Paving Therapeutic Avenues for FOXG1 Syndrome: Untangling Genotypes and Phenotypes from a Molecular Perspective

por Akol, Ipek, Gather, Fabian, Vogel, Tanja
Publicado 2022

DOT1L deletion impairs the development of cortical parvalbumin-expressing interneurons

por Cheffer, Arquimedes, Garcia-Miralles, Marta, Maier, Esther, Akol, Ipek, Franz, Henriette, Srinivasan, Vandana Shree Vedartham, Vogel, Tanja
Publicado 2023

Nucleophosmin 1 cooperates with the methyltransferase DOT1L to preserve peri-nucleolar heterochromatin organization by regulating H3K27me3 levels and DNA repeats expression

por Izzo, Annalisa, Akol, Ipek, Villarreal, Alejandro, Lebel, Shannon, Garcia-Miralles, Marta, Cheffer, Arquimedes, Bovio, Patrick, Heidrich, Stefanie, Vogel, Tanja
Publicado 2023

Multimodal epigenetic changes and altered NEUROD1 chromatin binding in the mouse hippocampus underlie FOXG1 syndrome

por Akol, Ipek, Izzo, Annalisa, Gather, Fabian, Strack, Stefanie, Heidrich, Stefanie, Ó hAilín, Darren, Villarreal, Alejandro, Hacker, Christine, Rauleac, Tudor, Bella, Chiara, Fischer, Andre, Manke, Thomas, Vogel, Tanja
Publicado 2023