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 (189)

Journal Article
Tavella, S.; Biticchi, R.; Schito, A.; Minina, E.; Di Martino, D.; Pagano, A.; Vortkamp, A.; Horton, W. A.; Cancedda, R.; Garofalo, S.: Targeted expression of SHH affects chondrocyte differentiation, growth plate organization, and Sox9 expression. Journal of Bone and Mineral Research 19 (10), pp. 1678 - 1688 (2004)
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Harvey, M.; Shink, E.; Tremblay, M.; Gagné, B.; Raymond, C.; Labbé, M.; Walther, D. J.; Bader, M.; Barden, N.: Support for the Involvement of TPH2 Gene in Affective Disorders. Molecular Psychiatry 9 (11), pp. 980 - 981 (2004)
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Thiele, H.; Sakano, M.; Kitagawa, H.; Sugahara, K.; Rajab, A.; Höhne, W.; Ritter, H.; Leschik, G.; Nürnberg, P.; Mundlos, S.: Loss of chondroitin 6-O-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvement. Proceedings of the National Academy of Sciences 101 (27), pp. 10155 - 10160 (2004)
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I. Roig, I.; Liebe, B.; Egozcue, J.; Cabero, L. l.; Garcia, M.; Scherthan, H.: Female-specific features of recombinational double-stranded DNA repair in relation to synapsis and telomere dynamics in human oocytes. Chromosoma: Biology of the Nucleus 113 (1), pp. 22 - 23 (2004)
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Bartels, C. F.; Bükülmez, H.; Padayatti, P.; Rhee, D. K.; van Ravenswaaij-Arts, C.; Pauli, R. M.; Mundlos, S.; Chitayat, D.; Shih, L.-Y.; Al-Gazali, L. I. et al.; Kant, S.; Cole, T.; Morton, J.; Cormier-Daire, V.; Faivre, L.; Lees, M.; Kirk, J.; Mortier, G. R.; Leroy, J.; Zabel, B.; Kim, C. A.; Crow, Y.; Braverman, N. E.; van den Akker, F.; Warman, M. L.: Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux. American Journal of Human Genetics 75 (1), pp. 27 - 34 (2004)
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Hakenberg, J.; Schmeier, S.; Kowald, A.; Klipp, E.; Leser, U.: Finding kinetic parameters using text mining. OMICS: A Journal of Integrative Biology 8 (2), pp. 131 - 152 (2004)
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Kahlem, P.; Sultan, M.; Herwig, R.; Steinfath, M.; Balzereit, D.; Eppens, B.; Saran, N. G.; Pletcher, M. T.; South, S. T.; Stetten, G. et al.; Lehrach, H.; Reeves, R. H.; Yaspo, M.-L.: Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of Down Syndrome. Genome Research 14 (7), pp. 1258 - 1267 (2004)
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Khare, D.; Ziegelin, G.; Lanka, E.; Heinemann, U.: Sequence-specific DNA binding determined by contacts outside the helix-turn-helix motif of the ParB homolog KorB. Nature Structural & Molecular Biology 11 (7), pp. 656 - 663 (2004)
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Khorasani, M. Z.; Hennig, S.; Imre, G.; Asakawa, S.; Palczewski, S.; Berger, A.; Hori, H.; Naruse, K.; Mitani, H.; Shima, A. et al.; Lehrach, H.; Wittbrodt, J.; Kondoh, H.; Shimizu, N.; Himmelbauer, H.: A first generation physical map of the medaka genome in BACs essential for positional cloning and clone-by-clone based genomic sequencing. Mechanisms of Development 121 (7-8), pp. 903 - 913 (2004)
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Poustka, A. J.; Kühn, A.; Radosavljevic, V.; Wellenreuther, R.; Lehrach, H.; Panopoulou, G.: On the origin of the chordate central nervous system: expression of onecut in the sea urchin embryo. Evolution and Development 6 (4), pp. 227 - 236 (2004)
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Quiring, R.; Wittbrodt, B.; Henrich, T.; Ramialison, M.; Burgtorf, C.; Lehrach, H.; Wittbrodt, J.: Large-scale expression screening by automated whole-mount in situ hybridization. Mechanisms of Development 121 (7-8), pp. 971 - 976 (2004)
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Rickert, A. M.; Borodina, T. A.; Kuhn, E. J.; Lehrach, H.; Sperling, S.: Refinement of single-nucleotide polymorphism genotyping methods on human genomic DNA: amplifluor allele-specific polymerase chain reaction versus ligation detection reaction-TaqMan. Analytical Biochemistry 330 (2), pp. 288 - 297 (2004)
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Scheid, S.; Spang, R.: A stochastic downhill search algorithm for estimating the local false discovery rate. IEEE ACM Transactions on Computational Biology and Bioinformatics 1 (3), pp. 98 - 108 (2004)
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Wilharm, G.; Lehmann, V.; Krauss, K.; Lehnert, B.; Richter, S.; Ruckdeschel, K.; Heesemann, J.; Trülzsch, K.: Yersinia enterocolitica type III secretion depends on the proton motive force but not on the flagellar motor components MotA and MotB. Infection and Immunity 72 (7), pp. 4004 - 4009 (2004)
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Wilharm, G.; Lehmann, V.; Neumayer, W.; Trček, J.: Yersinia enterocolitica type III secretion: Evidence for the ability to transport proteins that are folded prior to secretion. BMC Microbiology 4, p. 27 - 27 (2004)
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Gurok, U.; Steinhoff, C.; Lipkowitz, B.; Ropers, H.-H.; Scharff, C.; Nuber, U. A.: Gene expression changes in the course of neural progenitor cell differentiation. Journal of Neuroscience 24 (26), pp. 5982 - 6002 (2004)
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Walter, S.; Sandig, K.; Hinkel, G. K.; Mitulla, B.; Ounap, K.; Sims, G.; Sitska, M.; Utermann, B.; Viertel, P.; Kalscheuer, V. M. et al.; Bartsch, O.: Subtelomere FISH in 50 children with mental retardation and minor anomalies, identified by a checklist, detects 10 rearrangements including a de novo balanced translocation of chromosomes 17p13.3 and 20q13.33. American Journal of Medical Genetics 128A (4), pp. 364 - 373 (2004)
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Antebi, A.: Inside insulin signaling, communication is key to long life. Science of Aging Knowledge Environment 2004 (23), p. pe25 - pe25 (2004)
Journal Article
Koziel, L.; Kunath, M.; Kelly, O. G.; Vortkamp, A.: Ext1-dependent heparan sulfate regulates the range of Ihh signaling during endochondral ossification. Developmental Cell 6 (6), pp. 801 - 813 (2004)
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Horváth, R.; Lochmüller, H.; Hoeltzenbein, M.; Müller-Höcker, J.; Schoser, B. G.; Pongratz, D.; Jaksch, M.: Spontaneous recovery of a childhood onset mitochondrial myopathy caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene. Journal of Medical Genetics 41 (6), p. e75 - e75 (2004)
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