![]() ![]() | NORONHA, A., MODAMIO CHAMARRO, J., JAROSZ, Y., GUERARD, E., Sompairac, N., PRECIAT GONZALEZ, G. A., DANIELSDOTTIR, A. D., KRECKE, M., MERTEN, D., HARALDSDOTTIR, H., HEINKEN, A. K., HEIRENDT, L., MAGNUSDOTTIR, S., RAVCHEEV, D., SAHOO, S., GAWRON, P., FRISCIONI, L., GARCIA SANTA CRUZ, B., Prendergast, M., ... THIELE, I. (2018). The Virtual Metabolic Human database: integrating human and gut microbiome metabolism with nutrition and disease. Nucleic Acids Research. doi:10.1093/nar/gky992 ![]() |
Nguyen, H., Riess, A., KRÜGER, M., Bauer, P., Singer, S., Schneider, M., Enders, H., & Dufke, A. (2009). Mosaic Trisomy 21/Monosomy 21 in a Living Female Infant. Cytogenetic and Genome Research, 125 (1), 26-32. doi:10.1159/000218745 ![]() |
RUNTE, M., Varon, R., Horn, D., Horsthemke, B., & Buiting, K. (2005). Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader–Willi syndrome. Human Genetics, 116 (3), 228-230. doi:10.1007/s00439-004-1219-2 ![]() |
Toulany, M., Dittmann, K., KRÜGER, M., Baumann, M., & Rodemann, H. (2005). Radioresistance of K-Ras mutated human tumor cells is mediated through EGFR-dependent activation of PI3K-AKT pathway. Radiotherapy and Oncology, 76 (2), 143-150. doi:10.1016/j.radonc.2005.06.024 ![]() |
RUNTE, M., Kroisel, P., Gillessen-Kaesbach, G., Varon, R., Horn, D., Cohen, M., Wagstaff, J., Horsthemke, B., & Buiting, K. (2004). SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome. Human Genetics, 114 (6), 553-561. doi:10.1007/s00439-004-1104-z ![]() |
RUNTE, M. (2003). Identifizierung und Expressionsanalyse der SNURF-SNRPN Sense – UBE3A Antisense Transkriptionseinheit in der Prader-Willi-/Angelman-Syndrom-Region auf Chromosom 15 [Doctoral thesis, Universität Essen]. ORBilu-University of Luxembourg. https://orbilu.uni.lu/handle/10993/20853 |
RUNTE, M., Faerber, C., Lich, C., Zeschnigk, M., Buchholz, T., Smith, A., Van Maldergem, L., Buerger, J., Muscatelli, F., Gillessen-Kaesbach, G., Horsthemke, B., & Buiting, K. (2001). Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15. European Journal of Human Genetics, 9 (7), 519-526. doi:10.1038/sj.ejhg.5200661 ![]() |
RUNTE, M., Huettenhofer, A., Groß, S., Kiefmann, M., Horsthemke, B., & Buiting, K. (2001). The IC-SNURF–SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A. Human Molecular Genetics, 10 (23), 2687-2700. doi:10.1093/hmg/10.23.2687 ![]() |
Klein, W., Tromm, A., Griga, T., Fricke, H., Folwaczny, C., Hocke, M., Eitner, K., Marx, M., RUNTE, M., & Epplen, J. T. (2000). The IL-10 gene is not involved in the predisposition to inflammatory bowel disease. Electrophoresis, 21 (17), 3578-3582. doi:10.1002/1522-2683(200011)21:17<3578::AID-ELPS3578>3.0.CO;2-Z ![]() |
RUNTE, M., Dekomien, G., & Epplen, J. T. (2000). Evaluation of RDS/Peripherin and ROM1 as candidate genes in generalised progressive retinal atrophy and exclusion of digenic inheritance. Animal Genetics, 31 (3), 223-227. doi:10.1046/j.1365-2052.2000.00633.x ![]() |
Dekomien, G., RUNTE, M., Goedde, R., & Epplen, J. T. (2000). Generalized progressive retinal atrophy of Sloughi dogs is due to an 8-bp insertion in exon 21 of the PDE6B gene. CytoGenetics and Cell Genetics, 90 (3-4), 261-267. doi:10.1159/000056785 ![]() |