Researcher Portfolio
Marks, Matthias
Dept. of Developmental Genetics (Head: Bernhard G. Herrmann), Max Planck Institute for Molecular Genetics, Max Planck Society
Researcher Profile
Position: Dept. of Developmental Genetics (Head: Bernhard G. Herrmann), Max Planck Institute for Molecular Genetics, Max Planck Society
Researcher ID: https://pure.mpg.de/cone/persons/resource/persons50423
Publications
: Weitensteiner, V., Zhang, R., Bungenberg, J., Marks, M., Gehlen, J., Ralser, D. J., Hilger, A. C., Sharma, A., Schumacher, J., Gembruch, U., Merz, W. M., Becker, A., Altmüller, J., Thiele, H., Herrmann, B. G., Odermatt, B., Ludwig, M., & Reutter, H. (2018). Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene. Birth Defects Research, 110(7), 587-597. doi:10.1002/bdr2.1200. [PubMan] : Lange, L., Marks, M., Liu, J., Wittler, L., Bauer, H., Piehl, S., Bläß, G., Timmermann, B., & Herrmann, B. G. (2017). Pattering and gastrulation deffects caused by the tw18 lethal are due to loss of Ppp2r1a. Biology Open, 6(6), 752-764. doi:10.1242/bio.023200. [PubMan] : Riemer, P., Rydenfelt, M., Marks, M., van Eunen, K., Thedieck, K., Herrmann, B. G., Blüthgen, N., Sers, C., & Morkel, M. (2017). Oncogenic ß-catenin and PIK3CA instruct network states and cancer phenotypes in intestinal organoids. The Journal of Cell Biology: JCB, 216(6), 1567-1577. doi:10.1083/jcb.201610058. [PubMan] : Sudheer, S., Liu, J., Marks, M., Koch, F., Anurin, A., Scholze, M., Senft, A. D., Wittler, L., Macura, K., Grote, P., & Herrmann, B. G. (2016). Different Concentrations of FGF Ligands, FGF2 or FGF8 Determine Distinct States of WNT-Induced Presomitic Mesoderm. Stem Cells, 34(7), 1790-800. doi:10.1002/stem.2371. [PubMan] : Marks, M., Pennimpede, T., Lange, L., Grote, P., Herrmann, B. G., & Wittler, L. (2016). Analysis of the Fam181 gene family during mouse development reveals distinct strain-specific expression patterns, suggesting a role in nervous system development and function. Gene, 575(2 Pt 2), 438-451. doi:10.1016/j.gene.2015.09.035. [PubMan] : Schwartz, B., Marks, M., Wittler, L., Werber, M., Währisch, S., Nordheim, A., Herrmann, B. G., & Grote, P. (2014). SRF is essential for mesodermal cell migration during elongation of the embryonic body axis. Mechanisms of Development, 133, 23-35. doi:10.1016/j.mod.2014. [PubMan] : Marks, M. (2014). Investigations into Expression and Function of the Murine Fam181 Gene Family. PhD Thesis, Free University Berlin, Faculty of Biology, Chemistry and Pharmacy, Berlin. [PubMan]