Publications

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Kowald, A.; Klipp, E.: Alternative pathways might mediate toxicity of high concentrations of superoxide dismutase. Annals of the New York Academy of Sciences 1019, pp. 370 - 374 (2004)

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Meierhofer, D.; Mayr, J. A.; Foetschl, U.; Berger, A.; Fink, K.; Schmeller, N.; Hacker, G. W.; Hauser-Kronberger, C.; Kofler, B.; Sperl, W.: Decrease of mitochondrial DNA content and energy metabolism in renal cell carcinoma. Carcinogenesis 25 (6), pp. 1005 - 1010 (2004)

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publisher-version

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Scharff, C.; White, S. A.: Genetic components of vocal learning. Annals of the New York Academy of Sciences 1016, pp. 325 - 347 (2004)

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Skarnes, W. C.; von Melchner, H.; Wurst, W.; Hicks, G.; Nord, A. S.; Cox, T.; Young, S. G.; Ruiz, P.; Soriano, P.; Tessier-Lavigne, M. et al.; Conklin, B. R.; Stanford, W. L.; Rossant, J.: A public gene trap resource for mouse functional genomics. Nature Genetics 36 (6), pp. 543 - 544 (2004)

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Shi, W.; van den Hurk, J. A. J. M.; Alamo-Bethencourt, V.; Mayer, W.; Winkens, H. J.; Ropers, H.-H.; Cremers, F. P. M.; Fundele, R.: Choroideremia gene product affects trophoblast development and vascularization in mouse extra-embryonic tissues. Developmental Biology 272 (1), pp. 53 - 65 (2004)

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DNA sequence and comparative analysis of chimpanzee chromosome 22. Nature 429 (6990), pp. 382 - 388 (2004)

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Freude, K.; Hoffmann, K.; Jensen, L.-R.; Delatycki, M. B.; des Portes, V.; Moser, B.; Hamel, B.; van Bokhoven, H.; Moraine, C.; Fryns, J.-P. et al.; Chelly, J.; Gécz, J.; Lenzner, S.; Kalscheuer, V. M.; Ropers, H.-H.: Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation. American Journal of Human Genetics 75 (2), pp. 305 - 309 (2004)

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Rosenberg, E. H.; Almeida, L. S.; Kleefstra, T.; deGrauw, R. S.; Yntema, H. G.; Bahi, N.; Moraine, C.; Ropers, H.-H.; Fryns, J.-P.; deGrauw, T. J. et al.; Jakobs, C.; Salomons, G. S.: High prevalence of SLC6A8 deficiency in X-linked mental retardation. American Journal of Human Genetics 75, pp. 97 - 105 (2004)

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Ehrenhofer-Murray, A. E.: Chromatin dynamics at DNA replication, transcription and repair. European Journal of Biochemistry 271 (12), pp. 2335 - 2349 (2004)

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Revenkova, E.; Eijpe, M.; Heyting, C.; Hodges, C. A.; Hunt, P. A.; Liebe, B.; Scherthan, H.; Jessberger, R.: Cohesin SMC1b is required for meiotic chromosome dynamics, sister chromatid cohesion and DNA recombination. Nature Cell Biology 6 (6), pp. 555 - 562 (2004)

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Mulvihill, E. R.; Jaeger, J.; Sengupta, R.; Ruzzo, W. L.; Reimer, C.; Lukito, S.; Schwartz, S. M.: Atherosclerotic plaque smooth muscle cells have a distinct phenotype. Arteriosclerosis, Thrombosis, and Vascular Biology: an Official Journal of the American Heart Association 24 (7), pp. 1283 - 1289 (2004)

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Anokhina, M. M.; Barta, A.; Nierhaus, K. H.; Spiridonova, V. A.; Kopylov, A. M.: Mapping of the second tetracycline binding site on the ribosomal small subunit of E.coli. Nucleic Acids Research 32 (8), pp. 2594 - 2597 (2004)

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Kramer, A.; Feilner, T.; Possling, A.; Radchuk, V.; Weschke, W.; Buerkle, L.; Kersten, B.: Identification of barley CK2alpha targets by using the protein microarray technology. Phytochemistry: an International Journal of Plant Biochemistry 65 (12), pp. 1777 - 1784 (2004)

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Stacher, E.; Ullmann, R.; Halbwedl, I.; Gogg-Kammerer, M.; Boccon-Gibod, L.; Nicholson, A. G.; Sheppard, M. N.; Carvalho, L.; Franca, M. T.; MacSweeney, F. et al.; Morresi-Hauf, A.; Popper, H. H.: Atypical goblet cell hyperplasia in congenital cystic adenomatoid malformation as a possible preneoplasia for pulmonary adenocarcinoma in childhood: A genetic analysis. Human Pathology 35 (5), pp. 565 - 570 (2004)

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Jung, R.; Wendeler, M. W.; Danevad, M.; Himmelbauer, H.; Gessner, R.: Phylogenetic origin of LI-cadherin revealed by protein and gene structure analysis. Cellular and Molecular Life Science 61 (10), pp. 1157 - 1166 (2004)

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Rajab, A.; Kunze, J.; Mundlos, S.: Spondyloepiphyseal dysplasia omani type: A new recessive type of SED with progressive spinal involvement. American Journal of Medical Genetics 126A (4), pp. 413 - 419 (2004)

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Ramirez, A.; Faupel, J.; Goebel, I.; Stiller, A.; Beyer, S.; Stockle, C.; Hasan, C.; Bode, U.; Kornak, U.; Kubisch, C.: Identification of a novel mutation in the coding region of the grey-lethal gene OSTM1 in human malignant infantile osteopetrosis. Human Mutation 23 (5), pp. 471 - 476 (2004)

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Takacs, C. M.; Amore, G.; Oliveri, P.; Poustka, A. J.; Wang, D.; Burke, R. D.; Peterson, K. J.: Expression of an NK2 homeodomain gene in the apical ectoderm defines a new territory in the early sea urchin embryo. Developmental Biology 269 (1), pp. 152 - 164 (2004)

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Timmermann, B.; Sauer, S.; Dahl, A.; Reinhardt, R.: Genetische Variabilität des Menschen: Hochdurchsatz- Technologien und Datenanalyse. Laborwelt 5 (5), pp. 31 - 32 (2004)

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Krenn, V.; Petersen, I.; Haeupl, T.; Koepenik, A.; Blind, C.; Dietel, M.; Konthur, Z.; Skriner, K.: Array technology and proteomics in autoimmune diseases. Proteomics in Pathology, Research and Practice, pp. 95 - 103 (2004)

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Journal Article (189)