Journal Article (1120)

701.
Journal Article
Shehata, S. N.; Deak, M.; Morrice, N. A.; Ohta, E.; Hunter, R. W.; Kalscheuer, V. M.; Sakamoto, K.: Cyclin Y phosphorylation- and 14-3-3-binding-dependent activation of PCTAIRE-1/CDK16. Biochemical Journal 469 (3), pp. 409 - 420 (2015)
702.
Journal Article
Stange, K.; Ott, C. E.; Schmidt-von Kegler, M.; Gillesen-Kaesbach, G.; Mundlos, S.; Dathe, K.; Seemann, P.: Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations? JOURNAL OF HUMAN GENETICS 60 (8), pp. 419 - 425 (2015)
703.
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Flöttmann, R.; Wagner, J.; Kobus, K.; Curry, C. J.; Savarirayan, R.; Nishimura, G.; Yasui, N.; Spranger, J.; Van Esch, H.; Lyons, M. J. et al.; DuPont, B. R.; Dwivedi, A.; Klopocki, E.; Horn, D.; Mundlos, S.; Spielmann, M.: Microdeletions on 6p22.3 are associated with mesomelic dysplasia Savarirayan type. Journal of Medical Genetics 52 (7), pp. 476 - 483 (2015)
704.
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Francioli, L. C.; Polak, P. P.; Koren, A.; Menelaou, A.; Chun, S.; Renkens, I.; Genome of the Netherlands, C.; van Duijn, C. M.; Swertz, M.; Wijmenga, C. et al.; van Ommen, G.; Slagboom, P. E.; Boomsma, D. I.; Ye, K.; Guryev, V.; Arndt, P. F.; Kloosterman, W. P.; de Bakker, P. I.; Sunyaev, S. R.: Genome-wide patterns and properties of de novo mutations in humans. Nature Genetics 47 (7), pp. 822 - 826 (2015)
705.
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Pasqualini, L.; Bu, H.; Puhr, M.; Narisu, N.; Rainer, J.; Schlick, B.; Schäfer, G.; Angelova, M.; Trajanoski, Z.; Börno, S. T. et al.; Schweiger, M. R.; Fuchsberger, C.; Klocker, H.: miR-22 and miR-29a are members of the androgen receptor cistrome modulating LAMC1 and Mcl-1 in prostate cancer. Molecular Endocrinology 29 (7), pp. 1037 - 1054 (2015)
706.
Journal Article
Jolly, L. A.; Nguyen, L. S.; Domingo, D.; Sun, Y.; Barry, S.; Hancarova, M.; Plevova, P.; Vlckova, M.; Havlovicova, M.; Kalscheuer, V. M. et al.; Graziano, C.; Pippucci, T.; Bonora, E.; Sedlacek, Z.; Gecz, J.: HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain. Human Molecular Genetics 24 (12), pp. 3335 - 3347 (2015)
707.
Journal Article
Chaban, Y.; Lurz, R.; Brasilès, S.; Cornilleau, C.; Karreman, M.; Zinn-Justin, S.; Tavares, P.; Orlova, E. V.: Structural rearrangements in the phage head-to-tail interface during assembly and infection. Proceedings of the National Academy of Sciences of the United States of America 112 (22), pp. 7009 - 7014 (2015)
708.
Journal Article
Hammerl, J. A.; Roschanski, N.; Lurz, R.; Johne, R.; Lanka, E.; Hertwig, S.: The Molecular Switch of Telomere Phages: High Binding Specificity of the PY54 Cro Lytic Repressor to a Single Operator Site. Viruses 7 (6), pp. 2771 - 2793 (2015)
709.
Journal Article
Bernal Ulloa, S. M.; Heinzmann, J.; Herrmann, D.; Timmermann, B.; Baulain, U.; Großfeld, R.; Diederich, M.; Lucas-Hahn, A.; Niemann, H.: Effects of different oocyte retrieval and in vitro maturation systems on bovine embryo development and quality. Zygote 23 (3), pp. 367 - 377 (2015)
710.
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Grote, P.; Herrmann, B. G.: Long noncoding RNAs in organogenesis: Making the difference. Trends in Genetics 31 (6), pp. 329 - 335 (2015)
711.
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Hossini, A. M.; Megges, M.; Prigione, A.; Lichtner, B.; Toliat, M. R.; Wruck, W.; Schröter, F.; Nuernberg, P.; Kroll, H.; Makrantonak, E. et al.; Zoubouli, C. C.; Adjaye, J.: Erratum: Induced pluripotent stem cell-derived neuronal cells from a sporadic Alzheimer's disease donor as a model for investigating AD-associated gene regulatory networks. BMC Genomics 16, p. 84 (2015)
712.
Journal Article
Maass, P. G.; Aydin, A.; Luft, F. C.; Schachterle, C.; Weise, A.; Stricker, S.; Lindschau, C.; Vaegler, M.; Qadri, F.; Toka, H. R. et al.; Schulz, H.; Krawitz, P. M.; Parkhomchuk, D.; Hecht, J.; Hollfinger, I.; Wefeld-Neuenfeld, Y.; Bartels-Klein, E.; Muhl, A.; Kann, M.; Schuster, H.; Chitayat, D.; Bialer, M. G.; Wienker, T. F.; Ott, J.; Rittscher, K.; Liehr, T.; Jordan, J.; Plessis, G.; Tank, J.; Mai, K.; Naraghi, R.; Hodge, R.; Hopp, M.; Hattenbach, L. O.; Busjahn, A.; Rauch, A.; Vandeput, F.; Gong, M.; Ruschendorf, F.; Hübner, N.; Haller, H.; Mundlos, S.; Bilginturan, N.; Movsesian, M. A.; Klussmann, E.; Toka, O.; Bahring, S.: PDE3A mutations cause autosomal dominant hypertension with brachydactyly. Nature Genetics 47 (6), pp. 647 - 653 (2015)
713.
Journal Article
Shaw, M.; Yap, T. Y.; Henden, L.; Bahlo, M.; Gardner, A.; Kalscheuer, V. M.; Haan, E.; Christie, L.; Hackett, A.; Gecz, J.: Identical by descent L1CAM mutation in two apparently unrelated families with intellectual disability without L1 syndrome. European Journal of Medical Genetics 58 (6-7), pp. 364 - 368 (2015)
714.
Journal Article
Starick, S. R.; Ibn-Salem, J.; Jurk, M.; Hernandez, C.; Love, M. I.; Chung, H.-R.; Vingron, M.; Thomas-Chollier, M.; Meijsing, S. H.: ChIP-exo signal associated with DNA-binding motifs provides insight into the genomic binding of the glucocorticoid receptor and cooperating transcription factors. Genome Res 25 (6), pp. 825 - 835 (2015)
715.
Journal Article
Sukalo, M.; Tilsen, F.; Kayserili, H.; Muller, D.; Tuysuz, B.; Ruddy, D. M.; Wakeling, E.; Orstavik, K. H.; Snape, K. M.; Trembath, R. et al.; De Smedt, M.; van der Aa, N.; Skalej, M.; Mundlos, S.; Wuyts, W.; Southgate, L.; Zenker, M.: DOCK6 mutations are responsible for a distinct autosomal-recessive variant of Adams-Oliver syndrome associated with brain and eye anomalies. Human Mutations 36 (6), pp. 593 - 598 (2015)
716.
Journal Article
Schafer, S.; Adami, E.; Heinig, M.; Rodrigues, K. E.; Kreuchwig, F.; Silhavy, J.; van Heesch, S.; Simaite, D.; Rajewsky, N.; Cuppen, E. et al.; Pravenec, M.; Vingron, M.; Cook, S. A.; Hubner, N.: Translational regulation shapes the molecular landscape of complex disease phenotypes. Nat Commun 6, 6:7200 (2015)
717.
Journal Article
Fuhr, L.; Rousseau, M.; Plauth, A.; Schroeder, F. C.; Sauer, S.: Amorfrutins Are Natural PPARgamma Agonists with Potent Anti-inflammatory Properties. Journal of Natural Products 78 (5), pp. 1160 - 1164 (2015)
718.
Journal Article
Lupiáñez, D. G.; Kraft, K.; Heinrich, V.; Krawitz, P.; Brancati, F.; Klopocki, E.; Horn, D.; Kayserili, H.; Opitz, J. M.; Laxova, R. et al.; Santos-Simarro, F.; Gilbert-Dussardier, B.; Wittler, L.; Borschiwer, M.; Haas, S. A.; Osterwalder, M.; Franke, M.; Timmermann, B.; Hecht, J.; Spielmann, M.; Visel, A.; Mundlos, S.: Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions. Cell 161 (5), pp. 1012 - 1025 (2015)
719.
Journal Article
Milenkovic, A.; Brandl, C.; Milenkovic, V. M.; Jendryke, T.; Sirianant, L.; Wanitchakool, P.; Zimmermann, S.; Reiff, C. M.; Horling, F.; Schrewe, H. et al.; Schreiber, R.; Kunzelmann, K.; Wetzel, C. H.; Weber, B. H. F.: Bestrophin 1 is indispensable for volume regulation in human retinal pigment epithelium cells. Proceedings of the National Academy of Sciences of the United States of America 112 (20), pp. E2630 - E2639 (2015)
720.
Journal Article
Kähler, C.; Guenther, A.; Uhlich, A.; Krobitsch, S.: PRMT1-mediated arginine methylation controls ATXN2L localization. Experimental Cell Research 334 (1), pp. 114 - 125 (2015)
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