The Fuchs corneal dystrophy-associated CTG repeat expansion in the TCF4 gene affects transcription from its alternative promoters

por Sirp, Alex, Leite, Kristian, Tuvikene, Jürgen, Nurm, Kaja, Sepp, Mari, Timmusk, Tõnis
Publicado 2020

Functional consequences of TCF4 missense substitutions associated with Pitt-Hopkins syndrome, mild intellectual disability, and schizophrenia

por Sirp, Alex, Roots, Kaisa, Nurm, Kaja, Tuvikene, Jürgen, Sepp, Mari, Timmusk, Tõnis
Publicado 2021

Daughterless, the Drosophila orthologue of TCF4, is required for associative learning and maintenance of the synaptic proteome

por Tamberg, Laura, Jaago, Mariliis, Säälik, Kristi, Sirp, Alex, Tuvikene, Jürgen, Shubina, Anastassia, Kiir, Carl Sander, Nurm, Kaja, Sepp, Mari, Timmusk, Tõnis, Palgi, Mari
Publicado 2020

Isoform-Specific Reduction of the Basic Helix-Loop-Helix Transcription Factor TCF4 Levels in Huntington’s Disease

por Nurm, Kaja, Sepp, Mari, Castany-Pladevall, Carla, Creus-Muncunill, Jordi, Tuvikene, Jürgen, Sirp, Alex, Vihma, Hanna, Blake, Derek J., Perez-Navarro, Esther, Timmusk, Tõnis
Publicado 2021