BRAF V600E, TERT promoter mutations and CDKN2A/B homozygous deletions are frequent in epithelioid glioblastomas: a histological and molecular analysis focusing on intratumoral heterogeneity-Reference-Cited by-同舟云学术

BRAF V600E, TERT promoter mutations and CDKN2A/B homozygous deletions are frequent in epithelioid glioblastomas: a histological and molecular analysis focusing on intratumoral heterogeneity

Published:2017-12-05 Issue:5 Volume:28 Page:663-673
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:Brain Pathology

Author:

Nakajima Nozomi¹,Nobusawa Sumihito¹^ORCID,Nakata Satoshi¹²,Nakada Mitsutoshi³,Yamazaki Tatsuya¹,Matsumura Nozomi¹,Harada Kenichi⁴,Matsuda Hadzki⁵,Funata Nobuaki⁶,Nagai Shoichi⁷,Nakamura Hideo⁸,Sasaki Atsushi⁹,Akimoto Jiro¹⁰,Hirato Junko¹¹,Yokoo Hideaki¹

Affiliation:

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

2. Department of Neurosurgery Gunma University Graduate School of Medicine Maebashi Japan

3. Department of Neurosurgery Kanazawa University Graduate School of Medical Sciences Kanazawa Japan

4. Department of Human Pathology Kanazawa University Graduate School of Medical Sciences Kanazawa Japan

5. Department of Neurosurgery Dokkyo Medical University Mibu Japan

6. Department of Pathology Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital Tokyo Japan

7. Department of Neurosurgery Faculty of Medicine University of Toyama Toyama Japan

8. Department of Neurosurgery Kumamoto University Graduate School of Medical Sciences Kumamoto Japan

9. Department of Pathology Saitama Medical University Moroyama Japan

10. Department of Neurosurgery Tokyo Medical University Tokyo Japan

11. Department of Pathology Gunma University Hospital Maebashi Japan

Publisher

Wiley

Subject

Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bpa.12572

Reference41 articles.

1. Epithelioid Glioblastomas and Anaplastic Epithelioid Pleomorphic Xanthoastrocytomas-Same Entity or First Cousins?

2. Frequent IDH1/2 mutations in intracranial chondrosarcoma: a possible diagnostic clue for its differentiation from chordoma

3. A combination of TERT promoter mutation and MGMT methylation status predicts clinically relevant subgroups of newly diagnosed glioblastomas

4. Clinical, radiological, histological and molecular characteristics of paediatric epithelioid glioblastoma

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