What do we know about IDH1/2 mutations so far, and how do we use it? Craig Horbinski Review 20 March 2013 Pages: 621 - 636
The role of mast cells in neuroinflammation Sofie NelissenEvi LemmensSven Hendrix Review 13 February 2013 Pages: 637 - 650
Meningeal hemangiopericytoma and solitary fibrous tumors carry the NAB2-STAT6 fusion and can be diagnosed by nuclear expression of STAT6 protein Leonille SchweizerChristian KoelscheAndreas von Deimling Original Paper 11 April 2013 Pages: 651 - 658
Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas Adam M. FontebassoJeremy SchwartzentruberJacek Majewski Original Paper Open access 16 February 2013 Pages: 659 - 669
In human glioblastomas transcript elongation by alternative polyadenylation and miRNA targeting is a potent mechanism of MGMT silencing Simone KrethElisabeth LimbeckFriedrich W. Kreth Original Paper 23 January 2013 Pages: 671 - 681
EGFR wild-type amplification and activation promote invasion and development of glioblastoma independent of angiogenesis Krishna M. TalasilaAnke SoentgerathHrvoje Miletic Original Paper Open access 22 February 2013 Pages: 683 - 698
Early intraneuronal accumulation and increased aggregation of phosphorylated Abeta in a mouse model of Alzheimer’s disease Sathish KumarOliver WirthsJochen Walter Original Paper 24 March 2013 Pages: 699 - 709
Loss of vesicular dopamine release precedes tauopathy in degenerative dopaminergic neurons in a Drosophila model expressing human tau Ting-Han WuYu-Ning LuHui-Yun Chang Original Paper Open access 15 March 2013 Pages: 711 - 725
Epigenetic regulation of cholinergic receptor M1 (CHRM1) by histone H3K9me3 impairs Ca2+ signaling in Huntington’s disease Junghee LeeYu Jin HwangHoon Ryu Original Paper 02 March 2013 Pages: 727 - 739
Corticobasal degeneration with olivopontocerebellar atrophy and TDP-43 pathology: an unusual clinicopathologic variant of CBD Naomi KouriKenichi OshimaDennis W. Dickson Original Paper 31 January 2013 Pages: 741 - 752
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson’s disease and multiple system atrophy? Aoife P. KielyYasmine T. AsiJanice L. Holton Case Report Open access 12 February 2013 Pages: 753 - 769