Vos, B.; Borghgraef, M.; Chelly, J.; Des Portes, V. et al.; Van Bokhoven, H.; Hamel, B.; Ropers, H.-H.; Kalscheuer, V.; Raynaud, M.; Moraine, C.; Marynen, P.; Froyen, G.: Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: Clinical study and mutation analysis of the NXF5 gene. American Journal of Medical Genetics Part A 119A (3), S. 367 - 374 (2003)

Trelles-Sticken, E.; Loidl, J.; Scherthan, H.: Increased ploidy and KAR3 and SIR3 disruption alter the dynamics of meiotic chromosomes and telomeres. Journal of Cell Science 116 (12), S. 2431 - 2442 (2003)

Dieterich, C.; Herwig, R.; Vingron, M.: Exploring potential target genes of signaling pathways by predicting conserved transcription factor binding sites. Bioinformatics 19 (Suppl. 2), S. ii50 - ii56 (2003)

Agmon, I.; Auerbach, T.; Baram, D.; Bartels, H.; Bashan, A.; Berisio, R.; Fucini, P.; Hansen, H. A. S.; Harms, J.; Kessler, M. et al.; Peretz, M.; Schluenzen, F.; Yonath, A.; Zarivach, R.: On peptide bond formation, translocation, nascent protein progression and the regulatory properties of ribosomes - Delivered on 20 October 2002 at the 28th FEBS Meeting in Istanbul. European Journal of Biochemistry 270 (12), S. 2543 - 2556 (2003)

Arndt, P. F.; Burge, C. B.; Hwa, T.: DNA sequence evolution with neighbor-dependent mutation. Journal of Computational Biology 10 (3-4), S. 313 - 322 (2003)

Kalscheuer, V. M.; Tao, J.; Donnelly, A.; Hollway, G.; Schwinger, E.; Kubart, S.; Menzel, C.; Hoeltzenbein, M.; Tommerup, N.; Eyre, H. et al.; Harbord, M.; Haan, E.; Sutherland, G. R.; Ropers, H.-H.; Gécz, J.: Disruption of the Serine/Threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation. American Journal of Human Genetics 72 (6), S. 1401 - 1411 (2003)

Klempa, B.; Ulrich, R.; Meisel, H.; Krüger, D. H.; Schmidt, H. A.; Kaluz, S.; Labuda, M.; Hjelle, B.: Genetic interaction between Dobrava and Saaremaa hantaviruses: Now or millions of years ago? (Author's Reply). Journal of Virology 77 (12), S. 7157 - 7158 (2003)

Panopoulou, G.; Hennig, S.; Groth, D.; Krause, A.; Poustka, A. J.; Herwig, R.; Vingron, M.; Lehrach, H.: New evidence for genome-wide duplications at the origin of vertebrates using an amphioxus gene set and completed animal genomes. Genome Research 13 (6), S. 1056 - 1066 (2003)

Ropers, H.-H.; Hoeltzenbein, M.; Kalscheuer, V.; Yntema, H.; Hamel, B.; Fryns, J.-P.; Chelly, J.; Partington, M.; Gecz, J.; Moraine, C.: Nonsyndromic X-linked mental retardation: where are the missing mutations? Trends in Genetics 19 (6), S. 316 - 320 (2003)

Sauer, S.; Lehrach, H.; Reinhardt, R.: MALDI mass spectrometry analysis of single nucleotide polymorphisms by photocleavage and charge-tagging. Nucleic Acids Research 31 (11), e63 (2003)

Margot, J. B.; Ehrenhofer-Murray, A. E.; Leonhardt, H.: Interactions within the mammalian DNA methyltransferase family. BMC Molecular Biology 4, 7 (2003)

Kaynak, B.; von Heydebreck, A.; Mebus, S.; Seelow, D.; Hennig, S.; Vogel, J.; Sperling, H.-P.; Pregla, R.; Alexi-Meskishvili, V.; Hetzer, R. et al.; Lange, P. E.; Vingron, M.; Lehrach, H.; Sperling, S.: Genome-wide array analysis of normal and malformed human hearts. Circulation 107 (19), S. 2467 - 2474 (2003)

Stock, M.; Schafer, H.; Stricker, S.; Gross, G.; Mundlos, S.; Otto, F.: Expression of galectin-3 in skeletal tissues is controlled by Runx2. Journal of Biological Chemistry 278 (19), S. 17360 - 17367 (2003)

Spang, R.: Diagnostic signatures from microarrays: a bioinformatics concept for personalized medicine. BIOSILICO 1 (2), S. 64 - 68 (2003)

Bienvenu, T.; Poirier, K.; Van Esch, H.; Hamel, B.; Moraine, C.; Fryns, J. P.; Ropers, H. H.; Beldjord, C.; Yntema, H. G.; Chelly, J.: Rare polymorphic variants of the AGTR2 gene in boys with non-specific mental retardation. Journal of Medical Genetics 40 (5), S. 357 - 359 (2003)

Hertwig, S.; Klein, I.; Lurz, R.; Lanka, E.; Appel, B.: PY54, a linear plasmid prophage of Yersinia enterocolitica with covalently closed ends. Molecular Microbiology 48 (4), S. 989 - 1003 (2003)

Höltje, M.; Winter, S.; Walther, D.; Pahner, I.; Hörtnagl, H.; Ottersen, O. P.; Bader, M.; Ahnert-Hilger, G.: The vesicular monoamine content regulates VMAT2 activity through Gq in mouse platelets. Journal of Biological Chemistry 278 (18), S. 15850 - 15858 (2003)

Pesch, K.; Zeitz, C.; Fries, J. E.; Muenscher, S.; Pusch, C. M.; Kohler, K.; Berger, W.; Wissinger, B.: Isolation of the mouse nyctalopin gene Nyx and expression studies in mouse and rat retina. Investigative Ophthalmology & Visual Science 44 (5), S. 2260 - 2266 (2003)

Savvides, S. N.; Yeo, H.-J.; Beck, M. R.; Blaesing, F.; Lurz, R.; Lanka, E.; Buhrdorf, R.; Fischer, W.; Haas, R.; Waksman, G.: VirB11 ATPases are dynamic hexameric assemblies: new insights into bacterial type IV secretion. EMBO Journal 22 (9), S. 1969 - 1980 (2003)

Stock, M.; Schäfer, H.; Stricker, S.; Gross, G.; Mundlos, S.; Otto, F.: Expression of galectin-3 in skeletal tissues is controlled by Runx2. Journal of Biological Chemistry 278 (19), S. 17360 - 17367 (2003)