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Tuemer, Z.; Henriksen, A.M.; Bache, I.; Brixen, K.; Kalschauer, V. M.; Illum, N.; Rasmussen, K.; Larsen, L.A.; Tommerup, N.: : Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome. American Journal of Medical Genetics: Part A 135 (3), S. 339 - 341 (2005)

Henrich, T.; Ramialison, M.; Wittbrodt, B.; Assouline, B.; Bourrat, F.; Berger, A.; Himmelbauer, H.; Sasaki, T.; Shimizu, N.; Westerfield, M. et al.; Kondoh, H.; Wittbrodt, J.: MEPD: a resource for medaka gene expression patterns. Bioinformatics 21 (14), S. 3195 - 3197 (2005)

Shpanchenko, O. V.; Zvereva, M. I.; Ivanov, P. V.; Bugaeva, E. Y.; Rozov, A. S.; Bogdanov, A. A.; Kalkum, M.; Isaksson, L. A.; Nierhaus, K. H.; Dontsova, O. A.: Stepping tmRNA through the ribosome. Journal of Biological Chemistry 280 (18), S. 18368 - 18374 (2005)

Borg, I.; Freude, K.; Kuebart, S.; Hoffmann, K.; Menzel, C.; Laccone, F.; Firth, H.; Ferguson-Smith, M. A.; Tommerup, N.; Ropers, H.-H. et al.; Sargan, D.; Kalscheuer, V. M.: Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome. European Journal of Human Genetics 13 (8), S. 921 - 927 (2005)

Roepcke, S.; Grossmann, S.; Rahmann, S.; Vingron, M.: T-Reg Comparator: an analysis tool for the comparison of position weight matrices. Web Server Issue, S. W438 - W341 (2005)

Schnütgen, F.; De-Zolt, S.; Van Sloun, P.; Hollatz, M.; Floss, T.; Hansen, J.; Altschmied, J.; Seisenberger, C.; Ghyselinck, N. B.; Ruiz, P. et al.; Chambon, P.; Wurst, W.; von Melchner, H.: Genomewide production of multipurpose alleles for the functional analysis of the mouse genome. Proceedings of the National Academy of Sciences of the United States of America (Washington, DC) 102 (20), S. 7221 - 7226 (2005)

Cepok, S.; Zhou, D.; Srivastava, R.; Nessler, S.; Stei, S.; Büssow, K.; Sommer, N.; Hemmer, B.: Identification of Epstein-Barr virus proteins as putative targets of the immune response in multiple sclerosis. Journal of Clinical Investigation (New York, NY) 115 (5), S. 1352 - 1360 (2005)

Resch-Genger, U.; Hoffmann, K.; Nietfeld, W.; Engel, A.; Neukammer, J.; Nitschke, R.; Ebert, P.; Macdonald, R.: How to improve quality assurance in fluorometry: fluorescence-inherent sources of error and suited fluorescence standards. Journal of Fluorescence 15 (3), S. 337 - 362 (2005)

Roig, I.; Robles, P.; Garcia, R.; Martínez-Flores, I.; Cabero, L. l.; Egozcue, J.; Liebe, B.; Scherthan, H.; Garcia, M.: Chromosome 18 pairing behavior in human trisomic oocytes. Presence of an extra chromosome extends bouquet stage. Reproduction: the Journal of the Society for Reproduction and Fertility 129 (5), S. 565 - 575 (2005)

Toedling, J.; Schmeier, S.; Heinig, M.; Georgi, B.; Roepcke, S.: MACAT—microarray chromosome analysis tool. Bioinformatics 21 (9), S. 2112 - 2113 (2005)

Ziegelin, G.; Tegtmeyer, N.; Lurz, R.; Hertwig, S.; Hammerl, J.; Appel, B.; Lanka, E.: The repA gene of the linear Yersinia enterocolitica prophage PY54 functions as a circular minimal replicon in Escherichia coli. Journal of Bacteriology 187 (10), S. 3445 - 3454 (2005)

Roepcke, S.; Fiziev, P.; Seeburg, P. H.; Vingron, M.: SVC: structured visualization of evolutionary sequence conservation. Web Server Issue, S. W271 - W273 (2005)

Schröder, G.; Lanka, E.: The mating pair formation system of conjugative plasmids—A versatile secretion machinery for transfer of proteins and DNA. Plasmid 54 (1), S. 1 - 25 (2005)

Jaeger, J.; Weichenhan, D.; Ivandic, B.; Spang, R.: Early diagnostic marker panel determination for microarray based clinical studies. Statistical Applications in Genetics and Molecular Biology 4 (1), S. Article 9 - Article 9 (2005)

Steller, S.; Angenendt, P.; Cahill, D. J.; Heuberger, S.; Lehrach, H.; Kreutzberger, J.: Bacterial protein microarrays for identification of new potential diagnostic markers for Neisseria meningitidis infections. PROTEOMICS 5 (8), S. 2048 - 2055 (2005)

Horváth, J.; Fliegauf, M.; Olbrich, H.; Kispert, A.; King, S. M.; Mitchison, H.; Zariwala, M. A.; Knowles, M. R.; Sudbrak, R.; Fekete, G. et al.; Neesen, J.; Reinhardt, R.; Omran, H.: Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients. American Journal of Respiratory Cell and Molecular Biology 33 (1), S. 41 - 47 (2005)

Horváth, J.; Fliegauf, M.; Olbrich, H.; Kispert, A.; King, S. M.; Mitchison, H.; Zariwala, M. A.; Knowles, M. R.; Sudbrak, R.; Fekete, G. et al.; Neesen, J.; Reinhardt, R.; Omran, H.: Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients. American Journal of Respiratory Cell and Molecular Biology 33 (1), S. 41 - 47 (2005)

Backsch, C.; Rudolph, B.; Kuehne-Hei, R.; Kalscheuer, V.; Bartsch, O.; Jansen, L.; Beer, K.; Meyer, B.; Schneider, A.; Duerst, M.: A region on human chromosome 4 (q35.1-->qter) induces senescence in cell hybrids and is involved in cervical carcinogenesis. Genes Chromosomes & Cancer 43 (12), S. 260 - 267 (2005)

Greber, B.; Tandara, H.; Lehrach, H.; Himmelbauer, H.: Comparison of PCR-based mutation detection methods and application for identification of mouse Sult1a1 mutant embryonic stem cell clones using pooled templates. Human Mutation 25 (5), S. 483 - 490 (2005)