Meningeal SWI/SNF related, matrix‐associated, actin‐dependent regulator of chromatin, subfamily B member 1 (SMARCB1)‐deficient tumours: an emerging group of meningeal tumours-Reference-Cited by-同舟云学术

Meningeal SWI/SNF related, matrix‐associated, actin‐dependent regulator of chromatin, subfamily B member 1 (SMARCB1)‐deficient tumours: an emerging group of meningeal tumours

Published:2016-12-28 Issue:5 Volume:43 Page:433-449
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathol Appl Neurobiol

Author:

Dadone B.¹²,Fontaine D.³,Mondot L.⁴,Cristofari G.⁵,Jouvet A.⁶,Godfraind C.⁷,Varlet P.⁸,Ranchère‐Vince D.⁹,Coindre J.‐M.¹⁰,Gastaud L.¹¹,Baudoin C.⁵,Peyron A.‐C.²⁵,Thyss A.¹¹,Coutts M.¹²,Michiels J.‐F.¹,Pedeutour F.²⁵,Burel‐Vandenbos F.¹,

Affiliation:

1. Central Laboratory of Pathology of Nice University Hospital France

2. Laboratory of Solid Tumors Genetics Nice University Hospital France

3. Department of Neurosurgery Nice University Hospital France

4. Department of Radiology Nice University Hospital France

5. Institute for Research on Cancer and Aging of Nice (IRCAN) CNRS UMR 7284/INSERM U1081 University of Nice Sophia‐Antipolis Nice France

6. Department of Pathology and Neuropathology Groupement Hospitalier Est Lyon Bron France

7. Department of Pathology University Hospital of Clermont‐Ferrand Clermont‐Ferrand France

8. Department of Neuropathology Sainte‐Anne Hospital Paris France

9. Department of Biopathology Centre Léon Bérard Lyon France

10. Department of Pathology Institut Bergonié Bordeaux France

11. Department of Oncology Centre Antoine Lacassagne Nice France

12. Department of Pathology West Kent Cancer Centre Maidstone UK

Funder

Institut National Du Cancer

Publisher

Wiley

Subject

Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nan.12364

Reference55 articles.

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5. Genomic Analysis Using High-Density Single Nucleotide Polymorphism-Based Oligonucleotide Arrays and Multiplex Ligation-Dependent Probe Amplification Provides a Comprehensive Analysis of INI1/SMARCB1 in Malignant Rhabdoid Tumors

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