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Huels, C.; Muellner, S.; Meyer, E.; Cahill, D. J.: The impact of protein biochips and microarrays on the drug development process. Drug Discovery Today 7 (18), pp. 119 - 124 (2002)

Gitton, Y.; Dahmane, N.; Baik, S.; i Altaba, A. R.; Neidhardt, L.; Scholze, M.; Herrmann, B. G.; Kahlem, P.; Benkhala, A.; Schrinner, S. et al.; Yildirimman, R.; Herwig, R.; Lehrach, H.; Yaspo, M.-L.: A gene expression map of human chromosome 21 orthologues in the mouse. Nature 420 (6917), pp. 586 - 590 (2002)

Grünweller, A.; Ehrenhofer-Murray, A. E.: A Novel Yeast Silencer: The 2µ Origin of Saccharomyces cerevisiae Has HST3-, MIG1- and SIR-Dependent Silencing Activity. Genetics 162 (1), pp. 59 - 71 (2002)

Lenzner, S.; Prietz, S.; Feil, S.; Nuber, U. A.; Ropers, H. H.; Berger, W.: Global Gene Expression Analysis in a Mouse Model for Norrie Disease: Late Involvement of Photoreceptor Cells. Investigative Ophthalmology & Visual Science 43 (9), pp. 2825 - 2833 (2002)

Minina, E.; Kreschel, C.; Naski, M. C.; Ornitz, D. M.; Vortkamp, A.: Interaction of FGF, Ihh/Pthlh, and BMP Signaling Integrates Chondrocyte Proliferation and Hypertrophic Differentiation. Developmental Cell 3 (3), pp. 439 - 449 (2002)

Fuchs, T.; Malecova, B.; Linhart, C.; Sharan, R.; Khen, M.; Herwig, R.; Shmulevich, D.; Elkon, R.; Steinfath, M.; O'Brien, J. K. et al.; Radelof, U.; Lehrach, H.; Lancet, D.; Shamir, R.: DEFOG: A Practical Scheme for Deciphering Families of Genes. Genomics 80 (3), pp. 295 - 302 (2002)

Otto, E.; Hoefele, J.; Ruf, R.; Mueller, A. M.; Hiller, K. S.; Wolf, M. T. F.; Schuermann, M. J.; Becker, A.; Birkenhäger, R.; Sudbrak, R. et al.; Hennies, H. C.; Nürnberg, P.; Hildebrandt, F.: A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in Evolution. American Journal of Human Genetics 71 (5), pp. 1161 - 1167 (2002)

Otto, E.; Hoefele, J.; Ruf, R.; Mueller, A. M.; Hiller, K. S.; Wolf, M. T. F.; Schuermann, M. J.; Becker, A.; Birkenhäger, R.; Sudbrak, R. et al.; Hennies, H. C.; Nürnberg, P.; Hildebrandt, F.: A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in Evolution. American Journal of Human Genetics 71 (5), pp. 1161 - 1167 (2002)

Heinrich, J.; Schultz, J.; Bosse, M.; Ziegelin, G.; Lanka, E.; Mölling, K.: Linear closed mini DNA generated by the prokaryotic cleaving-joining enzyme TelN is functional in mammalian cells. Journal of Molecular Medicine 80 (10), pp. 648 - 654 (2002)

Heiser, V.; Engemann, S.; Bröcker, W.; Dunke, I.; Boeddrich, A.; Waelter, S.; Nordhoff, E.; Lurz, R.; Schugardt, N.; Rautenberg, S. et al.; Herhaus, C.; Barnickel, G.; Böttcher, H.; Lehrach, H.; Wanker, E. E.: Identification of benzothiazoles as potential polyglutamine aggregation inhibitors of Huntington's disease by using an automated filter retardation assay. Proceedings of the National Academy of Sciences 99 (Suppl. 4), pp. 16400 - 16406 (2002)

Heiser, V.; Engemann, S.; Bröcker, W.; Dunkel, I.; Boeddrich, A.; Waelter, S.; Nordhoff, E.; Lurz, R.; Schugardt, N.; Rautenberg, S. et al.; Herhaus, C.; Barnickel, G.; Böttcher, H.; Lehrach, H.; Wanker, E. E.: Identification of benzothiazoles as potential polyglutamine aggregation inhibitors of Huntington’s disease by using an automated filter retardation assay. Self-Perpetuating Structural States in Biology, Disease, and Genetics, pp. 16400 - 16406 (2002)

Grützner, F.; Roest Crollius, H.; Lütjens, G.; Jaillon, O.; Weissenbach, J.; Ropers, H. H.; Haaf, T.: Four-Hundred Million Years of Conserved Synteny of Human Xp and Xq Genes on Three Tetraodon Chromosomes. Genome Research 12 (9), pp. 1316 - 1322 (2002)

Katzke, S.; Booms, P.; Tiecke, F.; Palz, M.; Pletschacher, A.; Türkmen, S.; Neumann, L. M.; Pregla, R.; Leitner, C.; Schramm, C. et al.; Lorenz, P.; Hagemeier, C.; Fuchs, J.; Skovby, F.; Rosenberg, T.; Robinson, P. N.: TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies. Human Mutation 20 (3), pp. 197 - 208 (2002)

Robinson, P. N.; Booms, P.; Katzke, S.; Ladewig, M.; Neumann, L. M.; Palz, M.; Pregla, R.; Tiecke, F.; Rosenberg, T.: Mutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathies. Human Mutation 20 (3), pp. 153 - 161 (2002)

Möncke-Buchner, E.; Reich, S.; Mücke, M.; Reuter, M.; Messer, W.; Wanker, E.; Krüger, D. H.: Counting CAG repeats in the Huntington’s disease gene by restriction endonuclease EcoP15I cleavage. Nucleic Acxids Research 30 (16), p. e83 - e83 (2002)

Möncke-Buchner, E.; Reich, S.; Mücke, M.; Reuter, M.; Messer, W.; Wanker, E.; Krüger, D. H.: Counting CAG repeats in the Huntington’s disease gene by restriction endonuclease EcoP15I cleavage. Nucleic Acids Research 30 (16), p. e83 - e83 (2002)

Liebermeister, W.: Linear modes of gene expression determined by independent component analysis. Bioinformatics 18 (1), pp. 51 - 60 (2002)

Kasulke, D.; Seitz, S.; Ehrenhofer-Murray, A. E.: A Role for the Saccharomyces cerevisiae RENT Complex Protein Net1 in HMR Silencing. Genetics 161 (4), pp. 1411 - 1423 (2002)

Kalkum, M.; Eisenbrandt, R.; Lurz, R.; Lanka, E.: Tying rings for sex. Trends in Microbiology 10 (8), pp. 382 - 387 (2002)

Kalkum, M.; Eisenbrandt, R.; Lurz, R.; Lanka, E.: Tying rings for sex. 8, pp. 382 - 387 (2002)