Max Planck Publications of Lastname Lab

The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.

Journal Article (9)

Journal Article

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)

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Journal Article

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)

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Journal Article

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)

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Journal Article

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)

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Journal Article

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)

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Journal Article

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)

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Journal Article

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)

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Journal Article

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)

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Journal Article

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)

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Book Chapter (2)

Book Chapter

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)

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Book Chapter

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)

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Thesis - Diploma (1)

Thesis - Diploma

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

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