mRNA Cap Methylation in Pluripotency and Differentiation

por Grasso, Laura, Suska, Olga, Davidson, Lindsay, Gonatopoulos-Pournatzis, Thomas, Williamson, Ritchie, Wasmus, Lize, Wiedlich, Simone, Peggie, Mark, Stavridis, Marios P., Cowling, Victoria H.
Publicado 2016

Elevated O‐GlcNAc Levels Activate Epigenetically Repressed Genes and Delay Mouse ESC Differentiation Without Affecting Naïve to Primed Cell Transition

por Speakman, Christopher M., Domke, Tanja C.E., Wongpaiboonwattana, Wikrom, Sanders, Kelly, Mudaliar, Manikhandan, van Aalten, Daan M.F., Barton, Geoffrey J., Stavridis, Marios P.
Publicado 2014

A missense mutation in the catalytic domain of O‐GlcNAc transferase links perturbations in protein O‐GlcNAcylation to X‐linked intellectual disability

por Pravata, Veronica M., Gundogdu, Mehmet, Bartual, Sergio G., Ferenbach, Andrew T., Stavridis, Marios, Õunap, Katrin, Pajusalu, Sander, Žordania, Riina, Wojcik, Monica H., van Aalten, Daan M. F.
Publicado 2019

Negative-feedback regulation of FGF signalling by DUSP6/MKP-3 is driven by ERK1/2 and mediated by Ets factor binding to a conserved site within the DUSP6/MKP-3 gene promoter

por Ekerot, Maria, Stavridis, Marios P., Delavaine, Laurent, Mitchell, Michael P., Staples, Christopher, Owens, David M., Keenan, Iain D., Dickinson, Robin J., Storey, Kate G., Keyse, Stephen M.
Publicado 2008

Catalytic deficiency of O-GlcNAc transferase leads to X-linked intellectual disability

por Pravata, Veronica M., Muha, Villo, Gundogdu, Mehmet, Ferenbach, Andrew T., Kakade, Poonam S., Vandadi, Vasudha, Wilmes, Ariane C., Borodkin, Vladimir S., Joss, Shelagh, Stavridis, Marios P., van Aalten, Daan M. F.
Publicado 2019

An O-GlcNAc transferase pathogenic variant linked to intellectual disability affects pluripotent stem cell self-renewal

por Omelková, Michaela, Fenger, Christina Dühring, Murray, Marta, Hammer, Trine Bjørg, Pravata, Veronica M., Bartual, Sergio Galan, Czajewski, Ignacy, Bayat, Allan, Ferenbach, Andrew T., Stavridis, Marios P., van Aalten, Daan M. F.
Publicado 2023

An intellectual disability syndrome with single-nucleotide variants in O-GlcNAc transferase

por Pravata, Veronica M., Omelková, Michaela, Stavridis, Marios P., Desbiens, Chelsea M., Stephen, Hannah M., Lefeber, Dirk J., Gecz, Jozef, Gundogdu, Mehmet, Õunap, Katrin, Joss, Shelagh, Schwartz, Charles E., Wells, Lance, van Aalten, Daan M. F.
Publicado 2020

An ERK5–KLF2 signalling module regulates early embryonic gene expression and telomere rejuvenation in stem cells

por Brown, Helen A., Williams, Charles A.C., Zhou, Houjiang, Rios-Szwed, Diana, Fernandez-Alonso, Rosalia, Mansoor, Saria, McMulkin, Liam, Toth, Rachel, Gourlay, Robert, Peltier, Julien, Dieguez-Martinez, Nora, Trost, Matthias, Lizcano, Jose M., Stavridis, Marios P., Findlay, Greg M.
Publicado 2021