Max Planck Publications

Gerisch, B.; Weitzel, C.; Kober-Eisermann, C.; Rottiers, V.; Antebi, A.: A hormonal signaling pathway influencing C. elegans metabolism, reproductive development, and life span. Developmental Cell 1 (6), pp. 841 - 51 (2001)

Daiber, A.; Nauser, T.; Takaya, N.; Kudo, T.; Weber, P.; Hultschig, C.; Shoun, H.; Ullrich, V.: Isotope effects and intermediates in the reduction of NO by P450NOR. Journal of Inorganic Biochemistry 88 (3 - 4), pp. 343 - 352 (2001)

Brunner, B.; Hornung, U.; Shan, Z.; Nanda, I.; Kondo, M.; Zend-Ajusch, E.; Haaf, T.; Ropers, H. H.; Shima, A.; Schmid, M. et al.; Kalscheuer, V. M.; Schartl, M.: Genomic organization and expression of the doublesex-related gene cluster in vertebrates and detection of putative regulatory regions for DMRT1. Genomics 77 (1-2), pp. 8 - 17 (2001)

Fritz, B.; Aslan, M.; Kalscheuer, V.; Ramsing, M.; Saar, K.; Fuchs, B.; Rehder, H.: Low incidence of UPD in spontaneous abortions beyond the 5th gestational week. Eur J Hum Genet 9 (12), pp. 910 - 6 (2001)

Mergenthaler, S.; Hitchins, M. P.; Blagitko-Dorfs, N.; Monk, D.; Wollmann, H. A.; Ranke, M. B.; Ropers, H. H.; Apostolidou, S.; Stanier, P.; Preece, M. A. et al.; Eggermann, T.; Kalscheuer, V. M.; Moore, G. E.: Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression? Am J Hum Genet 68 (2), pp. 543 - 5 (2001)

Mergenthaler, S.; Sharp, A.; Ranke, M. B.; Kalscheuer, V. M.; Wollmann, H. A.; Eggermann, T.: Gene dosage analysis in Silver-Russell syndrome: use of quantitative competitive PCR and dual-color FISH to estimate the frequency of duplications in 7p11.2-p13. Genet Test 5 (3), pp. 261 - 6 (2001)

Sudbrak, R.; Wieczorek, G.; Nuber, U. A.; Mann, W.; Kirchner, R.; Erdogan, F.; Brown, C. J.; Wohrle, D.; Sterk, P.; Kalscheuer, V. M. et al.; Berger, W.; Lehrach, H.; Ropers, H. H.: X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications. Hum Mol Genet 10 (1), pp. 77 - 83 (2001)

Tonnies, H.; Stumm, M.; Wegner, R. D.; Chudoba, I.; Kalscheuer, V.; Neitzel, H.: Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics. Cytogenet Cell Genet 93 (3-4), pp. 188 - 94 (2001)

Volleth, M.; Stumm, M.; Mohnike, K.; Kalscheuer, V. M.; Jakubiczka, S.; Wieacker, P.: Preferential inactivation of a dupX(q23 --> q27-28) chromosome in a girl with mental retardation and dysmorphy. Hum Hered 52 (3), pp. 177 - 82 (2001)

Eickhoff, H.; Schneider, U.; Nordhoff, E.; Nyarsik, L.; Zehetner, G.; Nietfeld, W.; Lehrach, H.: Technology Development for DNA Chips. In: DNA Arrays: Technologies and Experimental Strategies, pp. 1 - 9 (Ed. Grigorenko, E. V.). CRC Press, Boca Raton [et al] (2001)

Blaha, G.; Nierhaus, K. H.: Features and functions of the ribosomal E site. In: The Ribosome, pp. 135 - 146. Cold Spring Harbor Laboratory Press, Cold Spring Harbor (2001)

Hirsch, D.: Untersuchungen zu Auswirkungen von Missensemutationen im Nijmegen-Breakage-Syndrom-Gen NBN. Diploma, Freie Universität, Berlin (2001)