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.
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Plasmids from Article
| ID | Plasmid | Purpose |
|---|---|---|
| 73047 | pCAG mFoxg1-GFP T271A | C-terminal fusion of gfp Mouse Foxg1 T271A |
| 73048 | pCAG mFoxg1-GFP wildtype | C-terminal fusion of gfp Mouse wildtype Foxg1 |
| 73049 | pCIG AKT3 E17K;K177M | Human AKT3 E17K;K177M |
| 73050 | pCIG AKT3 E17K | Human AKT3 E17K |
| 73051 | pCIG AKT3 K177M | Human AKT3 K177M |
| 73052 | pCIG AKT3 S472A | Human AKT3 S472A |
| 73053 | pCIG AKT3 S472E | Human AKT3 S472E |
| 73055 | pCIG PIK3CA E545K | Human PIK3CA E545K |
| 73056 | pCIG PIK3CA Wildtype | Human PIK3CA Wildtype |
| 73057 | pCAG mFoxg1-GFP T271E | C-terminal GFP fusion of Mouse Foxg1 T271E |