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Title
Characteristics of gliomas in patients with somatic IDH mosaicism
Authors
Keywords
IDH mutation, Glioma, Somatic mosaicism, Ollier, Maffucci
Journal
Acta Neuropathologica Communications
Volume 4, Issue 1, Pages -
Publisher
Springer Nature
Online
2016-03-31
DOI
10.1186/s40478-016-0302-y
References
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Related references
Note: Only part of the references are listed.- Insulator dysfunction and oncogene activation in IDH mutant gliomas
- (2015) William A. Flavahan et al. NATURE
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- (2015) Jeanette E. Eckel-Passow et al. NEW ENGLAND JOURNAL OF MEDICINE
- Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas
- (2015) NEW ENGLAND JOURNAL OF MEDICINE
- MutantIDHis sufficient to initiate enchondromatosis in mice
- (2015) Makoto Hirata et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- ATRX and IDH1-R132H immunohistochemistry with subsequent copy number analysis and IDH sequencing as a basis for an “integrated” diagnostic approach for adult astrocytoma, oligodendroglioma and glioblastoma
- (2014) David E. Reuss et al. ACTA NEUROPATHOLOGICA
- A case of radiologically multicentric but genetically identical multiple glioblastomas
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- Reduced H3K27me3 and DNA Hypomethylation Are Major Drivers of Gene Expression in K27M Mutant Pediatric High-Grade Gliomas
- (2013) Sebastian Bender et al. CANCER CELL
- IDH2 and TP53 mutations are correlated with gliomagenesis in a patient with Maffucci syndrome
- (2013) Kunihiko Moriya et al. CANCER SCIENCE
- Induction of sarcomas by mutant IDH2
- (2013) C. Lu et al. GENES & DEVELOPMENT
- Inhibition of PRC2 Activity by a Gain-of-Function H3 Mutation Found in Pediatric Glioblastoma
- (2013) P. W. Lewis et al. SCIENCE
- Multifocal supratentorial diffuse glioma in a young patient with Ollier disease
- (2012) P. Pearce et al. JOURNAL OF CLINICAL NEUROSCIENCE
- IDH mutation impairs histone demethylation and results in a block to cell differentiation
- (2012) Chao Lu et al. NATURE
- Transformation by the (R)-enantiomer of 2-hydroxyglutarate linked to EGLN activation
- (2012) Peppi Koivunen et al. NATURE
- IDH1 mutation is sufficient to establish the glioma hypermethylator phenotype
- (2012) Sevin Turcan et al. NATURE
- SNP Array Analysis Reveals Novel Genomic Abnormalities Including Copy Neutral Loss of Heterozygosity in Anaplastic Oligodendrogliomas
- (2012) Ahmed Idbaih et al. PLoS One
- Gliomatosis cerebri in a patient with Ollier disease
- (2011) Ruth A. Mitchell et al. JOURNAL OF CLINICAL NEUROSCIENCE
- IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours
- (2011) M Fernanda Amary et al. JOURNAL OF PATHOLOGY
- Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2
- (2011) M Fernanda Amary et al. NATURE GENETICS
- Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
- (2011) Twinkal C Pansuriya et al. NATURE GENETICS
- Inherited predisposition to glioma
- (2011) A. P. Kyritsis et al. NEURO-ONCOLOGY
- IDH1 or IDH2 mutations predict longer survival and response to temozolomide in low-grade gliomas
- (2010) C. Houillier et al. NEUROLOGY
- Pediatric thalamic glioblastoma associated with Ollier disease (multiple enchondromatosis): a rare case of concurrence
- (2009) Adrianna Ranger et al. Journal of Neurosurgery-Pediatrics
- IDH1andIDH2Mutations in Gliomas
- (2009) Hai Yan et al. NEW ENGLAND JOURNAL OF MEDICINE
- Cerebellar anaplastic astrocytoma in a teenager with Ollier Disease
- (2008) Mohammad Sami Walid et al. JOURNAL OF NEURO-ONCOLOGY
- Maffucci syndrome associated with a pituitary adenoma and a probable brainstem tumor
- (2008) Joana Ruivo et al. JOURNAL OF NEUROSURGERY
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