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KRÜGER Maren

University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB) > LCSB Operations > Scienteens Lab

Main Referenced Co-authors
Buiting, K (3)
Epplen, Jörg T (3)
Horsthemke, B (3)
Dekomien, Gabriele (2)
Horn, D (2)
Main Referenced Disciplines
Genetics & genetic processes (9)
Oncology (1)
Biochemistry, biophysics & molecular biology (1)
Biotechnology (1)

Publications (total 11)

The most downloaded
391 downloads
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 https://hdl.handle.net/10993/37074

The most cited

322 citations (Scopus®)

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 https://hdl.handle.net/10993/20847

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer reviewed

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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