Our publications listed in the Puplication Repository of the Max Planck Society (PuRe)

Journal Article (140)

61.
Journal Article
Kariminejad, A.; Kariminejad, R.; Tzschach, A.; Ullmann, R.; Ahmed, A.; Asghari-Roodsari, A.; Salehpour, S.; Afroozan, F.; Ropers, H.-H.; Kariminejad, M. H.: Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy of MSX2 with craniosynostosis. American Journal of Medical Genetics Part A 149 (7), pp. 1544 - 1549 (2009)
62.
Journal Article
Ott, C.-E.; Bauer, S.; Manke, T.; Ahrens, S.; Rödelsperger, C.; Grünhagen, J.; Kornak, U.; Duda, G.; Mundlos, S.; Robinson, P. N.: Promiscuous and depolarization-induced immediate-early response genes are induced by mechanical strain of osteoblasts. Journal of Bone and Mineral Research 24 (7), pp. 1247 - 1262 (2009)
63.
Journal Article
Raile, K.; Klopocki, E.; Holder, M.; Wessel, T.; Galler, A.; Deiss, D.; Müller, D.; Riebel, T.; Horn, D.; Maringa, M. et al.; Weber, J.; Ullmann, R.; Grüters, A.: Expanded clinical spectrum in hepatocyte nuclear factor 1B-maturity-onset diabetes of the young. Journal of Clinical Endocrinology & Metabolism 94 (7), pp. 2658 - 2664 (2009)
64.
Journal Article
Ralser, M.; Wamelink, M. M. C.; Latkolik, S.; Jansen, E. E. W.; Lehrach, H.; Jakobs, C.: Correspondence: Metabolic reconfiguration precedes transcriptional regulation in the antioxidant response. Nature biotechnology 27 (7), pp. 604 - 605 (2009)
65.
Journal Article
Schimmelmann, B. G.; Friedel, S.; Nguyen, T. T.; Sauer, S.; Ganz Vogel, C. I.; Konrad, K.; Wilhelm, C.; Sinzig, J.; Renner, T. J.; Romanos, M. et al.; Palmason, H.; Dempfle, A.; Walitza, S.; Freitag, C.; Meyer, J.; Linder, M.; Schäfer, H.; Warnke, A.; Lesch, K. P.; Herpertz-Dahlman, B.; Hinney, A.; Hebebrand, J.: Exploring the genetic link between RLS and ADHD. Journal of Psychiatric Research 43 (10), pp. 941 - 945 (2009)
66.
Journal Article
Chung, H.-R.; Vingron, M.: Comparison of sequence-dependent tiling array normalization approaches. BMC Bioinformatics 10, p. 204 - 204 (2009)
67.
Journal Article
Milenković, T.; Filippis, I.; Lappe, M.; Pržulj, N.: Optimized null model for protein structure networks. PLoS ONE 4 (6), p. e5967 - e5967 (2009)
68.
Journal Article
Ye, K.; Schulz, M. H.; Long, Q.; Apweiler, R.; Ning, Z.: Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads. Bioinformatics 25 (21), pp. 2865 - 2871 (2009)
69.
Journal Article
Hucthagowder, V.; Morava, E.; Kornak, U.; Lefeber, D. J.; Fischer, B.; Dimopoulou, A.; Aldinger, A.; Choi, J.; Davis, E. C.; Abuelo, D. N. et al.; Adamowicz, M.; Al-Aama, J.; Basel-Vanagaite, L.; Fernandez, B.; Greally, M. T.; Gillessen-Kaesbach, G.; Kayserili, H.; Lemyre, E.; Tekin, M.; Türkmen, S.; Tuysuz, B.; Yüksel-Konuk, B.; Mundlos, S.; Van Maldergem, L.; Wevers, R. A.; Urban, Z.: Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival. Human Molecular Genetics 18 (12), pp. 2149 - 2165 (2009)
70.
Journal Article
Schinke, T.; Schilling, A. F.; Baranowsky, A.; Seitz, S.; Marshall, R. P.; Linn, T.; Blaeker, M.; Huebner, A. K.; Schulz, A.; Simon, R. et al.; Gebauer, M.; Priemel, M.; Kornak, U.; Perkovic, S.; Barvencik, F.; Beil, F. T.; Del Fattore, A.; Frattini, A.; Streichert, T.; Pueschel, K.; Villa, A.; Debatin, K.-M.; Rueger, J. M.; Teti, A.; Zustin, J.; Sauter, G.; Amling, M.: Impaired gastric acidification negatively affects calcium homeostasis and bone mass. Nature Medicine 15, pp. 674 - 681 (2009)
71.
Journal Article
Shoichet, S. A.; Waibel, S.; Endruhn, S.; Sperfeld, A. D.; Vorwerk, B.; Mümlller, I.; Erdogan, F.; Ludolph, A. C.; Ropers, H.-H.; Ullmann, R.: Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization. Amyotrophic Lateral Sclerosis 10 (3), pp. 162 - 169 (2009)
72.
Journal Article
Tzschach, A.: Genetik der nichtsyndromalen geistigen Behinderung. Medizinische Genetik 21 (2), pp. 231 - 236 (2009)
73.
Journal Article
Tzschach, A.; Ramel, C.; Kron, A.; Seipel, B.; Wüster, C.; Cordes, U.; Liehr, T.; Hoeltzenbein, M.; Menzel, C.; Ropers, H.-H. et al.; Ullmann, R.; Kalscheuer, V.; Decker, J.; Steinberger, D.: Hypergonadotropic hypogonadism in a patient with inv ins (2;4). International Journal of Andrology 32 (3), pp. 226 - 230 (2009)
74.
Journal Article
Zatkova, A.; Merk, S.; Wendehack, M.; Bilban, M.; Muzik, E. M.; Muradyan, A.; Haferlach, C.; Haferlach, T.; Wimmer, K.; Fonatsch, C. et al.; Ullmann, R.: AML/MDS with 11q/MLL amplification show characteristic gene expression signature and interplay of DNA copy number changes. Genes, Chromosomes and Cancer 48 (6), pp. 510 - 520 (2009)
75.
Journal Article
Zuccotti, M.; Merico, V.; Sacchi, L.; Bellone, M.; Brink, T. C.; Stefanelli, M.; Redi, C. A.; Bellazzi, R.; Adjaye, J.; Garagna, S.: Oct-4 regulates the expression of Stella and Foxj2 at the Nanog locus: implications for the developmental competence of mouse oocytes. Human Reproduction 24 (9), pp. 2225 - 2237 (2009)
76.
Journal Article
Türkmen, S.; Guo, G.; Garshasbi, M.; Hoffmann, K.; Alshalah, A. J.; Mischung, C.; Kuss, A.; Humphrey, N.; Mundlos, S.; Robinson, P. N.: CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait. PLoS Genetics 5, p. e1000487 - e1000487 (2009)
77.
Journal Article
Schweiger, M. R.; Kerick, M.; Timmermann, B.; Albrecht, M. W.; Borodina, T.; Parkhomchuk, D.; Zatloukal, K.; Lehrach, H.: Genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (FFPE) tumor tissues for copy-number- and mutation-analysis. PLoS ONE 4 (5), p. e5548 - e5548 (2009)
78.
Journal Article
Geibela, S.; Banchenkoa, S.; Engela, M.; Lanka, E.; Saenger, W.: Structure and function of primase RepB' encoded by broad-host-range plasmid RSF1010: that replicates exclusively in leading-strand mode. Proceedings of the National Academy of Sciences 106 (19), pp. 7810 - 7815 (2009)
79.
Journal Article
Jürgens, A. S.; Kolanczyk, M.; Moebest, D. C. C.; Zemojtel, T.; Lichtenauer, U.; Duchniewicz, M.; Gantert, M. P.; Hecht, J.; Hattenhorst, U.; Burdach, S. et al.; Dorn, A.; Kamps, M. P.; Beuschlein, F.; Räpple, D.; Scheele, J. S.: PBX1 is dispensable for neural commitment of RA-treated murine ES cells. In Vitro Cellular & Developmental Biology - Animal 45 (5-6), pp. 252 - 263 (2009)
80.
Journal Article
Scheele, J. S.; Kolanczyk, M.; Gantert, M.; Zemojtel, T.; Dorn, A.; Sykes, D. B.; Möbest, D. C. C.; Kamps, M. P.; Räpple, D.: The Spt-Ada-Gcn5-acetyltransferase complex interaction motif of E2a is essential for a subset of transcriptional and oncogenic properties of E2a-Pbx1. Leukemia & Lymphoma 50 (5), pp. 816 - 828 (2009)
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