A Bioinformatic Investigation into a Unique Human FOXM1 Exon Variant and Its Relevance to Gyrencephaly
Therefore, we conclude that the FOXM1 transcript variant comprising the exon 9 sequence in its entirety could be more appropriately reclassified as a human-specific cortical folding variant not found in other species. This research lays the foundation for further investigating the role of FOXM1 exon 9 in human gyrification and brain development.
Authors
- A.C. Johnstone (ORCID: https://orcid.org/0000-0003-0736-9751)
- Mikaela Barresi (ORCID: https://orcid.org/0000-0001-5365-5113)
- Mary Tolcos (ORCID: https://orcid.org/0000-0001-6105-4553)
Institutions
- RMIT University (AU)
Publication Details
- Journal
- Developmental Neuroscience
- Published
- 2025-04-22
- DOI
- https://doi.org/10.1159/000545713
- Primary Topic
- FOXO transcription factor regulation
- Type
- article
- Field-Weighted Citation Impact
- 0.00