S. Franck

CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy

Michael D. Wilson, R. Weksberg, S. Seneca, 2017, American journal of human genetics.

Endogenous suppression of WNT signalling in human embryonic stem cells leads to low differentiation propensity towards definitive endoderm

Laura Prochazka, P. Zandstra, Joel Östblom, 2020, Scientific Reports.

The role of the reprogramming method and pluripotency state in gamete differentiation from patient-specific human pluripotent stem cells

B. Heindryckx, K. Sermon, G. Pennings, 2018, Molecular human reproduction.

Sustained intrinsic WNT and BMP4 activation impairs hESC differentiation to definitive endoderm and drives the cells towards extra-embryonic mesoderm

K. Sermon, C. Spits, M. Geens, 2021, Scientific Reports.

Constitutional activation of BMP4 and WNT signalling in hESC results in impaired mesendoderm differentiation

K. Sermon, C. Spits, M. Geens, 2020, bioRxiv.

Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicing

M. Swanson, C. Spits, P. Hilven, 2022, Biology open.

MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells.

J. Vermeesch, K. Sermon, C. Spits, 2020, Human Molecular Genetics.

MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells

J. Vermeesch, K. Sermon, C. Spits, 2020, bioRxiv.