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