Publikationen von Matthias Marks

Weitensteiner, V.; Zhang, R.; Bungenberg, J.; Marks, M.; Gehlen, J.; Ralser, D. J.; Hilger, A. C.; Sharma, A.; Schumacher , J.; Gembruch, U. et al.; Merz, W. M.; Becker, A.; Altmüller, J.; Thiele, H.; Herrmann, B. G.; Odermatt , B.; Ludwig, M.; Reutter, H.: 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), S. 587 - 597 (2018)

Lange, L.; Marks, M.; Liu, J.; Wittler, L.; Bauer, H.; Piehl, S.; Bläß, G.; Timmermann, B.; Herrmann, B. G.: Pattering and gastrulation deffects caused by the tw18 lethal are due to loss of Ppp2r1a. Biology Open 6 (6), S. 752 - 764 (2017)

Riemer, P.; Rydenfelt, M.; Marks, M.; van Eunen, K.; Thedieck, K.; Herrmann, B. G.; Blüthgen, N.; Sers, C.; Morkel, M.: Oncogenic ß-catenin and PIK3CA instruct network states and cancer phenotypes in intestinal organoids. The Journal of Cell Biology: JCB 216 (6), S. 1567 - 1577 (2017)

Sudheer, S.; Liu, J.; Marks, M.; Koch, F.; Anurin, A.; Scholze, M.; Senft, A. D.; Wittler, L.; Macura, K.; Grote, P. et al.; Herrmann, B. G.: Different Concentrations of FGF Ligands, FGF2 or FGF8 Determine Distinct States of WNT-Induced Presomitic Mesoderm. Stem Cells 34 (7), S. 1790 - 800 (2016)

Marks, M.; Pennimpede, T.; Lange, L.; Grote, P.; Herrmann, B. G.; Wittler, L.: 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), S. 438 - 451 (2016)

Schwartz, B.; Marks, M.; Wittler, L.; Werber, M.; Währisch, S.; Nordheim, A.; Herrmann, B. G.; Grote, P.: SRF is essential for mesodermal cell migration during elongation of the embryonic body axis. Mechanisms of Development 133, S. 23 - 35 (2014)

Marks, M.: Investigations into Expression and Function of the Murine Fam181 Gene Family. Dissertation, Free University Berlin, Faculty of Biology, Chemistry and Pharmacy, Berlin (2014)