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...

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Bibliografski detalji

Glavni autori:	Jennie C. Holmberg, Victoria A. Riley, Aidan M. Sokolov, Luke J. Fisher, David M. Feliciano
Format:	Artigo
Jezik:	Inglês
Izdano:	MDPI AG 2026-03-01
Serija:	Kinases and Phosphatases
Teme:	<i>Tsc2</i> <i>Tsc1</i> Tuberin Tuberous Sclerosis Complex TSC mTOR
Online pristup:	https://www.mdpi.com/2813-3757/4/1/6
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