Disparate and shared transcriptomic signatures associated with cortical atrophy in genetic bvFTD.
Journal
medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986
Informations de publication
Date de publication:
27 Jul 2024
27 Jul 2024
Historique:
medline:
31
8
2024
pubmed:
31
8
2024
entrez:
30
8
2024
Statut:
epublish
Résumé
Cortical atrophy in behavioral variant frontotemporal degeneration (bvFTD) exhibits spatial heterogeneity across genetic subgroups, potentially driven by distinct biological mechanisms. Using an integrative imaging-transcriptomics approach, we identified disparate and shared transcriptomic signatures associated with cortical thickness in
Identifiants
pubmed: 39211858
doi: 10.1101/2024.07.25.24310894
pmc: PMC11361203
pii:
doi:
Types de publication
Journal Article
Preprint
Langues
eng