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An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development.
Baek ST, Copeland B, Yun EJ, Kwon SK, Guemez-Gamboa A, Schaffer AE, Kim S, Kang HC, Song S, Mathern GW, Gleeson JG
Nat Med. 2015 Dec;21(12):1445-54. doi: 10.1038/nm.3982. Epub 2015 Nov 2. PubMed Article

Plasmids from Article

ID Plasmid Purpose
73047pCAG mFoxg1-GFP T271AC-terminal fusion of gfp Mouse Foxg1 T271A
73048pCAG mFoxg1-GFP wildtypeC-terminal fusion of gfp Mouse wildtype Foxg1
73049pCIG AKT3 E17K;K177MHuman AKT3 E17K;K177M
73050pCIG AKT3 E17KHuman AKT3 E17K
73051pCIG AKT3 K177MHuman AKT3 K177M
73052pCIG AKT3 S472AHuman AKT3 S472A
73053pCIG AKT3 S472EHuman AKT3 S472E
73055pCIG PIK3CA E545KHuman PIK3CA E545K
73056pCIG PIK3CA WildtypeHuman PIK3CA Wildtype
73057pCAG mFoxg1-GFP T271EC-terminal GFP fusion of Mouse Foxg1 T271E

Antibodies from Article