Suchergebnisse

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), S. 1678 - 1688 (2004)

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), S. 980 - 981 (2004)

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), S. 10155 - 10160 (2004)

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), S. 22 - 23 (2004)

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), S. 27 - 34 (2004)

Hakenberg, J.; Schmeier, S.; Kowald, A.; Klipp, E.; Leser, U.: Finding kinetic parameters using text mining. OMICS: A Journal of Integrative Biology 8 (2), S. 131 - 152 (2004)

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), S. 1258 - 1267 (2004)

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), S. 656 - 663 (2004)

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), S. 903 - 913 (2004)

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), S. 227 - 236 (2004)

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), S. 971 - 976 (2004)

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), S. 288 - 297 (2004)

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), S. 98 - 108 (2004)

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), S. 4004 - 4009 (2004)

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, S. 27 - 27 (2004)

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), S. 5982 - 6002 (2004)

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), S. 364 - 373 (2004)

Antebi, A.: Inside insulin signaling, communication is key to long life. Science of Aging Knowledge Environment 2004 (23), S. pe25 - pe25 (2004)

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), S. 801 - 813 (2004)

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), S. e75 - e75 (2004)