Journal Article (144)

21.
Journal Article
Börno, S.; Fischer, A.; Kerick, M.; Falth, M.; Laible, M.; Brase, J. C.; Kuner, R.; Dahl, A.; Grimm, C.; Sayanjali, B. et al.; Isau, M.; Röhr, C.; Wunderlich, A.; Timmermann, B.; Claus, R.; Plass, C.; Graefen, M.; Simon, R.; Demichelis, F.; Rubin, M. A.; Sauter, G.; Schlomm, T.; Sültmann, H.; Lehrach, H.; Schweiger, M. R.: Genome-wide DNA methylation events in TMPRSS2-ERG fusion-negative prostate cancers implicate an EZH2-dependent mechanism with miR-26a hypermethylation. Cancer Discovery 2 (11), pp. 1024 - 1035 (2012)
22.
Journal Article
Fischer, B.; Dimopoulou, A.; Egerer, J.; Gardeitchik, T.; Kidd, A.; Jost, D.; Kayserili, H.; Alanay, Y.; Tantcheva-Poor, I.; Mangold, E. et al.; Daumer-Haas, C.; Phadke, S.; Peirano, R. I.; Heusel, J.; Desphande, C.; Gupta, N.; Nanda, A.; Felix, E.; Berry-Kravis, E.; Kabra, M.; Wevers, R. A.; van Maldergem, L.; Mundlos, S.; Morava, E.; Kornak, U.: Further characterization of ATP6V0A2-related autosomal recessive cutis laxa. Human Genetics 131 (11), pp. 1761 - 1773 (2012)
23.
Journal Article
Hucho, T.; Suckow, V.; Joseph, E. K.; Kuhn, J.; Schmoranzer, J.; Dina, O. A.; Chen, X.; Karst, M.; Bernateck, M.; Levine, J. D. et al.; Ropers, H.-H.: Ca++/CaMKII switches nociceptor-sensitizing stimuli into desensitizing stimuli. Journal of Neurochemistry: official journal of the International Society for Neurochemistry 123 (4), pp. 589 - 601 (2012)
24.
Journal Article
Sharma, M.; Ioannidis, J. P.; Aasly, J. O.; Annesi, G.; Brice, A.; Bertram, L.; Bozi, M.; Barcikowska, M.; Crosiers, D.; Clarke, C. E. et al.; Facheris, M. F.; Farrer, M.; Garraux, G.; Gispert, S.; Auburger, G.; Vilarino-Guell, C.; Hadjigeorgiou, G. M.; Hicks, A. A.; Hattori, N.; Jeon, B. S.; Jamrozik, Z.; Krygowska-Wajs, A.; Lesage, S.; Lill, C. M.; Lin, J. J.; Lynch, T.; Lichtner, P.; Lang, A. E.; Libioulle, C.; Murata, M.; Mok, V.; Jasinska-Myga, B.; Mellick, G. D.; Morrison, K. E.; Meitnger, T.; Zimprich, A.; Opala, G.; Pramstaller, P. P.; Pichler, I.; Park, S. S.; Quattrone, A.; Rogaeva, E.; Ross, O. A.; Stefanis, L.; Stockton, J. D.; Satake, W.; Silburn, P. A.; Strom, T. M.; Theuns, J.; Tan, E. K.; Toda, T.; Tomiyama, H.; Uitti, R. J.; Van Broeckhoven, C.; Wirdefeldt, K.; Wszolek, Z.; Xiromerisiou, G.; Yomono, H. S.; Yueh, K. C.; Zhao, Y.; Gasser, T.; Maraganore, D.; Krüger, R.: A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of Medical Genetics (London) 49 (11), pp. 721 - 726 (2012)
25.
Journal Article
Sudheer, S.; Bhushan, R.; Fauler, B.; Lehrach, H.; Adjaye, J.: FGF inhibition directs BMP4-mediated differentiation of human embryonic stem cells to syncytiotrophoblast. Stem Cells and Development 21 (16), pp. 2987 - 3000 (2012)
26.
Journal Article
Wollrab, C.; Heitkam, T.; Holtgrawe, D.; Weisshaar, B.; Minoche, A. E.; Dohm, J. C.; Himmelbauer, H.; Schmidt, T.: Evolutionary reshuffling in the Errantivirus lineage Elbe within the Beta vulgaris genome. The Plant Journal 72 (4), pp. 636 - 51 (2012)
27.
Journal Article
Kamburov, A.; Grossmann, A.; Herwig, R.; Stelzl, U.: Cluster-based assessment of protein-protein interaction confidence. BMC Bioinformatics, p. 13:262 - 13:262 (2012)
28.
Journal Article
Rubelt, F.; Sievert, V.; Knaust, F.; Diener, C.; Lim, T. S.; Klipp, E.; Reinhardt, R.; Lehrach, H.; Konthur, Z.: Onset of Immune Senescence Defined by Unbiased Pyrosequencing of Human Immunoglobulin mRNA Repertoires. PLoS One (accepted)
29.
Journal Article
Berillo, O.; Khailenko, V.; Ivashchenko, A.; Perlmuter-Shoshany, L.; Bolshoy, A.: miRNA and tropism of human parvovirus B19. Computational Biology and Chemistry 40 (0), pp. 1 - 6 (2012)
30.
Journal Article
El Khassawna, T.; Toben, D.; Kolanczyk, M.; Schmidt-Bleek, K.; Koennecke, I.; Schell, H.; Mundlos, S.; Duda, G. N.: Deterioration of fracture healing in the mouse model of NF1 long bone dysplasia. Bone 51 (4), pp. 651 - 660 (2012)
31.
Journal Article
Geffers, L.; Herrmann, B. G.; Eichele, G.: Web-based digital gene expression atlases for the mouse. Mammalian Genome 23, pp. 525 - 538 (2012)
32.
Journal Article
Mangold, E.; Reutter, H.; Leon-Cachon, R. B.; Ludwig, K. U.; Herms, S.; Chacon-Camacho, O.; Ortiz-Lopez, R.; Paredes-Zenteno, M.; Arizpe-Cantu, A.; Munoz-Jimenez, S. G. et al.; Nowak, S.; Kramer, F. J.; Wienker, T. F.; Nothen, M. M.; Knapp, M.; Rojas-Martinez, A.: Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate. European Journal of Oral Science 120 (5), pp. 373 - 377 (2012)
33.
Journal Article
Moschidou, D.; Mukherjee, S.; Blundell, M. P.; Drews, K.; Jones, G. N.; Abdulrazzak, H.; Nowakowska, B.; Phoolchund, A.; Lay, K.; Ramasamy, T. S. et al.; Cananzi, M.; Nettersheim, D.; Sullivan, M.; Frost, J.; Moore, G.; Vermeesch, J. R.; Fisk, N. M.; Thrasher, A. J.; Atala, A.; Adjaye, J.; Schorle, H.; De Coppi, P.; Guillot, P. V.: Valproic acid confers functional pluripotency to human amniotic fluid stem cells in a transgene-free approach. Molecular Therapy 20 (10), pp. 1953 - 1967 (2012)
34.
Journal Article
Peifer, M.; Fernandez-Cuesta, L.; Sos, M. L.; George, J.; Seidel, D.; Kasper, L. H.; Plenker, D.; Leenders, F.; Sun, R.; Zander, T. et al.; Menon, R.; Koker, M.; Dahmen, I.; Muller, C.; Di Cerbo, V.; Schildhaus, H. U.; Altmuller, J.; Baessmann, I.; Becker, C.; de Wilde, B.; Vandesompele, J.; Bohm, D.; Ansen, S.; Gabler, F.; Wilkening, I.; Heynck, S.; Heuckmann, J. M.; Lu, X.; Carter, S. L.; Cibulskis, K.; Banerji, S.; Getz, G.; Park, K. S.; Rauh, D.; Grutter, C.; Fischer, M.; Pasqualucci, L.; Wright, G.; Wainer, Z.; Russell, P.; Petersen, I.; Chen, Y.; Stoelben, E.; Ludwig, C.; Schnabel, P.; Hoffmann, H.; Muley, T.; Brockmann, M.; Engel-Riedel, W.; Muscarella, L. A.; Fazio, V. M.; Groen, H.; Timens, W.; Sietsma, H.; Thunnissen, E.; Smit, E.; Heideman, D. A.; Snijders, P. J.; Cappuzzo, F.; Ligorio, C.; Damiani, S.; Field, J.; Solberg, S.; Brustugun, O. T.; Lund-Iversen, M.; Sanger, J.; Clement, J. H.; Soltermann, A.; Moch, H.; Weder, W.; Solomon, B.; Soria, J. C.; Validire, P.; Besse, B.; Brambilla, E.; Brambilla, C.; Lantuejoul, S.; Lorimier, P.; Schneider, P. M.; Hallek, M.; Pao, W.; Meyerson, M.; Sage, J.; Shendure, J.; Schneider, R.; Buttner, R.; Wolf, J.; Nurnberg, P.; Perner, S.; Heukamp, L. C.; Brindle, P. K.; Haas, S.; Thomas, R. K.: Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer. Nature Genetics 44 (10), pp. 1104 - 1110 (2012)
35.
Journal Article
Spielmann, M.; Brancati, F.; Krawitz, P. M.; Robinson, P. N.; Ibrahim, D. M.; Franke, M.; Hecht, J.; Lohan, S.; Dathe, K.; Nardone, A. M. et al.; Ferrari, P.; Landi, A.; Wittler, L.; Timmermann, B.; Chan, D.; Mennen, U.; Klopocki, E.; Mundlos, S.: Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locus. American Journal of Human Genetics 91 (4), pp. 629 - 635 (2012)
36.
Journal Article
Huang, L.; Jolly, L. A.; Willis-Owen, S.; Gardner, A.; Kumar, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M. et al.; Hackett, A.; Field, M.; Froyen, G.; Hu, H. C.; Haas, S.; Ropers, H.-H.; Kalscheuer, V. M.; Corbett, M. A.; Gecz, J.: A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability. The American Journal of Human Genetics 91 (4), pp. 694 - 702 (2012)
37.
Journal Article
Kämpjärvi, K.; Mäkinen, N.; Kilpivaara, O.; Arola, J.; Heinonen, H.-R.; Böhm, J.; Abdel-Wahab, O.; Lehtonen, H. J.; Pelttari, L. M.; Mehine, M. et al.; Schrewe, H.; Nevanlinna, H.; Levine, R. L.; Hokland, P.; Böhling, T.; Mecklin, J.-P.; Bützow, R.; Aaltonen, L. A.; Vahteristo, P.: Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer. British Journal of Cancer 107, pp. 1761 - 1765 (2012)
38.
Journal Article
Wittler, L.; Hilger, A.; Proske, J.; Pennimpede, T.; Draaken, M.; Ebert, A.-K.; Rösch, W.; Stein, R.; Nöthen, M. M.; Reutter, H. et al.; Ludwig, M.: Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadias. Gene 506 (2), pp. 392 - 395 (2012)
39.
Journal Article
Parsons, M. J.; Grimm, C.; Paya-Cano, J. L.; Fernandes, C.; Liu, L.; Philip, V. M.; Chesler, E. J.; Nietfeld, W.; Lehrach, H.; Schalkwyk, L. C.: Genetic variation in hippocampal microRNA expression differences in C57BL/6 J X DBA/2 J (BXD) recombinant inbred mouse strains. BMC Genomics 13, p. 476 (2012)
40.
Journal Article
Zanni, G.; Cali, T.; Kalscheuer, V. M.; Ottolini, D.; Barresi, S.; Lebrun, N.; Montecchi-Palazzi, L.; Hu, H.; Chelly, J.; Bertini, E. et al.; Brini, M.; Carafoli, E.: Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis. Proceedings of the National Academy of Sciences of the United States of America 109 (36), pp. 14514 - 14519 (2012)
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