An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development-Reference-Cited by-同舟云学术

An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development

Published:2015-11-02 Issue:12 Volume:21 Page:1445-1454
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Baek Seung Tae^ORCID,Copeland Brett,Yun Eun-Jin,Kwon Seok-Kyu,Guemez-Gamboa Alicia,Schaffer Ashleigh E,Kim Sangwoo,Kang Hoon-Chul,Song Saera,Mathern Gary W,Gleeson Joseph G

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm.3982.pdf

Reference61 articles.

1. Lee, J.H. et al. De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly. Nat. Genet. 44, 941–945 (2012).

2. Poduri, A., Evrony, G.D., Cai, X. & Walsh, C.A. Somatic mutation, genomic variation and neurological disease. Science 341, 1237758 (2013).

3. Aronica, E., Becker, A.J. & Spreafico, R. Malformations of cortical development. Brain Pathol. 22, 380–401 (2012).

4. Blümcke, I. et al. The clinicopathologic spectrum of focal cortical dysplasias: a consensus classification proposed by an ad hoc task force of the ILAE Diagnostic Methods Commission. Epilepsia 52, 158–174 (2011).

5. Taylor, D.C., Falconer, M.A., Bruton, C.J. & Corsellis, J.A. Focal dysplasia of the cerebral cortex in epilepsy. J. Neurol. Neurosurg. Psychiatry 34, 369–387 (1971).

Cited by 104 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A spectrum of AKT3 activating mutations cause focal malformations of cortical development (FMCDs) in cortical organoids;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2024-08

2. Neurocognitive, Clinical and Reelin Activity in Rehabilitation Using Neurofeedback Therapy in Patients with Schizophrenia;Journal of Clinical Medicine;2024-07-10

3. Broadening the scope of multigene panel analysis for adult epilepsy patients;Epilepsia Open;2024-07

4. Balloon cells in malformations of cortical development: friends or foes?;Acta Epileptologica;2024-06-14

5. Focal cortical dysplasia II caused by brain somatic mutation of IRS-1 is associated with ERK signaling pathway activation;Cerebral Cortex;2024-06