Single-cell DNA-methylation analysis reveals epigenetic chimerism in preimplantation embryos

by Lorthongpanich, C., Cheow, L., Balu, S., Quake, S.R., Knowles, B.B., Burkholder, W.F., Solter, D., Messerschmidt, D.M.
Published 2016

Global translation during early development depends on the essential transcription factor PRDM10

by Han, B.Y., Seah, M.K.Y., Brooks, I.R., Quek, D.H.P., Huxley, D.R., Foo, C.-S., Lee, L.T., Wollmann, H., Guo, H., Messerschmidt, D.M., Guccione, E.
Published 2021

Loss of maternal Trim28 causes male-predominant early embryonic lethality

by Kumar, A.S, Seah, M.K.Y, Ling, K.Y, Wang, Y, Tan, J.H.L, Nitsch, S, Lim, S.L, Lorthongpanich, C, Wollmann, H, Low, D.H.P, Guccione, E, Messerschmidt, D.M
Published 2020

PRDM15 loss of function links NOTCH and WNT/PCP signaling to patterning defects in holoprosencephaly

by Mzoughi, S., Di Tullio, F., Low, D.H.P., Motofeanu, C.-M., Ong, S.L.M., Wollmann, H., Wun, C.M., Kruszka, P., Muenke, M., Hildebrandt, F., Dunn, N.R., Messerschmidt, D.M., Guccione, E.
Published 2021

A genetic and developmental pathway from STAT3 to the OCT4-NANOG circuit is essential for maintenance of ICM lineages in vivo

by Do, D.V., Ueda, J., Messerschmidt, D.M., Lorthongpanich, C., Zhou, Y., Feng, B., Guo, G., Lin, P.J., Hossain, M.Z., Zhang, W., Moh, A., Wu, Q., Robson, P., Ng, H.H., Poellinger, L., Knowles, B.B., Solter, D., Fu, X.-Y.
Published 2014