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...
I tiakina i:
| Ngā kaituhi matua: | , , , , |
|---|---|
| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
MDPI AG
2026-03-01
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| Rangatū: | Kinases and Phosphatases |
| Ngā marau: | |
| Urunga tuihono: | https://www.mdpi.com/2813-3757/4/1/6 |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
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