Oncogenic PI3K mutations are as common asAKT1andSMOmutations in meningioma

Author:

Abedalthagafi Malak,Bi Wenya Linda,Aizer Ayal A.,Merrill Parker H.,Brewster Ryan,Agarwalla Pankaj K.,Listewnik Marc L.,Dias-Santagata Dora,Thorner Aaron R.,Van Hummelen Paul,Brastianos Priscilla K.,Reardon David A.,Wen Patrick Y.,Al-Mefty Ossama,Ramkissoon Shakti H.,Folkerth Rebecca D.,Ligon Keith L.,Ligon Azra H.,Alexander Brian M.,Dunn Ian F.,Beroukhim Rameen,Santagata Sandro

Funder

King Abdulaziz City for Science and Technology (KACST)

Saudi Arabia

Brain Science Foundation

Pediatric Brain and Spinal Cancer Research

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Neurology (clinical),Oncology

Reference37 articles.

1. The 2007 WHO Classification of Tumours of the Central Nervous System

2. A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor

3. Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas;Lekanne Deprez;Am J Hum Genet,1994

4. Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas

5. Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma;Wellenreuther;Am J Pathol,1995

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