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Shultz, L. D.; Lyons, B. L.; Burzenski, L. M.; Gott, B.; Samuels, R.; Schweitzer, P. A.; Dreger, C.; Herrmann, H.; Kalscheuer, V.; Olins, A. L. et al.; Olins, D. E.; Sperling, K.; Hoffmann, K.: Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huet anomaly. Human Molecular Genetics 12 (1), pp. 61 - 69 (2003)

Sudbrak, R.; Reinhardt, R.; Hennig, S.; Lehrach, H.; Gunther, E.; Walter, L.: Comparative and evolutionary analysis of the rhesus macaque extended MHC class II region. Immunogenetics 54 (10), pp. 699 - 704 (2003)

Walther, D. J.: Die Serotonin-Biosynthese im Zentralen Nervensystem wird von einem neuronenspezifischen Tryptophan-Hydroxylase-Isoenzym geschwindigkeitsbestimmend katalysiert. BIOspektrum 9 (2), pp. 184 - 186 (2003)

Wilson, D. N.; Nierhaus, K. H.: The ribosome through the looking glass. Angewandte Chemie-International Edition 42 (30), pp. 3464 - 3486 (2003)

Yamaguchi, K.; Subramanian, A. R.: Proteomic identification of all plastid-specific ribosomal proteins in higher plant chloroplast 30S ribosomal subunit - PSRP-2 (U1A-type domains), PSRP-3 alpha/beta (ycf65 homologue) and PSRP-4 (Thx homologue). European Journal of Biochemistry 270 (2), pp. 190 - 205 (2003)

Heiser, V.; Engernann, S.; Brocker, W.; Dunkel, I.; Boeddrich, A.; Waelter, S.; Nordhoff, E.; Lurz, R.; Schugardt, N.; Rautenberg, S. et al.; Herhaus, C.; Barnickel, G.; Boettcher, 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 of the United States of America 99 (Suppl. 4), pp. 16400 - 16406 (2002)

Sudbrak, R.; Reinhardt, R.; Hennig, S.; Günther, E.; Walter, L.: Comparative and evolutionary analysis of the rhesus macaque extended MHC class II region. Immunogenetics 54 (10), pp. 699 - 704 (2002)

Herwig, R.; Schulz, B.; Weisshaar, B.; Hennig, S.; Steinfath, M.; Drungowski, M.; Stahl, D.; Wruck, W.; Menze, A.; O'Brien, J. et al.; Lehrach, H.; Radelof, U.: Construction of a 'unigene' cDNA clone set by oligonucleotide fingerprinting allows access to 25 000 potential sugar beet genes. The Plant Journal 32 (5), pp. 845 - 857 (2002)

Klipp, E.; Heinrich, R.; Holzhütter, H.-G.: Prediction of temporal gene expression. Metabolic opimization by re-distribution of enzyme activities. European Journal of Biochemistry 269 (22), pp. 1432 - 1033 (2002)

Laumonnier, F.; Ronce, N.; Hamel, B. C. J.; Thomas, P.; Jespinasse, J.; Raynaud, M.; Paringaux, C.; Bokhoven, H. v.; Kalscheuer, V.; Fryns, J.-P. et al.; Chelly, J.; Moraine, C.; Briault, S.: Transcription Factor SOX3 Is Involved in X-Linked Mental Retardation with Growth Hormone Deficiency. American Journal of Human Genetics 71 (6), pp. 1450 - 1455 (2002)

Rabus, R.; Kube, M.; Beck, A.; Widdel, F.; Reinhardt, R.: Genes involved in the anaerobic degradation of ethylbenzene in a denitrifying bacterium, strain EbN1. Archives of Microbiology 178 (6), pp. 506 - 516 (2002)

Regierer, B.: Large scale automated genome and proteome analysis in plants – GABI-LAPP. Genomeexpress 4, pp. 3 - 5 (2002)

Regierer, B.: GABI-LAPP - Large-scale Automated Plant Proteomics in GABI. Genomeexpress 4 (2), pp. 3 - 5 (2002)

Regierer, B.; Fernie, A. R.; Springer, F.; Perez-Melis, A.; Leisse, A.; Koehl, K.; Willmitzer, L.; Geigenberger, P.; Kossmann, J.: Starch content and yield increase as a result of altering adenylate pools in transgenic plants. Nature Biotechnology 20 (12), pp. 1256 - 1260 (2002)

Arap, W.; Kolonin, M. G.; Trepel, M.; Lahdenranta, J.; Cardó-Vila, M.; Giordano, R. J.; Mintz, P. J.; Ardelt, P. U.; Yao, V. J.; Vidal, C. I. et al.; Chen, L.; Flamm, A.; Valtanen, H.; Weavind, L. M.; Hicks, M. E.; Pollock, R. E.; Botz, G. H.; Bucana, C. D.; Koivunen, E.; Cahill, D.; Troncoso, P.; Baggerly, K. A.; Pentz, R. D.; Do, K.-A.; Logothetis, C. J.; Pasqualin, R.: Steps toward mapping the human vasculature by phage display. Nature Medicine 8 (2), pp. 121 - 127 (2002)

Horváth, R.; Scharfe, C.; Hoeltzenbein, M.; Do, B. H.; Schröder, C.; Warzok, R.; Vogelgesang, S.; Lochmüller, H.; Müller-Höcker, J.; Gerbitz, K. D. et al.; Oefner, P. J.; Jaksch, M.: Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene. Journal of Medical Genetics 39 (11), pp. 812 - 816 (2002)

Kunath, M.; Lüdecke, H.-J.; Vortkamp, A.: Expression of Trps1 during mouse embryonic development. Gene Expression Patterns 2 (1-2), pp. 119 - 122 (2002)

Morava, É.; Kárteszi, J.; Weisenbach, J.; Caliebe, A.; Mundlos, S.; Méhes, K.: Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia. European Journal of Pediatrics 161 (11), pp. 619 - 622 (2002)

Steinhoff, C.; Prior, A.; Reichmann, G.; Seifert, H.-H.; Schulz, W. A.: Activity of E2F-dependent promoters in bladder carcinoma cells and their use for tumour-specific targeting of p53-induced apoptosis. International Journal of Oncology 21 (5), pp. 1033 - 1040 (2002)

Unger, S.; Mornet, E.; Mundlos, S.; Blaser, S.; Cole, D. E.: Severe cleidocranial dysplasia can mimic hypophosphatasia. European Journal of Pediatrics 161 (11), pp. 623 - 626 (2002)