SomaticAKT1mutations cause meningiomas colocalizing with a characteristic pattern of cranial hyperostosis

Molecular genetics of meningiomas: a systematic review of the current literature and potential basis for future treatment paradigms

(2016) Martin H. Pham et al.   Neurosurgical Focus

Complex interactions between the components of the PI3K/AKT/mTOR pathway, and with components of MAPK, JAK/STAT and Notch-1 pathways, indicate their involvement in meningioma development

(2014) Elias A. El-Habr et al.   VIRCHOWS ARCHIV

A Limited Form of Proteus Syndrome With Bilateral Plantar Cerebriform Collagenomas and Varicose Veins Secondary to a MosaicAKT1Mutation

(2014) Jamie S. Wee et al.   JAMA Dermatology

AKT1E17K mutations cluster with meningothelial and transitional meningiomas and can be detected by SFRP1 immunohistochemistry

(2013) Felix Sahm et al.   ACTA NEUROPATHOLOGICA

Genomic sequencing of meningiomas identifies oncogenic SMO and AKT1 mutations

(2013) Priscilla K Brastianos et al.   NATURE GENETICS

Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO

(2013) V. E. Clark et al.   SCIENCE

A Mosaic Activating Mutation inAKT1Associated with the Proteus Syndrome

(2011) Marjorie J. Lindhurst et al.   NEW ENGLAND JOURNAL OF MEDICINE

Hyperostosing meningiomas of the cranial vault with and without tumor mass

(2010) Andrea Talacchi et al.   ACTA NEUROCHIRURGICA

Meningioma causing hyperostosis of the cranial convexity in a child

(2010) Adem Yılmaz et al.   JOURNAL OF CLINICAL NEUROSCIENCE

Fibroblast growth factor receptor–3 expression in meningiomas with stimulation of proliferation by the phosphoinositide 3 kinase–Akt pathway

(2009) Mahlon D. Johnson et al.   JOURNAL OF NEUROSURGERY