Pogoda, HM., Riedl-Quinkertz, I., Hammerschmidt, M. (2023). Direct BMP signaling to chordoblasts is required for the initiation of segmented notochord sheath mineralization in zebrafish vertebral column development. Front Endocrinol (Lausanne). 14:1107339. doi: 10.3389/fendo.2023.1107339
Pogoda, HM., Riedl-Quinkertz, I., Löhr, H., Waxman, J.S., Dale, R.M., Topczewski, J., Schulte-Merker, S., Hammerschmidt, M. (2018). Direct activation of chordoblasts by retinoic acid is required for segmented centra mineralization during zebrafish spine development. Development 2018 145: dev159418 doi: 10.1242/dev.15941
Jeradi, S. and Hammerschmidt, M. (2016). Retinoic acid-induced premature osteoblast-to-preosteocyte transitioning has multiple effects on calvarial development. Development 143: 1205-1216
Talbot, J.C., Walker, M.B., Carney, T.C., Huycke, T.R., Yan, Y.-L., Bremiller, R.A., Gai, L., DeLaurier, A., Postlethwait, J.H., Hammerschmidt, M. and Kimmel, C.B. (2012). Fras1 shapes endodermal pouch 1 and stabilizes zebrafish pharyngeal skeletal development. Development 139: 2804-2813
Asharani, P.V., Keupp, K., Semler, O., Wang, W., Li, Y., Thiele, H., Yigit, G., Pohl, E., Becker, J., Frommolt, P., Sonntag, C., Altmüller, J., Zimmermann, K., Greenspan, D.S., Akarsu, N.A., Netzer, C., Schönau, E., Wirth, R, Hammerschmidt, M., Nürnberg, P., Wollnik, B. and Carney, T.J. (2012). Attenuated. BMP1 function compromises osteogenesis, leading to bone fragility in humans and zebrafish. Am. J. Hum. Genet. 90: 661-674
Laue, K., Pogoda, H.-M., Daniel PB, van Haeringen A, Alanay Y, von Ameln S, Rachwalski M, Morgan T, Gray MJ, Breuning MH, Sawyer GM, Sutherland-Smith AJ, Nikkels PG, Kubisch C, Bloch W, Wollnik B, Hammerschmidt, M.*, Roberston, S.P.* (2011). Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid. Am. J. Hum. Genet. 89: 595-606 (* joint corresponding authors)
Li, Y., Laue, K., Temtamy, S., Aglan, M., Kotan, L.D., Yigit, G., Husniye, C., Pawlik, B., Nürnberg, G., Wakeling, E.L., Quarrell, O.W., Baessmann, I., Lanktree, M.B., Yilmaz, M., Hegele, R.A., Amr, K., May, K.W., Nürnberg, P., Topaoglu, A.K., Hammerschmidt, M.* and Wollnik, B.* (2010). Temtamy preaxial brachydactyly syndrome is caused by loss-of-function mutations in Chondroitin synthase 1, a potential target of BMP signaling. Am. J. Hum. Genet. 87: 757-767 (* joint corresponding authors)
Laue, K., Jänicke, M., Plaster, N., Sonntag, C. and Hammerschmidt, M. (2008). Restriction of retinoic acid activity by Cyp26b1 is required for proper timing and patterning of osteogenesis during zebrafish development. Development 135: 3775-3787
Laue, K., Dejaut, S., Crump, J. G., Plaster, N., Roehl, H. H., Kimmel, C. B., Schneider, R. and Hammerschmidt, M. (2008). The multidomain protein Brpf1 binds histones and is required for hox gene expression and segmental identity. Development 135: 1935-1946
Nowak, M. and Hammerschmidt, M. (2006). Ubc9 is required for mitosis and cell survival during zebrafish development. Mol. Biol. Cell 17: 5324-5336
Plaster, N., Sonntag, C., Busse, C.E. and Hammerschmidt, M. (2006). p53 deficiency rescues apoptosis and differentiation of multiple cell types in zebrafish flathead mutants deficient for zygotic DNA polymerase d1. Cell Death Diff. 13: 223-235
