Loss of <i>Tsc2</i> in Neonatal V-SVZ Neural Stem Cells Causes Rare Malformations
Tuberous Sclerosis Complex (TSC) is a genetic disorder caused by mutations that inactivate <i>TSC1</i> or <i>TSC2</i> genes. <i>TSC1</i> or <i>TSC2</i> mutations activate the mammalian target of rapamycin complex 1 (mTORC1) protein kinase pathway. Although many patients inherit a single copy of a mu...
Guardado en:
| Autores principales: | , , , , |
|---|---|
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
MDPI AG
2026-03-01
|
| Colección: | Kinases and Phosphatases |
| Materias: | |
| Acceso en línea: | https://www.mdpi.com/2813-3757/4/1/6 |
| Etiquetas: |
Sin Etiquetas, Sea el primero en etiquetar este registro!
|