Intratumoral Heterogeneity of Genomic Imbalance in a Case of Epithelioid Glioblastoma withBRAFV600E Mutation

Author:

Nobusawa Sumihito1,Hirato Junko2,Kurihara Hideyuki3,Ogawa Akira4,Okura Naoki5,Nagaishi Masaya16,Ikota Hayato1,Yokoo Hideaki1,Nakazato Yoichi17

Affiliation:

1. Department of Human Pathology; Gunma University Graduate School of Medicine; Maebashi Japan

2. Department of Pathology; Gunma University Hospital; Maebashi Japan

3. Department of Neurosurgery; National Hospital Organization Takasaki General Medical Center; Takasaki Japan

4. Department of Pathology; National Hospital Organization Takasaki General Medical Center; Takasaki Japan

5. Department of Radiology; Graduate School of Medicine; University of Tokyo; Tokyo Japan

6. Department of Neurosurgery; Koshigaya Hospital; Dokkyo University School of Medicine; Koshigaya Japan

7. Department of Pathology; Hidaka Hospital; Takasaki Japan

Publisher

Wiley

Subject

Clinical Neurology,Pathology and Forensic Medicine,General Neuroscience

Reference37 articles.

1. Frequent IDH1/2 mutations in intracranial chondrosarcoma: a possible diagnostic clue for its differentiation from chordoma;Arai;Brain Tumor Pathol,2012

2. Clinicopathological characteristics and treatment of rhabdoid glioblastoma;Babu;J Neurosurg,2013

3. The somatic genomic landscape of glioblastoma;Brennan;Cell,2013

4. Clinical, radiological, histological, and molecular characteristics of paediatric epithelioid;Broniscer;Neuropathol Appl Neurobiol,2013

5. The t(1;3) breakpoint-spanning genes LSAMP and NORE1 are involved in clear cell renal cell carcinoma;Chen;Cancer Cell,2003

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