• Daughterless, the Drosophila orthologue of TCF4, is required for associative learning and maintenance of the synaptic proteomeTamberg, Laura; Jaago, Mariliis; Säälik, Kristi; Sirp, Alex; Tuvikene, Jürgen; Šubina, Anastassia; Kiir, Carl Alexander; Nurm, Kaja; Sepp, Mari; Timmusk, Tõnis; Palgi, MariDisease Models & Mechanisms2020 / art. dmm042747, 15 p. : ill https://doi.org/10.1242/dmm.042747 https://www.scopus.com/sourceid/19400157151 https://www.scopus.com/record/display.uri?eid=2-s2.0-85089787837&origin=inward&txGid=00501db0e094da2f52c76cc77ed39410 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=DIS%20MODEL%20MECH&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000568787400004
• The Fuchs corneal dystrophy-associated CTG repeat expansion in the TCF4 gene affects transcription from its alternative promotersSirp, Alex; Leite, Kristian; Tuvikene, Jürgen; Nurm, Kaja; Sepp, Mari; Timmusk, TõnisScientific reports2020 / art. 18424 https://doi.org/10.1038/s41598-020-75437-3 https://www.scopus.com/sourceid/21100200805 https://www.scopus.com/record/display.uri?eid=2-s2.0-85094182890&origin=inward&txGid=22248f09f3e4ee0047f2c77e4e88d16f https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SCI%20REP-UK&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000587650700010
• Functional consequences of TCF4 missense substitutions associated with Pitt-Hopkins syndrome, mild intellectual disability, and schizophreniaSirp, Alex; Roots, Kaisa; Nurm, Kaja; Tuvikene, Jürgen; Sepp, Mari; Timmusk, TõnisThe journal of biological chemistry2021 / art. 101381 https://doi.org/10.1016/j.jbc.2021.101381 https://www.scopus.com/sourceid/17592 https://www.scopus.com/record/display.uri?eid=2-s2.0-85120786755&origin=inward&txGid=2a0e0ea8f34df3f954eb5a2f4f4332a6 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=J%20BIOL%20CHEM&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000748311800006
• The intellectual disability and schizophrenia associated transcription factor TCF4 is regulated by neuronal activity and protein kinase ASepp, Mari; Vihma, Hanna; Nurm, Kaja; Urb, Mari; Page, Stephanie Cerceo; Roots, Kaisa; Hark, Anu; Maher, Brady J.; Pruunsild, Priit; Timmusk, TõnisJournal of neuroscience2017 / p. 10516-10527 : ill https://doi.org/10.1523/JNEUROSCI.1151-17.2017 https://www.scopus.com/sourceid/16764 https://www.scopus.com/record/display.uri?eid=2-s2.0-85032376205&origin=inward&txGid=2ec7b1a903971f17f293c42510158560 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=J%20NEUROSCI&year=2023 https://www.webofscience.com/wos/woscc/full-record/WOS:000490188200001
• Isoform-specific reduction of the basic helix-Loop-helix transcription factor TCF4 levels in Huntington's diseaseNurm, Kaja; Sepp, Mari; Castany-Pladevall, Carla; Creus-Muncunill, Jordi; Tuvikene, Jürgen; Sirp, Alex; Vihma, Hanna; Blake, Derek J.; Perez-Navarro, Esther; Timmusk, TõniseNeuro2021 / 53 p. : ill https://doi.org/10.1523/ENEURO.0197-21.2021 https://www.scopus.com/sourceid/21100782808 https://www.scopus.com/record/display.uri?eid=2-s2.0-85117035817&origin=inward&txGid=0456efa44ef3b7987b5d28a44aafbbda https://jcr.clarivate.com/jcr-jp/journal-profile?journal=ENEURO&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000708032800001
• Transcription factors FOXO3 and TCF4 in Huntington’s disease = Transkriptisoonifaktorid FOXO3 ja TCF4 Huntingtoni tõvesNurm, Kaja2021 https://www.ester.ee/record=b5469637*est https://digikogu.taltech.ee/et/Item/07ffb222-9e0b-46ba-ace9-81f821b153a6 https://doi.org/10.23658/taltech.55/2021